A Marine Carotenoid of Fucoxanthinol Accelerates the Growth of Human Pancreatic Cancer PANC-1 Cells.
Masaru TerasakiShouta TakahashiRyuta NishimuraAtsuhito KubotaHiroyuki KojimaTohru OhtaJunichi HamadaYasuhiro KuramitsuHayato MaedaKazuo MiyashitaMami TakahashiMichihiro MutohPublished in: Nutrition and cancer (2021)
Fucoxanthin and its metabolite fucoxanthinol (FxOH), highly polar xanthophylls, exert strong anticancer effects against many cancer cell types. However, the effects of Fx and FxOH on pancreatic cancer, a high mortality cancer, remain unclear. We herein investigated whether FxOH induces apoptosis in human pancreatic cancer cells. FxOH (5.0 μmol/L) significantly promoted the growth of human pancreatic cancer PANC-1 cells, but induced apoptosis in human colorectal cancer DLD-1 cells. A microarray-based gene analysis revealed that the gene sets of cell cycle, adhesion, PI3K/AKT, MAPK, NRF2, adipogenesis, TGF-β, STAT, and Wnt signals in PANC-1 cells were markedly altered by FxOH. A western blot analysis showed that FxOH up-regulated the expression of integrin β1 and PPARγ as well as the activation of pFAK(Tyr397), pPaxillin(Tyr31), and pAKT(Ser473) in PANC-1 cells, but exerted the opposite effects in DLD-1 cells. Moreover, the expression of FYN, a downstream target of integrin subunits, was up-regulated (7.4-fold by qPCR) in FxOH-treated PANC-1 cells. These results suggest that FxOH accelerates the growth of PANC-1 cells by up-regulating the expression of integrin β1, FAK, Paxillin, FYN, AKT, and PPARγ.
Keyphrases
- induced apoptosis
- cell cycle arrest
- signaling pathway
- endoplasmic reticulum stress
- pi k akt
- oxidative stress
- cell proliferation
- cell cycle
- endothelial cells
- poor prognosis
- squamous cell carcinoma
- cell death
- type diabetes
- epithelial mesenchymal transition
- coronary artery disease
- long non coding rna
- genome wide
- cystic fibrosis
- transcription factor
- south africa
- adipose tissue
- cardiovascular events
- young adults
- pseudomonas aeruginosa
- single molecule
- staphylococcus aureus
- lymph node metastasis