The Breakthrough Toby Robins Breast Cancer Research Centre, Institute of Cancer Research, Mary-Jean Mitchell Green Building, Chester Beatty Laboratories, Fulham Road, London SW3 6JB, UK.
Curr Opin Cell Biol. 2010 Dec;22(6):872-81. doi: 10.1016/j.ceb.2010.08.025. Epub 2010 Sep 29.
The processes of dying are as tightly regulated as those of growth and proliferation, and together they establish a finely tuned balance that ensures proper organ size and function. Failure in the regulation of these responses lies at the heart of many human diseases. Certain members of the inhibitor of apoptosis (IAP) protein family function as important gatekeepers of cell death and survival. While IAPs can regulate cell death by controlling caspases, they also modulate other signalling processes that impact on cell viability. Probably the most important contribution of IAPs to cell survival and tumorigenesis resides in the ability of a number of IAPs to act as ubiquitin-E3 ligases regulating NF-κB signalling. Here, we discuss the latest insights into the ubiquitin-related roles of IAPs and how this contributes to the survival of cells and the organism.
凋亡抑制蛋白(IAP)家族的某些成员作为细胞死亡和存活的重要守门员,其功能是调节细胞死亡和存活的重要守门员。虽然 IAP 可以通过控制半胱天冬酶来调节细胞死亡,但它们也调节其他影响细胞活力的信号转导过程。IAP 对细胞存活和肿瘤发生的最重要贡献可能在于许多 IAP 能够作为调节 NF-κB 信号的泛素-E3 连接酶发挥作用。在这里,我们讨论了 IAP 与泛素相关的作用的最新见解,以及这如何有助于细胞和生物体的存活。