| Literature DB >> 33590779 |
Masaru Terasaki1,2, Shouta Takahashi1, Ryuta Nishimura1, Atsuhito Kubota1, Hiroyuki Kojima1,2, Tohru Ohta2, Junichi Hamada2, Yasuhiro Kuramitsu2, Hayato Maeda3, Kazuo Miyashita4, Mami Takahashi5, Michihiro Mutoh6.
Abstract
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.Entities:
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Year: 2021 PMID: 33590779 DOI: 10.1080/01635581.2020.1863994
Source DB: PubMed Journal: Nutr Cancer ISSN: 0163-5581 Impact factor: 2.900