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人参皂苷代谢物通过调节 AMP 激活的蛋白激酶诱导 MCF-7 乳腺癌细胞凋亡。

Ginseng saponin metabolite induces apoptosis in MCF-7 breast cancer cells through the modulation of AMP-activated protein kinase.

机构信息

Department of Marine Life Science, Jeju National University, Jeju-si 690-756, Republic of Korea.

出版信息

Environ Toxicol Pharmacol. 2010 Sep;30(2):134-40. doi: 10.1016/j.etap.2010.04.008. Epub 2010 May 10.

Abstract

Previous studies have shown that the ginseng saponin metabolite, Compound K (20-O-d-glucopyranosyl-20(S)-protopanaxadiol, IH901), suppresses proliferation of various cancers and induces apoptosis. AMP-activated protein kinase (AMPK) is a sensor of cellular energy states and is involved in apoptosis of cancer cells. We hypothesized that Compound K may exert cytotoxicity in MCF-7 human breast cancer cells through modulation of AMPK, followed by a decrease in cyclooxygenase-2 (COX-2) expression. Compound K inhibited cell growth, induced apoptosis via generation of reactive oxygen species (ROS), as well as decreasing COX-2 expression and prostaglandin E(2) (PGE(2)) levels. These effects of Compound K were induced via an AMPK-dependent pathway and were abrogated by a specific AMPK inhibitor. These results suggest that Compound K induced apoptosis by modulating AMPK-COX-2 signaling in MCF-7 human breast cancer cells.

摘要

先前的研究表明,人参皂苷代谢物,化合物 K(20-O-β-D-吡喃葡萄糖基-20(S)-原人参二醇,IH901),可抑制多种癌症的增殖并诱导细胞凋亡。AMP 激活的蛋白激酶(AMPK)是细胞能量状态的传感器,参与癌细胞的凋亡。我们假设化合物 K 可能通过调节 AMPK,随后降低环氧化酶-2(COX-2)的表达,在 MCF-7 人乳腺癌细胞中发挥细胞毒性作用。化合物 K 通过产生活性氧(ROS)抑制细胞生长,诱导细胞凋亡,同时降低 COX-2 表达和前列腺素 E2(PGE2)水平。化合物 K 的这些作用是通过 AMPK 依赖的途径诱导的,并被特异性 AMPK 抑制剂阻断。这些结果表明,化合物 K 通过调节 MCF-7 人乳腺癌细胞中的 AMPK-COX-2 信号通路诱导细胞凋亡。

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