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首页> 外文期刊>Journal of Gastrointestinal Cancer >Chemopreventive Effects of Non-steroidal Anti-inflammatory Drugs in Early Neoplasm of Experimental Colorectal Cancer: an Apoptosome Study
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Chemopreventive Effects of Non-steroidal Anti-inflammatory Drugs in Early Neoplasm of Experimental Colorectal Cancer: an Apoptosome Study

机译:非甾体类抗炎药在实验性大肠癌早期肿瘤中的化学预防作用:细胞凋亡研究。

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摘要

Apoptosis is a highly regulated mechanism of cell death where pro-apoptotic proteins and caspases play an important role. Activation of pro-caspases at a definite time is essential to control the whole caspase cascade. Mitochondrion contains some pro-apoptotic proteins, which need to come out in cytoplasm for apoptotic function such as Cytochrome c (Cyt c), while the Bcl-2 protein family works as the guard of mitochondrial membrane and prevents the escape of Cyt c. Once Cyt c is out in cytoplasm, it binds with Apaf-1 (another pro-apoptotic protein also essential for proper cell differentiation) and pro-caspase-9, forming the Apoptosome complex. In this study, the role of two non-steroidal anti-inflammatory drugs (NSAIDs), Diclofenac and Celecoxib, in experimentally induced early neoplasm of colon via apoptosome mechanism had been studied. It has been recognized that the prolonged use of NSAIDs has its effect on reducing the risk of colorectal cancer through apoptotic pathways. However, the role of NSAIDs in respect of apoptosome is not clear.
机译:凋亡是细胞死亡的高度调节的机制,其中促凋亡蛋白和胱天蛋白酶在其中起重要作用。在特定时间激活前胱天蛋白酶对控制整个胱天蛋白酶级联至关重要。线粒体含有一些促凋亡蛋白,这些蛋白需要凋亡才能在细胞质中释放出来,例如细胞色素c(Cyt c),而Bcl-2蛋白家族起着线粒体膜的保护作用,并阻止Cyt c逃逸。一旦Cyt c进入细胞质,它就会与Apaf-1(另一种促凋亡蛋白,对于正常的细胞分化也是必不可少的)和pro-caspase-9结合,形成凋亡小体复合物。在这项研究中,已经研究了两种非甾体抗炎药(双氯芬酸和塞来昔布)通过凋亡机制在实验性诱导结肠早期肿瘤中的作用。已经认识到,长期使用NSAID具有通过凋亡途径降低结直肠癌风险的作用。但是,NSAID在凋亡方面的作用尚不清楚。

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