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首页> 外文期刊>Cell cycle >The roles of synoviolin in crosstalk between endoplasmic reticulum stress-induced apoptosis and p53 pathway.
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The roles of synoviolin in crosstalk between endoplasmic reticulum stress-induced apoptosis and p53 pathway.

机译:滑膜增生蛋白在内质网应激诱导的细胞凋亡与p53通路之间的串扰中的作用。

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摘要

Endopalsmic reticulum (ER) is specialized organelle to maintain the integrity of secreted and membranous proteins. ER also senses so-called "ER stress", which is a result of various internal and external stresses, and triggers apoptosis when the diverse attempts to accommodate with the stress are in fail. The impairment these ER functions has been implicated in several human diseases, in which aberrant ER stress induced apoptosis is observed. We discuss about another disease model related with ER mediated apoptosis based on the recent studies about Synoviolin, an E3 ubiquitin ligase inherently utilized for ER associated degradation (ERAD). In addition to its canonical role in ERAD, Synoviolin targets tumor suppressor gene p53 for proteasomal degradation, suggesting the crosstalk between ERAD and p53 mediated apoptotic pathway under ER stress. Together with the anti-apoptotic property of Synoviolin previously elucidated by both in vitro and in vivo analyses, its new function in p53 regulation may provide a new insight into the pathomechanism of proliferative diseases such as cancer or rheumatoid arthritis.
机译:眼睑内质网(ER)是专门的细胞器,可维持分泌和膜蛋白的完整性。 ER还感觉到所谓的“ ER压力”,这是各种内部和外部压力的结果,并在适应压力的各种尝试失败时触发了细胞凋亡。这些ER功能的损害与几种人类疾病有关,其中观察到异常的ER应激诱导的细胞凋亡。我们基于有关Synoviolin的最新研究,讨论与ER介导的细胞凋亡相关的另一种疾病模型,Synoviolin是固有用于ER相关降解(ERAD)的E3泛素连接酶。 Synoviolin除了在ERAD中具有典型作用外,还针对肿瘤抑制基因p53进行蛋白酶体降解,这表明ER应激下ERAD与p53介导的凋亡途径之间存在串扰。连同先前在体外和体内分析中阐明的Synoviolin的抗凋亡特性一起,其在p53调节中的新功能可能为增生性疾病如癌症或类风湿性关节炎的发病机理提供新的见解。

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