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Article

Screening of Promising Chemotherapeutic Candidates from Plants against Human Adult T-Cell Leukemia/Lymphoma (VII): Active Principles from Thuja occidentalis L.

by
Daisuke Nakano
1,
Kenji Ishitsuka
2,
Madoka Ishihara
1,
Ryota Tsuchihashi
1,
Masafumi Okawa
1,*,
Kazuo Tamura
3 and
Junei Kinjo
1
1
Faculty of Pharmaceutical Sciences, Fukuoka University, Fukuoka 814-0180, Japan
2
Division of Hematology and Rheumatology, Graduate School of Medical and Dental Sciences, Kagoshima University, Kagoshima 890-8544, Japan
3
Division of Medical Oncology, Hematology and Infectious Disease, Department of Internal Medicine, Fukuoka University, Fukuoka 814-0180, Japan
*
Author to whom correspondence should be addressed.
Molecules 2021, 26(24), 7619; https://doi.org/10.3390/molecules26247619
Submission received: 18 November 2021 / Revised: 8 December 2021 / Accepted: 13 December 2021 / Published: 15 December 2021
(This article belongs to the Special Issue Medicinal Plants and Industrial Crops: Phytochemistry and Metabolic Diseases)
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Abstract

:
During the screening of novel chemotherapeutic candidates from plants against adult T-cell leukemia/lymphoma, we identified that the extracts of Thuja occidentalis (Cupressaceae) showed potent anti-proliferative activity in MT-1 and MT-2 cells. Therefore, we attempted to isolate the active components from this plant. We isolated and identified 32 compounds (1–32; eight lignans, 18 terpenoids, and six flavonoids) from the extracts of the leaves and cones. Their structures were determined by spectroscopic analysis. Several of the isolated compounds inhibited the growth of both cell lines. Lignans showed more potent activity than other classes of compounds. A comparison of the activities of compounds 1–8 revealed that the presence of a trans-lactone (linkage of C-6 to C-7) correlated with increased activity. Diterpenes showed moderate activity, and the presence of a ketone moiety at the C-7 position correlated with increased activity in compounds 12–21. In addition, biflavones showed moderate activity, and the presence of methoxy functions appeared to influence the activity of these compounds. Several lignans were lead compound of anti-cancer reagent (etoposide). In conclusion, not only lignans, but also diterpenes and/or biflavones, may be promising candidates for the treatment of adult T-cell leukemia/lymphoma.

1. Introduction

Adult T-cell leukemia/lymphoma (ATL) is a malignancy of mature peripheral T-lymphocytes associated with human T-cell lymphotropic virus type I (HTLV-1). Conventional chemotherapeutic regimens used to treat other types of malignant lymphoma have been administered to ATL patients, but the therapeutic outcomes of acute- and lymphoma-type ATL remain very poor [1]. Therefore, we conducted a search for novel chemotherapeutic candidates for the treatment of ATL in plant extracts and tested these compounds in two cell lines. MT-1 cells were established from the peripheral blood tumor cells of ATL patients [2], and MT-2 cells were established from cord blood T-cells by co-cultivation of normal human cord lymphocytes and peripheral blood tumor cells from an ATL patient [3].
We previously reported the screening of 582 extracts and the isolation of active constituents (withanolides, cardenolides, aporphine alkaloids, phenanthroindolizidine alkaloids, quinolone alkaloids, and coumarins) for testing in MT-1 and MT-2 cell lines [4,5,6,7,8,9,10]. In a previous paper, induction of apoptosis by 24,25-dihydrowithanolide D determined by cytometric APO2.7-PC5 assay and evidenced by PARP cleavage [6], calotropin (cardenolide) induced apoptosis in MT-1 and MT-2 cells in a concentration-dependent manner, and the cell cycle experiments demonstrated that calotropin arrested MT-1 and MT-2 cells at the G2/M phase [7], accumulation of Sub-G1 cells were observed in MT-1 and MT-2 cells treated by liriodenine (aporphine alkaloid), suggesting induction of apoptosis [8]. Herein, following the results of our previous screening program [5], we report the isolation of active compounds from Thuja occidentalis, a plant belonging to the family Cupressaceae. T. occidentalis is native to North America and widely cultivated as ornamental tree known as white cedar [11]. Previous phytochemical studies on T. occidentalis have resulted in the isolation of several diterpenes (dehydroabietane, neothujic acids III and IV), lignans [(−)-matairesinol, (−)-thujaplicatin methyl ether, (−)-wikstromol, epi-pinoresinol], monoterpenes (α-thujone, β-thujone, fenchone), and a sesquiterpene alcohol [(+)-occidentalol] [12]. In traditional medicine, T. occidentalis has been used in the treatment of liver diseases, bronchitis, psoriasis, enuresis, amenorrhea, cystitis, uterine carcinomas, diarrhea, and rheumatism [13]. Thujone exerts proapoptotic and antiinvasive effects on GBM cells. They confirm the potential of α-thujone for the treatment of glioblastoma multiforme [14]. In in vivo studies, α/β-thujone promotes the regression of neoplasia and inhibited the angiogenic markers (VEGF, Ang-4, and CD31) into the tumor [15]. The aqueous extract and the polysaccharide fraction of T. occidentalis reduced production of proinflammatory cytokines (TNF-α and IL-6), decreased immunostaining of COX-2 and iNOS, and inhibited oxidative stress [16].

2. Results and Discussion

2.1. Screening of Antiproliferative Activities of Cupressaceae Plants against MT-1 and MT-2 Cells

Table 1 summarizes the anti-proliferative activities of several Cupressaceae plant extracts based on their activity in MT-1 and MT-2 cells. Despite variation in potency, anti-proliferative activity was exhibited by nine of the 10 extracts. In a preliminary test, the most potent anti-proliferative activity in MT-1 and MT-2 cells was exhibited by leaf extract following by the cone extract of T. occidentalis; therefore, we attempted to isolate the active compounds from these extracts. In addition, we attempted to isolate an extract from the cones of T. occidentalis.

2.2. Isolation of Compounds from the Extracts of T. occidentalis

Extraction of the leaves of T. occidentalis was performed with MeOH under reflux, and the extract was initially partitioned between n-hexane and 80% MeOH. The n-hexane layer and 80% MeOH layer were subjected to columns to isolate the compounds. Conversely, extraction of the cones of T. occidentalis was performed with MeOH under reflux and the extracts were subjected to columns to isolate the compounds.
The extracts were subjected to several chromatographic purification steps to obtain compounds 3–9, 11–18, 20–27, and 29–32 from the leaves; compounds 1–3, 6, 9–10, 19–20, and 27–29 were extracted from the cones (Figure 1). Compounds 1–32 had been previously identified and the physical data of these compounds are in accordance to those reported [17,18,19,20,21,22,23,24,25,26,27,28,29,30,31,32,33,34,35,36,37,38,39,40].

2.3. Determination of Anti-Proliferative Activity

The anti-proliferative effects of compounds 1–32 are listed in Table 2. In addition, doxorubicin (clinically used antineoplastic drug) and etoposide (semisynthetic derivative of podophyllotoxin) were used as positive control.
Almost all of the isolated lignans (1–8) inhibited the growth of both tumor cell lines. But all compounds had weaker antiproliferative activity than positive control except compound 3. The trans-lactone moiety in compounds 1 and 3 increased their anti-proliferative activity compared with compounds 2 and 4, which do not possess a trans-lactone moiety. The presence of a hydroxyl group at position 7α in compounds 1 and 2 appeared to decrease the activity of these compounds compared with compounds 3 and 4. Furthermore, the presence of a ketone moiety at position C-7 in compound 5 was associated with decreased activity in comparison to compound 4, which lacked this moiety. Comparison of compounds 3 and 6 indicated that, the linkage of C-6 to C-7 appeared to enhance the activity (Figure 2).
Compared with compounds 6, 7, and 8, the presence of substituents (OH and OAc) influenced the activities.
Several of the isolated terpenoid compounds inhibited the proliferation of cell lines. The presence of a double bond at position C-8 in compound 16 appeared to enhance its activity compared with compound 13, which did not have a double bond at this position. Compared with compounds 15 and 16, the presence of a ketone moiety at position C-7 enhanced the activity. Similarly, compared with compounds 18, 19, and 20, the substituents (OH and ketone) influenced their activities (Figure 3).
Several of the isolated flavonoids (25–30) inhibited the proliferation of cell lines. Comparison of compounds 25, 26, 27, 28, and 29, indicated the presence of one or two methoxy groups appeared to influence the activity of the compounds.
The EC50 value of compound 3 against MT-1 and MT-2 cell growth showed that compound 3 had the highest activity compared with the other compounds. Compounds 19 and 20 showed moderate activity in the current study. In previous studies, compound 19 showed cytotoxic activity in LOVO cells [32] and compound 20 showed cytotoxic activity in Hela cells and A549 cells [41]. In addition, both compounds have shown inhibition against Herpes Simplex Virus type 2 (HSV-2) [42]. Compounds 26 and 27 had moderate activity; these biflavones have shown anti-cancer properties in medulloblastoma, leukemia, osteosarcoma, colon, lung, neck, prostate, breast, cervical, ovarian, and kidney cancers [43]. Compound 27 inhibited the growth of Daoy and D283 cell lines, and induced G2/M cell cycle arrest in Daoy cells. Moreover, compound 27 reduced the expression of Wnt target genes, including Axin2 and cyclin D1, and inhibited the survival of MB cells [44].

2.4. Apoptosis Analysis

We analyzed the ability of the extracted compounds to induce apoptosis. The following experiments were studied for compound 3 which was the most active and compound 26 which was the most active except for lignans. Annexin V-positive cells were used to investigate the effects of deoxypodophyllotoxin (3) and isoginkgetin (26) on apoptosis. The proportion of annexin V-positive cells after the 72 h treatment with deoxypodophyllotoxin (3) and isoginkgetin (26) is shown in Figure 4 and Figure 5, respectively. The distribution of apoptotic cells, which were located in the upper-right (late apoptotic/dead cells) and lower-right (early apoptotic cells) quadrants, was increased in cells treated with deoxypodophyllotoxin (3) and isoginkgetin (26). The concentration of deoxypodophyllotoxin (3) was changed 2 nM to 10 nM increased the early apoptotic cells from 23.20% to 70.32%, the concentration of isoginkgetin (26) was changed 1.4 µM to 35 µM increased the early apoptotic cells from 24.35% to 55.35%. In the case MT-2 had a similar tendency. Therefore, deoxypodophyllotoxin (3) and isoginkgetin (26) significantly induced apoptosis in MT-1 and MT-2 cells.

3. Materials and Methods

3.1. General Experimental Procedures

The 1H-NMR (600 MHz) and 13C-NMR (150 MHz) spectra were measured in CDCl3 or DMSO-d6 using a JNM-ECZ600R spectrometer (JEOL, Tokyo, Japan) at room temperature, and the chemical shifts given as a δ (ppm) scale with tetramethylsilane (TMS) as the internal standard. The FAB-MS was measured using a JEOL JMS-HX110 mass spectrometer and acquired in a glycerol matrix. HPLC was conducted using a Waters machine equipped with a 1525 binary pump and a 2489 UV/Vis detector (Waters, Massachusetts, USA). Separation was carried out using a Cosmosil 5C18 MS-II column (20.0 mm × 250 mm, ODS, 5 µm; Nacalai Tesque, Kyoto, Japan). Apoptosis analyses were carried out using a Muse Cell Analyzer (Merck KGaA, Darmstadt, Germany).

3.2. Plant Materials

The plant materials used in this study were taken from the medicinal plant garden of Fukuoka University, located in Fukuoka, Japan. Voucher specimens were deposited in the Laboratory of Pharmacognosy of Fukuoka University, Fukuoka, Japan (FUN-0270).

3.3. Extraction and Isolation

The samples were powdered, and the compounds were extracted in accordance with the procedure described in a previous paper [4]. Extraction of the leaves of T. occidentalis (4860 g) was performed with MeOH under reflux. The extract (72.6 g) was initially partitioned using n-hexane and 80% MeOH. The n-hexane phase was subjected to a Diaion HP-20 column using 85% MeOH, 90% MeOH, 95% MeOH, 100% MeOH, and MeOH:acetone (4:1) to obtain fraction (fr.) LH1, LH2, LH3, LH4, and LH5, respectively. The fr. LH1 was subjected to a silica gel column using hexane:acetone (9:1) to obtain fr. LH1-1. The fr. LH1-1 was subjected to a silica gel column using hexane:EtOAc (3:1 and 2:1) to obtain fr. LH1-1-1 and compound 13 (1.9 mg). The fr. LH1-1-1 was subjected to HPLC purification using 55% MeCN to obtain compound 17 (22.0 mg). The fr. LH2 was subjected to a silica gel column using hexane:acetone (30:1, 10:1, and 5:1) to obtain fr. LH2-1, LH2-2, and LH2-3. The fr. LH2-1 was subjected to a silica gel column using hexane to obtain fr. LH2-1-1 and LH2-1-2. The fr. LH2-1-1 was subjected to a silica gel column using hexane:acetone (11:1) to obtain fr. LH2-1-1-1. The fr. LH2-1-1-1 was subjected to HPLC purification using 80% MeCN to obtain compound 21 (13.2 mg) and compound 22 (46.4 mg). The fr. LH2-1-2 was subjected to an ODS column using 60% MeOH to obtain compound 14 (517.0 mg). The fr. LH2-2 was subjected to a silica gel column using hexane:acetone (10:1) to obtain fr. LH2-2-1. The fr. LH2-2-1 was subjected to HPLC purification using 90% MeCN to obtain compound 15 (10.9 mg). The fr. LH2-3 was subjected to a silica gel column using hexane:acetone (4:1 and 3:1) to obtain fr. LH2-3-1 and LH2-3-2, respectively. The fr. LH2-3-1 was subjected to a silica gel column using CHCl3:MeOH (30:1) to obtain fr. LH2-3-1-1. The fr. LH2-3-1-1 was subjected to HPLC purification using 60% MeCN to obtain compound 20 (20.5 mg). The fr. LH2-3-2 was subjected to a silica gel column using CHCl3:MeOH (25:1) to obtain fr. LH2-3-2-1. The fr. LH2-3-2-1 was subjected to HPLC purification using 50% MeCN to obtain compound 16 (18.0 mg). The fr. LH3 was subjected to a silica gel column using hexane:acetone (95:1) to obtain fr. LH3-1. The fr. LH3-1 was subjected to HPLC purification using 80% MeCN to obtain compound 18 (19.8 mg). The fr. LH4 was subjected to a silica gel column using hexane:EtOAC (10:1) and CHCl3:MeOH:H2O (17:3:0.3) to obtain fr. LH4-1 and LH4-2, respectively. The fr. LH4-1 was subjected to a silica gel column using hexane:acetone (50:1) to obtain fr. LH4-1-1. The fr. LH4-1-1 was subjected to HPLC purification using 85% MeCN to obtain compound 11 (13.6 mg). The fr. LH4-2 was subjected to a silica gel column using acetone to obtain compound 32 (18.0 mg). The fr. LH5 was subjected to a silica gel column using hexane:EtOAc (5:1) to obtain fr. LH5-1. The fr. LH5-1 was subjected to a silica gel column using hexane:acetone (10:1) to obtain fr. LH5-1-1. The fr. LH5-1-1 was subjected to HPLC purification using MeOH to obtain compound 31 (26.3 mg).
The 80% MeOH phase was subjected to a Diaion HP-20 column using MeOH, MeOH:acetone (3:2), and acetone to obtain fr. LM1, LM2, LM3, and LM4. The fr. LM1 was subjected to an MCI gel column using 80% MeOH, 90% MeOH, and acetone to obtain fr. LM1-1, LM1-2, and LM1-3, respectively. The fr. LM1-1 was subjected to a silica gel column using hexane:acetone (5:1) to obtain fr. LM1-1-1. The fr. LM1-1-1 was subjected to a silica gel column using hexane:EtOAc (2:1) to obtain fr. LM1-1-1-1. The fr. LM1-1-1-1 was subjected to a silica gel column using CHCl3:MeOH (100:1) to obtain fr. LM1-1-1-1-1. The fr. LM1-1-1-1-1 was subjected to HPLC purification using 40% MeCN to obtain compound 9 (2.5 mg). The fr. LM1-2 was subjected to a silica gel column using hexane:acetone (6:1, 5:1, 3:1, 2:1, and acetone) to obtain fr. LM1-2-1, LM1-2-2, LM1-2-3, LM1-2-4, and LM1-2-5, respectively. The fr. LM1-2-1 was subjected to a silica gel column using CHCl3:MeOH (84:1) to obtain compound 24 (6.2 mg). The fr. LM1-2-2 was subjected to a silica gel column using hexane:acetone (13:2) to obtain fr. LM1-2-2-1. The fr. LM1-2-2-1 was subjected to an ODS column using 77% MeOH to obtain compound 12 (22.0 mg). The fr. LM1-2-3 was subjected to a silica gel column using CHCl3 and CHCl3:MeOH (100:1) to obtain compound 7 (6.7 mg) and fr. LM1-2-3-1, respectively. The fr. LM1-2-3-1 was subjected to HPLC purification using 50% MeCN to obtain compound 8 (5.7 mg). The fr. LM1-2-4 was subjected to a silica gel column using hexane:acetone (2:1) to obtain fr. LM1-2-4-1. The fr. LM1-2-4-1 was subjected to a silica gel column using CHCl3 to obtain fr. LM1-2-4-1-1. The fr. LM1-2-4-1-1 was subjected to HPLC purification using 40% MeCN to obtain compound 23 (4.1 mg). The fr. LM1-2-5 was subjected to a silica gel column using CHCl3:MeOH:H2O (9:1:0.1) to obtain fr. LM1-2-5-1. The fr. LM1-2-5-1 was subjected to an ODS column using 30% MeCN to obtain compound 25 (9.2 mg). The fr. LM1-3 was subjected to HPLC purification using 50% MeCN to obtain compound 27 (45.7 mg) and compound 26 (6.5 mg). The fr. LM2 was subjected to a silica gel column using hexane:EtOAC (3:2) to obtain fr. LM2-1. The fr. LM2-1 was subjected to a silica gel column using hexane:acetone (3:1 and 5:2) to obtain compound 6 (23.9 mg), compound 3 (730 mg), and fr. LM2-1-1. The fr. LM2-1-1 was subjected to HPLC purification using 35% MeCN to obtain compound 4 (2.7 mg) and compound 5 (4.3 mg). The fr. LM3 was subjected to a silica gel column using hexane:EtOAc (1:1) to obtain fr. LM3-1. The fr. LM3-1 was subjected to a silica gel column using CHCl3:MeOH (80:1) to obtain fr. LM3-1-1. The fr. LM3-1-1 was subjected to HPLC purification using 50% MeCN to obtain compound 29 (2.2 mg). The fr. LM4 was subjected to a silica gel column using CHCl3:MeOH (15:1) to obtain fr. LM4-1. The fr. LM4-1 was subjected to HPLC purification using 45% MeCN to obtain compound 30 (4.6 mg).
Extraction of the cones of T. occidentalis (688 g) was performed with MeOH under reflux. The extract (72.6 g) was subjected to a Diaion HP-20 column using 80% MeOH, 100% MeOH, and acetone to obtain fr. C1, C2, and C3, respectively. The fr. C1 was subjected to a silica gel column using CHCl3:MeOH:H2O (9:1:0.1) to obtain fr. C1-1. The fr. C1-1 was subjected to a silica gel column using hexane:acetone (8:1, 7:1, and 2:1) to obtain fr. C1-1-1, C-1-1-2, and C1-1-3, respectively. The fr. C1-1-1 was subjected to HPLC purification using 50% MeCN to obtain compound 9 (3.2 mg). The fr. C1-1-2 was subjected to a silica gel column using CHCl3:MeOH (80:1) to obtain fr. C1-1-2-1. The fr. C1-1-2-1 was subjected to HPLC purification using 50% MeCN to obtain compound 10 (14.0 mg) and compound 19 (3.0 mg). The fr. C1-1-3 was subjected to a silica gel column using hexane:EtOAc (2:3) to obtain fr. C1-1-3-1. The fr. C1-1-3-1 was subjected to HPLC purification using 30% MeCN to obtain compound 2 (2.8 mg). The fr. C2 was subjected to a silica gel column using CHCl3:MeOH (20:1) to obtain fr. C2-1. The fr. C2-1 was subjected to a silica gel column using hexane:acetone (8:1, 6:1, and 4:1) to obtain fr. C2-1-1, C2-1-2, and C2-1-3, respectively. The fr. C2-1-1 was subjected to a silica gel column using hexane:EtOAc (7:2) to obtain fr. C2-1-1-1. The fr. C2-1-1-1 was subjected to HPLC purification using 60% MeCN to obtain compound 20 (9.2 mg). The fr. C2-1-2 was subjected to a silica gel column using CHCl3:MeOH (40:1) to obtain fr. C2-1-2-1. The fr. C2-1-2-1 was subjected to HPLC purification using 55% MeCN to obtain compound 1 (10.5 mg). The fr. C2-1-3 was subjected to a silica gel column using hexane:EtOAc (2:1) to obtain fr. C2-1-3-1. The fr. C2-1-3-1 was subjected to HPLC purification using 40% MeCN to obtain compound 3 (63.0 mg) and compound 6 (16.2 mg). The fr. C3 was subjected to a silica gel column using hexane:EtOAc (1:1) to obtain fr. C3-1. The fr. C3-1 was subjected to a silica gel column using CHCl3:MeOH (25:1) to obtain fr. C3-1-1 and C3-1-2. The fr. C3-1-1 was subjected to HPLC purification using 60% MeCN to obtain compound 29 (3.1 mg) and compound 28 (2.0 mg). The fr. C3-1-2 was subjected to HPLC purification using 45% MeCN to obtain compound 27 (5.3 mg).

3.4. Identification of Compounds

Compounds 1–32 were identified as podophyllotoxin (1) [17], picropodophyllotoxin (2) [17], deoxypodophyllotoxin (3) [18], deoxypicropodophyllotoxin (4) [19], picropodophyllone (5) [20], (−)-yatein (6) [21], podorhizol (7) [22], podorhizol acetate (8) [23], oplopanone (9) [24], oplodiol (10) [25], phytol (11) [26], 7α-hydroxysandaracopimaric acid (12) [18], 7-oxo-epi-pimara-15-en-18-oic acid (13) [27,28], isopimaric acid (14) [29], macrophypene C (15) [30], 7-oxo-epi-pimara-8,15-dien-19-oic acid (16) [28], 7-oxo-epi-pimara-15-ene-18-oic acid methyl ester (17) [28], 4-epi-dehydroabietinol (18) [31], 8,11,13-abietatriene-7α, 18-diol (19) [32], 7-oxodehydroabietinol (20) [33], ferruginol (21) [34], (+)-totarol (22) [35], E-communic acid (23) [18], (+)-cupressic acid (24) [36], amentoflavone (25) [37], isoginkgetin (26) [37], ginkgetin (27) [37], 7,4′,4′″-trimethyl-amentoflavone (28) [38], 7,4′,7″- trimethyl-amentoflavone (29) [38], hinokiflavone (30) [37], β-sitosterol (31) [39], and β-sitosterol glycoside (32) [40], respectively, based on the comparison of their physical data with those reported in the literature (Tables S1–S5).

3.5. Cell Culture

Two HTLV-1-infected T-cell lines, MT-1 and MT-2, were kindly provided by Dr Isao Miyoshi of Kochi University in Nankoku, Japan. Culture conditions were as previously described [5]. The cells were cultured in RPMI-1640 medium with L-glutamine and sodium bicarbonate containing 15% fetal bovine serum (Biowest, Nuaille, France) and 1% kanamycin. Cells were cultured at 37 °C in humidified 5% CO2/95% air.

3.6. Measurement of Anti-Proliferative Effects against MT-1 and MT-2 Cells

Viability was determined using the MTT assay. The MT-1 and MT-2 cells were maintained in RPMI-1640 medium containing fetal bovine serum (15%). A 50-μL aliquot of the cell suspension (5000 cells per well) and 50 μL of the test sample solution or suspension were plated in flat-bottomed microtiter wells (extract final concentration: 100, 10, 1, 0.1 μg/mL, and control; compound final concentration: between 10 pg/mL and 100 μg/mL, and control) and incubated for 72 h at 37 °C in a humidified atmosphere containing 5% CO2. After cultivation, 10 μL of 3-(4,5)-dimethyl-2-thiazoyl-2,5-diphenyl-2H-tetrazolium bromide (MTT reagent) solution was added to the microtiter wells. After incubation for 4 h at 37 °C, 100 μL of isopropanol was added to solubilize the MTT-formazan product. The absorbance at 450 nm was measured with a microplate reader.

3.7. Apoptosis Analysis

Detection of apoptosis was performed using The Muse Annexin V & Dead Cell Assay Kit (Merck, Darmstadt, Germany) according to the manufacturer’s protocol. MT-1 and MT-2 cells incubated in the presence or absence of compound 3 and 26 for 72 h were collected by centrifugation (310× g at 4 °C for 10 min), suspended in 100 μL of RPMI 1640 medium, and incubated with 100 μL of Annexin V reagent at room temperature for 20 min. Cells were measured by a Muse Cell Analyzer (Merck, Darmstadt, Germany).

4. Conclusions

In conclusion, as part of our investigations of Cupressaceae plants, extracts of T. occidentalis showed potent inhibitory effects against MT-1 and MT-2 cell lines. We isolated 32 compounds (eight lignans, 18 terpenoids, and six flavonoids) from the extract and examined their structure–activity relationships. Almost all of the isolated lignans inhibited the growth of both tumor cell lines. Several diterpene compounds had moderate activity, of which some have been previously reported to exhibit cytotoxicity in cancer cells. Moreover, several flavonoids showed moderate activity; some of these biflavones have been reported to show anti-cancer properties in some cancers and may induce cell cycle arrest, and inhibitory activities against amyloid-β peptide 42 cytotoxicity in PC-12 cells [45]. We continue to search the biflavone and components of other Cupressaceae plants. We also demonstrated that deoxypodophyllotoxin (3) and isoginkgetin (26) enhanced apoptosis. Therefore, not only lignans but also diterpenes and/or biflavones may be promising candidates for the treatment of ATL.

Supplementary Materials

The following are available online, contain 13C-NMR data of compounds (Table S1: 13C-NMR spectroscopic (CDCl3) of compounds 1–8. Table S2: 13C-NMR spectroscopic (CDCl3) of compounds 9–11. Table S3: 13C-NMR spectroscopic (CDCl3) of compounds 12–24. Table S4: 13C-NMR spectroscopic (DMSO-d6) of compounds 25–30. Table S5: 13C-NMR spectroscopic (CDCl3) of compounds 31 and 32.)

Author Contributions

Conceptualization, J.K., K.I. and K.T.; methodology, J.K. and D.N.; formal analysis, D.N., M.I. and R.T.; investigation, D.N. and M.I.; resources, M.O.; data curation, D.N. and M.I.; writing—original draft preparation, D.N.; writing—review and editing, J.K., M.O., R.T. and K.I.; visualization, D.N. and M.I.; supervision, J.K., M.O. and K.I.; project administration, J.K. All authors have read and agreed to the published version of the manuscript.

Funding

This work was supported by Japan Society for the Promotion of Science JSPS KAKENHI Grant Number JP19K16403.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Acknowledgments

We thank Georgia Lenihan-Geels, from Edanz (https://jp.edanz.com/ac, last accessed on 15 December 2021) for editing a draft of this manuscript.

Conflicts of Interest

The authors declare no conflict of interest.

Sample Availability

Samples of the compounds are not available from the authors.

References

  1. Ishitsuka, K.; Tamura, K. Treatment of adult T-cell leukemia/lymphoma: Past, present, and future. Eur. J. Haematol. 2008, 80, 185–196. [Google Scholar] [CrossRef] [PubMed]
  2. Miyoshi, I.; Kubonishi, I.; Sumida, M.; Hiraki, S.; Tsubota, T.; Kimura, I.; Miyamoto, K.; Sato, J. A novel T-cell line derived from adult T-cell leukemia. GANN Jpn. J. Cancer Res. 1980, 71, 155–156. [Google Scholar]
  3. Miyoshi, I.; Kubonishi, I.; Yoshimoto, S.; Akagi, T.; Ohtsuki, Y.; Shiraishi, Y.; Nagata, K.; Hinuma, Y. Type C virus particles in a cord T-cell line derived by cocultivating normal human cord leukocytes and human leukaemic T cells. Nature 1981, 294, 770–771. [Google Scholar] [CrossRef] [PubMed]
  4. Kinjo, J.; Nakano, D.; Fujioka, T.; Okabe, H. Screening of promising chemotherapeutic candidates from plants extracts. J. Nat. Med. 2016, 70, 335–360. [Google Scholar] [CrossRef] [Green Version]
  5. Nakano, D.; Ishitsuka, K.; Hatsuse, T.; Tsuchihashi, R.; Okawa, M.; Okabe, H.; Tamura, K.; Kinjo, J. Screening of promising chemotherapeutic candidates against human adult T-cell leukemia/lymphoma from plants: Active principles structure–activity relationships with withanolides. J. Nat. Med. 2011, 65, 559–567. [Google Scholar] [CrossRef]
  6. Nakano, D.; Ishitsuka, K.; Katsuya, H.; Kunami, N.; Nogami, R.; Yoshimura, Y.; Matsuda, M.; Kamikawa, M.; Tsuchihashi, R.; Okawa, M.; et al. Screening of promising chemotherapeutic candidates from plants against human adult T-cell leukemia/lymphoma (II): Apoptosis of antiproliferactive principle (24,25-dihydrowithanolide D) against ATL cell lines and structure–activity relationships with withanolides isolated from solanaceous plants. J. Nat. Med. 2012, 66, 415–420. [Google Scholar]
  7. Nakano, D.; Ishitsuka, K.; Takashima, M.; Arima, R.; Satou, A.; Tsuchihashi, R.; Okawa, M.T.; Tamura, K.; Kinjo, J. Screening of promising chemotherapeutic candidates from plants against human adult T-cell leukemia/lymphoma (VI): Cardenolides from Asclepias curassavica. Biol. Pharm. Bull. 2020, 43, 1609–1614. [Google Scholar] [CrossRef]
  8. Nakano, D.; Ishitsuka, K.; Kamikawa, M.; Matsuda, M.; Tsuchihashi, R.; Okawa, M.; Okabe, H.; Tamura, K.; Kinjo, J. Screening of promising chemotherapeutic candidates from plants against human adult T-cell leukemia/lymphoma (III). J. Nat. Med. 2013, 67, 894–903. [Google Scholar] [CrossRef] [PubMed]
  9. Nakano, D.; Ishitsuka, K.; Mizuki, I.; Tsuchihashi, R.; Okawa, M.; Okabe, H.; Tamura, K.; Kinjo, J. Screening of promising chemotherapeutic candidates from plants against human adult T-cell leukemia/lymphoma (IV): Phenanthroindolizidine alkaloids from Tylophora tanakae leaves. J. Nat. Med. 2015, 69, 397–401. [Google Scholar] [CrossRef]
  10. Nakano, D.; Ishitsuka, K.; Matsuda, N.; Kouguchi, A.; Tsuchihashi, R.; Okawa, M.; Okabe, H.; Tamura, K.; Kinjo, J. Screening of promising chemotherapeutic candidates from plants against human adult T-cell leukemia/lymphoma (V): Coumarins and alkaloids from Boenninghausenia japonica and Ruta graveolens. J. Nat. Med. 2017, 71, 170–180. [Google Scholar] [CrossRef]
  11. Alves, L.D.S.; Figueiredo, C.B.M.; Silva, C.C.A.R.; Marques, G.S.; Ferreira, P.A.; Soares, M.F.R.; Silva, R.M.F.; Rolim-Neto, P.J. Thuja occidentalis L. (Cupressaceae): Review of botanical, phytochemical, pharmacological and toxicological aspects. Int. J. Pharm. Sci. Res. 2014, 5, 1163–1177. [Google Scholar]
  12. Chang, L.C.; Song, L.L.; Park, E.J.; Luyengi, L.; Lee, K.J.; Farnsworth, N.R.; Pezzuto, J.M.; Kinghorn, A.D. Bioactive constituents of Thuja occidentalis. J. Nat. Prod. 2000, 63, 1235–1238. [Google Scholar] [CrossRef]
  13. Sonia, C.; Alina, C.; Neli, K.O.; Ioan, D.; Anca, H.; Coralia, C. Thuja occidentalis L. (Cupressaceae): Ethnobotany, phytochemistry and biological activity. Molecules 2020, 25, 5416. [Google Scholar]
  14. Pudełek, M.; Catapano, J.; Kochanowski, P.; Mrowiec, K.; Janik-Olchawa, N.; Czyz, J.; Ryszawy, D. Therapeutic potential of monoterpene α-thujone, the main compound of Thuja occidentalis L. essential oil, against malignant glioblastoma multiforme cells in vitro. Fitoterapia 2019, 134, 172–181. [Google Scholar] [CrossRef]
  15. Torres, A.; Vargas, Y.; Uribe, D.; Carrasco, C.; Torres, C.; Rocha, R.; Oyarzun, C.; Martin, R.S.; Quezada, C. Pro-apoptotic and anti-angiogenic properties of the α/β-thujone fraction from Thuja occidentalis on glioblastoma cells. J. Neurooncol. 2016, 128, 9–19. [Google Scholar] [CrossRef] [PubMed]
  16. Silva, I.S.; Nicolau, L.A.D.; Sousa, F.B.M.; de Araújo, S.; Oliveira, A.P.; Araújo, T.S.L.; Souza, L.K.M.; Martins, C.S.; Aquino, P.E.A.; Carvalho, L.L.; et al. Evaluation of anti-inflammatory potential of aqueous extract and polysaccharide fraction of Thuja occidentalis Linn. in mice. Int. J. Biol. Macromol. 2017, 105, 1105–1116. [Google Scholar] [CrossRef] [PubMed]
  17. Zhao, L.; Tian, X.; Fan, P.C.; Zhan, Y.J.; Shen, D.W.; Jin, Y. Separation, determination and identification of the diastereoisomers of podophyllotoxin and its esters by high-performance liquid chromatography/tandem mass spectrometry. J. Chromatogr. A 2008, 1210, 168–177. [Google Scholar] [CrossRef]
  18. Muto, N.; Tomokuni, T.; Haramoto, M.; Takemoto, H.; Nakanishi, T.; Inatomi, Y.; Murata, H.; Inada, A. Isolation of apoptosis- and differentiation- inducing substances toward human promyelocytic leukemia HL-60 cells from leaves of Juniperus taxifolia. Biosci. Biotechnol. Biochem. 2008, 72, 477–484. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  19. San Feliciano, A.; Medarde, M.; Lopes, J.L.; Puebla, P.; Miguel del Corral, J.M.; Barrero, A.F. Lignans from Juniperus thurifera. Phytochemistry 1989, 28, 2863–2866. [Google Scholar] [CrossRef]
  20. Lei, M.; Hu, R.J.; Wang, Y.G. Mild and selective oxidation of alcohols to aldehydes and ketones using NaIO4/TEMPO/NaBr system under acidic conditions. Tetrahedron 2006, 62, 8928–8932. [Google Scholar] [CrossRef]
  21. Tomioka, K.; Ishiguro, T.; Koga, K. Stereoselective reactions. X. total synthesis of optically pure antitumor lignans, bursran. Chem. Pharm. Bull. 1985, 33, 4333–4337. [Google Scholar] [CrossRef] [Green Version]
  22. Giordano, T.; Marcelo, F.A.; Fernando, C. Diastereoselective synthesis of b-piperonyl-γ-butyrolactones from morita-baylis-hillman adducts. Highly efficient synthesis of (±)-yatein, (±)-podorhizol and (±)-epi-podorhizol. J. Braz. Chem. Soc. 2010, 21, 2327–2339. [Google Scholar]
  23. San Feliciano, A.; Miguel del Corral, J.M.; Gordaliza, M.; Castro, A. Lignans from Juniperus sabina. Phytochemistry 1990, 29, 1335–1338. [Google Scholar] [CrossRef]
  24. Su, W.C.; Fang, J.M.; Cheng, Y.S. Sesquiterpenes from leaves of Cryptomeria japonica. Phytochemistry 1995, 39, 603–607. [Google Scholar]
  25. Jung, K.Y.; Kim, D.S.; Oh, S.R.; Lee, I.S.; Lee, J.J.; Lee, H.K.; Shin, D.H.; Kim, E.H.; Cheong, C.J. Sesquiterpene components from the flower buds og Magnolia fargesii. Arch. Pharm. Res. 1997, 20, 363–367. [Google Scholar] [CrossRef]
  26. Goodman, R.A.; Oldfield, E.; Allerhand, A. Assignments in the natural-abundance carbon-13 nuclear magnetic resonance spectrum of chlorophyll and a study of segmental motion in neat phytol. J. Am. Chem. Soc. 1973, 95, 7553–7558. [Google Scholar] [CrossRef]
  27. Werner, H.; Palaniappan, K. Ent-pimaranes, ent-kauranes, heliangolides and other constituents of three Helianthus species. Phytochemistry 1984, 23, 1453–1459. [Google Scholar]
  28. Urones, J.G.; Marcos, I.S.; Ferreras, J.F.; Barcala, P.B. Terpenoids from Nepta tuberosa subsp. Reticulata (II). Phytochemistry 1988, 27, 523–526. [Google Scholar] [CrossRef]
  29. Sakar, M.K.; Er, N.; Ercil, D.; Olmo, E.D.; San Feliciano, A. (−)-Desoxypodophyllotoxin and diterpenoids from juniperus nana willd. berries. Acta. Pharm. Turc. 2002, 44, 213–219. [Google Scholar]
  30. Xu, J.; Sun, Y.; Wang, M.; Ren, Q.; Li, S.; Wang, H.; Sun, X.; Jin, D.-Q.; Sun, H.; Ohizumi, Y.; et al. Bioactive diterpenoids from the leaves of Callicarpa macrophylla. J. Nat. Prod. 2015, 78, 1563–1569. [Google Scholar] [CrossRef]
  31. Fraga, M.F.; Hernandez, M.G.; Artega, J.M.; Suarez, S. The microbiological transformation of the diterpenes dehydroabietanol and teideadiol by Mucor plumbeus. Phytochemistry 2003, 63, 663–668. [Google Scholar] [CrossRef]
  32. Yang, X.W.; Feng, L.; Li, S.M.; Liu, X.H.; Li, Y.L.; Wu, L.; Shen, Y.H.; Tian, J.M.; Zhang, X.; Liu, X.R.; et al. Isolation, structure, and bioactivities of abiesadines A-Y, 25 new diterpenes from Abies georgei Orr. Bioorg. Med. Chem. 2010, 18, 744–754. [Google Scholar] [CrossRef]
  33. Tanaka, R.; Ohtsu, H.; Matsunaga, S. Abietane diterpene acids and other constituents from the leaves of Larix kaempferi. Phytochemistry 1997, 46, 1051–1057. [Google Scholar] [CrossRef]
  34. Ryu, Y.B.; Jeong, H.J.; Kim, J.H.; Kim, Y.M.; Park, J.Y.; Kim, D.; Naguyen, T.T.H.; Park, S.J.; Chang, J.S.; Park, K.H.; et al. Biflavonoids from Torreya nucifera displaying SARS-CoV 3CLpro inhibition. Bioorg. Med. Chem. 2010, 18, 7940–7947. [Google Scholar] [CrossRef] [PubMed]
  35. Marcos, L.S.; Cubillo, M.A.; Moro, R.F.; Diez, D.; Basabe, P.; Sanz, F.; Urones, J.G. Synthesis of (+)-totarol. Tetrahedron Lett. 2003, 44, 8831–8835. [Google Scholar] [CrossRef]
  36. Liu, C.M.; Zhou, H.B.; Zhang, W.D. terpenoids from stems and leaves of Cupressus gigantea. Chin. J. Nat. Med. 2010, 8, 405–410. [Google Scholar] [CrossRef]
  37. Markham, K.R.; Sheppard, C.; Geiger, H. 13C NMR studies of some naturally occurring amentoflavone and hinokiflavone bioflavonoids. Phytochemstry 1987, 26, 3335–3337. [Google Scholar] [CrossRef]
  38. Fonseca, F.N.; Ferreira, A.J.S.; Sartorelli, P.; Lopes, N.P.; Floh, E.I.S.; Handro, W.; Kato, M.J. Phenylpropanoid derivatives and biflavones at different stages of differentiation and development of Araucaria angustifolia. Phytochemistry 2000, 55, 575–580. [Google Scholar] [CrossRef]
  39. Nono, R.N.; Barboni, L.; Teponno, R.B.; Quassinti, L.; Bramucci, M.; Vitali, L.A.; Petrelli, D.; Lupidi, G.; Tapondjou, A.L. Antimicrobial, antioxidant, anti-inflammatory activities and phytoconstituents of extracts from the roots of Dissotis thollonii Cogn.(Melastomataceae). S. Afr. J. Bot. 2014, 93, 19–26. [Google Scholar] [CrossRef]
  40. Shaheen, F.; Muhanmmad, A.; Rubeena, S.; Irfanullah; Sarah, B. Spectral assignments and reference data. Magn. Reson. Chem. 2001, 39, 399–405. [Google Scholar]
  41. Moujir, L.M.; Seca, A.M.L.; Araujo, L.; Silva, A.M.S.; Barreto, M.C. A new natural spiro heterocyclic compound and the cytotoxic activity of the secondary metabolites from Juniperus brevifolia leaves. Fitoterapia 2011, 82, 225–229. [Google Scholar] [CrossRef] [PubMed]
  42. Lee, S.A.G.; Liliana, A.B.G.; Miguel, A.G. Anti HHV-1 and HHV-2 activity in vitro of abietic and dehydroabietic acid derivatives. Pharmacologyonline 2012, 1, 36–42. [Google Scholar]
  43. Muhammad, A.; Azhar, R.; Ghulam, H.; Muhammad, A.S.; Muhammad, K.Z.; Haseeb, A.; Iqra, S.; Ammara, R.; Maleeha, M.; Sevki, A.; et al. Ginkgetin: A natural biflavone with versatile pharmacological activities. Food. Chem. Toxicol. 2020, 145, 111642. [Google Scholar]
  44. Ye, Z.N.; Yu, M.Y.; Kong, L.M.; Wang, W.H.; Yang, Y.F.; Liu, J.Q.; Qiu, M.H.; Li, Y. Biflavone ginkgetin, a novel wnt inhibitor, suppresses the growth of medulloblastoma. Nat. Prod. Bioprospect. 2015, 5, 91–97. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  45. Sasaki, H.; Kitoh, Y.; Tsukada, M.; Miki, K.; Koyama, K.; Juliawaty, L.D.; Hakim, E.H.; Takahashi, K.; Kinoshita, K. Inhibitory activities of bioflavonoids against amyloid-b peptide 42 cytotoxicity in PC-12 cells. Bioorganic Med. Chem. Lett. 2015, 25, 2831–2833. [Google Scholar] [CrossRef] [PubMed]
Molecules 26 07619 g001 550
Figure 1. Compounds from T. occidentalis.
Figure 1. Compounds from T. occidentalis.
Molecules 26 07619 g001
Molecules 26 07619 g002 550
Figure 2. Structure–activity relationships of lignans.
Figure 2. Structure–activity relationships of lignans.
Molecules 26 07619 g002
Molecules 26 07619 g003 550
Figure 3. Structure–activity relationships of diterpenoids.
Figure 3. Structure–activity relationships of diterpenoids.
Molecules 26 07619 g003
Molecules 26 07619 g004 550
Figure 4. Deoxypodophyllotoxin (3) induced cell apoptosis in MT-1 and MT-2 cells.
Figure 4. Deoxypodophyllotoxin (3) induced cell apoptosis in MT-1 and MT-2 cells.
Molecules 26 07619 g004
Molecules 26 07619 g005 550
Figure 5. Isoginkgetin (26) induced cell apoptosis in MT-1 and MT-2 cells.
Figure 5. Isoginkgetin (26) induced cell apoptosis in MT-1 and MT-2 cells.
Molecules 26 07619 g005
Table
Table 1. Anti-proliferative activities of the tested plant extracts.
Table 1. Anti-proliferative activities of the tested plant extracts.
FamilyScientific NamePartsEC50 (µg/mL)
MT-1MT-2
CupressaceaeBiota orientalisLeaves>100>100
Stems>100>100
Juniperus chinensis var. kaizuka HortLeaves43.461.1
Stems18.110.8
Juniperus rigidaLeaves14.013.2
Stems>100>100
Thuja occidentalisLeaves1.651.38
Stems5.514.21
Cones1.740.50
Thujopsis dolabrataAerial parts2.400.76
The presented data are the mean of three independent experiments.
Table
Table 2. Anti-proliferative activity of compounds 1–32, doxorubicin, and etoposide standards (EC50).
Table 2. Anti-proliferative activity of compounds 1–32, doxorubicin, and etoposide standards (EC50).
CompoundEC50 (µM)
MT-1MT-2
10.1150.134
20.9701.3
30.00580.0033
40.200.12
543.716.5
60.7500.675
79.467.98
80.6110.175
9>476>476
10109118
1163.9125
12174200
13>314>314
1412164.9
15>301172
16142133
17>301>301
18109.530.49
1925.819.2
2017.722.3
21103125
2211930.0
2374.6140.9
24228109
2588.1135.8
265.262.45
277.075.78
28>172>172
29>172>172
308.979.78
31>234>234
32>169>169
doxorubicin0.0150.013
etoposide0.0510.065
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Nakano, D.; Ishitsuka, K.; Ishihara, M.; Tsuchihashi, R.; Okawa, M.; Tamura, K.; Kinjo, J. Screening of Promising Chemotherapeutic Candidates from Plants against Human Adult T-Cell Leukemia/Lymphoma (VII): Active Principles from Thuja occidentalis L. Molecules 2021, 26, 7619. https://doi.org/10.3390/molecules26247619

AMA Style

Nakano D, Ishitsuka K, Ishihara M, Tsuchihashi R, Okawa M, Tamura K, Kinjo J. Screening of Promising Chemotherapeutic Candidates from Plants against Human Adult T-Cell Leukemia/Lymphoma (VII): Active Principles from Thuja occidentalis L. Molecules. 2021; 26(24):7619. https://doi.org/10.3390/molecules26247619

Chicago/Turabian Style

Nakano, Daisuke, Kenji Ishitsuka, Madoka Ishihara, Ryota Tsuchihashi, Masafumi Okawa, Kazuo Tamura, and Junei Kinjo. 2021. "Screening of Promising Chemotherapeutic Candidates from Plants against Human Adult T-Cell Leukemia/Lymphoma (VII): Active Principles from Thuja occidentalis L." Molecules 26, no. 24: 7619. https://doi.org/10.3390/molecules26247619

APA Style

Nakano, D., Ishitsuka, K., Ishihara, M., Tsuchihashi, R., Okawa, M., Tamura, K., & Kinjo, J. (2021). Screening of Promising Chemotherapeutic Candidates from Plants against Human Adult T-Cell Leukemia/Lymphoma (VII): Active Principles from Thuja occidentalis L. Molecules, 26(24), 7619. https://doi.org/10.3390/molecules26247619

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