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岩藻黄质醇诱导人结肠癌细胞失巢凋亡

Induction of Anoikis in Human Colorectal Cancer Cells by Fucoxanthinol.

作者信息

Terasaki Masaru, Maeda Hayato, Miyashita Kazuo, Mutoh Michihiro

机构信息

a School of Pharmaceutical Sciences, Health Sciences University of Hokkaido , Kanazawa, Ishikari-Tobetsu, Hokkaido , Japan.

b Faculty of Agriculture and Life Science, Hirosaki University , Hirosaki, Aomori , Japan.

出版信息

Nutr Cancer. 2017 Oct;69(7):1043-1052. doi: 10.1080/01635581.2017.1339814. Epub 2017 Oct 9.

Abstract

Fucoxanthin (Fx), one of the major xanthophylls in brown algae, is known to be effective for colorectal cancer (CRC) chemoprevention through inhibiting cell growth, cell cycle and caspase activation. Recently, we observed fucoxanthinol (FuOH), an anti-cancer active metabolite of Fx, treatment of human CRC cells resulted in plenty of living floating cells several hours after exposure, and induced apoptosis. In the present study, we investigated whether FuOH induced anchorage-dependent apoptosis, that is "anoikis", along with integrin signal suppression in human CRC cells. We found that cells exposed to 2.5 μM FuOH clearly showed anti-proliferative and apoptotic effects to DLD-1 cells, human CRC cells. FuOH treatment of DLD-1 cells led to an increase in anoikis-like changes represented by Calcein AM negative/ethidium homodimer-1 positive cell and living floating cells. Moreover, FuOH decreased FAK activation, and altered integrin β1 expression and distribution after 6 h treatment. After 24 h, the cells decreased PPARγ expression and Akt activation and increased integrin β1 expression. Our findings suggested that FuOH can induce anoikis in CRC cells through suppression of integrin signals in human CRC cells.

摘要

岩藻黄质(Fx)是褐藻中主要的叶黄素之一,已知其通过抑制细胞生长、细胞周期和半胱天冬酶激活对结直肠癌(CRC)化学预防有效。最近,我们观察到岩藻黄醇(FuOH),一种Fx的抗癌活性代谢产物,处理人CRC细胞后数小时会产生大量活的漂浮细胞,并诱导细胞凋亡。在本研究中,我们调查了FuOH是否会在人CRC细胞中诱导锚定依赖性凋亡,即“失巢凋亡”,以及整合素信号抑制。我们发现,暴露于2.5μM FuOH的细胞对人CRC细胞系DLD-1细胞明显表现出抗增殖和凋亡作用。用FuOH处理DLD-1细胞导致以钙黄绿素AM阴性/碘化丙啶-1阳性细胞和活的漂浮细胞为代表的失巢凋亡样变化增加。此外,FuOH处理6小时后降低了粘着斑激酶(FAK)激活,并改变了整合素β1的表达和分布。24小时后,细胞降低了过氧化物酶体增殖物激活受体γ(PPARγ)表达和蛋白激酶B(Akt)激活,并增加了整合素β1表达。我们的研究结果表明,FuOH可通过抑制人CRC细胞中的整合素信号来诱导CRC细胞发生失巢凋亡。

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