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维甲酰苯胺抑制 Notch-1:结肠癌发生的治疗靶点。

Notch-1 inhibition by Withaferin-A: a therapeutic target against colon carcinogenesis.

机构信息

Department of Clinical Sciences, College of Health Sciences, University of Kentucky, Lexington, Kentucky 40536-0200, USA.

出版信息

Mol Cancer Ther. 2010 Jan;9(1):202-10. doi: 10.1158/1535-7163.MCT-09-0771. Epub 2010 Jan 6.

Abstract

Notch signaling plays a crucial role in the development of colon cancer; targeting the Notch pathway may sensitize colon cancers to various adjuvant agents. The focus of our current study is to identify natural compounds that target Notch signaling and that might be beneficial for the prevention and treatment of colon cancer. Withaferin-A (WA) is a bioactive compound derived from Withania somnifera, which inhibits Notch-1 signaling and downregulates prosurvival pathways, such as Akt/NF-kappaB/Bcl-2, in three colon cancer cell lines (HCT-116, SW-480, and SW-620). In addition, WA downregulated the expression of mammalian target of rapamycin signaling components, pS6K and p4E-BP1, and activated c-Jun-NH(2)-kinase-mediated apoptosis in colon cancer cells. We also established the molecular link between Notch/Akt/mammalian target of rapamycin signaling by complementary approaches (i.e., overexpression of Notch-1 or inhibition of Notch-1 by small interfering RNA). Our results suggest that WA inhibits Notch-mediated prosurvival signaling, which facilitates c-Jun-NH(2)-kinase-mediated apoptosis in colon cancer cell lines. These results underscore the anticancer activity of WA, which exhibits potential for further development for targeted chemotherapy and/or chemoprevention strategies in the context of colon cancer.

摘要

Notch 信号通路在结肠癌的发生发展中起着至关重要的作用;靶向 Notch 通路可能会使结肠癌对各种辅助药物敏感。我们目前的研究重点是确定靶向 Notch 信号通路的天然化合物,这些化合物可能对结肠癌的预防和治疗有益。Withaferin-A (WA) 是一种从印度人参中提取的生物活性化合物,它可以抑制 Notch-1 信号通路,并下调 Akt/NF-kappaB/Bcl-2 等存活途径,在三种结肠癌细胞系(HCT-116、SW-480 和 SW-620)中。此外,WA 下调了哺乳动物雷帕霉素靶蛋白信号成分 pS6K 和 p4E-BP1 的表达,并激活了结肠癌细胞中的 c-Jun-NH(2)-kinase 介导的细胞凋亡。我们还通过互补方法(即 Notch-1 的过表达或通过小干扰 RNA 抑制 Notch-1)建立了 Notch/Akt/哺乳动物雷帕霉素靶蛋白信号之间的分子联系。我们的研究结果表明,WA 抑制 Notch 介导的存活信号,这有助于结肠癌细胞系中 c-Jun-NH(2)-kinase 介导的细胞凋亡。这些结果突出了 WA 的抗癌活性,这为进一步开发针对结肠癌的靶向化疗和/或化学预防策略提供了潜力。

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