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Article

Anticancer Activities of Novel Nicotinamide Phosphoribosyltransferase Inhibitors in Hematological Malignancies

by
Paulina Biniecka
1,
Saki Matsumoto
1,
Axel Belotti
1,
Jessie Joussot
2,
Jian Fei Bai
2,
Somi Reddy Majjigapu
2,
Paul Thoueille
3,
Dany Spaggiari
3,
Vincent Desfontaine
3,
Francesco Piacente
4,
Santina Bruzzone
4,
Michele Cea
5,6,
Laurent A. Decosterd
3,
Pierre Vogel
2,
Alessio Nencioni
5,6,
Michel A. Duchosal
1,7,* and
Aimable Nahimana
1,*
1
Central Laboratory of Hematology, Department of Medical Laboratory and Pathology, Lausanne University Hospital and University of Lausanne, 1011 Lausanne, Switzerland
2
Laboratory of Glycochemistry and Asymmetric Synthesis, Swiss Federal Institute of Technology (EPFL), 1015 Lausanne, Switzerland
3
Service and Laboratory of Clinical Pharmacology, Department of Laboratory Medicine and Pathology, Lausanne University Hospital and University of Lausanne, 1011 Lausanne, Switzerland
4
Department of Experimental Medicine, Section of Biochemistry, University of Genoa, 16132 Genoa, Italy
5
Department of Internal Medicine and Medical Specialties, University of Genoa, 16132 Genoa, Italy
6
Ospedale Policlinico San Martino IRCCS, Department of Internal Medicine, University of Genoa, 16132 Genoa, Italy
7
Service of Hematology, Department of Oncology, Lausanne University Hospital and University of Lausanne, 1011 Lausanne, Switzerland
*
Authors to whom correspondence should be addressed.
Molecules 2023, 28(4), 1897; https://doi.org/10.3390/molecules28041897
Submission received: 12 December 2022 / Revised: 20 January 2023 / Accepted: 2 February 2023 / Published: 16 February 2023
(This article belongs to the Special Issue Recent Advances in Development of Small Molecules to Fight Cancer)
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Abstract

:
Targeting cancer cells that are highly dependent on the nicotinamide adenine dinucleotide (NAD+) metabolite is a promising therapeutic strategy. Nicotinamide phosphoribosyltransferase (NAMPT) is the rate-limiting enzyme catalyzing NAD+ production. Despite the high efficacy of several developed NAMPT inhibitors (i.e., FK866 (APO866)) in preclinical studies, their clinical activity was proven to be limited. Here, we report the synthesis of new NAMPT Inhibitors, JJ08, FEI191 and FEI199, which exhibit a broad anticancer activity in vitro. Results show that these compounds are potent NAMPT inhibitors that deplete NAD+ and NADP(H) after 24 h of drug treatment, followed by an increase in reactive oxygen species (ROS) accumulation. The latter event leads to ATP loss and mitochondrial depolarization with induction of apoptosis and necrosis. Supplementation with exogenous NAD+ precursors or catalase (ROS scavenger) abrogates the cell death induced by the new compounds. Finally, in vivo administration of the new NAMPT inhibitors in a mouse xenograft model of human Burkitt lymphoma delays tumor growth and significantly prolongs mouse survival. The most promising results are collected with JJ08, which completely eradicates tumor growth. Collectively, our findings demonstrate the efficient anticancer activity of the new NAMPT inhibitor JJ08 and highlight a strong interest for further evaluation of this compound in hematological malignancies.

1. Introduction

Cancer cells have very high nutrient and energy demands in order to sustain their constant growth and rapid cell proliferation. Their metabolic reprogramming has recently emerged as an important cancer hallmark [1,2]. First described by Otto Warburg, a particular characteristic of cancerous cells resides in their preference towards aerobic glycolysis over oxidative phosphorylation [3]. However, this preference does not exclude the involvement of oxidative metabolism. Malignant cells rely on ATP and oncometabolite production from the mitochondrial tricarboxylic acid (TCA) cycle as much as they rely on glycolysis for their survival and proliferation [4].
Nicotinamide adenine dinucleotide (NAD+) is the main co-factor associated with cellular energetics and mediates redox reactions in crucial metabolic pathways, such as glycolysis, the TCA cycle and oxidative phosphorylation [5]. Additionally, it serves as a substrate for several NAD-degrading enzymes, including poly ADP-ribose polymerases (PARPs), mono (ADP-ribose) transferases (ARTs), NAD-ases/ADP ribosyl cyclases/cyclic ADP-ribose hydrolases (CD38/CD157) and sirtuins (SIRT). Subsequently, through these enzymes, NAD+ is involved in numerous biological processes, such as cellular proliferation, signaling and adhesion, calcium mobilization, cell cycle control, stress response, DNA damage, genomic integrity and transcriptional regulation [6]. NAD+ results from different molecular pathways, de novo from tryptophan, from nicotinic acid/nicotinic acid riboside (NA/NAR) through the Preiss–Handler pathway or through salvage pathways from nicotinamide/nicotinamide riboside (NAM/NR) and reduced nicotinamide riboside (NRH) [7,8]. In mammalian cells, NAM/NA are the most commonly used precursors to synthesize NAD+. Nicotinamide phosphoribosyltransferase (NAMPT) is the rate-limiting enzyme that catalyzes the phosphoribosylation of NAM to produce nicotinamide mononucleotide (NMN) [9,10]. Then, the latter is converted to NAD+, a process catalyzed by NMN adenyltransferase. Furthermore, NAMPT expression is upregulated in most cancer cells [11,12,13] and is associated with tumor progression [14,15]. Thus, targeting NAMPT has emerged as a promising strategy to eliminate malignant cells selectively, as they highly rely on NAD+ synthesis [16,17]. The first NAMPT inhibitor, FK866, also known as APO866 (Figure 1), was described by Hasmann et al. [18]. Its high killing ability on multiple cancer cell lines was observed in several preclinical studies [19,20,21,22,23]. This observation has provided a rationale for testing FK866 (APO866) and another NAMPT inhibitor CHS-828 (also known as GMX-1778, Figure 1) in clinical trials on hematological and solid malignancies (NCT00435084, NCT00432107, NCT00431912, NCT00457574 and NCT00724841). Despite their high anticancer activity observed in several preclinical studies, these inhibitors did not achieve the same efficacy in clinical trials. The clinical results showed a few dose-limiting toxicities and no significant tumor response [24,25,26]. The orally available NAMPT inhibitors KPT-9274 and OT-82 (Figure 1) have been tested as potential drugs in patients with solid tumors or with relapsed/refractory lymphoma [27,28]. Up to now, none of the published NAMPT inhibitors have become an anticancer agent. Thus, there is still a strong need for developing new potent and highly efficient NAMPT inhibitors.
We report here the synthesis of the three new NAMPT inhibitors: JJ08, FEI191 and FEI199. We test them for their potential antitumor activities toward hematological malignancies. We show that these compounds are potent NAMPT inhibitors that profoundly deplete NAD(H) and NADP(H) after 24 h of incubation, which is followed by a strong, time-dependent increase in ROS production including cytosolic/mitochondrial superoxide anions and hydrogen peroxide. That increase correlates with ATP depletion and mitochondrial depolarization. We provide evidence that JJ08, FEI191 and FEI199 exhibit cell death at low nanomolar concentrations towards several hematopoietic malignant cells. Treatment of mouse xenografts with the three new NAMPT inhibitors significantly prolonged mouse survival. JJ08 presented the most promising results as it abolished tumor growth completely.

2. Results

2.1. Synthesis of New Potent NAMPT Inhibitors

Within the European Health 7th framework project PANACREAS (grant agreement ID: 256986) we have synthesized a series of novel FK866 (APO866) analogues and shown that some of them are very toxic toward pancreatic cell lines [29]. Applying an analogous synthetic route to that reported for the synthesis of FK866 [29], we have prepared ((E)-N-(4-(1-(furan-2-carbonyl)piperidin-4-yl)butyl)-3-(pyridin-3-yl)acrylamide) (JJ08) which exchanges the benzamide moiety of FK866 for a furan-2-carboxamide group. The synthesis starts with the reduction of the HCl salt of 4-(piperidin-4-yl)butyric acid (1) into alcohol 2. The latter reacted with 2-furanoyl chloride and triethylamine, giving the corresponding carboxamide 3. A Mitsunobu displacement of the alcoholic moiety of 3 with phathalimide gave 4. Selective liberation of the primary amine 5 was realized by treatment with hydrazine chlorhydrate in ethanol. Amide coupling of 5 with (E)-3-(pyridin-3-yl) provided JJ08 (Scheme 1).
FEI191 ((Z)-2-cyano-1-(5-(1-(furan-2-carbonyl)piperidin-4-yl)pentyl)-3-phenylguanidine) and FEI199 ((Z)-2-cyano-1-((E)-5-(1-(furan-2-carbonyl)piperidin-4-yl)pent-2-en-1-yl)-3-phenylguanidine) are compounds in which the (pyridine-3-yl)acrylamide moiety of JJ08 has been exchanged for a (pyridin-4-yl)cyanoguanidine moiety and the C4-tether for C5-tethers. These compounds can be seen as chimeric derivatives of CHS-828. The synthesis of FEI191 (Scheme 2) starts with the commercially available tert-butyl 4-(3-hydroxypropyl)piperidine-1-carboxylate (6), a primary alcohol that undergoes Dess–Martin oxidation into the corresponding aldehyde 7. Wittig–Horner–Emmons olefination of 7 furnished the (E)-ene-ester 8 that was reduced into the corresponding (E)-allylic alcohol 9 by di(isobutyl)aluminum hydride in CH2Cl2. Catalytic hydrogenation of 8 provided ester 10, which was reduced into the corresponding alcohol 11. Mitsunobu displacement of the primary alcohol 11 with phthalimide gave 12. The piperidine moiety of 12 was deprotected selectively on treatment with aqueous HCl in dioxane furnishing chlorhydrate 13, which was converted into carboxamide 14 with 2-furoic chloride and trimethylamine. Selective liberation of the primary amine with hydrazine gave 15, which was treated with phenyl (Z)-N′-cyano-N-(pyridin-4-yl)carbamimidate to provide FEI191.
The synthesis of FEI199 starts with allylic alcohol 9 obtained above (Scheme 2). Over four steps, and without purification of the intermediate products, crude 16 was obtained in 55% yield. The preparations followed the same procedures as those for the conversion of 11 into 15. Treatment of 16 with phenyl (Z)-N′-cyano-N-(pyridin-4-yl)carbamimidate provided FEI199 (Scheme 3).
The detailed synthesis and characterization of JJ08, FEI191 and FEI199 can be found in Supplementary Materials, p. 3–13.

2.2. JJ08, FEI191 and FEI199 Are Potent NAMPT Inhibitors That Efficiently Deplete Intracellular NAD+ Content

First, we assessed whether the novel compounds are indeed NAMPT inhibitors by examining their capacity to inhibit in vitro NAMPT activity. Using FK866 (APO866), a prototype of NAMPT inhibitors, as a positive control, JJ08, FEI191 and FEI199 were tested in an NAMPT enzymatic inhibition assay. Figure 2 indicates that they were all potent NAMPT inhibitors, showing full inhibition of NAMPT. The direct consequence of NAMPT inhibition is the decrease in intracellular NAD+ content. Hence, we investigated whether treatment of hematopoietic malignant cells with the selected NAMPT inhibitors led to NAD+ depletion. To this end, we performed a time course analysis of intracellular NAD+ levels on four hematological cancer cell lines, including ML2, Jurkat, Namalwa and RPMI8226, which were treated with the selected compounds. As reported in Figure 3A–D, all tested NAMPT inhibitors fully depleted the NAD+ cell content within the first 24 h after treatment. Notably, in ML2 cells, an additional 8 h time point was recorded, indicating a fast drop in NAD+ levels (Figure 3A).
Taken together, these results indicate that all tested compounds are potent NAMPT inhibitors.

2.3. JJ08, FEI191 and FEI199 Induce Different Types of Cell Death in Several Hematological Malignancies in NAD+ Dependent Manner

NAD+ depletion has been proposed as a promising strategy to eliminate hematological malignancies [19,23,28,30,31]. We measured the cytotoxic activities of JJ08, FEI191 and FEI199 in the four aforementioned hematological cancer cell lines. The cell growth inhibitory effects were compared to that of FK866 (APO866). As summarized in Table 1, the half-maximal inhibitory concentration (IC50) values of the tested inhibitors were in the low nanomolar range. Among them, FEI199 was the most potent, with a measured IC50 that was lower than 0.3 nM in all malignancies.
To assess whether apoptosis is involved in the NAMPT inhibitor-induced cytotoxicity, malignant cells were first treated with the compounds for 96 h and subsequently double stained with ANXN/7AAD and analyzed by flow cytometry. As shown for ML2 cells and additional different malignant hematopoietic cell lines, all the inhibitors induced early (ANXN+/7AAD-) and late apoptotic (7AAD+) cell death at drug concentrations ranging between 0.1 and 10 nM. FEI199 induced maximal cell killings at very low concentrations (≤0.5 nM) on all tested cell lines, whereas at similar concentrations, FK866 (APO866) and JJ08 induced cell death at only between 20 and 75%, depending on the cell line (Figure 4A–D). Moreover, FEI191 and FEI199 induced more late apoptotic/necrotic (7AAD+) than early apoptotic cell death (ANXN+/7AAD-) compared with APO866. To provide additional evidence of the involvement of apoptosis in the cell death induced by the new NAMPT inhibitors, we assessed the activation of various caspases, including CASP-3, CASP-8 and CASP-9. Hematopoietic malignant cells were treated for 72 h with the compounds and caspase activation was assessed using the specific CaspGLOW™ Red Active probes specific for each caspase and flow cytometry. The results show a strong increase in CASP-3, CASP-8 and CASP-9 activities in treated versus untreated cells (Figure 5), suggesting that caspase-dependent apoptosis contributes to the antitumor activity of the tested compounds.
Another possible type of cell death is necrosis, which correlates with the release of the cytosolic enzymes, especially lactate dehydrogenase (LDH), into the extracellular space. Therefore, the detection of LDH in the medium is used as a marker of necrotic cell death [32]. Accordingly, we monitored necrotic cell death in time-dependent analyses, as well as the drug effect on cell proliferation in ML2 and Jurkat cells cultured with or without the new NAMPT inhibitors. As shown in Figure 6A,B, LDH release in the medium significantly increased over time in leukemic cells treated with the NAMPT inhibitors compared to untreated ones, whereas cell proliferation decreased over time and only approximately 40% of proliferating cells remained at 48 h after treatment (Figure 6C,D). These finding show the involvement of necrotic cell death in treatment with NAMPT inhibitors.
To demonstrate that the antitumor activity of the new NAMPT inhibitors was due to NAD+ depletion, we evaluated the ability of NAM and NA (precursors involved in the NAD+ biosynthesis), as well as NAD+, to abrogate the cell death caused by our compounds. Extracellular supplementation in excess with NAD+ or its precursors fully restored the viability of the cells despite the presence of the inhibitors (Figure 7). Interestingly, the supplementation with NA (but not with NAM or NAD+) did not protect Namalwa cells from cell death in response to treatment with the NAMPT inhibitors (Figure 7C). This can be explained by the fact that Namalwa cells have a naturally very low expression of the nicotinic acid phosphoribosyltransferase (NAPRT) gene [33], which is required to utilize NA in NAD+ biosynthesis.
Collectively, these results indicate that the new NAMPT inhibitors induce both apoptotic and necrotic cell death in an NAD+-dependent manner in several human hematopoietic malignant cells.

2.4. Treatment with JJ08, FEI191 and FEI199 Induces High Levels of ROS Production and ATP Depletion in Hematological Malignant Cells

The first consequence of NAMPT inhibition is NAD+ depletion, which occurs within 24 h and will subsequently result in a profound decrease in NADP(H). To verify this hypothesis, we evaluated the intracellular NADP(H) content in myeloid leukemia cells upon treatment with NAMPT inhibitors. As shown in Figure 8, treatment with the compounds significantly depleted NADP(H) cell content compared to untreated cells. Since NADPH, a powerful cell antioxidant, is directly involved in redox reactions and is essential to maintain cellular homeostasis, its depletion is expected to generate high levels of oxidative stress. Therefore, cytosolic and mitochondrial superoxide anions, as well as intracellular hydrogen peroxide, were measured in hematopoietic malignant cells treated with the new compounds, using DHE, MitoSOX and carboxy-H2DCFDA probes, respectively. In accordance with our hypothesis, Figure 9 shows that the new NAMPT inhibitors increased the levels of various ROS in all treated cell types. High ROS production is known to be detrimental for the cells, since it oxidizes proteins, lipids and cell organelles, including mitochondria, resulting in ATP depletion [19,34] and ultimately leading to cell death [35]. As expected, the treatment of hematopoietic malignant cells with the new NAMPT inhibitors led to an ATP loss in a time-dependent manner (Figure 10A), which was followed by mitochondrial membrane depolarization (Figure 10B), that ultimately resulted in cell death at 96 h (Figure 10C). To provide strong evidence that high levels of ROS production are the main driver of these events that led to cell death, we monitored cell death in hematopoietic malignant cells treated with these compounds in the presence or absence of catalase, a potent H2O2 scavenger [36,37]. As shown in Figure 11, the supplementation with catalase did not prevent NAD+ depletion in ML2 cells (Figure 11A), but it fully abrogated the loss in ATP (Figure 11B) and MMP (Figure 11C), as well as the ultimate cell death (Figure 11D), in response to all of the tested NAMPT inhibitors. Moreover, the supplementation with catalase also prevented the cell death caused by NAMPT inhibitors at 72 h in Jurkat and RPMI8226 cell lines (Figure 11E–G).
Collectively, these results indicate that all of the tested NAMPT inhibitors significantly depleted cellular NADP(H) content, resulting in a burst of ROS production. In turn, this induces the loss of ATP, which is followed by mitochondrial membrane depolarization and ultimately leads to cell death. Importantly, oxidative stress appears to be the main cause of cancer cell death after NAMPT inhibitor treatment.

2.5. The Therapeutic Activity of JJ088 in SCID Mice Bearing Burkitt Lymphoma Is Superior to That of FEI191 and FEI199

The promising results presented above led us to explore the potential therapeutic efficacy of the new NAMPT inhibitors in a mouse xenograft model of Burkitt lymphoma. To this end, NAMPT inhibitors (10 mg/kg) were administered intraperitoneally (I.P.) to mice with established Namalwa tumors (human Burkitt lymphoma cell line) and tumor growth was monitored over time. As shown in Figure 12, treatment with the new NAMPT inhibitors exerted a significant therapeutic effect (Figure 12A) and significantly prolonged overall mice survival compared to untreated control animals (Figure 12B, log-rank test, P < 0.05). Interestingly, treatment with JJ08 completely eradicated tumor growth 5 days after administration. Instead, FEI191 and FEI199 did not stop tumor progression, but significantly delayed it compared to the vehicle-injected group (Figure 12A), suggesting that the in vitro efficiencies of FEI191 and FEI199 do not translate into equally potent in vivo activities. To understand why FEI191 and FEI199 were less efficient in abrogating tumor growth than JJ08, pharmacokinetics (PK) studies were carried out. Plasma concentrations of the compounds were monitored in mice (n=3) after I.P. administration for up to 24 h (Supplementary Materials, Figure S1). Then, PK parameters were derived and are presented in Table 2. The PK values of FK866 (APO866), which is known to effectively abrogate tumor growth in vivo, are shown as a reference [19]. The measured compound concentrations used for the PK data analysis are given in Supplementary Materials, Table S1. Notably, the concentrations of FEI199 measured after 8 h and 24 h were excluded, as the analytical responses were below the lower limit of quantification of the method. For FEI191, concentrations measured at 8 h and 24 h were also excluded from the PK data analysis due to carryover issues.
The four compounds showed broadly similar PK profiles, but FK866 (APO866) distinctively appeared to provide the best systemic exposure (i.e., AUC0-24). In addition, the plasma concentrations of APO866 were less variable between the mice samples (Table S1). The maximum plasma concentrations (Cmax) of JJ08 and APO866 were comparable, while the AUC0-24 of JJ08 appeared to be approximately 2-fold lower than that of APO866. This difference is mainly due to the early time points, which contribute significantly to the calculated AUC0-24 values. Similarly, the calculated apparent drug clearance (CL/F) for JJ08 was found to be 2-fold higher, whereas its half-life (T1/2) appeared to be two times shorter as compared to APO866, indicating that JJ08 was cleared faster from circulation. Finally, based on the calculated apparent terminal volume of distribution (Vz/F), both JJ08 and APO866 compounds seemed to be well absorbed into tissues and/or highly metabolized.
Regarding FEI191 and FEI199, the terminal rate constant, λz, value (and therefore, T1/2 and Vz/F) could not be assessed because their terminal phases were insufficiently characterized due to analytical issues, as discussed above. However, the maximal concentrations (Cmax) were lower than those of APO866 or JJ08 and the clearance of FEI191 and FEI199 proved to be more than 4-fold higher, suggesting faster drug elimination.
Taken together, our in vivo data indicate that the new NAMPT inhibitors delayed and/or prevented tumor growth in a mouse Burkitt lymphoma model, with JJ08 being the most potent anticancer agent. Furthermore, JJ08 had very similar PK parameters to APO866, whereas both FEI compounds exhibited lower concentrations in the blood after administration, which could explain their lower anticancer activities in vivo.

3. Discussion

In this study, we report the synthesis and evaluation of the therapeutic efficacies of three novel NAMPT inhibitors, JJ08, FEI191 and FEI199, in hematological malignancies. We show that the new compounds have a broad antitumor activity against various hematological malignancies. In agreement with our previous studies on APO866, a prototype NAMPT inhibitor [19,36,38,39], we found that the new NAMPT inhibitors are highly toxic towards leukemia (AML and ALL), lymphoma (Burkitt) and multiple myeloma (MM) cells. Mechanistically, these compounds caused a strong NAD+ depletion that led to exhaustion of NADPH, which in turn resulted in a burst of oxidative stress. The high levels of ROS induced by these compounds disrupted the mitochondrial membrane integrity, causing ATP depletion and cell death. Scavenging ROS production with catalase abrogated cell death induced by NAMPT inhibitors, despite NAD+ depletion, pointing out the major contribution of oxidative stress to the antitumor activity of APO866 and of the new NAMPT inhibitors. In addition, we demonstrated that the new NAMPT inhibitors induced different types of cell death, including both caspase-dependent and caspase-independent apoptosis, but also necrotic cell death. Therefore, their mode of action described in this study is similar to that reported previously for NAMPT inhibitors [19,30,36,38,39,40,41],indicating that although these compounds have different chemical structures, they have common mechanisms involved with cell death.
Importantly, in vivo administration of the new NAMPT inhibitors as a single agent prevented and/or delayed tumor growth in an animal model of human Burkitt lymphoma and significantly prolonged median survival, thereby underlining the therapeutic potential of these molecules. It is noteworthy to mention that JJ08 fully eradicated tumor growth and allowed mouse disease-free survival. In line with the in vivo data, JJ08, as well as APO866, exhibited the best PK properties when compared to those of both FEI compounds.
The search for new NAMPT inhibitors is motivated by the need to identify novel drugs that counter cancer progression and thereby increase patient life expectancy and quality of life, a goal of a high priority. In this endeavor, the development of anticancer therapies targeting the NAMPT-mediated NAD+ biosynthetic pathway represents a promising strategy and should have broad clinical implications. We and others have demonstrated that NAMPT inhibitors exhibit high efficacy against a wide range of human solid tumors and blood cancers, without significant toxicity to laboratory animal models [19,29,36,42,43,44,45,46,47,48,49]. In an effort to discover new anticancer agents, we here have identified three novel NAMPT inhibitors with broad and strong anti-leukemic/lymphoma activity. Among them, JJ08 exhibited a promising profile as an overall potent antitumor agent both in vitro and in vivo, despite the fact that in vitro, FEI191 and FEI199 had higher antitumor activity than JJ08. This discrepancy between in vitro and in vivo studies is most probably related to the worse PK profiles of FEI compounds. Indeed, PK analyses showed that FEI compounds were rapidly cleared out of body circulation compared to JJ08 (or APO866). Moreover, the calculated clearance of FEI compounds was at least 4-fold higher, the Cmax was lower and their AUCs were approximately 2-to-9-fold smaller than those of JJ08 (or APO866). The apparent volume of distribution calculated for all molecules indicated that they are highly absorbed into the tissues and/or highly metabolized. The calculated clearance for all compounds indirectly suggested that these novel NAMPT inhibitors are molecules with high hepatic excretion. Further studies aiming at improving the PK properties of novel NAMPT inhibitors are needed.
To put our results in a global context, one should keep in mind that the striking antitumor activity of NAMPT inhibitors reported in several studies is closely correlated with their in vitro experimental conditions. For instance, RPMI medium widely used for cell culture contains only nicotinamide as an NAD+ precursor. In our study, and in many preclinical studies, the major (if not the only) source of NAD+ synthesis was also nicotinamide, indicating that only one route of NAD+ synthesis, namely, the salvage pathway, is activated within these experimental settings. In a real life situation, where many NAD+ precursors could be present in a tumor environment, blocking only one pathway of NAD+ synthesis would not be sufficient and this could greatly contribute to the loss of the therapeutic efficacy of NAMPT inhibitors. In agreement with this scenario, we and others have demonstrated that the levels and/or presence of NAD+ precursors (other than nicotinamide) considerably affect the antitumor efficiency of NAMPT inhibitors [39,50]. The loss of the efficacy of NAMPT inhibitors in the latter circumstance was mainly due to the activation of the alternative NAD+ production pathways. We also showed that gut microbiota played a crucial role in host NAD+ metabolism, as they contribute to resistance to NAMPT inhibitors [39]. These observations should be taken into consideration in future clinical trials, for instance, the nature and level of NAD+ precursors or alternatively targeting more than one route of NAD+ synthesis should be investigated.
In this study, we showed that the novel NAMPT inhibitors delayed or eradicated the tumor growth and thus significantly prolonged xenografted mouse survival, without evident signs of toxicity including loss of body weight, lethargy, rough coat or premature death. However, in clinical trials, the common dose-limiting toxicities were thrombocytopenia and a variety of gastrointestinal symptoms [24,25,26,51]. Therefore, the strategies to limit off-target toxicities need to be refined. FEI191 and FEI199 had high activities in vitro. Therapeutic modalities to significantly boost their in vivo activities and reduce their systemic associated toxicities should be explored. In this line, the next generation of NAMPT inhibitors can be conjugated to antibodies (creating antibody–drug conjugates, or ADCs). In this drug delivery system, the inhibitor is conjugated to the antibody that targets the antigens/proteins specifically expressed in cancer cells, thus allowing specific inhibitor delivery. Using such a strategy, several investigators [52,53,54] have demonstrated the antitumor efficacy of ADCs with NAMPT inhibitors in different mouse xenograft models. Only mild, reversible hematologic side effects were observed with ADCs in toxicological in vivo studies, with no signs of retinal or cardiac toxicities, as reported for NAMPT inhibitors alone in preclinical studies [52]. These findings open a new era in clinical trials to specifically target and improve the therapeutic window of NAMPT inhibition.

4. Conclusions

In summary, we have synthesized three novel NAMPT inhibitors: JJ08, FEI191 and FEI199. They are strong growth inhibitors of cancer cells from numerous hematological malignancies. Our in vitro and in vivo data demonstrate that these compounds are potent anticancer agents. JJ08 shows the best efficacy and is well tolerated in the mouse xenograft model of Burkitt lymphoma. We propose that JJ08 should undergo further clinical development for the treatment of hematologic malignancies.

5. Materials and Methods

5.1. Cell Lines and Culture Conditions

Four hematological cell lines (ML2—acute myeloid leukemia; Jurkat—acute lymphoblastic leukemia; Namalwa—Burkitt lymphoma; and RPMI8226—multiple myeloma) were purchased from DSMZ (German Collection of Microorganisms and Cell Cultures, Braunschweig, Germany) or ATCC.
All cells were cultured in RPMI medium (Invitrogen AG, 61870-01) supplemented with 10% heat inactivated fetal calf serum (Amimed, 2-01F30-I) and 1% penicillin/streptomycin at 37 °C (Amimed, 4-01F00-H) in a humidified atmosphere of 95% air and 5% CO2.

5.2. NAMPT Enzymatic Activity Assay

The ability of FK866 (APO866) analogues to inhibit NAMPT activity was assessed with an NAMPT Activity Assay Kit (Colorimetric) (Abcam, ab221819, Cambridge, UK) according to the manufacturer’s instructions. Briefly, NAMPT inhibitors were dissolved in DMSO to a final concentration of 1 µM and distributed in a 96-well plate in duplicate. Then, a reaction mix containing assay buffer, ATP, NMNAT1, NAM, PRPP and ddH2O was added and the plate was incubated at 30 °C for 60 min. After, to measure the generated NAD+, a mix of WST-1, ADH, diaphorase and ethanol was added to the wells. The absorbance was measured in kinetic mode at 450 nm on a microplate reader for 45 min at 30 °C.

5.3. Flow Cytometry Analyses

The cellular effects of FK866 (APO866) and the new NAMPT inhibitors, JJ08, FEI191 and FEI199, on hematopoietic malignant cells were evaluated using a Beckman Coulter Cytomics Gallios flow cytometer (Beckman Coulter International S.A., Nyon, Switzerland). The measured parameters included cell death, mitochondrial membrane potential (MMP), reactive oxygen species (ROS) production and caspase activation.

5.4. Characterization of Cell Death

To determine the cell death induced by NAMPT inhibitors, malignant cells were stained with ANNEXIN-V (ANXN, eBioscience, BMS306FI/300) and 7-aminoactinomycin D (7AAD, Immunotech, A07704) as described by the manufacturer and analyzed using flow cytometry. Dead cells were identified as ANXN+7AAD+ /7AAD+ and early apoptotic cells as ANXN+ 7AAD-. Specific cell death induced by inhibitors was calculated using the following formula: percent of cell death induced by compound = [(S – C) / (100 – C)] × 100; where S = treated sample cell death and C = untreated sample cell death.

5.5. Analysis of Mitochondrial Membrane Potential

Mitochondrial membrane depolarization was determined using tetramethylrhodamine methyl ester (TMRM, ThermoFisher Scientific, T668) according to the manufacturer’s protocol. TMRM is a cationic, cell-permeant, red-orange fluorescent dye that accumulates in polarized mitochondria, but it is released after their depolarization. Untreated or treated cells were harvested, centrifuged and resuspended in culture medium containing 50 nM TMRM, and then incubated at 37 °C for 30 min in the dark. Cells were washed twice with PBS and immediately analyzed using flow cytometry.

5.6. Detection of Cellular and Mitochondrial Reactive Oxygen Species (ROS)

Various types of ROS were determined in untreated and drug-treated hematopoietic malignant cells by flow cytometry using live-cell permeant specific fluorogenic probes. Dihydroethidium (DHE, Marker Gene Technologies, M1241) was used as probe for detection of the cytosolic superoxide anion (cO2•-), MitoSox (Molecular Probes, M36008) was used as probe for detection of the mitochondrial superoxide anion (mO2•-) and 6-carboxy-2,7-dichlorodihydrofluorescein diacetate (carboxy-H2DCFDA; Molecular Probes, C-400) was used as probe for detection of H2O2. DHE was oxidized to red fluorescent ethidium by cytosolic superoxide and MitoSOX was selectively targeted to mitochondria, where it was oxidized by superoxide and exhibited red fluorescence. Carboxy-H2DCFDA was cleaved by esterase to yield DCFH, a polar nonfluorescent product, but in the presence of hydrogen peroxide, the latter is oxidized to a green fluorescent product, dichlorofluorescent (DCF). For cell staining, cells were centrifuged and the pellets were resuspended in PBS with a final concentration of 5 μM for each probe. The mixture was incubated in the dark at 37 °C for 15 min. Then, the cell suspension was analyzed using flow cytometry within 20 min.

5.7. Detection of Caspases Activation

Activation of various caspases was assessed using flow cytometry and specific CaspGLOW™ Red Active (BioVision, K190, Cambridge, UK) for following caspases: CASP3 (BioVision Inc., BV-K193-100), CASPASE 8 (CASP8; BioVision Inc., BV-K198-100) and CASPASE 9 (CASP9; BioVision Inc., BV-K199-25). The CaspGLOW assays offer a convenient way for measuring activated caspases in living cells. The assay uses a specific inhibitor for each caspase conjugated to sulforhodamine as a fluorescent marker, which is cell permeable, nontoxic and irreversibly binds in specific manner to activated caspase in apoptotic cells. The red fluorescence label allows for direct detection of activated caspase in apoptotic cells by flow cytometry. Cell staining was performed according to the manufacturer’s information and analyzed.

5.8. Quantification of Intracellular NAD+, NADP(H) and ATP Contents

Cells (1 × 106/mL) in the log growth phase were seeded in a 6-well plate in the presence or absence of the NAMPT inhibitors. At each time point, 800 µL of cells was centrifuged at 900 g (2000 rpm) for 5 min and washed with cold PBS. Then, the supernatant was discarded and cells were resuspended in 300 µL of lysis buffer (20 mM NaHCO3, 100 mM Na2CO3) and kept at –80 °C for at least 4 h before analysis.
Total NAD+ content was measured in cell lysates using a biochemical assay described previously [18]. Briefly, cell lysates (20 µL) were plated in a 96-well flat bottom plate. A standard curve was generated using a 1:3 serial dilution in lysis buffer of a β-NAD+ stock solution. Cycling buffer (160 µL) was added into each well and the plate was incubated for 5 min at 37 °C. Afterwards, ethanol (20 µL), pre-warmed to 37 °C, was added into each well and the plate was incubated for an additional 5 min at 37 °C. The absorbance was measured in kinetic mode at 570 nm after 5, 10, 15, 20 and 30 min at 37 °C on a spectrophotometer. The amount of NAD+ in each sample was normalized to the protein content for each test sample at each time point.
The NADP+ and NADPH contents in the cells were determined separately using an NADP/NADPH-GloTM kit (Promega, G9081, Madison, WI, USA) and according to the manufacturer’s protocol.
The total ATP cell content was quantified using an ATP determination Kit (Life Technologies, A22066, Carlsbad, CA, USA) according to the manufacturer’s instructions.

5.9. Detection of Necrotic Cell Death with LDH Assay

The LDH release quantification was performed using a colorimetric CyQUANT LDH Cytotoxicity Assay (Invitrogen, C20300, Carlsbad, CA, USA). Lactate dehydrogenase (LDH) is a cytosolic enzyme that is released into the cell culture medium upon the disruption of the plasma membrane, indicating the necrotic type of death. LDH is quantified in the media in enzymatic reactions. Firstly, LDH catalyzes the conversion of lactate to pyruvate with the accompanying reduction of NAD+ to NADH. Then, the added diaphorase oxidizes NADH, which leads to the reduction of a tetrazolium salt to a red formazan. The amount of formulated formazan is directly proportional to the total LDH released into the media. Here, cells (1 × 105/mL) in the log growth phase were seeded in a 24-well plate in the presence or absence of NAMPT inhibitors. At each time point, 100 µL of cells was transferred to a 96-well plate and the reaction mixture from the kit was added. The plate was then incubated at RT for 30 min and protected from light. Afterwards, the stop solution was added and the absorbance was measured at 490 nm with a spectrophotometer. The higher the absorbance intensity in the sample, the more LDH is released to the culture medium.

5.10. Cell Proliferation Determination

The cell proliferation was assessed with alamarBlue® reagent (Bio-Rad, BUF012B, Hercules, CA, USA), which is based on REDOX reaction by viable cells. Specifically, resazurin sodium salt is reduced by the reducing environment of metabolically active cells to the highly fluorescence resorufin sodium salt. Cells were seeded in a 24-well plate (1 × 105/mL) and treated with NAMPT inhibitors. After incubation, at each time point, 200 µL of cells was transferred to a 96-well plate and alamarBlue® dye (20 µL) was added, then the plate was incubated for 4 h in 37 °C in the dark. At the end, the absorbance at 570 and 600 nm was measured. Proliferation is depicted as a percentage of the control.

5.11. Therapeutic Efficacy Evaluation of Novel NAMPT Inhibitors Using a Mouse Xenograft Model of Human Burkitt Lymphoma

The new NAMPT inhibitors (JJ08, FEI191 and FEI199 (in comparison with lead compound, FK866 (APO866))) were evaluated in vivo in a mouse xenograft model of human Burkitt lymphoma. Twenty non-leaky C.B.-17 SCID mice (8 to 10 weeks old; Iffa Credo, L’Arbresle, France) were housed in micro-isolator cages in a specific pathogen-free room in the animal facility at the University Hospital of Lausanne. Firstly, the mice spent one week alone to acclimatize to their new environment. All animals were handled according to the institutional regulations and with the prior approval of the animal ethic committee of the University of Lausanne. Manipulations were performed in sterile conditions under a laminar flow hood. Firstly, Namalwa cells (1 × 107) were injected subcutaneously into the mouse flank side. Once the tumors became palpable and reached a size between 100 and 150 mm3, mice (n = five/ group) were randomized into control and treated groups. The drugs were administered intraperitoneally (10 mg/kg body weight) in 200 µL 0.9% saline twice a day for 4 days, repeated weekly over 3 weeks. The control group was treated only with 200 µL 0.9% saline. Every day, the animals were monitored for any signs of illness, and in cases where the tumor size reached a diameter of 15 mm, they were sacrificed immediately.

5.12. Analytical Method of Pharmacokinetic Studies In Vivo

Concentration measurements in mice EDTA plasma samples were performed using a Vanquish Flex ultra-high-performance liquid chromatography (UHPLC) system attached to a TSQ QuantisTM triple quadrupole mass spectrometer (MS) (ThermoFisher Scientific, Waltham, MA, USA). The chromatographic column was a Luna Omega Polar C18 3 µm, 50 × 2.1 mm from Phenomenex (Torrance, CA, USA), kept at 40 °C in a UHPLC oven. The mobile phase was made of water and acetonitrile (ACN) with 0.1% formic acid in each. The gradient program ranged from 20 to 95% ACN in 1.5 min and the total method duration (including equilibration for the next injection) was 3 min. The flow rate and injection volume were 0.5 mL/min and 5 µL, respectively.
For the sample preparation, 90 µL of ACN was added to an aliquot of 30 µL of mouse plasma for protein precipitation. The mixture was then centrifugated at 14,000 rpm and the supernatant was directly injected in the UHPLC–MS.

5.13. Pharmacokinetic Analyses

Drug plasma concentrations were measured at selected time points after intraperitoneal administration in mice (sacrificed mice in triplicates for each time point). Samples were analyzed on two separate occasions for each sampling. Then, pharmacokinetic (PK) parameters were computed using standard non-compartmental calculations for geometric means of the measured concentrations using the “PKNCA R Package” (R version 4.0.2, R Development Core Team, http://www.r-project.org/ access date: 4 February 2023).
The area under the curve (AUC0-24) was calculated for the four drugs using the trapezoidal and log-trapezoidal rule when appropriate. The terminal rate constant (λz) was approximated using the slope of the terminal phase, while the half-life (T1/2) was calculated as ln(2)/λz, the apparent clearance (CL/F) as the dose divided by AUC0-24 and the apparent volume of distribution (Vz/F) as (CL/F)/λz.

5.14. Statistical Analysis

All experiments were performed in triplicate and data are expressed as means with the standard error of the mean (SEM), unless otherwise noted. Unpaired t-tests were performed to test differences in pre- and post-treatment malignant cells. The Kaplan–Meier survival method using a long rank test was applied for the analyses of animal survival studies. GraphPad Prism version 9.1.0 (GraphPad Software, San Diego, CA, USA) was used for statistical analysis. p values less than 0.05 were considered statistically significant.

Supplementary Materials

The following supporting information can be downloaded at: https://www.mdpi.com/article/10.3390/molecules28041897/s1, Information on chemical synthesis of JJ08 and its characterization, p. 3; Information on chemical synthesis of FEI191, FEI199 and their characterizations, p.7; Figure S1: Geometric means of plasma concentrations of NAMPT inhibitors after intraperitoneal administration of drugs at 20 mg/kg; Table S1: Measured concentrations of JJ08, APO866, FEI-191 and FEI-199.

Author Contributions

P.B. designed and executed the biological experiments, analyzed the data and wrote the paper. S.M. and A.B. performed the experiments, analyzed the data and drafted the manuscript. J.F.B., S.R.M. and P.V. synthesized and characterized the new NAMPT inhibitors and wrote the paper. J.J. participated in the synthesis of the JJ08 compound. P.T., D.S., V.D. and L.A.D. performed the P.K. studies and wrote the paper. F.P., S.B., M.C. and A.N. (Alessio Nencioni) analyzed the results and wrote the paper. M.A.D. designed and analyzed experiments, coordinated the project and wrote the paper. A.N. (Aimable Nahimana) designed, executed and analyzed experiments, coordinated the project and wrote the paper. All authors have read and agreed to the published version of the manuscript.

Funding

This work was supported by a grant from Fondation Dubois-Ferrière Dinu Lipatti (A.N. (Aimable Nahimana)), by the Fondation Emma Muschamp (A.N.) (Aimable Nahimana, by the Seventh Framework Program PANACREAS (GA #256986 to S.B., P.V., A.N. (Alessio Nencioni), A.N. (Aimable Nahimana) and M.A.D.) and by the European FP7 project INTEGRATA (#813284-1 to SB, PV, A.N. (Aimable Nahimana), A.N. (Alessio Nencioni) and M.A.D.).

Institutional Review Board Statement

The animal study protocol was approved by the Ethics Committee of the University of Lausanne (Cantonal number VD3039x1a and National number 31354).

Informed Consent Statement

Not applicable.

Data Availability Statement

The data presented in this study are available on request from the corresponding author.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Pavlova, N.N.; Thompson, C.B. The Emerging Hallmarks of Cancer Metabolism. Cell Metab. 2016, 23, 27–47. [Google Scholar] [CrossRef] [Green Version]
  2. Hanahan, D.; Weinberg, R.A. Hallmarks of cancer: The next generation. Cell 2011, 144, 646–674. [Google Scholar] [CrossRef] [Green Version]
  3. Warburg, O. On the origin of cancer cells. Science 1956, 123, 309–314. [Google Scholar] [CrossRef] [PubMed]
  4. DeBerardinis, R.J.; Chandel, N.S. We need to talk about the Warburg effect. Nat. Metab. 2020, 2, 127–129. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  5. Yaku, K.; Okabe, K.; Hikosaka, K.; Nakagawa, T. NAD Metabolism in Cancer Therapeutics. Front. Oncol. 2018, 8, 622. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  6. Kincaid, J.W.; Berger, N.A. NAD metabolism in aging and cancer. Exp. Biol. Med. 2020, 245, 1594–1614. [Google Scholar] [CrossRef]
  7. Nikiforov, A.; Kulikova, V.; Ziegler, M. The human NAD metabolome: Functions, metabolism and compartmentalization. Crit. Rev. Biochem. Mol. Biol. 2015, 50, 284–297. [Google Scholar] [CrossRef] [Green Version]
  8. Reiten, O.K.; Wilvang, M.A.; Mitchell, S.J.; Hu, Z.; Fang, E.F. Preclinical and clinical evidence of NAD(+) precursors in health, disease, and ageing. Mech. Ageing Dev. 2021, 199, 111567. [Google Scholar] [CrossRef]
  9. Revollo, J.R.; Grimm, A.A.; Imai, S. The NAD biosynthesis pathway mediated by nicotinamide phosphoribosyltransferase regulates Sir2 activity in mammalian cells. J. Biol. Chem. 2004, 279, 50754–50763. [Google Scholar] [CrossRef] [Green Version]
  10. Rongvaux, A.; Shea, R.J.; Mulks, M.H.; Gigot, D.; Urbain, J.; Leo, O.; Andris, F. Pre-B-cell colony-enhancing factor, whose expression is up-regulated in activated lymphocytes, is a nicotinamide phosphoribosyltransferase, a cytosolic enzyme involved in NAD biosynthesis. Eur. J. Immunol. 2002, 32, 3225–3234. [Google Scholar] [CrossRef]
  11. Gallí, M.; Van Gool, F.; Rongvaux, A.; Andris, F.; Leo, O. The Nicotinamide Phosphoribosyltransferase: A Molecular Link between Metabolism, Inflammation, and Cancer. Cancer Res. 2010, 70, 8. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  12. Garten, A.; Schuster, S.; Penke, M.; Gorski, T.; de Giorgis, T.; Kiess, W. Physiological and pathophysiological roles of NAMPT and NAD metabolism. Nat. Rev. Endocrinol. 2015, 11, 535–546. [Google Scholar] [CrossRef] [PubMed]
  13. Lucena-Cacace, A.; Otero-Albiol, D.; Jiménez-García, M.P.; Muñoz-Galvan, S.; Carnero, A. NAMPT Is a Potent Oncogene in Colon Cancer Progression that Modulates Cancer Stem Cell Properties and Resistance to Therapy through Sirt1 and PARP. J Clin. Cancer Res. 2018, 24, 1202–1215. [Google Scholar] [CrossRef] [Green Version]
  14. Sawicka-Gutaj, N.; Waligórska-Stachura, J.; Andrusiewicz, M.; Biczysko, M.; Sowiński, J.; Skrobisz, J.; Ruchała, M. Nicotinamide phosphorybosiltransferase overexpression in thyroid malignancies and its correlation with tumor stage and with survivin/survivin DEx3 expression. Tumour Biol. 2015, 36, 7859–7863. [Google Scholar] [CrossRef] [Green Version]
  15. Nakajima, T.E.; Yamada, Y.; Hamano, T.; Furuta, K.; Gotoda, T.; Katai, H.; Kato, K.; Hamaguchi, T.; Shimada, Y. Adipocytokine levels in gastric cancer patients: Resistin and visfatin as biomarkers of gastric cancer. J. Gastroenterol. 2009, 44, 685–690. [Google Scholar] [CrossRef] [PubMed]
  16. Galli, U.; Colombo, G.; Travelli, C.; Tron, G.C.; Genazzani, A.A.; Grolla, A.A. Recent Advances in NAMPT Inhibitors: A Novel Immunotherapic Strategy. Front. Pharmacol. 2020, 11, 656. [Google Scholar] [CrossRef]
  17. Heske, C.M. Beyond Energy Metabolism: Exploiting the Additional Roles of NAMPT for Cancer Therapy. Front. Oncol. 2020, 9, 1514. [Google Scholar] [CrossRef] [Green Version]
  18. Hasmann, M.; Schemainda, I. FK866, a highly specific noncompetitive inhibitor of nicotinamide phosphoribosyltransferase, represents a novel mechanism for induction of tumor cell apoptosis. Cancer Res. 2003, 63, 7436–7442. [Google Scholar]
  19. Nahimana, A.; Attinger, A.; Aubry, D.; Greaney, P.; Ireson, C.; Thougaard, A.V.; Tjornelund, J.; Dawson, K.M.; Dupuis, M.; Duchosal, M.A. The NAD biosynthesis inhibitor APO866 has potent antitumor activity against hematologic malignancies. Blood 2009, 113, 3276–3286. [Google Scholar] [CrossRef]
  20. Cagnetta, A.; Caffa, I.; Acharya, C.; Soncini, D.; Acharya, P.; Adamia, S.; Pierri, I.; Bergamaschi, M.; Garuti, A.; Fraternali, G.; et al. APO866 Increases Antitumor Activity of Cyclosporin-A by Inducing Mitochondrial and Endoplasmic Reticulum Stress in Leukemia Cells. Clin. Cancer Res. 2015, 21, 3934–3945. [Google Scholar] [CrossRef] [Green Version]
  21. Yang, P.; Zhang, L.; Shi, Q.J.; Lu, Y.B.; Wu, M.; Wei, E.Q.; Zhang, W.P. Nicotinamide phosphoribosyltransferase inhibitor APO866 induces C6 glioblastoma cell death via autophagy. Die Pharmazie 2015, 70, 650–655. [Google Scholar] [PubMed]
  22. Barraud, M.; Garnier, J.; Loncle, C.; Gayet, O.; Lequeue, C.; Vasseur, S.; Bian, B.; Duconseil, P.; Gilabert, M.; Bigonnet, M.; et al. A pancreatic ductal adenocarcinoma subpopulation is sensitive to FK866, an inhibitor of NAMPT. Oncotarget 2016, 7, 53783–53796. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  23. Cea, M.; Zoppoli, G.; Bruzzone, S.; Fruscione, F.; Moran, E.; Garuti, A.; Rocco, I.; Cirmena, G.; Casciaro, S.; Olcese, F.; et al. APO866 activity in hematologic malignancies: A preclinical in vitro study. Blood 2009, 113, 6035–6037, author reply 6037–6038. [Google Scholar] [CrossRef] [PubMed]
  24. Hovstadius, P.; Larsson, R.; Jonsson, E.; Skov, T.; Kissmeyer, A.M.; Krasilnikoff, K.; Bergh, J.; Karlsson, M.O.; Lönnebo, A.; Ahlgren, J. A Phase I study of CHS 828 in patients with solid tumor malignancy. Clin. Cancer Res. 2002, 8, 2843–2850. [Google Scholar]
  25. Ravaud, A.; Cerny, T.; Terret, C.; Wanders, J.; Bui, B.N.; Hess, D.; Droz, J.P.; Fumoleau, P.; Twelves, C. Phase I study and pharmacokinetic of CHS-828, a guanidino-containing compound, administered orally as a single dose every 3 weeks in solid tumours: An ECSG/EORTC study. Eur. J. Cancer 2005, 41, 702–707. [Google Scholar] [CrossRef]
  26. Holen, K.; Saltz, L.B.; Hollywood, E.; Burk, K.; Hanauske, A.-R. The pharmacokinetics, toxicities, and biologic effects of FK866, a nicotinamide adenine dinucleotide biosynthesis inhibitor. Investig. New Drugs 2008, 26, 45–51. [Google Scholar] [CrossRef]
  27. Naing, A.; Leong, S.; Pishvaian, M.J.; Razak, A.R.A.; Mahipal, A.; Berlin, J.; Cho, D.; Senapedis, W.; Shacham, S.; Kauffman, M.; et al. A first in human phase 1 study of KPT-9274, a first in class dual inhibitor of PAK4 and NAMPT, in patients with advanced solid malignancies or NHL. Ann. Oncol. 2017, 28, v125. [Google Scholar] [CrossRef] [Green Version]
  28. Korotchkina, L.; Kazyulkin, D.; Komarov, P.G.; Polinsky, A.; Andrianova, E.L.; Joshi, S.; Gupta, M.; Vujcic, S.; Kononov, E.; Toshkov, I.; et al. OT-82, a novel anticancer drug candidate that targets the strong dependence of hematological malignancies on NAD biosynthesis. Leukemia 2020, 34, 1828–1839. [Google Scholar] [CrossRef] [Green Version]
  29. Bai, J.-F.; Majjigapu, S.R.; Sordat, B.; Poty, S.; Vogel, P.; Elías-Rodríguez, P.; Moreno-Vargas, A.J.; Carmona, A.T.; Caffa, I.; Ghanem, M.; et al. Identification of new FK866 analogues with potent anticancer activity against pancreatic cancer. Eur. J. Med. Chem. 2022, 239, 114504. [Google Scholar] [CrossRef]
  30. Kozako, T.; Aikawa, A.; Ohsugi, T.; Uchida, Y.-i.; Kato, N.; Sato, K.; Ishitsuka, K.; Yoshimitsu, M.; Honda, S.-i. High expression of NAMPT in adult T-cell leukemia/lymphoma and anti-tumor activity of a NAMPT inhibitor. Eur. J. Pharmacol. 2019, 865, 172738. [Google Scholar] [CrossRef]
  31. Mitchell, S.R.; Larkin, K.; Grieselhuber, N.R.; Lai, T.-H.; Cannon, M.; Orwick, S.; Sharma, P.; Asemelash, Y.; Zhang, P.; Goettl, V.M.; et al. Selective targeting of NAMPT by KPT-9274 in acute myeloid leukemia. Blood Adv. 2019, 3, 242–255. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  32. Chan, F.K.-M.; Moriwaki, K.; De Rosa, M.J. Detection of necrosis by release of lactate dehydrogenase activity. Methods Mol. Biol. 2013, 979, 65–70. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  33. Klijn, C.; Durinck, S.; Stawiski, E.W.; Haverty, P.M.; Jiang, Z.; Liu, H.; Degenhardt, J.; Mayba, O.; Gnad, F.; Liu, J.; et al. A comprehensive transcriptional portrait of human cancer cell lines. Nat. Biotechnol. 2015, 33, 306–312. [Google Scholar] [CrossRef] [PubMed]
  34. Stein, L.R.; Imai, S. The dynamic regulation of NAD metabolism in mitochondria. Trends Endocrinol. Metab. 2012, 23, 420–428. [Google Scholar] [CrossRef] [Green Version]
  35. Redza-Dutordoir, M.; Averill-Bates, D.A. Activation of apoptosis signalling pathways by reactive oxygen species. BBA 2016, 1863, 2977–2992. [Google Scholar] [CrossRef]
  36. Ginet, V.; Puyal, J.; Rummel, C.; Aubry, D.; Breton, C.; Cloux, A.J.; Majjigapu, S.R.; Sordat, B.; Vogel, P.; Bruzzone, S.; et al. A critical role of autophagy in antileukemia/lymphoma effects of APO866, an inhibitor of NAD biosynthesis. Autophagy 2014, 10, 603–617. [Google Scholar] [CrossRef] [Green Version]
  37. Liou, G.-Y.; Storz, P. Reactive oxygen species in cancer. Free Radic Res. 2010, 44, 479–496. [Google Scholar] [CrossRef] [Green Version]
  38. Cloux, A.J.; Aubry, D.; Heulot, M.; Widmann, C.; ElMokh, O.; Piacente, F.; Cea, M.; Nencioni, A.; Bellotti, A.; Bouzourène, K.; et al. Reactive oxygen/nitrogen species contribute substantially to the antileukemia effect of APO866, a NAD lowering agent. Oncotarget 2019, 10, 6723–6738. [Google Scholar] [CrossRef] [Green Version]
  39. ElMokh, O.; Matsumoto, S.; Biniecka, P.; Bellotti, A.; Schaeuble, K.; Piacente, F.; Gallart-Ayala, H.; Ivanisevic, J.; Stamenkovic, I.; Nencioni, A.; et al. Gut microbiota severely hampers the efficacy of NAD-lowering therapy in leukemia. Cell Death Dis. 2022, 13, 320. [Google Scholar] [CrossRef]
  40. Cea, M.; Cagnetta, A.; Fulciniti, M.; Tai, Y.T.; Hideshima, T.; Chauhan, D.; Roccaro, A.; Sacco, A.; Calimeri, T.; Cottini, F.; et al. Targeting NAD+ salvage pathway induces autophagy in multiple myeloma cells via mTORC1 and extracellular signal-regulated kinase (ERK1/2) inhibition. Blood 2012, 120, 3519–3529. [Google Scholar] [CrossRef] [Green Version]
  41. Cagnetta, A.; Cea, M.; Calimeri, T.; Acharya, C.; Fulciniti, M.; Tai, Y.T.; Hideshima, T.; Chauhan, D.; Zhong, M.Y.; Patrone, F.; et al. Intracellular NAD+ depletion enhances bortezomib-induced anti-myeloma activity. Blood 2013, 122, 1243–1255. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  42. Ghanem, M.S.; Monacelli, F.; Nencioni, A. Advances in NAD-Lowering Agents for Cancer Treatment. Nutrients 2021, 13, 1665. [Google Scholar] [CrossRef] [PubMed]
  43. Olesen, U.H.; Christensen, M.K.; Björkling, F.; Jäättelä, M.; Jensen, P.B.; Sehested, M.; Nielsen, S.J. Anticancer agent CHS-828 inhibits cellular synthesis of NAD. Biochem. Biophys. Res. Commun. 2008, 367, 799–804. [Google Scholar] [CrossRef]
  44. Zhao, G.; Green, C.F.; Hui, Y.-H.; Prieto, L.; Shepard, R.; Dong, S.; Wang, T.; Tan, B.; Gong, X.; Kays, L.; et al. Discovery of a Highly Selective NAMPT Inhibitor That Demonstrates Robust Efficacy and Improved Retinal Toxicity with Nicotinic Acid Coadministration. Mol. Cancer Ther. 2017, 16, 2677–2688. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  45. Del Nagro, C.; Xiao, Y.; Rangell, L.; Reichelt, M.; O’Brien, T. Depletion of the central metabolite NAD leads to oncosis-mediated cell death. J. Biol. Chem. 2014, 289, 35182–35192. [Google Scholar] [CrossRef] [Green Version]
  46. Beauparlant, P.; Bédard, D.; Bernier, C.; Chan, H.; Gilbert, K.; Goulet, D.; Gratton, M.O.; Lavoie, M.; Roulston, A.; Turcotte, E.; et al. Preclinical development of the nicotinamide phosphoribosyl transferase inhibitor prodrug GMX1777. Anticancer Drugs 2009, 20, 346–354. [Google Scholar] [CrossRef]
  47. Okumura, S.; Sasaki, T.; Minami, Y.; Ohsaki, Y. Nicotinamide phosphoribosyltransferase: A potent therapeutic target in non-small cell lung cancer with epidermal growth factor receptor-gene mutation. J. Thorac. Oncol. 2012, 7, 49–56. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  48. Drevs, J.; Löser, R.; Rattel, B.; Esser, N. Antiangiogenic potency of FK866/K22.175, a new inhibitor of intracellular NAD biosynthesis, in murine renal cell carcinoma. Anticancer Res. 2003, 23, 4853–4858. [Google Scholar]
  49. Johanson, V.; Arvidsson, Y.; Kölby, L.; Bernhardt, P.; Swärd, C.; Nilsson, O.; Ahlman, H. Antitumoural effects of the pyridyl cyanoguanidine CHS 828 on three different types of neuroendocrine tumours xenografted to nude mice. Neuroendocrinology 2005, 82, 171–176. [Google Scholar] [CrossRef]
  50. Shats, I.; Williams, J.G.; Liu, J.; Makarov, M.V.; Wu, X.; Lih, F.B.; Deterding, L.J.; Lim, C.; Xu, X.; Randall, T.A.; et al. Bacteria Boost Mammalian Host NAD Metabolism by Engaging the Deamidated Biosynthesis Pathway. Cell Metab. 2020, 31, 564–579.e7. [Google Scholar] [CrossRef] [PubMed]
  51. von Heideman, A.; Berglund, Å.; Larsson, R.; Nygren, P. Safety and efficacy of NAD depleting cancer drugs: Results of a phase I clinical trial of CHS 828 and overview of published data. Cancer Chemother. Pharmacol. 2010, 65, 1165–1172. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  52. Neumann, C.S.; Olivas, K.C.; Anderson, M.E.; Cochran, J.H.; Jin, S.; Li, F.; Loftus, L.V.; Meyer, D.W.; Neale, J.; Nix, J.C.; et al. Targeted Delivery of Cytotoxic NAMPT Inhibitors Using Antibody-Drug Conjugates. Mol. Cancer Ther. 2018, 17, 2633–2642. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  53. Böhnke, N.; Berger, M.; Griebenow, N.; Rottmann, A.; Erkelenz, M.; Hammer, S.; Berndt, S.; Günther, J.; Wengner, A.M.; Stelte-Ludwig, B.; et al. A Novel NAMPT Inhibitor-Based Antibody–Drug Conjugate Payload Class for Cancer Therapy. Bioconjug. Chem. 2022, 33, 1210–1221. [Google Scholar] [CrossRef] [PubMed]
  54. Karpov, A.S.; Abrams, T.; Clark, S.; Raikar, A.; D’Alessio, J.A.; Dillon, M.P.; Gesner, T.G.; Jones, D.; Lacaud, M.; Mallet, W.; et al. Nicotinamide Phosphoribosyltransferase Inhibitor as a Novel Payload for Antibody-Drug Conjugates. ACS Med. Chem. Lett. 2018, 9, 838–842. [Google Scholar] [CrossRef]
Molecules 28 01897 g001 550
Figure 1. Chemical structures of NAMPT inhibitors. JJ08 is an FK866 (APO866) analogue with a furan-2-carboxamide group instead of a benzamide group (tail group). With their cyanoguanidine moieties, FEI191 and FEI199 can be seen as analogues of CHS-828 and they also contain a furan-2-carboxamide tail group.
Figure 1. Chemical structures of NAMPT inhibitors. JJ08 is an FK866 (APO866) analogue with a furan-2-carboxamide group instead of a benzamide group (tail group). With their cyanoguanidine moieties, FEI191 and FEI199 can be seen as analogues of CHS-828 and they also contain a furan-2-carboxamide tail group.
Molecules 28 01897 g001
Molecules 28 01897 sch001 550
Scheme 1. Synthesis of JJ08.
Scheme 1. Synthesis of JJ08.
Molecules 28 01897 sch001
Molecules 28 01897 sch002 550
Scheme 2. Synthesis of FEI191.
Scheme 2. Synthesis of FEI191.
Molecules 28 01897 sch002
Molecules 28 01897 sch003 550
Scheme 3. Synthesis of FEI199.
Scheme 3. Synthesis of FEI199.
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Figure 2. New compounds with a potent NAMPT inhibitory activity. Compounds were added in 1 µM final concentration to purified NAMPT and incubated with co-substrates, resulting in a reduction of tetrazolium salt (WST-1) to colorful formazan. The amount of formed dye is directly proportional to the enzyme activity. The absorbance of the dye was detected at OD 450 nm.
Figure 2. New compounds with a potent NAMPT inhibitory activity. Compounds were added in 1 µM final concentration to purified NAMPT and incubated with co-substrates, resulting in a reduction of tetrazolium salt (WST-1) to colorful formazan. The amount of formed dye is directly proportional to the enzyme activity. The absorbance of the dye was detected at OD 450 nm.
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Figure 3. New NAMPT inhibitors induce profound depletion of intracellular NAD+. ML2 (A), Jurkat (B), Namalwa (C) and RPMI8226 (D) cells were incubated with NAMPT inhibitors for 96 h. Intracellular NAD+ content was measured in a time-dependent manner as indicated on the x-axis. NAD+ levels were first normalized to the total protein and then to the control at each time point.
Figure 3. New NAMPT inhibitors induce profound depletion of intracellular NAD+. ML2 (A), Jurkat (B), Namalwa (C) and RPMI8226 (D) cells were incubated with NAMPT inhibitors for 96 h. Intracellular NAD+ content was measured in a time-dependent manner as indicated on the x-axis. NAD+ levels were first normalized to the total protein and then to the control at each time point.
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Figure 4. NAMPT inhibitors induce cell death in hematological malignancies in a dose-dependent manner, with FEI199 being the most potent. A dose-dependent analysis of cell death induced by NAMPT inhibitors on ML2 (A), Jurkat (B), Namalwa (C) and RPMI8226 (D) cell lines. The cells were treated with various concentrations of NAMPT inhibitors for 96 h and cell death was assessed by flow cytometry using ANXN and 7AAD staining. The percentages of early apoptotic cells (ANXN+ 7AAD−) are shown as white columns and those of late apoptotic cells (7AAD+) are shown as solid black columns. Data are means ± SD, n ≥ 3.
Figure 4. NAMPT inhibitors induce cell death in hematological malignancies in a dose-dependent manner, with FEI199 being the most potent. A dose-dependent analysis of cell death induced by NAMPT inhibitors on ML2 (A), Jurkat (B), Namalwa (C) and RPMI8226 (D) cell lines. The cells were treated with various concentrations of NAMPT inhibitors for 96 h and cell death was assessed by flow cytometry using ANXN and 7AAD staining. The percentages of early apoptotic cells (ANXN+ 7AAD−) are shown as white columns and those of late apoptotic cells (7AAD+) are shown as solid black columns. Data are means ± SD, n ≥ 3.
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Figure 5. Treatment with NAMPT inhibitors induces strong activation of caspase –3, –8 and –9. ML2 (A–C) and Jurkat (D–F) cells were treated with 10 nM of NAMPT inhibitors for 72 h and activated forms of CASP-3, CASP-8 and CASP-9 were detected using a fluorescent-specific probe for each caspase and flow cytometry. Data are representative of at least three independent experiments and the graphs show mean fluorescence intensity (MFI). * p < 0.005.
Figure 5. Treatment with NAMPT inhibitors induces strong activation of caspase –3, –8 and –9. ML2 (A–C) and Jurkat (D–F) cells were treated with 10 nM of NAMPT inhibitors for 72 h and activated forms of CASP-3, CASP-8 and CASP-9 were detected using a fluorescent-specific probe for each caspase and flow cytometry. Data are representative of at least three independent experiments and the graphs show mean fluorescence intensity (MFI). * p < 0.005.
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Figure 6. NAMPT inhibitors induce necrotic cell death and decrease cell proliferation in hematological malignancies. A time-dependent analysis of LDH release on ML2 (A) and Jurkat (B) cells treated with NAMPT inhibitors (10 nM) was assessed according to the manufacturer’s instructions. Cell proliferation was assessed on ML2 (C) and Jurkat (D) cells based on the ability of metabolically active cells to reduce resazurin sodium salt to a highly fluorescence product using AlamarBlue reagent. The absorbance of both products was measured with a spectrophotometer at the appropriate wavelength. Data are ± SD, n = 3, * p < 0.05, ** p < 0.01, **** p < 0.0001 (CTRL vs. inhibitors treated groups).
Figure 6. NAMPT inhibitors induce necrotic cell death and decrease cell proliferation in hematological malignancies. A time-dependent analysis of LDH release on ML2 (A) and Jurkat (B) cells treated with NAMPT inhibitors (10 nM) was assessed according to the manufacturer’s instructions. Cell proliferation was assessed on ML2 (C) and Jurkat (D) cells based on the ability of metabolically active cells to reduce resazurin sodium salt to a highly fluorescence product using AlamarBlue reagent. The absorbance of both products was measured with a spectrophotometer at the appropriate wavelength. Data are ± SD, n = 3, * p < 0.05, ** p < 0.01, **** p < 0.0001 (CTRL vs. inhibitors treated groups).
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Figure 7. Supplementation with NAD, NAM and NA abrogates the killing effect of NAMPT inhibitors. ML2 (A), Jurkat (B), Namalwa (C) and RPMI8226 (D) cells were incubated for 96 h with NAMPT inhibitors in the presence or absence of NAD (0.5 mM), NAM (1 mM) or NA (10 µM). Cell death was assessed as mentioned in Figure 4. Data are ± SD, n = 3, * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001 (inhibitors treated vs. NAD, NAM and NA groups).
Figure 7. Supplementation with NAD, NAM and NA abrogates the killing effect of NAMPT inhibitors. ML2 (A), Jurkat (B), Namalwa (C) and RPMI8226 (D) cells were incubated for 96 h with NAMPT inhibitors in the presence or absence of NAD (0.5 mM), NAM (1 mM) or NA (10 µM). Cell death was assessed as mentioned in Figure 4. Data are ± SD, n = 3, * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001 (inhibitors treated vs. NAD, NAM and NA groups).
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Figure 8. New NAMPT inhibitors severely deplete NADP(H) cell content in hematopoietic malignant cells. ML2 cells were incubated with NAMPT inhibitors for 96 h. A time-dependent analysis of intracellular NADP+/NADPH content was performed according to the manufacturer’s instructions. NADP+/NADPH levels were first normalized to the total protein and then to control at each time point.
Figure 8. New NAMPT inhibitors severely deplete NADP(H) cell content in hematopoietic malignant cells. ML2 cells were incubated with NAMPT inhibitors for 96 h. A time-dependent analysis of intracellular NADP+/NADPH content was performed according to the manufacturer’s instructions. NADP+/NADPH levels were first normalized to the total protein and then to control at each time point.
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Figure 9. NAMPT inhibitors induce high levels of ROS production upon cell death in malignant cells. ML2 and Jurkat cells were treated with APO866, JJ08, FEI191 and FEI199 for 72 h. Mitochondrial (A) and cytosolic (B) superoxide anions and hydrogen peroxide (C) were detected by flow cytometry using MitoSOX, DHE and H2DCFDA fluorescent probes, respectively. The percentage of positive cells is proportional to the amount of produced superoxide anions. Data are ± SD, n = 3, ** p < 0.01, *** p < 0.001 (CTRL vs. inhibitors treated groups).
Figure 9. NAMPT inhibitors induce high levels of ROS production upon cell death in malignant cells. ML2 and Jurkat cells were treated with APO866, JJ08, FEI191 and FEI199 for 72 h. Mitochondrial (A) and cytosolic (B) superoxide anions and hydrogen peroxide (C) were detected by flow cytometry using MitoSOX, DHE and H2DCFDA fluorescent probes, respectively. The percentage of positive cells is proportional to the amount of produced superoxide anions. Data are ± SD, n = 3, ** p < 0.01, *** p < 0.001 (CTRL vs. inhibitors treated groups).
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Figure 10. JJ08, FEI191 and FEI199 deplete intracellular ATP content (A), induce the loss of MMP (B) and ultimately cause cell death (C). ML2, Jurkat, Namalwa and RPMI8226 cells were treated with NAMPT inhibitors for 96 h. Intracellular ATP content, MMP and cell death were measured in a time-dependent fashion. ATP levels were first normalized to protein content and then to control at each time point. MMP was detected by flow cytometry using TMRM staining, and cell death was analyzed as described in Figure 4. Data are ± SD, n = 3.
Figure 10. JJ08, FEI191 and FEI199 deplete intracellular ATP content (A), induce the loss of MMP (B) and ultimately cause cell death (C). ML2, Jurkat, Namalwa and RPMI8226 cells were treated with NAMPT inhibitors for 96 h. Intracellular ATP content, MMP and cell death were measured in a time-dependent fashion. ATP levels were first normalized to protein content and then to control at each time point. MMP was detected by flow cytometry using TMRM staining, and cell death was analyzed as described in Figure 4. Data are ± SD, n = 3.
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Figure 11. Catalase supplementation abrogates the killing effect of NAMPT inhibitors but not NAD+ depletion in tested cell lines, except for Namalwa cells. Catalase (1000 U / ml) was added 1 h before the inhibitors. Kinetic analyses of intracellular NAD+, ATP, MMP and cell death were assessed on the ML2 cell line (A–D). Cell death was assessed as described in Figure 4, at 72 h on ML2 (E), Jurkat (F) and RPMI8226 (G). Data are ± SD, n = 3, * p < 0.05, ** p < 0.01, *** p < 0.001 (inhibitors treated vs. catalase treated groups).
Figure 11. Catalase supplementation abrogates the killing effect of NAMPT inhibitors but not NAD+ depletion in tested cell lines, except for Namalwa cells. Catalase (1000 U / ml) was added 1 h before the inhibitors. Kinetic analyses of intracellular NAD+, ATP, MMP and cell death were assessed on the ML2 cell line (A–D). Cell death was assessed as described in Figure 4, at 72 h on ML2 (E), Jurkat (F) and RPMI8226 (G). Data are ± SD, n = 3, * p < 0.05, ** p < 0.01, *** p < 0.001 (inhibitors treated vs. catalase treated groups).
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Figure 12. JJ08 eradicates tumor growth and significantly prolongs the survival in a xenograft mouse model of human Burkitt lymphoma. Tumor size (A) and survival rate (B) of mice xenografted with Namalwa cells treated or untreated with NAMPT inhibitors were monitored for 21 days. Twenty-five 6-to-8-week-old C.B.-17 SCID mice were transplanted subcutaneously with Namalwa cells (107). Once tumors reached a volume of approximately 100–150 mm3, at day 14, mice were randomized into five groups of animals (n = 5) with similar body weight. Control groups received vehicle (pink line) and JJ08 (10 mg/kg; light blue line), FEI191 (10 mg/kg; red line), FEI199 (10 mg/kg; green line) or APO866 (10 mg/kg; blue line) were administered as described in the Materials and Methods section. Day 1 on the graphs corresponds to the beginning of the treatment (when the tumor volume reached >100 mm3). Error bars = SD. * p < 0.05, ** p < 0.01, *** p < 0.001. Data were analyzed by the Kaplan–Meier survival analysis with log-rank test.
Figure 12. JJ08 eradicates tumor growth and significantly prolongs the survival in a xenograft mouse model of human Burkitt lymphoma. Tumor size (A) and survival rate (B) of mice xenografted with Namalwa cells treated or untreated with NAMPT inhibitors were monitored for 21 days. Twenty-five 6-to-8-week-old C.B.-17 SCID mice were transplanted subcutaneously with Namalwa cells (107). Once tumors reached a volume of approximately 100–150 mm3, at day 14, mice were randomized into five groups of animals (n = 5) with similar body weight. Control groups received vehicle (pink line) and JJ08 (10 mg/kg; light blue line), FEI191 (10 mg/kg; red line), FEI199 (10 mg/kg; green line) or APO866 (10 mg/kg; blue line) were administered as described in the Materials and Methods section. Day 1 on the graphs corresponds to the beginning of the treatment (when the tumor volume reached >100 mm3). Error bars = SD. * p < 0.05, ** p < 0.01, *** p < 0.001. Data were analyzed by the Kaplan–Meier survival analysis with log-rank test.
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Table
Table 1. NAMPT inhibitors induce cell death in various cell lines of hematological malignancies. IC50 (nM) after 96 h of treatment with NAMPT inhibitors.
Table 1. NAMPT inhibitors induce cell death in various cell lines of hematological malignancies. IC50 (nM) after 96 h of treatment with NAMPT inhibitors.
APO866JJ08FEI191FEI199
ML20.410.510.310.21
JURKAT0.470.850.450.25
NAMALWA0.580.580.450.29
RPMI82260.230.300.250.12
ML2: acute myeloid leukemia; Jurkat: acute lymphoblastic leukemia; NMLW: Burkitt lymphoma; RPMI8226: multiple myeloma.
Table
Table 2. Pharmacokinetic parameters of JJ08, FEI191 and FEI199 in female SCID mice following intraperitoneal administration.
Table 2. Pharmacokinetic parameters of JJ08, FEI191 and FEI199 in female SCID mice following intraperitoneal administration.
APO866JJ08FEI191FEI199
Cmax (ng/mL)28,02824,302268312,031
Tmax (h)0.170.170.170.17
T1/2 (h)3.746.58--
AUC0-24 (ng*h/mL)16,42675631820 *3718 *
CL/F (mL/h)2453220108
Vz/F (mL)131502--
Cmax: maximum concentration; Tmax: time to reach maximum concentration; T1/2: half-life of the compounds; AUC0-24: area under the plasma concentration–time curve over the last 24 h dosing interval; CL/F: apparent drug clearance; Vz/F: apparent terminal volume of distribution. * AUC was calculated from PK measurements up to 8 h. However, given the low concentrations, terminal exposure is not expected to induce significant changes in calculated exposure.
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Biniecka, P.; Matsumoto, S.; Belotti, A.; Joussot, J.; Bai, J.F.; Majjigapu, S.R.; Thoueille, P.; Spaggiari, D.; Desfontaine, V.; Piacente, F.; et al. Anticancer Activities of Novel Nicotinamide Phosphoribosyltransferase Inhibitors in Hematological Malignancies. Molecules 2023, 28, 1897. https://doi.org/10.3390/molecules28041897

AMA Style

Biniecka P, Matsumoto S, Belotti A, Joussot J, Bai JF, Majjigapu SR, Thoueille P, Spaggiari D, Desfontaine V, Piacente F, et al. Anticancer Activities of Novel Nicotinamide Phosphoribosyltransferase Inhibitors in Hematological Malignancies. Molecules. 2023; 28(4):1897. https://doi.org/10.3390/molecules28041897

Chicago/Turabian Style

Biniecka, Paulina, Saki Matsumoto, Axel Belotti, Jessie Joussot, Jian Fei Bai, Somi Reddy Majjigapu, Paul Thoueille, Dany Spaggiari, Vincent Desfontaine, Francesco Piacente, and et al. 2023. "Anticancer Activities of Novel Nicotinamide Phosphoribosyltransferase Inhibitors in Hematological Malignancies" Molecules 28, no. 4: 1897. https://doi.org/10.3390/molecules28041897

APA Style

Biniecka, P., Matsumoto, S., Belotti, A., Joussot, J., Bai, J. F., Majjigapu, S. R., Thoueille, P., Spaggiari, D., Desfontaine, V., Piacente, F., Bruzzone, S., Cea, M., Decosterd, L. A., Vogel, P., Nencioni, A., Duchosal, M. A., & Nahimana, A. (2023). Anticancer Activities of Novel Nicotinamide Phosphoribosyltransferase Inhibitors in Hematological Malignancies. Molecules, 28(4), 1897. https://doi.org/10.3390/molecules28041897

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