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Review

Seaweed Secondary Metabolites In Vitro and In Vivo Anticancer Activity

by
Djenisa H. A. Rocha
1,
Ana M. L. Seca
1,2 and
Diana C. G. A. Pinto
1,*
1
Department of Chemistry & QOPNA-Organic Chemistry, Natural Products and Food Stuffs, University of Aveiro, Campus de Santiago, 3810-193 Aveiro, Portugal
2
cE3c-Centre for Ecology, Evolution and Environmental Changes, Azorean Biodiversity Group & Faculty of Sciences and Technology, University of Azores, Rua Mãe de Deus, 9501-321 Ponta Delgada, Portugal
*
Author to whom correspondence should be addressed.
Mar. Drugs 2018, 16(11), 410; https://doi.org/10.3390/md16110410
Submission received: 14 October 2018 / Revised: 22 October 2018 / Accepted: 23 October 2018 / Published: 26 October 2018
(This article belongs to the Special Issue Discovery and Application of Macroalgae-Derived Natural Products)
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Abstract

:
Isolation, finding or discovery of novel anticancer agents is very important for cancer treatment, and seaweeds are one of the largest producers of chemically active metabolites with valuable cytotoxic properties, and therefore can be used as new chemotherapeutic agents or source of inspiration to develop new ones. Identification of the more potent and selective anticancer components isolated from brown, green and red seaweeds, as well as studies of their mode of action is very attractive and constitute a small but relevant progress for pharmacological applications. Several researchers have carried out in vitro and in vivo studies in various cell lines and have disclosed the active metabolites among the terpenoids, including carotenoids, polyphenols and alkaloids that can be found in seaweeds. In this review the type of metabolites and their cytotoxic or antiproliferative effects will be discussed additionally their mode of action, structure-activity relationship and selectivity will also be revealed. The diterpene dictyolactone, the sterol cholest-5-en-3β,7α-diol and the halogenated monoterpene halomon are among the reported compounds, the ones that present sub-micromolar cytotoxicity. Additionally, one dimeric sesquiterpene of the cyclolaurane-type, three bromophenols and one halogenated monoterpene should be emphasized because they exhibit half maximal inhibitory concentration (IC50) values between 1–5 µM against several cell lines.

Graphical Abstract

1. Introduction

Cancer is one of the deadliest diseases, and its influence on European and USA mortality is 20% and 14% respectively [1]. It is estimated that in 2018 the numbers will reach values of 18 million new cases and 10 million deaths [1] and it is expected that, in the near future, this numbers will increase [2]. Lung cancer is the most common, both in terms of incidence and mortality, followed by female breast and colorectal cancers. These types of cancers account, each, for nearly 2 million diagnoses in 2018 [1,3]. The top three more frequent cancers diagnosed in women are the breast, lung and colorectal cancers [3], being the lung cancer responsible for more deaths. Whereas in men lung cancer is also the leading cause of death and the more frequent cancer diagnosed, followed by prostate and colorectal cancers [1].
Although significant advances are being made, fully effective cancer therapy is a far way from being achieved [4,5,6]. The cancer heterogeneity [7], and the development of resistance to anticancer drugs [8] constitute one of the major problems to be overcome. In fact, the treatment of cancer usually comprises a combination of therapies, in accordance with the characteristics and stage of the tumor, including surgery, radio and/or chemotherapy and most recently immunotherapy [9,10,11]. Thus, currently, the development of drugs for a specific cancer-related target, combined with an effective understanding of the drug relationship with human tumor biology became the key in the effort to cure cancer [12].
One of the main sources of drugs are natural compounds, which have demonstrated considerable potential in the cancer therapy [13,14]. In fact, at least one-third of the current top twenty drugs are derived from natural sources, including plants and marine species, and among the 175 small molecules approved to treat cancer, 49% are either natural compounds or directly derived therefrom [15].
Seaweeds or macroalgae are photosynthetic organisms that play a key role in ocean biodiversity and productivity and comprise green algae (Chlorophyta), brown algae (Phaeophyta) and red algae (Rhodophyta). Furthermore, seaweeds are also a source of unique secondary metabolites that showed very interesting bioactivities [16,17,18,19,20]. Due to its nutritional value, seaweeds have also been used as food in many countries of East Asia (Japan, Korea, and China) and in the Celtic cultures of Europe (Ireland, Scotland and Brittany), and used as additive in cosmetic and food industries [21,22].
In the last two decades, seaweed chemical profiles have demonstrated that they are rich in terpenoids, alkaloids, polyphenols, steroids, pigments and polysaccharides and some biological assays showed that several of these metabolites have promising pharmacological activities [23,24,25,26] including in cancer therapy [27,28,29].
This review aims to highlight the secondary metabolites isolated from seaweeds with the highest cytotoxic/antiproliferative activity. Their activity level, chemical structures, putative mechanisms of action will be discussed. Moreover, the reported in vivo studies will be emphasized. It is important to highlight that this is not an exhaustive review but rather an author’s selection, where the compounds whose biological activity and mechanism of action suggest that they have significant therapeutic potential. Thus, the discussed and cited studies involve seaweed secondary metabolites exhibiting cytotoxic activities lower than 15 µM. Exceptions can also be mentioned if they are rare cases or the mechanism of action is elucidated.

2. Secondary Metabolites from Seaweeds with in Vitro Cytotoxic Activity

2.1. Mono-, Sesqui-, Diterpenes and Sterols

Epidemiological and experimental studies suggest that terpenoids may be helpful to curb the growth of a variety of cancer cells, including mammary, skin, lung, forestomach, colon, pancreatic and prostate carcinomas cells and open more opportunities for cancer therapy [30,31].
The search for anticancer terpenoids from seaweeds in the last 30 years resulted in a significant number of compounds with relevant cytotoxic activity against a large number of cancer cell lines, highlighted on Table 1 and whose chemical structures are presented in Figure 1.
From the 33 compounds shown in Table 1, 19 were isolated from brown seaweeds, whereas the remaining were isolated from red seaweeds. One third exhibit moderate activity (10 μM < IC50 <15 μM) against the cancer cell lines tested, while nearly 20 compounds exhibit significant cytotoxic activity, with IC50 values between 1 and 10 μM, at least against one of the cancer cell line tested. Among the latter, compounds 20 (laurebiphenyl) and 31 [(1E,5E,7E)-3,4-erythro-1-bromo--7-dichromethyl-3-methyl-3,4,8-trichlorooctatriene] can be emphasized, as they exhibit IC50 values between 1–5 µM (Table 1).
The detailed analysis of the results compiled in Table 1 allowed choosing compound 22 (cholest-5-en-3β,7α-diol) as the most interesting one, due to the lower IC50 values (<0.5 μM) against several cell lines. Additionally, also exhibited significant activity (IC50 values 5–9 µM) against gastric and colon cancer lines. Compounds 11 (dictyolactone) and 33 (halomon) also should be highlighted due to their strong activity (IC50 = 0.99 and 0.92 µM, respectively) against human non-small cell lung carcinoma cells (NSCLCN6-L16) and colon cancer cell line (HCT-116).
Unfortunately, very few compounds (only 6 out of 33) were subjected to selectivity studies and the more active ones, mentioned above, are not included in this lot. Debromoplysinol (23) and isoaplysin (24) are the most selective compounds, exhibiting cancer cell selectivity index of 4.1 and 3.8, respectively, which means nearly four times more selective to the prostate carcinoma cells than to mammary epithelial no-tumoral cells.
The results obtained in cytotoxic evaluations of hydroazulene skeleton type diterpenes isolated from the marine brown alga Polycladia myrica (S.G. Gmelin) Draima, Ballesteros, F. Rousseau & T. Thibaut (syn. Cystoseira myrica (S.G. Gmelin) C. Agardh), where compounds 1–3 (Figure 1) were included, suggest that the presence of free hydroxyl groups is irrelevant [32].
Cytotoxicity of several meroditerpenes in different phases of the HeLa cell line growth cycle conducted by Gouveia et al. demonstrated that the HeLa cell line in log phase is 3.6 times more sensitive to cystoazorol A 4 than in lag phase [34]. Moreover, compound 4 showed a selectivity index higher than taxol, compound used as a positive control in the study [34].
From the Mediterranean brown algae Dilophus ligulatus (Kützing) Feldmann, which is the second genus that provides more compounds with interesting cytotoxic activity, can be emphasized the diterpenoids 5–11 that exhibit IC50 values lower than 15 µM (Table 1). For example, murine leukemia cells (P-388) and P-388 doxorubicin resistant cell lines exhibit similar sensitivity (IC50 = 3.64 to 13.3 µM and IC50 = 5.95 to 12.9 µM, respectively) to diterpenes 6–9 and 11 [35]. Furthermore, compounds 6–11 exhibit higher cytotoxic activity against NSCLCN6-L16 (IC50 0.99–6.85 μM) than mercaptopurine (IC50 6.57–19.7 μM), an effective anticancer drug used as positive control [35].
Both flabellinol 13 and flabellinone 14 (Figure 1), two polycyclic diterpenoids fused to an oxidized ring and biosynthetically related, were cytotoxic against NCI-H460 (IC50 9 and 14 μM, respectively). The action mechanism is related with their ability to block the sodium channel activity [37]. From the brown algae Taonia atomaria (Woodward) J. Agardh collected in Central Aegean Sea were isolated two cyclic meroditerpenoids, atomarianone A 15 and atomarianone B 16, that are epimers at C-7 and both are analogues of flabellinone 14 (Figure 1). The different relative configuration at C-10 suggests that they are formed in a different diterpene cyclization pathway, nevertheless both exhibit significant cytotoxicity against two different lung cancer cell lines (Table 1) [38].
The antiproliferative properties of six meroditerpenoids were evaluated against human and non-human cancer cell lines and against no-tumoral cell line by Pereira et al. [39]. Epitaondiol 17 and stypotriol triacetate 18 (Figure 1) were the most active compounds, being the thrice-cloned neuroblastoma SH-SY5Y the most susceptible cell line tested (IC50 12.2 and 14 µM, respectively), though much less active than vincristine (IC50 = 0.03 µM) used as positive control [39]. Furthermore, compounds 17 and 18 have lower selective index than other compounds tested, once at 25 µM have more than 50% of proliferation inhibition on non-cancer Chinese hamster fibroblasts cell line (V79) [39].
The red alga of the genus Laurencia is collected in different parts of the world, but typically inhabit tropical oceans and are recognized for the biosynthesis of a high diversity of secondary metabolites, especially terpenoids mainly sesquiterpenoids, sterols and acetogennins. Some of these metabolites exhibit important pharmacological effects, from which cytotoxic can be highlighted [54,55,56]. From the compounds indicated in Table 1, five (20–24) were isolated from Laurencia species, the third genus with more compounds presented in Table 1 (after the genera Plocamium and Dilophus). Among the compounds isolated, the most active one is cholest-5-en-3β,7α-diol 22, the ones with the broadest action spectrum are laurebiphenyl 20, cholest-5-en-3β,7α-diol 22 and debromoaplysinol 23, and the most selective one is debromoaplysinol 23 (Table 1).
Isoaplysin 24 and debromoaplysinol 23 are two sesquiterpenes that differ in the presence of the C3a-hydroxymethyl instead of the C3a-bromomethyl moiety (Figure 1). Compound 23 displays enhanced selectivity and broad spectrum cytotoxicity relative to 24 which, according to the authors, suggests that the hydroxyl group could play a significant role in the cytotoxicity of this class of compounds [45]. However, these compounds also have different configuration around the C3 and C8b chiral centers and that could explain the activity displayed. In fact, it is also observed that the stereochemistry of the C8b chiral center can play an important role in the drug-ligand interactions. This is well demonstrated by the strong activity of debromoaplysinol 23 when compared with debromoepiaplysinol 21 (Figure 1, Table 1). Compound 21 was tested against 5 cancer cell lines (lung, hepatic, cervix, gastric and ileum cancer cell lines) and shown to be much less active (IC50 values greater than 15 µM) than compound 23 [44].
Plocamium is the genus with greater representativeness in Table 1 (8 secondary metabolites). The six halogenated monoterpenes 25–30 (Figure 1) isolated from the red macroalga Plocamium suhrii Kützing collected near Port Elizabeth, South Africa, showed great cytotoxicity (IC50 < 10 µM) against esophageal cancer cell line (WHCO1), even higher than the well-known clinical anticancer drug cisplatin (IC50 = 13 µM) [47]. Moreover, the low variation of the cytotoxicity level of compounds 25–30 against WHCO1 cell line (IC50 = 6.6 to 9.9 µM) shows that the C1 double bond configuration (comparing compound 25 and 27), the C4 chiral center configuration (comparing compounds 25 and 26), and the presence of bromine atoms in the structure (comparing compounds 27 and 28), have little or no effect on the compounds’ cytotoxicity.
Last year, was reported the isolation of halogenated monoterpenes 25, 31 and 32 from the red alga Plocamium cartilagineum (Linnaeus) P.S.Dixon (syn. Plocamium cartilagineum) collected in South Africa [48]. Additionally, the compounds’ cytotoxic effects were evaluated and stereoisomers 25 and 31 exhibit identical and significant cytotoxicity against colon cancer cell line (IC50 = 3.3 µM) and low effect against lung cancer cell line (NCI-H460) [48]. In the attempt to find the possible mechanism of action was confirmed that none of the compounds have activity as sodium channel blockers or activators [48].
Halomon [6(R)-bromo-3(S)-bromomethyl)-7-methyl-2,3,7-trichloro-1-octene] 33 (Figure 1), an halogenated monoterpene isolated for the first time from Portieria hornemannii (Lyngbye) P. C. Silva, showed high cytotoxic activity against renal-, brain-, colon-derived solid tumor cell lines while leukaemia and melanoma cells are less sensitive to this compound [53]. This interesting case of differential cytotoxicity led this compound for in vivo and preclinical drug development. Unfortunately, several constraints such as low and variable natural content, and poor in vivo results, has hampered the clinical development of this compound. Conversely, the high interest of scientific community in the isolation of enough halomon 33 material lead to the reinvestigation of Portieria hornemannii (Lyngbye) P. C. Silva and to the consequent isolate of other halogenated monoterpenes. This fact allowed some structure/activity relationship studies that demonstrated no crucial role of the halogen at C7 neither the C6 nor C7 hybridization to the activity while the halogen atoms at C6 and C2 are crucial for the high cytotoxicity [57]. The mechanism of action of halomon-type monoterpenes have not been completely elucidated but it was demonstrated that halomon 33 possess potent inhibitory activity of the DNA methyltransferase-1 (DNMT-1) (IC50 = 1.25 µM), an enzyme responsible for methylation of cytosine residues residing at CpG sites. In fact, in many cancers, promoters of tumor suppressor genes are silenced by hypermethylation at CpG sites, and thus, the inhibition of DNMT-1 could potentially reverse tumor growth [58]. In truth, the interest in halomon 33 never fainted; the first total synthesis was achieved in 1998, halomon 33 was obtained in 13 steps with an overall yield of 13% [59] and in 2000 Sotokawa et al. described the synthesis of the racemic halomon, in three-steps (25%) and poor selectivity [60]. Fifteen years later, the first selective method was described, which was also efficient [61]. Recently, halomon was synthesized using the previous method with some improvements in the enantioselectivity resulting also in preparation of several halomon-analogues and halogenated natural products [62]. Thus, conditions are created to advance with the clinical studies and/or development of new anticancer drugs based on the halomon scaffold.
Apart from the few cases mentioned above, the study of the compounds action mechanisms is vague. However, some studies on the mechanism of action of terpenoids extracted from seaweeds which are not indicated in Table 1 can be found in the literature. This means that the compounds showed lower activity or the IC50 value has not been reported. Nevertheless, information about possible mechanisms of action is important to understand the action of natural sesquiterpene. One example is the 14-keto-stypodiol diacetate 34 (Figure 2), a diterpenoid isolated from the seaweed Stypopodium flabelliforme with great structural similarity with compound 18 (Figure 1), whose cytotoxic effect on prostatic cancer cell proliferation (DU-145, IC50 = 24 µM), and its action mechanism was studied [63]. 14-Keto-stypodiol diacetate 34 acts on microtubule assembly inhibition, induces mitotic arrest and has strong inhibition effect on plasminogen activator secretion [63]. These events are all correlated and affect the cell invasive capacity [64,65]. Moreover, the identification of the signaling pathway influenced by the microtubule cytoskeleton [66] may offer a source of novel anticancer treatments.
Laurinterol 35 (Figure 2), is a marine sesquiterpene isolated from a red alga Laurencia (Laurencia okamurae Yamada) [55], L. pacifica [45], Laurencia nidifica J. Agardh [67] that structurally is very similar to a part of laurebiphenyl 20 (Figure 1). Laurinterol 35 was reported for the first time as potential anticancer metabolite against melanoma cells (B16F1) with IC50 value of 33.9 µM. and several studies were applied to understand its mechanism of action in B16F1 cells [55]. The results showed that 35 can induce apoptosis via activation of p53 transcription factor in melanoma cells and also increases the cell numbers in sub-G1 phase by DNA fragmentation [55].
Dactylone 36 (Figure 2), a natural marine halogenated sesquiterpenoid isolated from Laurencia glandulifera (Kützing) Kützing [68] was most recently evaluated for its effect on the mouse skin epidermal JB6P+Cl41 [69]. The dactylone 36 inhibits epidermal growth factor-induced transformation in JB6P+Cl41 cells, induces G1-S cell progression arrest and apoptosis of tumor cells. Also, decreases the expression of cyclin D3 and Cdk4 and cause the suppression of phosphorylation of the Rb protein of JB6P+Cl41 cells at Ser780, Ser807/811 and Ser795 in a dose-dependent manner. Similar inhibitory effects on phenotype expression were observed in the human tumor SK-MEL-28, HCT-116 and H460 cell lines [69]. Although this study didn’t present the IC50 values, they should, in our opinion, be presented herein because the cancer-preventive properties and some details of the dactylone 36 molecular mechanism of action can be important to understand the action of other natural sesquiterpene.
The last example, is mertensene 37 (Figure 2), a polyhalogenated monoterpene isolated from the red alga Pterocladiella capillacea (S.G. Gmelin) Santelices & Hommersand, that inhibit the viability of two human colorectal adenocarcinoma cell lines HT29 [70]. The results showed that mertensene 37 effect is correlated with the activation of mitogen-activated protein kinase (MAPK) extracellular signal–regulated kinase (ERK)-1/-2, serine/threonine-specific protein kinase (Akt) and nuclear factor-kappa B (NF-KB) pathways. In cell cycle mertensene-induced G2/M arrest which was associated with a decrease in the phosphorylated form of the anti-tumor transcription factor p53, retinoblastoma protein (Rb), cdc2 and chkp2. In apoptosis, mertensene triggers a caspase-dependent apoptosis by activation of caspase-3, the cleavage of poly (ADP-ribose) polymerase (PARP) and increased expression level of death receptor-associated protein TRADD [70].
The results discussed above confirm the role of terpenoids isolated from different species of brown and red alga as potential cancer chemotherapeutic and/or chemopreventive agents, against a large panel of cancer cells. However, deeper research to understand structure/activity relationships and to evaluate their cytotoxicity in no-tumoral cells is necessary. Furthermore, the most promising isolated metabolites should be evaluated in in vivo studies.

2.2. Carotenoid

Fucoxanthin 38 (Figure 3) is an orange-colored pigment tetraterpenoid belonging to xanthophylls subclass of carotenoids, that contributes to more than 10% of the total of carotenoids in nature, and being brown seaweeds their richest source in marine ecosystems [71,72,73]. Some of the examples of macroalgae that are excellent sources of this carotenoid are Undaria pinnatifida (Harvey) Suringar [74,75], Ectocarpus siliculosus (Dillwyn) Lyngbye [73], Saccharina japonica (Areschoug) C.E. Lane, C. Mayes, Druehl & G.W. Saunders (syn Laminaria japonica Areschoug) [76], Sargassum fulvellum (Turner) C. Agardh and Hizikia fusiformis (Harvey) Okamura [72].
The beneficial effects of fucoxanthin are widely described in the literature and are scientifically proven. In fact, the fucoxanthin have a very broad application ranging from prevention to treatment of cardiovascular diseases, oxidative stress, diabetes, obesity, hypertension, anti-inflammatory [20,24,25,77,78,79]. It also exhibits cytotoxic and anti-proliferative effects against a large number of cancer cell lines [80,81,82,83]. Fucoxanthin is clearly a great candidate for chemopreventive and/or chemotherapeutic use in the cancer battle. This can be concluded from the excellent review published by Satomi [83], where the antitumor and cancer-preventive effects of fucoxanthin are discussed and systematized. Herein we resume the main experimental evidences of fucoxanthin cytotoxic and/or antiproliferative effects (Table 2) as well as the main accepted wisdom about fucoxanthin mechanisms of action in different cancer cell lines.
The studies summarized in Table 2 suggest that fucoxanthin exerts its antiproliferative and cancer-preventing effects by modulating the expression of various cellular molecules and cellular signal transduction pathways, being the most cited mechanisms: (i) induction of G1 cell-cycle arrest, independent of the apoptosis induction. Involving also, one or more factors, such as the increase of p15INK4B, p21WAF1/CIP1 and p27KIP1 and connexin 32/43 expression, the activation of MAPK pathways, the decrease of myelocytomatosis (MYCN) proto-oncogene expression and suppression of NF-ĸB activity; (ii) induces a caspase dependent apoptosis accompanied by an increase of reactive oxygen species (ROS) generation and mitochondrial membrane permeability while occur decrease in B-cell lymphoma-extra large (BCL-xL), cellular inhibitors of apoptosis protein (CIAP)1, CIAP2, X-linked inhibitor of apoptosis protein (XIAP) and surviving proteins level, reduction in phosphoinositide 3-kinase (PI3K) and AKT activity and downregulation of signal transducer and activator of transcription 3 (STAT3)/epidermal growth factor receptor (EGFR ) signaling; (iii) induces metastasis inhibition by decrease the matrix metallopeptidase 9, cluster of differentiation 44 (CD44) and CXCR4.
In addition to the wide effects of fucoxanthin 38, the toxicological studies conducted in male and female mice showed that single doses (1000 or 2000 mg/kg) or repeated treatment (500 or 1000 mg/kg for 30 days) of this pigment, was neither toxic nor promotes histological alteration in mice [101].
The research involving fucoxanthin 38 is currently more focused on its use in combination therapy for the treatment of leukemia, aiming to solve adverse side effects such as the development of resistance and effects on no-tumor cells [102]. Other recent studies involve the development of new delivery systems such as encapsulation-based delivery systems [103,104] and combination with nanoparticles [105,106]. The objective of these new approaches is to overcome fucoxanthin 38 poor in vivo properties, such as low bioavailability and low chemical stability.
It is recognized that fucoxanthin 38 is metabolized to fucoxanthinol in the gastrointestinal tract by digestive enzymes, such as lipase and cholesterol esterase and then absorbed into intestinal cells [107]. Thus, fucoxanthinol seems to be the in vivo bioactive compound [82]. In fact, some authors studied the fucoxanthinol activity and described its ability to induces apoptosis on human colon adenocarcinoma cell line (CaCo-2), human breast adenocarcinoma cell line (MCF-7), human leukemia cell line (HL-60), human adenocarcinoma breast cell line (MDA-MB-231) [108,109], to promote antiproliferative effects on PC3 and T cell leukemia [110,111] and to induce apoptosis in body-cavity-based lymphoma cell line (BCBL-1) and primary effusion lymphoma cell line (TY-1) cells and G1 cell cycle arrest [112].

2.3. Phenolic Compounds

Phenolic compounds are composed of a single aromatic ring bearing one or more hydroxyl group to a polymeric structure of this simple unit and exhibit a large broad of biological activities [113,114,115]. The most common subclasses of polyphenols in seaweeds are halogenated phenols, catechins, flavonols, and phlorotannins, being this last more common in brown seaweed while bromophenols, polyphenolics compounds with one or more bromine substituents, are most commonly found in red seaweeds [28,113,116,117]. Polyphenols presence and concentrations in seaweeds can be linked to environmental factors [118,119], but is also dependent of the seaweed species [120,121].

2.3.1. Phlorotannins

Phlorotannins are described as polyphenolic secondary metabolites formed by polymerization of phloroglucinol 39 (Figure 4) monomer units highly hydrophilic and with a wide range of molecular sizes [113,122]. Based on their interlinkage, phlorotannins can be classified in subclasses, such as phlorethols, fucols, fucophlorethols, eckols, fuhalols and carmalols [122,123,124].
There is evidence that phlorotannins and its derivatives play important roles as anticancer metabolites, acting in different hallmarks of cancer such as proliferative signaling, metastasis, cell cycle, resistance to cell death, evasion, angiogenesis and evasion of growth suppressors. These metabolites can also be considered as chemopreventive agents due to their antioxidant effect, once oxidative stress may act in cancer initiation, promotion and progression [113,117,125,126].
From the brown seaweeds Ecklonia Cava Kjellman [127] and Ecklonia stolonifera Okamura [128] were isolated several phloroglucinol derivatives. One of them, dioxinodehydroeckol 40 (Figure 4), showed moderate antiproliferative activity against breast cancer cell lines, MCF-7 and MDA-MB-231, being MCF-7 more sensitive than MDA-MB-231. Dioxinodehydroeckol 40 inhibited 53% of MCF-7 cells proliferation at 10 µM [127] and induced the cells’ apoptosis through NF-κB dependent pathway, by an increase in the caspases-3 and -9 activities and cleavage of PARP, accompanied by activation of p53 and Bax and Bcl-2 inhibition [127]. The phlorotannin 40 (Figure 4), also exhibits protective activity against ultraviolet radiation B (UVB)-induced apoptosis of HaCaT cells (treatment of HaCaT cells post-UVB exposure with compound 40 allowed 72% less of cell death). Apparently, phlorotannin 40 can modulate the Bax/Bcl-2 and caspases expression [129]. This is an interesting result because indicates its potential to protect skin against UVB effects.
Dieckol 41 (Figure 4), the major component of Ecklonia Cava Kjellman [127], was described as an anti-metastatic compound, having the ability to regulate the metastasis-related genes action on MCF-7 cells, inhibiting the expression of MMP-9 (matrix metalloproteinase-9) and VEGF (vascular endothelial growth factor), and stimulated the expression of TIMP-1 and -2 (tissue inhibitor of metalloproteinase) [130]. This phlorotannin also exhibits a significant pro-apoptotic activity on the ovarian cancer cell line (SKOV3) associated with ROS production. The action mechanisms studied demonstrate that dieckol 41 triggered the activation of caspase-3, -8 and -9 via ROS production and the regulation of AKT and p38 signalling [131].
Phloroglucinol 39 (Figure 4), although is the base-unit of phlorotannins, was also assayed against breast cancer (MCF7, SKBR3 and BT549) stem-like cells which are largely responsible for return of breast cancer [132]. The authors demonstrated that treatment with phloroglucinol 39 suppresses sphere forming ability and anchorage-independent colony formation in breast cancer cells by decreasing the expression of Sox2, CD44, Oct4, Notch2 and β-catenin, the cancer stem-like cell regulators. Moreover, treatment with compound 39 sensitized breast cancer cells to anticancer drugs such as cisplatin, etoposide, and taxol as well as to ionizing radiation. This work proposed that phloroglucinol prevents disease relapse [132]. In the same year, the authors published another study highlighting the antimetastatic effects of phloroglucinol 39 on breast cancer cells (BT549 and MDA-MB-231) through inhibition of the PI3K/AKT and the rat sarcoma (RAS)/RAF-1/ERK mitogenic pathways thereby suppressing epithelial-mesenchymal cell transition [133].

2.3.2. Bromophenols

Since, the isolation of the first bromophenols from red algae Neorhodomela larix (Turner) Masuda (syn. Rhodomela larix (Turner) C. Agardh) [134], many novel bromophenols were isolated [135,136,137,138,139] and some of them, as it is indicated in Table 3, are very interesting cytotoxic compounds. The most interesting features will be discussed below and their structures are depicted in Figure 5.
The literature review carried out and summarized in Table 3 shows that there are 10 compounds belonging to the subclass of the bromophenols that exhibit cytotoxic activity with IC50 ≤ 15 µM. Among these, mention should be made to compounds 46, 48, and 50 for their relevant cytotoxicity (IC50 ≤ 9 µM) against a wide range of at least 6 cancer cell lines, and a particular emphasis to compound 51, which exhibits the highest cytotoxic activity against the six cancer cell lines, lung, gastric, breast, melanoma, ovarian and colon cell lines (IC50 ≤ 3.8 µM) (Figure 5 and Table 3). Compound 47 exhibit identical cytotoxic activity but only against 4 tumor cell lines (IC50 ≤ 3.8 µM against lung, gastric, breast and colon cancer cell lines). Compound 44 is the one with the lowest IC50 value in Table 3 (IC50 = 1.32 µM) against a colon cancer cell line, whereas compounds’ 51 and 47 present the lower values against a lung cancer cell line (IC50 = 1.6 and 1.8 µM respectively).
Unfortunately, from the works cited in Table 3 only the work performed by Lijun et al. evaluates the compounds selectivity [141]. They test the compounds, under the same experimental procedure, against the human embryo lung fibroblasts cell line.
The report of the values obtained with positive controls (anticancer drugs in clinical use) and evaluate in the same conditions is also rare. As far as we could find only Shoeib et al. report such data [137], however we should emphasize that the absence of these data significantly reduces the impact of the published results. The compounds 43 and 44 exhibit higher cytotoxic activity against HCT-116 (IC50 = 2.51 and 1.32 μM, respectively) than the 5-fluorouracil (IC50 = 4.93 μM), an effective anticancer drug used as positive control. On the other hand, HCT-116 cell line is 5-fold and 9-fold, respectively, more sensitive to the compounds 43 (ethyl ether lanosol) and 46 (n-propyl ether lanosol) than to compound 42 (methyl ether lanosol) while the human colon adenocarcinoma cell line (DLD-1) is much less sensitive to any of these compounds. Studies of structure-activity relationship showed that the activity is influenced by the number and position of bromine atoms, as well as the number of hydroxyl groups and aliphatic side chain [137].
Wu et al. [145] described the inhibitory effects of compound 47, bis (2,3-dibromo-4,5-dihydroxy-phenyl)-methane, in the proliferation, migration and invasion of hepatocellular carcinoma cells (BEL-7402). Exhibit a IC50 value of 15.9 μM and, at concentration of 9.1 µM, the cell adhesion to fibronectin and collagen IV as well as cell migration and invasion decrease significantly, while at 18.2 µM a complete inhibition of the migration and MMP-2 and MMP-9 expression occurs. Moreover, compound 47 inhibits the focal adhesion kinase (FAK), a protein required for cell transformation and invasion [145]. The compound 47 also inhibits multiple angiogenesis processes, including endothelial cell sprouting, migration, proliferation, and tube formation. It seems to be a potent and selective inhibitor of the tyrosine kinase receptor and exhibiting multi effects of inhibition. Moreover, at 10 μM inhibit the activities of FGFR2 and FGFR3, VEGFR2 and PDGFRα factors and decreases the phosphorylation of PKB/Akt and eNOS, as well as the NO production [146].
The inhibitory effect of compounds 48 and 49 against the protein tyrosine kinase (PTK) with over–expression of the proto-oncogene c-kit was evaluated and the results showed significant inhibition ratio of this protein (80.1% and 71.4% respectively) [147].
In 2012, Liu et al. [148] selected the compound 50 (bis(2,3-dibromo-4,5-dihydroxybenzyl) ether), a cytotoxicity compound against a wide range of cancer cell lines (IC50 ≤ 9 µM, Table 3), for detailed analysis of its effect on K562 cell line. The authors demonstrated that the mitochondrial pathway was involved in the bromophenol 50 induced apoptosis. In fact, bromophenol 50 induces S phase arrest and inhibits topoisomerase I activity followed by apoptosis. It is interesting to mention that compound 50, contrary to the mechanism of the topoisomerase I inhibitor campthotecin, was not able to stimulate the formation of topoisomerase I–DNA complex or able to intercalate DNA. These facts suggest a different inhibition mechanism [148]. Considering that the current topoisomerase I inhibitors exhibit significant side effects [149] and the uniqueness of compound 50 structure, its significant cytotoxic activity against a broad range of cancer cell lines coupled with its distinct mechanism of action, indicate that compound 50 may, undoubtedly, be a leading compound for the development of a new generation of anticancer topoisomerase I inhibitors.
Qi et al. also studied the bromophenol 50 effects on angiogenesis and detected that it can significantly repress the human umbilical vein endothelial cells (HUVEC) cells proliferation without induced apoptosis. Can also decrease migration and tube formation, without effect on the performed vascular tube, via inhibiting VEGF signal systems [150].

2.4. Alkaloids

Alkaloids isolated from seaweeds include indoles and indoles analogues, quinone, 2-phenylethylamine and 2,7-naphthyridine derivatives, however the most common ones belong to the indole and 2-phenylethylamine groups [151]. The indole type is concentrated in Rhodophyta (red seaweeds) while halogenated alkaloids, mainly bromine- and chloride-containing, are dominant in Chlorophyta (green seaweeds) [152]. Indole type alkaloids are also important because they represent a quarter of all alkaloids that are regarded as promising compounds in the development of new drugs.
The lophocladine B 52 (Figure 6) is a 2,7-naphthyridine alkaloid isolated from red alga Lophocladia sp. collected in the Fijan Islands [153]. The cytotoxicity of this molecule was evaluated against NCI-H460 (lung cancer cell line) and MDA-MB-435 (used by the authors as a human breast cancer model but currently considered as a human melanoma model [154]). Lophocladine B 52 exhibits significant cytotoxic effect against and MDA-MB-435 cell line (IC50 = 3.1 µM), causing a major reduction of cells in the G1 and S phases with G2/M cell cycle arrest [153]. Moreover, the analyses of lophocladine B 52 effects on cellular microtubes and actin filaments in A-10 cells (used as vascular smooth muscle cells model) showed that this metabolite acts as microtubules inhibitor with no loss of actin filament [153]. In the same year Lotter et al. reported that lophocladine B 52 is also able to inhibit human leukemia cells (HL-60) (IC50 = 1 µM) [155].
The well-known potential of the antitubulin compounds as effective anticancer agents, for example taxol and vincristine, spread the interest of the scientific community in the synthesis of lophocladine B 52 or derivatives, seeking new and more potent antitumor agents and/or structure activity relationship studies [155,156,157,158]. To date, only two of the synthesized compounds (simplified isoquinolines isoquinoline-triazole derivatives) exhibit better cytotoxicity (IC50 = 10.14 and 12.76 µM) than lophocladine B 52 against hepatic cancer (HepG2) and cervical cancer (HeLa) cell lines (IC50 = 89.5 and >100 µM) [158]. However, the synthesis of lophocladine B 52 allowed the conclusion that the cytotoxic level depends on the C1 substituent. For example, tert-amine is less potent than primary- and secondary-amines [157].
Indole alkaloids have exhibited a wide array of biological activities and the frameworks produced by marine species are often very different from those produced by terrestrial species [159,160,161]. One interesting example is the bisindole caulerpin or caulerpine 53 (Figure 6), isolated mainly from green algae genus Caulerpa [161,162] but also from Codium decorticatum (Woodward) M. Howe [163] and Halimeda incrassata (J. Ellis) J.V. Lamouroux [164]. And also found in some red algae such as Chondria armata (Kützing) Okamura [165], Laurencia dendroidea J. Agardh [syn. Laurencia majuscula (Harvey) A.H.S. Lucas] and Caloglossa leprieurii (Montagne) G. Martens [166].
Some of the abovementioned seaweeds are invasive species and the study of their chemical entities can contribute to suggesting a possible use for that biomasses, being the isolation of valuable chemicals one of the most explored uses. In this context, caulerpin 53 is among the most studied metabolites. Unfortunately, caulerpin 53 effects on cell growth/viability are not very interesting, IC50 values ≥ 20 µM against some cancer cell lines (T47-D, MCF-7, MDA-MB-231, PC3 DU145, HMEC, HCT116, HT29, LOVO and SW480) [167,168].
Even though, caulerpin 53 action mechanism was studied and it was proved that caulerpin 53 inhibits hypoxia-inducible factor 1 (HIF-1), an important target in cancer therapy [167]. The results suggested that caulerpin 53 at concentration of 10 µM and under hypoxic conditions blocked the induction of HIF-1α protein, the HIF-1 oxygen-regulated subunit, while at concentration of 30 µM, it disrupts mitochondrial ROS-regulated HIF-1 activation and downstream HIF-1 pathway [167]. Caulerpin 53 also exhibits effect on tumor cell migration once it suppressed the migration of metastatic MDA-MB-231 cells in a concentration-dependent manner, being the better results observed at 30 µM [167].
Caulerpin 53 overpowers the mitochondrial respiratory at complex II and increases ROS production in cisplatin-resistant C13 ovarian cancer cells, while it has no effect on the complexes I, III and IV [169], suggesting that some derivatives could be good candidates for the treatment of cisplatin-resistant cancer, once ovarian cancer cisplatin resistant cells are characterized by reduced oxygen consumption and increased dependence on glucose [170].
More recently, the anticancer effect of caulerpin 53 against LOVO cancer cell line was evaluated, and the results showed a cytotoxic effect with IC50 = 20 µM [168]. The mechanism of action study indicates that caulerpin 53 inhibits oxidative phosphorylation (OXPHOS), that is inhibits the metabolic pathway in which cells use enzymes to oxidize nutrients to release energy. LOVO cells are one example of those cells that are less glycolytic and more depended on OXPHOS to produce adenosine triphosphate (ATP). It was also demonstrated that in combination therapy, caulerpin 53 can be used with the glycolytic inhibitor 3-bromopyruvate to prevent LOVO cellular proliferation [168].

3. Secondary Metabolites from Seaweeds with In Vivo Antitumor Activity

Some of the secondary metabolites mentioned in the previous section were subjected to in vivo evaluations, not as much as it is recommended. Those studies, due to their significance, will be herein presented and discussed.
Preliminary in vivo evaluation of halomon 33 (Figure 1) showed that daily treatments (5× doses of 50 mg/kg) in an ip/ip xenograft model with highly aggressive U251 brain cancer showed 40% of success. However, research was stopped due to insufficient amount of halomon 33 to perform more essential tests. Both attempts to extract more material from the natural sources and development of efficient synthetic procedures demonstrate that the amount obtained could not be use by pharmaceutical industry [57].
The in vivo inhibitory effect of fucoxanthin 38 (Figure 3) in duodenal carcinogenesis was demonstrated using mice with duodenal carcinogenesis, which was induced by N-ethyl-N’-nitro-N-nitrosoguanidine. The mice were treated with fucoxanthin 38 [oral administration of 0.005% solution of fucoxanthin in drinking water], during 4 and 16 weeks. This in vivo study demonstrates that fucoxanthin 38 inhibits ornithine decarboxylase (ODC) activity [171], an enzyme whose activity is induced in response to cell growth stimuli and is highly expressed in diseases such as inflammation and cancer being not only a biomarker for cancer but also a potential target for its therapy [172].
Fucoxanthin 38 was also evaluated on melanin synthesis in vivo and was found that topical application (once a day to the back skin of the mice shortly after UVB irradiation) of an ointment (mixture of fucoxanthin at 0.01, 0.1 and 1% in white petrolatum) and oral treatment [fucoxanthin at 0.1, 1 and 10 mg/kg b.w. in water with 5% acacia, given once a day, 2 h before UVB irradiation (160 mJ/cm2) for seven days followed by increased UVB (320 mJ/cm2) irradiation for seven more days], suppressed skin mRNA expression related to melanogenesis [173]. Identical effect was observed on UV-induced skin pigmentation in guinea-pigs [173]. In conclusion these results suggest that fucoxanthin 38 exhibits in vivo anti-pigmentary activity, in UVB-induced melanogenesis, by topical or oral application. This effect of fucoxanthin 38 may be due to suppression of prostaglandin (PG) E2 synthesis and melanogenic stimulant receptors (neurotrophic, PGE2 and melanocyte stimulating hormone expression) [173].
Finally, fucoxanthin 38 at 25, 50 and 100 mg/kg b.w. oral administration dose, once per day for 1 week, exhibits the ability to induce apoptosis of sarcoma 180 (S180) [174]. The in vivo study was performed using male Kunming mice and the results indicated that treatment with fucoxanthin 38 remarkably reduce the expression of EGFR in the tumor tissue when compared with the model control group, suggesting that down-regulation of STAT3/EGFR signaling appeared to be involved in the in vivo anti-tumor effect and apoptosis induction [174].
Bald/c athymic female nude mouse with ovarian carcinoma induced by subcutaneously inoculating 5 × 106 SKOV3 cells, were used for in vivo studies of anticancer effects of dieckol 41 (Figure 4). For 4 consecutive weeks, the experimental group of mice is treated with dieckol 41 (50 and 100 mg/kg b.w.) or cisplatin (3 mg/kg b.w.) three times per week [131]. The results demonstrated that dieckol 41 suppressed tumor growths compared with the control group without any significant adverse effect in the SKOV3-bearing mouse model [131].
In 2017, the efficacy of dieckol 41 (oral admistration of 40 mg/kg b.w. dose for 15 weeks) as anticancer against N-nitrosodiethylamine (NDEA)-induced hepatocarcinogenesis in male albino Wistar rats was evaluated [175]. The treatment with dieckol 41 caused the suppression of the NDEA-initiated hepatocarcinogenesis by modulation of xenobiotic-metabolizing enzymes with modulation of cell proliferation and induction of apoptosis via the mitochondrial pathway. The inhibition of invasion and angiogenesis also observed was evidenced by the decrease of both MMP-2 and MMP-9 activities as well as the decrease of the vascular endothelial growth factor (VEGF) expression. Dieckol 41 also exerts anticancer effects via inhibition of the pro-inflammatory transcription factors NF-ĸb and COX2 [175].
Phloroglucinol 39 (Figure 4) (at 25 mg/kg b.w. dose administrated four times at alternate days) suppresses colony formation and in vivo tumorigenicity in BT549 breast cancer cells [132]. Tumor were formed by subcutaneous inoculation of 1 × 106 sphere-cultured BT549 breast cancer cells into athymic Bald/c female nude mice and phloroglucinol 39 decreased dramatically the tumor volume, suggesting that this secondary metabolite inhibits tumorigenic capacity by targeting cancer stem-like cells and/or non-cancer stem-like cells (CSCs) [132].
To study the phloroglucinol 39 effect on metastatic breast cancer (MDA-MB-231) in vivo, the model metastatic MDA-MB-231 cells injected into fourth mammary fat pad of NOD scid gamma (NSG) mice was used [133]. The treatment with phloroglucinol 39 (25 mg/kg b.w.) administrated four times on alternate days, attenuated the primary tumor formation in mammary fat pads, and attenuated the lung metastasis and the expression levels of vimentin (VIM) and SLUG proteins [133]. Similarly, to the in vitro data, treatment with phloroglucinol 39 decreased phosphorylation of AKT and ERK, consequently treated mice survive longer than the control mice [133].
The in vivo study to evaluate the activity of bromophenol 50 (Figure 5) was carry on zebrafish model, an ideal model used in screening of anti-angiogenic agents. At a concentration of 25 µM, bromophenol 50 inhibited the sub-intestinal vessel (SIV) formation in 49.5%, confirming it inhibitory activity against angiogenesis. The results also suggest that bromophenol 50 can, in concentration dependent manner, produce toxic effects towards the zebrafish development [150].
Our final example is the in vivo effect of caulerpin 53 (Figure 6), in combination with 3-bromopyruvate, on athymic nude mouse model bearing SW480 implanted xenografts. The combination therapy of 3-bromopyruvate and caulerpin 53 (30 mg/kg b.w.) displayed remarkable tumor regression. Complementary analysis demonstrated that proliferating cell nuclear antigen (PCNA) and phosphorylated mammalian target of rapamycin (p-mTOR) expression was significantly inhibited in this combined therapy, showing the key role of adenosine monophosphate-activated protein kinase (AMPK)/mTOR pathway in the anticancer activity of caulerpin 53 [168].

4. Conclusions

In this review the in vitro activities of 53 secondary metabolites isolated from brown, red and green seaweeds are presented and discussed. The mechanisms of action, structure/activity relationship and, in the cases that was possible, the in vivo studies were also discussed. From literature published in the last 30 years, were selected the secondary metabolites that exhibit cytotoxic activity against tumor cell lines with IC50 values lower than 15 µM. The compounds reported belong mainly to the terpenoids class, followed in much smaller number by compounds of bromophenols class, phlorotannins and alkaloids.
The diterpene 11 (dictyolactone), the sterol 22 (cholest-5-en-3β,7α-diol) and the halogenated monoterpene 33 (halomon) are the only reported compounds with sub-micromolar activity (IC50 ≤ 0.9 µM) against at least one cancer cell line, while laurebiphenyl 20, a dimeric sesquiterpene of the cyclolaurane-type, and the halogenated monoterpene 31, [(1E,5E,7E)-3,4-erythro-1-bromo-7- -dichromethyl-3-methyl-3,4,8-trichlorooctatriene] are relevant because they exhibit IC50 values between 1–5 µM against 6 cell lines (lung, cervix, gastric, hepatic, ileum, colon cancer cell lines). Of the remaining compounds, it is noteworthy the bromophenol 51, which exhibits high cytotoxic activity (IC50 ≤ 3.8 µM) against the lung, gastric, breast, colon, melanoma and ovarian cancer cell lines, the bis (2,3-dibromo-4,5-dihydroxy-phenyl)-methane 47 with identical cytotoxic activity against the first 4 tumoral cell lines and n-propyl ether lanosol 46 the most active bromophenol (IC50 = 1.32 µM against colon cancer cell line), in fact more active than the 5-fluorouracil. These are, as far as we could find, the most promising secondary metabolites isolated from seaweeds and reported in the literature.
It should be emphasized that most of the promising compounds outlined herein belong to classes of secondary metabolites that are not biosynthesized in terrestrial species, being the most evident ones the halogenated terpenes and bromophenols. This fact reinforces the importance of the marine environment in general and the seaweeds in particular as a source of potentials new anticancer drugs.
Nevertheless, several studies remain to be performed. Only a few compounds (only 9 out of 53 presented) were subjected to selectivity studies, and none of them correspond to the most promising ones. Also, the in vivo studies are scarce (5 out of 53 cytotoxic compounds reviewed), except for fucoxanthin 38, dieckol 41 and phloroglucinol 39. But this compound advanced studies can be explained because they are already recognized as having high pharmacological potential for the prevention/treatment for example cardiovascular diseases [20,25].
An added value of these compounds that can be detected by this literature survey is clearly shown by the in vitro and in vivo works demonstrating different mechanisms of action and targets. These facts suggest that the seaweeds’ secondary metabolites may be used to develop new anticancer agents with distinct ways of action.
Surprisingly, the most advanced studies on mechanisms of action and/or in vivo studies were not performed with the more promising compounds. Most likely because they are scarce in nature and/or their synthesis is not yet accomplished. Even so, we believe that some of the above-discussed compounds exhibit activities that justify greater attention from the scientific community.

Author Contributions

A.M.L.S. and D.C.G.A.P. conceived and revised the paper, D.H.A.R. made the research and wrote the first draft.

Funding

This research received no external funding.

Acknowledgments

We would like to thank also to University of Azores, University of Aveiro, Organic Chemistry Natural Products and Food Stuffs (QOPNA) unit, and Azorean Biodiversity Group (GBA) for technical support. We would also like to thank the Portuguese National Funds, through FCT—Fundação para a Ciência e a Tecnologia, and as applicable co-financed by the FEDER within the PT2020 Partnership Agreement by funding the Organic Chemistry Research Unit (QOPNA) (UID/QUI/00062/2013) and the cE3c centre (UID/BIA/00329/2013) for financial support. D.H.A. Rocha also thanks FCT for her grant (SFRH/BD/68991/2010).

Conflicts of Interest

The authors declare no conflict of interest. The founding sponsors had no role in the writing of the manuscript, and in the decision to publish it.

Abbreviations

AktSerine/Threonine-Specific Protein Kinase
AMPKAdenosine Monophosphate-Activated Protein Kinase
ATPAdenosine Triphosphate
BALB“Bagg Albino”
BaxB-Cell Lymphoma 2-Associated X Protein
BCBL-1Body-Cavity-Based Lymphoma Cell Line
BCL-xL B-Cell Lymphoma-Extra Large
BT549Human Carcinoma Breast Epithelial Cell Line
b.w.Body Weight
CD44Cluster of Differentiation 44
cdc2Cell Division Cycle Protein 2
CDK4Cyclin-Dependent Kinase 4
CpGCytosine Nucleotide Followed by A Guanine Nucleotide
CIAP Cellular Inhibitors of Apoptosis Protein
COXCyclooxygenase
CSCsCancer Stem-Like Cells
CTXCyclophosphamide
CXCR4CXC Motif Chemokine Receptor 4
DMSO Dimethyl Sulphoxide
DNADeoxyribonucleic Acid
DNMT-1 DNA Methyltransferase-1
EGFREpidermal Growth Factor Receptor
eNOS Endothelial Nitric Oxide Synthase
ERKExtracellular Signal–Regulated Kinase
FAKFocal Adhesion Kinase
FGFRFibroblast Growth Factor Receptor
G1 phaseGap 1 Phase
GTPGuanosine-5′-triphosphate
HaCaTAneuploid Immortal Keratinocyte Cell Line
HIF-1αHypoxia-Inducible Factor 1-Alpha
IC50The Half Maximal Inhibitory Concentration
K562 Human Chronic Myelogenous Leucemia Cell Line
LOVOHuman Colon (Supraclavicular Lymph Node Metastasis)
MMitosis
MAPKMitogen-Activated Protein Kinase
MDA-MB-231Human Adenocarcinoma Breast Cell Line
MMPMatrix Metalloproteinase
mRNAMessenger Ribonucleic Acid
MYCN Myelocytomatosis
NDEAN-nitrosodiethylamine
NF-ĸBNuclear Factor-kappa B
NODNonobese Diabetic
Notch-2Neurogenic Locus Notch Homolog Protein-2
NSGNOD Scid Gamma
Oct-4Octamer-Binding Transcription Factor 4
ODCOrnithine Decarboxylase
OXPHOSOxidative Phosphorylation
p15INK4B Cyclin-Dependent Kinase Inhibitor 4B
p21WAF1/CIP1 Cyclin-Dependent Kinase Inhibitor 1
p27KIP1Cyclin-Dependent Kinase Inhibitor 1B
p75NTRNeurotrophin Receptor p75
PARPPoly (ADP-Ribose) Polymerase
PCNA Proliferating Cell Nuclear Antigen
PDGFRαPlatelet-Derived Growth Factor Receptor α
p-mTORPhosphorylated Mammalian Target of Rapamycin
PI3KPhosphoinositide 3-Kinase
PTKProtein Tyrosine Kinase
RAF-1Murine Leukemia Viral Oncogene Homolog 1
RASRat Sarcoma
RbRetinoblastoma
ROSReactive Oxygen Species
S phaseSynthesis Phase
SCIDSevere Combined Immunodeficiency
SerSerine
SIVSub-Intestinal Vessel
SLUGHuman Embryonic Protein Snail Family Transcriptional Repressor 2
Sox2(Sex Determining Region Y)-Box 2
STAT3Signal Transducer and Activator of Transcription 3
SW480Human Colorectal Adenocarcinoma Cell Line
TIMPTissue Inhibitor of Metalloproteinase
TRADDTumour Necrosis Factor Receptor Superfamily Member 1A Associated via Death Domain
TY-1Primary Effusion Lymphoma Cell Line
U251Human Brain Glioblastoma Cell Line
UVBUltraviolet Radiation B
VEGFR2Vascular Endothelial Growth Factor Receptor 2
VIMVimentin
XIAPX-Linked Inhibitor of Apoptosis Protein

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Marinedrugs 16 00410 g001a 550Marinedrugs 16 00410 g001b 550
Figure 1. Chemical structure of the terpenoids 1–33 isolated from seaweeds that presented significant cytotoxic activity.
Figure 1. Chemical structure of the terpenoids 1–33 isolated from seaweeds that presented significant cytotoxic activity.
Marinedrugs 16 00410 g001aMarinedrugs 16 00410 g001b
Marinedrugs 16 00410 g002 550
Figure 2. Seaweed terpenoids, 34–37, with relevant studies on its cytotoxic action mechanism.
Figure 2. Seaweed terpenoids, 34–37, with relevant studies on its cytotoxic action mechanism.
Marinedrugs 16 00410 g002
Marinedrugs 16 00410 g003 550
Figure 3. Chemical structure of fucoxanthin isolated from seaweeds.
Figure 3. Chemical structure of fucoxanthin isolated from seaweeds.
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Marinedrugs 16 00410 g004 550
Figure 4. Chemical structure of phloroglucinol 39 and phlorotannins 40 and 41 isolated from seaweeds.
Figure 4. Chemical structure of phloroglucinol 39 and phlorotannins 40 and 41 isolated from seaweeds.
Marinedrugs 16 00410 g004
Marinedrugs 16 00410 g005 550
Figure 5. Chemical structure of bromophenols 42–51 isolated from seaweeds.
Figure 5. Chemical structure of bromophenols 42–51 isolated from seaweeds.
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Marinedrugs 16 00410 g006 550
Figure 6. Chemical structure of cytotoxic alkaloids isolated from seaweeds.
Figure 6. Chemical structure of cytotoxic alkaloids isolated from seaweeds.
Marinedrugs 16 00410 g006
Table
Table 1. Cytotoxic terpenoids isolated from seaweeds with half maximal inhibitory concentration (IC50) lower than 15 µM against tumoral cell lines.
Table 1. Cytotoxic terpenoids isolated from seaweeds with half maximal inhibitory concentration (IC50) lower than 15 µM against tumoral cell lines.
MetabolitesSources a [ref.]Cell Lines Tested (IC50 Value µM) [ref.]
1Cystoseira myrica (S.G.Gmelin) C.Agardh) [32]KA3IT (13.1); NIH3T3 b (19.7) [32]
2Cystoseira myrica (S.G.Gmelin) C.Agardh [32]KA3IT (13.7); NIH3T3 b (20.6) [32]
3Cystoseira myrica (S.G.Gmelin) C.Agardh [32]Dictyota dichotoma (Hudson) J.V.Lamouroux [33]KA3IT (14.4); NIH3T3 b (43.3) [32]
4Cystoseira abies-marina (S.G. Gmelin) C. Agardh [34]HeLa–Log phase (5.6); Vero b–Log phase (14.6) [34]
5Dilophus ligulatus (Kützing) Feldmann [35]P388 (4.33–4.79) [35]
6Dilophus ligulatus (Kützing) Feldmann [35]P388 (11.2); P388/DOX (12.9); NSCLCN6-L16 (6.61) [35]
7Dilophus ligulatus (Kützing) Feldmann [35]P388 (3.64); P388/DOX (5.95); KB (12.2); NSCLCN6-L16 (3.31) [35]
8Dilophus ligulatus (Kützing) Feldmann [35]P388 (7.42); P388/DOX (9.41); KB (14.3), NSCLCN6-L16 (6.85) [35]
9Dilophus ligulatus (Kützing) Feldmann [35]P388 (10.3); P388/DOX (10.8) KB (6.85); NSCLCN6-L16 (1.71) [35]
10Dilophus ligulatus (Kützing) Feldmann [35]P388 (13.3); KB (14.4); NSCLCN6-L16 (4.44) [35]
11Dilophus ligulatus (Kützing) Feldmann [35]P388 (9.26); P388/DOX (7.93) NSCLCN6-L16 (0.99) [35]
12Stypopodium zonale (J.V.Lamouroux) Papenfuss [36]HT-29 (5.83); H-116 (5.83); A549 (5.83) [36]
13Stypopodium flabelliforme Weber-van Bosse [37]NCI-H460 (9) [37]
14Stypopodium flabelliforme Weber-van Bosse [37]NCI-H460 (14) [37]
15 and 16Taonia atomaria (Woodward) J. Agardh [38]NSCLC-N6 (7.35); A549 (7.35) [38]
17Stypopodium flabelliforme Weber-van Bosse [39]SH-SY5Y (12.2) [39]
18Stypopodium flabelliforme Weber-van Bosse [39]SH-SY5Y (14) [39]
19Sargassum fallax Sonder [40]Sargassum yezoense (Yamada) Yoshida & T. Konno [41]P388 (14) [40]
20Laurencia tristicha Tseng, Chang, E.Z. et B.M. Xia [42]Laurencia nidifica J. Agardh [43]A549 (3.94); HeLa (3.77); BGC-823 (2.86); Bel7402 (4.48); HCT-8 (4.15) [42]
21Laurencia tristicha Tseng, Chang, E.Z. et B.M. Xia [44]HeLa (15.5) [44]
22Laurencia tristicha Tseng, Chang, E.Z. et B.M. Xia [44]HeLa (0.3); BGC-823 (5.1); Bel7402 (0.5); HCT-8 (0.5); HT29 (9.1) [44]
23Laurencia pacifica Kylin [45]Laurencia okamurae Yamada [46]DU145 (6.8); HT-29 (9.1); A431 (9.6); A2780 (10); BE2-C (13); MCF-7 (14); SMA (14); SJ-G2 (15); MCF10A b (28) [45]
24Laurencia pacifica Kylin [45]Laurencia okamurae Yamada [46]HT-29 (15); DU145 (12); MCF10A b (46) [45]
25Plocamium suhrii Kützing [47]Plocamium cartilagineum (Linnaeus) P.S.Dixon [48,49]WHCO1 (6.6) [47]; CFU (3.36) [48]
26Plocamium suhrii Kützing [47]Plocamium cartilagineum (Linnaeus) P.S.Dixon [48,49]WHCO1 (9.9) [47]
27Plocamium suhrii Kützing [47]WHCO1 (9.3) [47]
28Plocamium suhrii Kützing [47]Plocamium cartilagineum (Linnaeus) P.S.Dixon [49] Plocamium oregonum Doty [50]WHCO1 (8.5) [47]
29Plocamium suhrii Kützing [47]Plocamium corallorhiza (Turner) Hooker & Harvey [51]WHCO1 (7.9) [47]
30Plocamium suhrii Kützing [47]WHCO1 (8.4) [47]
31Plocamium cartilagineum (Linnaeus) P.S.Dixon [48,49]CFU (3.36) [48] HCT-116 (3.36) [52]
32Plocamium cartilagineum (Linnaeus) P.S.Dixon [48]NCI-H460 (13) [48]
33Portieria hornemannii (Lyngbye) P.C.Silva [53]HCT-116 (0.92) [52,53]
a In this table are indicated the seaweed Latin botanical name used by the authors, which, according to the database AlagaeBase (http://www.algaebase.org), does not always correspond to a currently accepted name; b No-tumoral cell line; A2780 = Ovarian cancer cell line; A431 = Human skin carcinoma cell line; A549 = human alveolar basal epithelial adenocarcinoma cell line; BE2-C = Neuroblastoma cancer cell line; Bel7402 = Hepatocellular carcinoma; BGC-823 = Human gastric cancer cell line; CFU = human colon cancer cell line; DU 145 = Human prostate carcinoma cell line; HCT-8 = Epithelial human ileum cell line; HCT 116 = Human colon carcinoma; HeLa = Cervix adenocarcinoma cell line; HT-29= Human colon cancer cell line; KA3IT = Virally transformed form mouse cancer cell line; KB = Human nasopharynx carcinoma; MCF 10A = Human mammary epithelial normal cell line; NCI-H460 = Human lung carcinoma cell line; NIH3T3 = Cell line murine, fibroblast; NSCLC-N6 = Squamous cell lung carcinoma; NSCLCN6-L16 = Human non-small cell lung carcinoma cells; P388 = Mouse leukemia cell line; P388/DOX = Doxorubicin resistant mouse leukaemia cell line; SH-SY5Y = Human bone marrow neuroblastoma cancer cell line; SJ-G2 = Human glioblastoma cancer cell line; SMA = Murine glioblastoma cancer cell line; Vero = Kidney no-tumoral cell line; WHCO1 = Oesophageal cancer cell line.
Table
Table 2. In vitro cytotoxic activity and action mechanism of fucoxanthin isolated from seaweeds.
Table 2. In vitro cytotoxic activity and action mechanism of fucoxanthin isolated from seaweeds.
Fucoxanthin SourceCell Line TestedLevel of ActivityActivity/MechanismTarget MoleculesRef.
Hizikia fusiformis (Harvey) OkamuraGOTO38% growth inhibition at 15.2 µMG1 cell cycle arrestN-myc[84]
Undaria pinnatifida (Harvey) SuringarHL-6046% cellular viability at 11.3 µMApoptosis inductionCaspase-3; caspase-7; caspase-9[85]
Unspecified sourcePC3, DU145, LNCapAt 20 µM cellular viability was 14.9% of PC3, 5% of DU145 and 9.8% of LNCap cell linesApoptosis inductionBcl-2; Bax; caspase-3[86,87]
Undaria pinnatifida (Harvey) SuringarCaCo-2, DLD-1, HT2936.8% cellular viability of CaCo-2 at 7.6 µMApoptosis and antiproliferative effectBcl-2[88]
Laminaria japonica AreschougWiDr, HCT116At 25 µM cell cycle arrest and phosphorylation of pRbCell cycle arrest G0/G1P21WAF1/Cip1[71]
Unspecified sourceHepG2, DU145IC50 = 3 µMCell cycle arrest G1GADD45A[89]
Laminaria japonica AreschougHepG2At 25 µM, inhibition in 29.5% of cell proliferation Cell cycle arrest G1Cyclin D[90]
Laminaria japonica AreschougEJ-1At 6.25 µM the cellular viability decreased to 52.62%Apoptosis inductionCaspase-3[91]
Undaria pinnatifida (Harvey) SuringarSK-Hep-1IC50 9.4 µMCell cycle arrest G1, apoptosis inductionConnexin 43; connexin-32[92]
Ishige okamurae Yendo HL-60Inhibition of proliferation in 65% at 15 µMApoptosis inductionCaspase-3; caspase-7; PARP; Bcl-xL[93]
Undaria pinnatifida (Harvey) SuringarMGC-803At 75 µM apoptosis inducing effects like Paclitaxel (1 µM)Cell cycle arrest G2/M, apoptosis inductionCyclinB1; survivin[94]
Unspecified sourceLNCapIC50 = 2.5 µMCell cycle arrest G1GADD45A; SAPK/JNK[95]
Undaria pinnatifida (Harvey) SuringarHUVECAt 5 µM inhibition of FGF-2 expression in 22%Inhibition of angiogenesisFGF-2; FGFR-1 [96]
Unspecified sourceT24Induced apoptosis at 40 µM and proliferation inhibition at 5–10 µMApoptosis induction; Cell cycle arrest G1Caspase-3; cyclin D1; cyclin E[97]
Unspecified sourceU87, U251At 25 µM the cellular viability decreased 52% and 43% in U87 and U251, respectivelyApoptosis induction. Inhibition of invasion and migrationCaspase-3; caspase-9; cleaved-PARP; P38-MMP-2/9[98]
Unspecified sourceSiHaStrong synergistic effect from combination with TRAILApoptosis inductionCaspase-3; Bcl-2; Bax[99]
Undaria pinnatifida (Harvey) SuringarSGC7901IC50 = 9.80 ± 0.94 (48 h)Apoptosis and autophagy inductionBeclin-1; caspase-3; Bcl-2[100]
Bcl-xL = B-cell lymphoma extra-large; CaCo-2 = Human colon adenocarcinoma cell line; DLD-1 = Human colon adenocarcinoma cell line; DU-145 = Human prostate carcinoma cell line; EJ-1= Human lymphoma; FGF = Fibroblast growth factors; GOTO = Human neuroblastoma cell line; HepG2 = Human liver hepatocarcinoma cell line; HCT-116 = Human colon carcinoma cell line; HL-60 = Human leukaemia cell line; HT-29 = Human colorectal adenocarcinoma cell lines; HUVEC = Human umbilical vein endothelial cells; LNCap = Human prostate carcinoma cell line; MGC-803 = Human gastric carcinoma cell line; N-myc = Proto-oncogene protein; P21WAF1/Cip1 = Cyclin-dependent kinase inhibitor 1; PARP = poly-ADP-ribose polymerase; PC-3 = Human prostate adenocarcinoma cell line; SAPK/JNK = c-Jun N-terminal kinases; SiHa = Human cervix uteri cell line; SGC7901 = Human gastric cancer cell line; SK-Hep-1 = Human endothelial adenocarcinoma cell line; T24 = Human bladder carcinoma cell line; U87 and U251 = Human primary glioblastoma cell line; WiDr = Human colorectal adenocarcinoma cell lines.
Table
Table 3. Bromophenols with potential cytotoxic activity isolated from seaweeds.
Table 3. Bromophenols with potential cytotoxic activity isolated from seaweeds.
MetabolitesSourcesCell Lines Tested (IC50 Value µM)
42Vertebrata lanosa (Linnaeus) T.A. Christensen [137], Neorhodomela larix (Turner) Masuda [134,140], Odonthalia corymbifera (S.G. Gmelin) Greville [135]DLD-1 (14.6); HCT-116 (14.1) [137]
43Vertebrata lanosa (Linnaeus) T.A.Christensen [137], Osmundaria serrata (Suhr) R.E. Norris [138]DLD-1 (13.5); HCT-116 (2.51) [137]
44Vertebrata lanosa (Linnaeus) T.A. Christensen [137]DLD-1 (12.4); HCT-116 (1.32) [137]
45Rhodomela confervoides (Hudson) P.C. Silva [141]KB (12.5); Bel7402 (12.9); A549 (14.4); HELF a (25.9) [141]
46Leathesia marina (Lyngbye) Decaisne [142,143]A549 (2.5); BGC823 (8.8); MCF-7 (2.7); Bel7402 (4.8); B16-BL6 (7.3); HT-1080 (6.6); A2780 (2.7) [142,143]
47Leathesia marina (Lyngbye) Decaisne [142], Rhodomela confervoides (Hudson) P.C. Silva [144]A549 (1.8); BGC823 (3.8); MCF-7 (2.7); HCT-8 (2.2) [142]
48Leathesia marina (Lyngbye) Decaisne [142,143]BGC823 (4.6); MCF-7(3.4); Bel7402 (5.5); HCT-8 (2.8); B16-BL6 (3.3), HT-1080 (7.2); A2780 (7.1) [142,143]
49Leathesia marina (Lyngbye) Decaisne [142,143]BGC823 (8.6); B16-BL6 (15.4); HT-1080 (10.3) [142,143]
50Leathesia marina (Lyngbye) Decaisne [142,143]A549 (5.4); MCF-7 (4.6); Bel7402 (7.4); HCT-8 (5.9); HT-1080 (8.2); A2780 (8.6) [142,143]
51Leathesia marina (Lyngbye) Decaisne [143]A549 (1.6); BGC823 (3.3); MCF-7 (2.5); HCT-8 (1.9); B16-BL6 (3.2); A2780 (3.8) [143]
a No-tumoral cell line A2780 = Ovarian carcinoma cell line; A549 = Human lung carcinoma cell line; B16-BL6 = Murine melanoma cell line; Bel7402 = Hepatocellular carcinoma cell line; BGC-823 = Human gastric cancer cell line; DLD-1 = Human colon adenocarcinoma cell line; HCT-8= Human colon adenocarcinoma cell line; HCT-116 = Human colon carcinoma cell line; HELF = Non-tumoral human embryo lung fibroblasts cell line; HT-1080 = Human fibrosarcoma cell line; KB = Human nasopharynx carcinoma; MCF-7= Human breast adenocarcinoma cell line.

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MDPI and ACS Style

Rocha, D.H.A.; Seca, A.M.L.; Pinto, D.C.G.A. Seaweed Secondary Metabolites In Vitro and In Vivo Anticancer Activity. Mar. Drugs 2018, 16, 410. https://doi.org/10.3390/md16110410

AMA Style

Rocha DHA, Seca AML, Pinto DCGA. Seaweed Secondary Metabolites In Vitro and In Vivo Anticancer Activity. Marine Drugs. 2018; 16(11):410. https://doi.org/10.3390/md16110410

Chicago/Turabian Style

Rocha, Djenisa H. A., Ana M. L. Seca, and Diana C. G. A. Pinto. 2018. "Seaweed Secondary Metabolites In Vitro and In Vivo Anticancer Activity" Marine Drugs 16, no. 11: 410. https://doi.org/10.3390/md16110410

APA Style

Rocha, D. H. A., Seca, A. M. L., & Pinto, D. C. G. A. (2018). Seaweed Secondary Metabolites In Vitro and In Vivo Anticancer Activity. Marine Drugs, 16(11), 410. https://doi.org/10.3390/md16110410

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