Table 3.
Experimental Model (In Vitro/In Vivo) |
Treatment (Dose, Route and Duration) |
Major Outcomes | Reference |
---|---|---|---|
CCSCs, CD44high/EpCAMhigh tumor cells and HT-29 human colorectal cancer cells | 0.1–5.0 µM fucoxanthinol from fucoxanthin (purity ≥ 98%) in tetrahydrofuran, treatment for 5 days | ↓ Cells viabilities; ↓ pAkt, PPARβ/δ and PPARγ; ↓ Colonospheres growth; ↑ Chromatin condensation; ↑ Nuclear fragmentations |
[48] |
NOD-SCID mice with tumors | 5 mg/kg b.w. fucoxanthinol from fucoxanthin (purity ≥ 98%) in tetrahydrofuran, orally every 3–4 days for 2 weeks | ↓ Csps tumorigenesis | |
Leukemia cell lines, K562 and TK6 | 0.1–10 μM in DMSO, treatment for 24 h | ↓ Cell viability and proliferation; ↓ Nuclei size; ↓ Anti-apoptotic protein (bcl-2 and caspase-3) |
[13] |
Breast cancer cells line, MDA-MB-231 and normal human skin fibroblast cells line |
10–50 μg/mL extracted from P. tenuis, C. sinuosa, I. stellate and D. indica in DMSO, treatment for 6–48 h | ↑ Death of cancer cells; ↓ Cell viability |
[51] |
Human gastric adenocarcinoma SGC-7901 or BGC-823 cells | 25–75 μM (purity ≥ 99%) extracted from Undaria pinnatifda in ethanol, pre-treatment for 24 h; paclitaxel 1 μM as positive control | ↑ Apoptotic cells; ↓ Cells cycle at S phase (SGC-7901) and G2/M phase (BGC-823); ↓ Mcl-1, STAT3 and p-STAT3 |
[53] |
Benzo(A)pyrene-induced lung cancer mice | N/A | ↑ Apoptosis (Caspase 9 and 3); ↓ Anti-apoptotic protein (Bcl2); ↓ Expression of PCNA |
[54] |
Human liver HepG2 cancer cell line | 10-40 μgmL−1 extracted from Chaetoceros calcitrans in DMSO, treatment for 72 h; doxorubicin as positive control | ↓ Proliferation; ↓ AKT1, ERK ½, JNK expression; ↑ BAX and BID gene; ↑ APAF and CYCS expression; ↓ Antioxidant genes (SOD1, SOD2, CAT) |
[55] |
Human breast cancer MDA-MB-231 cells | 25–100 μM extracted from U pinnatifida, treatment for 12–48 h | ↓ Lymphangiogenesis; ↓ VEGF-C, VEGF receptor-3, NF-κB, p-Akt and p-PI3K, micro-LVD |
[12] |
GBM1, A172 and C6 cell lines | 10–150 μM extracted from Phaeodactylum tricornutum, treatment for 24 h |
↓ Cell viability and proliferation and invasion; ↓ Angiogenesis and tubulogenesis; ↓ ATP levels; ↑ Apoptosis |
[52] |
AOM/DSS-induced carcinogenic mice | 30 mg/kg b.w. in palm oil, orally every 1 or 3 days for 3 weeks | ↑ Mucosal crypts and anoikis-like integrin 1low/-/cleaved caspase-3high cells; ↓ Integrin阝, pFAK, pPaxillin, αSMA |
[14] |
HeLa and SiHa cervical cancer cells | 0.1–25 µM, treatment for 48 h | ↓ Hela and SiHa cells (IC50: 1445 and 1641 µM, respectively) ↑ apoptosis; ↓ cell proliferation and colony formation; ↓ HIST1H3D and its mRNA, cell cycle at G0/G1 phase |
[56] |
Human non-small cell lung cancer A549, H1299, PC9 and small cell lung cancer H446 cell lines | 5–30 μM (purity ≥ 99%) extracted from Laminaria Japonica in ethanol, treatment for 48 h; diamminedichloroplatinum 5 mg/kg as positive control | ↓ Cells migration and invasion, metastasis; ↓ Expressions of Snail, Twist, Fibronectin, N-cadherin, MMP-2, PI3K, p-AKT and NF-Κb; ↑ Expression of TIMP-2 |
[60] |
C57BL/6J mice, orthotopic transplantations of cancer cells (KMPC44) | 3 mg/g b.w. in palm oil, orally for 2 weeks | ↓ Adenocarcinoma; ↓ CCL21/ CCR7 axis, Rho A, BTLA, N-cadherin, SMA, pFAK and pPaxillin |
[57] |
AOM/DSS-induced colorectal tumorigenesis in ApcMin/+ mice | 30 mg/kg b.w., orally for 5 weeks | ↑ Cleaved caspase-3; ↓ cyclin D1 expression; ↓ Bacteroidlales and Rikenellaceae; ↑ Lachnospiraceae |
[49] |
AOM/DSS-induced colorectal cancer mice | 50 mg/kg b.w., orally for 14 weeks | ↓ Ccr1, Cyclin D1, pSmad2, MAPK, PI3K/AKT, p53, RAS, STAT, TGF-β and Wnt | [50] |
TPA-induced skin cell transformation in Nfe2l2wild-type cells | N/A | ↓ ROS, oxidized GSSG/reduced GSH | [58] |
↑: upregulation; ↓: downregulation.