印度獐牙菜苦素A通过降解结直肠癌细胞系中的Mad2-Cdc20复合物来调节纺锤体组装检查点。

Withaferin A modulates the Spindle assembly checkpoint by degradation of Mad2-Cdc20 complex in colorectal cancer cell lines.

作者信息

Das Tania, Roy Kumar Singha, Chakrabarti Tulika, Mukhopadhyay Sibabrata, Roychoudhury Susanta

机构信息

Cancer Biology and Inflammatory Disorder Division, CSIR-Indian Institute of Chemical Biology, 4, Raja S.C. Mullick Road, Jadavpur, Kolkata 700032, India.

Cancer Biology and Inflammatory Disorder Division, CSIR-Indian Institute of Chemical Biology, 4, Raja S.C. Mullick Road, Jadavpur, Kolkata 700032, India.

出版信息

Biochem Pharmacol. 2014 Sep 1;91(1):31-9. doi: 10.1016/j.bcp.2014.06.022. Epub 2014 Jul 1.

Abstract

Withania somnifera L. Dunal (Ashwagandha) is used over centuries in the ayurvedic medicines in India. Withaferin A, a withanolide, is the major compound present in leaf extract of the plant which shows anticancer activity against leukemia, breast cancer and colorectal cancer. It arrests the ovarian cancer cells in the G2/M phase in dose dependent manner. In the current study we show the effect of Withaferin A on cell cycle regulation of colorectal cancer cell lines HCT116 and SW480 and its effect on cell fate. Treatment of these cells with this compound leads to apoptosis in a dose dependent manner. It causes the G2/M arrest in both the cell lines. We show that Withaferin A (WA) causes mitotic delay by blocking Spindle assembly checkpoint (SAC) function. Apoptosis induced by Withaferin A is associated with proteasomal degradation of Mad2 and Cdc20, an important constituent of the Spindle Checkpoint Complex. Further overexpression of Mad2 partially rescues the deleterious effect of WA by restoring proper anaphase initiation and keeping more number of cells viable. We hypothesize that Withaferin A kills cancer cells by delaying the mitotic exit followed by inducing chromosome instability.

摘要

印度人参(Withania somnifera L. Dunal)在印度阿育吠陀医学中已被使用了几个世纪。睡茄内酯A是该植物叶提取物中的主要化合物,对白血病、乳腺癌和结直肠癌具有抗癌活性。它以剂量依赖的方式使卵巢癌细胞停滞在G2/M期。在本研究中,我们展示了睡茄内酯A对结直肠癌细胞系HCT116和SW480细胞周期调控的影响及其对细胞命运的作用。用该化合物处理这些细胞会以剂量依赖的方式导致细胞凋亡。它使两种细胞系都出现G2/M期停滞。我们发现睡茄内酯A(WA)通过阻断纺锤体组装检查点(SAC)功能导致有丝分裂延迟。睡茄内酯A诱导的细胞凋亡与纺锤体检查点复合物的重要组成部分Mad2和Cdc20的蛋白酶体降解有关。进一步过表达Mad2可通过恢复正常的后期起始并使更多细胞存活来部分挽救WA的有害作用。我们推测睡茄内酯A通过延迟有丝分裂退出并随后诱导染色体不稳定来杀死癌细胞。

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