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Limiting the power of p53 through the ubiquitin proteasome pathway

机译:通过泛素蛋白酶体途径限制p53的功能

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摘要

The ubiquitin proteasome pathway is critical in restraining the activities of the p53 tumor suppressor. Numerous E3 and E4 ligases regulate p53 levels. Additionally, deubquitinating enzymes that modify p53 directly or indirectly also impact p53 function. When alterations of these proteins result in increased p53 activity, cells arrest in the cell cycle, senesce, or apoptose. On the other hand, alterations that result in decreased p53 levels yield tumor-prone phenotypes. This review focuses on the physiological relevance of these important regulators of p53 and their therapeutic implications.
机译:泛素蛋白酶体途径对于抑制p53肿瘤抑制因子的活性至关重要。许多E3和E4连接酶调节p53水平。另外,直接或间接修饰p53的去泛素化酶也影响p53的功能。当这些蛋白质的改变导致p53活性增加时,细胞就会在细胞周期中停滞,衰老或凋亡。另一方面,导致p53水平降低的改变会产生易发肿瘤的表型。这篇综述着重于这些重要的p53调节剂的生理相关性及其治疗意义。

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