Inhibition of NF-kappaB transcriptional activity enhances fucoxanthinol-induced apoptosis in colorectal cancer cells

Genes and Environment - Tập 41 Số 1 - Trang 1-8 - 2019
Tamura, Shuya1,2, Narita, Takumi1, Fujii, Gen3, Miyamoto, Shingo1,4, Hamoya, Takahiro1, Kurokawa, Yurie1, Takahashi, Maiko1, Miki, Kouhei1, Matsuzawa, Yui1, Komiya, Masami1, Terasaki, Masaru5, Yano, Tomohiro2, Mutoh, Michihiro1,6
1Epidemiology and Prevention Division, Research Center for Cancer Prevention and Screening, National Cancer Center, Tokyo, Japan
2Graduate School of Food and Nutritional Sciences, Toyo University, Gunma, Japan
3Central Radioisotope Division, National Cancer Center Research Institute, Tokyo, Japan
4Department of Cancer Cell Research, Sasaki Institute, Tokyo, Japan
5School of Pharmaceutical Sciences, Health Sciences University of Hokkaido, Ishikari-Tobetsu, Japan
6Division of Carcinogenesis and Cancer Prevention, National Cancer Center Research Institute, Tokyo, Japan

Tóm tắt

Evidence from epidemiological and experimental studies has shown that the etiology of colorectal cancer (CRC) is related to lifestyle, mainly diet. At the same time, there are many foods and beverages that have been shown to provide protection against CRC. We turned our attention to a traditional Japanese food, brown algae, that contains carotenoids and various functional polyphenols, especially fucoxanthin (FX) and fucoxanthinol (FxOH). Both FX and FxOH treatments induced apoptosis in a dose-dependent and time-dependent manner as detected by annexin V / propidium iodide and the presence of a subG1 population in human colon cancer HCT116 cells. This apoptotic effect of FxOH was stronger than that of FX. We also found that nuclear factor-kappa B (NF-κB) transcriptional activity was significantly increased by treatment with ≥5 μM FxOH. Thus, we cotreated the cells with FxOH plus NF-κB inhibitor, and the results demonstrated that this cotreatment strongly enhanced the induction of apoptosis compared with the effects of FxOH or NF-κB inhibitor treatment alone and resulted in X-linked inhibitor of apoptosis (IAP) downregulation. This study suggested that FxOH is a more potent apoptosis-inducing agent than FX and that its induction of apoptosis is enhanced by inhibiting NF-κB transcriptional activity via suppression of IAP family genes.

Tài liệu tham khảo

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