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首页> 外文期刊>International journal of biotechnology and bioengineering research >Insilico Analysis of PAC-1 as an Enhancer for Caspase-3 to Promote Apoptosis
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Insilico Analysis of PAC-1 as an Enhancer for Caspase-3 to Promote Apoptosis

机译:pac-1作为caspase-3的增强子的ininilico分析以促进凋亡

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摘要

Apoptosis is a selective process for deletion of cells. It is generally involved in embryogenesis. tissue remodeling and also to maintain organ size and function. Sequential activation of caspases plays an important role in programmed cell death. In the caspase family, caspase-3 is an important effector protease that cleaves many downstream proteins. Damage in apoplotic pathways promotes uncontrolled growth of cancer cell. Analyses on clinical researches indicate that anticancer drugs activate cascade of apoptotic pathways either by positively or negatively regulating cell death induction. PAC-1 is such a compound, synthesized chemically that selectively induces apoptosis in cancer cells. This article reviews the effect of PAC-1 computationally, as a promoter for caspase-3. Docking of caspase-3 proteins with the specific ligand i.e., compound PAC-1. showed high interaction. The result shows that the PAC-1 facilitates the activation of caspasc-3 and thus promotes the activation of apoptotic pathways and prevents the uncontrolled proliferation of cancer cells.
机译:凋亡是细胞缺失的选择性过程。它通常参与胚胎发生。组织重塑,并保持器官的大小和功能。胱天蛋白酶的顺序激活在程序性细胞死亡中起重要作用。在caspase家族中,caspase-3是裂解许多下游蛋白的重要效应蛋白酶。凋亡途径的损害促进了癌细胞的不受控制的生长。对临床研究的分析表明,抗癌药物通过积极或负调节细胞死亡诱导来激活凋亡途径的级联反应。 PAC-1是一种化学合成的化合物,可以选择性地诱导癌细胞凋亡。本文回顾了PAC-1在计算上的效果,作为caspase-3的启动子。与特定配体的caspase-3蛋白对接caspase-3蛋白,即化合物pac-1。显示高相互作用。结果表明,PAC-1促进了CASPASC-3的激活,从而促进了凋亡途径的激活,并防止了癌细胞的不受控制。

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