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人参皂苷Rg3通过激活Bcl-2相关X蛋白诱导人多发性骨髓瘤细胞凋亡。

Ginsenoside Rg3 induces apoptosis in human multiple myeloma cells via the activation of Bcl-2-associated X protein.

作者信息

Luo Yun, Zhang Ping, Zeng Han-Qing, Lou Shi-Feng, Wang Dao-Xin

机构信息

Department of Hematology, Second Affiliated Hospital of Chongqing Medical University, Chongqing 404000, P.R. China.

出版信息

Mol Med Rep. 2015 Sep;12(3):3557-3562. doi: 10.3892/mmr.2015.3802. Epub 2015 May 19.

Abstract

Ginsenoside Rg3 is one of the main constituents isolated from Panax ginseng, and exhibits cytotoxic effects against cancer cells. The present study aimed to investigate the effects of ginsenoside Rg3 on human multiple myeloma cells, and determine the underlying molecular mechanisms. The cells were exposed to ginsenoside Rg3 at various concentrations (0‑80 µM) for 48 h. A subsequent cell proliferation assay demonstrated that treatment with ginsenoside Rg3 resulted in a dose‑dependent inhibition of the proliferation of U266 and RPMI8226 cells. Furthermore, exposure to ginsenoside Rg3 led to a marked increase in the rate of apoptosis in the U266 cells, coupled with increased caspase‑3 activity. The ginsenoside Rg3‑treated cells also exhibited an elevation in the expression of B‑cell lymphoma 2‑associated X protein (Bax), a pro‑apoptotic protein. Notably, knockdown of Bax protected the U266 cells from Rg3‑induced apoptosis. Overall, these findings suggested that ginsenoside Rg3 induced apoptosis in multiple myeloma cells, at least partially, through upregulation of the expression of Bax.

摘要

人参皂苷Rg3是从人参中分离出的主要成分之一,对癌细胞具有细胞毒性作用。本研究旨在探讨人参皂苷Rg3对人多发性骨髓瘤细胞的影响,并确定其潜在的分子机制。将细胞暴露于不同浓度(0-80μM)的人参皂苷Rg3中48小时。随后的细胞增殖试验表明,人参皂苷Rg3处理导致U266和RPMI8226细胞增殖受到剂量依赖性抑制。此外,暴露于人参皂苷Rg3导致U266细胞凋亡率显著增加,同时半胱天冬酶-3活性增强。经人参皂苷Rg3处理的细胞还表现出促凋亡蛋白B细胞淋巴瘤2相关X蛋白(Bax)表达升高。值得注意的是,敲低Bax可保护U266细胞免受Rg3诱导的凋亡。总体而言,这些发现表明人参皂苷Rg3至少部分通过上调Bax表达诱导多发性骨髓瘤细胞凋亡。

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