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漆黄素通过p53介导的人肾癌Caki细胞中DR5表达上调诱导细胞凋亡。

Fisetin Induces Apoptosis Through p53-Mediated Up-Regulation of DR5 Expression in Human Renal Carcinoma Caki Cells.

作者信息

Min Kyoung-Jin, Nam Ju-Ock, Kwon Taeg Kyu

机构信息

Department of Immunology, School of Medicine, Keimyung University, 2800 Dalgubeoldaero, Dalseo-Gu, Daegu 704-701, Korea.

Department of Food Science and Biotechnology, Kyungpook National University, Daegu 41566, Korea.

出版信息

Molecules. 2017 Aug 2;22(8):1285. doi: 10.3390/molecules22081285.

Abstract

Fisetin is a natural compound found in fruits and vegetables such as strawberries, apples, cucumbers, and onions. Since fisetin can elicit anti-cancer effects, including anti-proliferation and anti-migration, we investigated whether fisetin induced apoptosis in human renal carcinoma (Caki) cells. Fisetin markedly induced sub-G1 population and cleavage of poly (ADP-ribose) polymerase (PARP), which is a marker of apoptosis, and increased caspase activation. We found that pan-caspase inhibitor (z-VAD-fmk) inhibited fisetin-induced apoptosis. In addition, fisetin induced death receptor 5 (DR5) expression at the transcriptional level, and down-regulation of DR5 by siRNA blocked fisetin-induced apoptosis. Furthermore, fisetin induced p53 protein expression through up-regulation of protein stability, whereas down-regulation of p53 by siRNA markedly inhibited fisetin-induced DR5 expression. In contrast, fisetin induced up-regulation of CHOP expression and reactive oxygen species production, which had no effect on fisetin-induced apoptosis. Taken together, our study demonstrates that fisetin induced apoptosis through p53 mediated up-regulation of DR5 expression at the transcriptional level.

摘要

非瑟酮是一种存在于草莓、苹果、黄瓜和洋葱等水果和蔬菜中的天然化合物。由于非瑟酮可引发抗癌作用,包括抗增殖和抗迁移,我们研究了非瑟酮是否能诱导人肾癌(Caki)细胞凋亡。非瑟酮显著诱导了亚G1期细胞群的形成以及聚(ADP - 核糖)聚合酶(PARP)的裂解,PARP是细胞凋亡的一个标志物,并且增加了半胱天冬酶的激活。我们发现泛半胱天冬酶抑制剂(z - VAD - fmk)抑制了非瑟酮诱导的细胞凋亡。此外,非瑟酮在转录水平诱导死亡受体5(DR5)表达,而通过小干扰RNA(siRNA)下调DR5可阻断非瑟酮诱导的细胞凋亡。此外,非瑟酮通过上调蛋白质稳定性诱导p53蛋白表达,而通过siRNA下调p53则显著抑制非瑟酮诱导的DR5表达。相反,非瑟酮诱导CHOP表达上调和活性氧生成增加,但这对非瑟酮诱导的细胞凋亡没有影响。综上所述,我们的研究表明,非瑟酮通过p53介导的转录水平上DR5表达上调诱导细胞凋亡。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/69f7/6151974/d0c49fa8baa5/molecules-22-01285-g001a.jpg

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