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含氮双膦酸盐通过抑制 Ras 信号通路和 Bim 介导的内在凋亡途径激活诱导造血肿瘤细胞凋亡。

Nitrogen-containing bisphosphonates induce apoptosis of hematopoietic tumor cells via inhibition of Ras signaling pathways and Bim-mediated activation of the intrinsic apoptotic pathway.

机构信息

Division of Pharmacotherapy, Kinki University School of Pharmacy, Kowakae, Higashi-Osaka 577-8502, Japan.

出版信息

Biochem Pharmacol. 2013 Jan 15;85(2):163-72. doi: 10.1016/j.bcp.2012.10.009. Epub 2012 Oct 17.

Abstract

Nitrogen-containing bisphosphonates (N-BPs) induce apoptosis in tumor cells by inhibiting the prenylation of small G-proteins. However, the details of the apoptosis-inducing mechanism remain obscure. The present study showed that the induction of apoptosis by N-BPs in hematopoietic tumor cells is mediated by mitochondrial apoptotic signaling pathways, which are activated by the suppression of geranylgeranyl pyrophosphate (GGPP) biosynthesis. Furthermore, N-BPs decreased the levels of phosphorylated extracellular signal-regulated kinase (ERK) and mTOR via suppression of Ras prenylation and enhanced Bim expression. The present results indicated that N-BPs induce apoptosis by decreasing the mitochondrial transmembrane potential, increasing the activation of caspase-9 and caspase-3, and enhancing Bim expression through inhibition of the Ras/MEK/ERK and Ras/mTOR pathways. The accumulation of N-BPs in bones suggests that they may act more effectively on tumors that have spread to bones or on Ras-variable tumors. This is the first study to show that the specific molecular pathways of N-BP-induced apoptosis.

摘要

含氮双膦酸盐(N-BPs)通过抑制小 G 蛋白的异戊烯化来诱导肿瘤细胞凋亡。然而,凋亡诱导机制的细节仍不清楚。本研究表明,N-BPs 通过抑制法尼基焦磷酸(GGPP)生物合成,激活线粒体凋亡信号通路,诱导造血肿瘤细胞凋亡。此外,N-BPs 通过抑制 Ras 异戊烯化和增强 Bim 表达,降低磷酸化细胞外信号调节激酶(ERK)和 mTOR 的水平。本研究结果表明,N-BPs 通过降低线粒体跨膜电位、增加 caspase-9 和 caspase-3 的激活以及增强 Bim 表达,诱导细胞凋亡,这是通过抑制 Ras/MEK/ERK 和 Ras/mTOR 通路实现的。N-BPs 在骨骼中的积累表明,它们可能对已扩散到骨骼的肿瘤或 Ras 可变肿瘤更有效。这是首次表明 N-BP 诱导凋亡的特定分子途径的研究。

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