Katsuumi Goro, Shimizu Ippei, Yoshida Yohko, Minamino Tohru
Nihon Rinsho. 2016 Sep;74(9):1491-1496.
Protein p53 is described as guardian of the genome contributing for the suppression of tumorigenesis. p53 is also known to be the critical regulator of cellular senescence. It is activated by various genomic stresses including telomere attrition, excessive mitogenic sig- naling and genotoxic agents(eg. reactive oxygen species), and mediates cellular senescence. Senescent cells develop growth arrest, associated with altered gene profiles. These changes induce chronic inflammation and organ dysfunction, promoting pathologies in age related disorders. In this review, we delineate the role of p53 induced cellular senescence in age related disorders, such as obesity/diabetes and heart failure.
蛋白质p53被描述为基因组的守护者,有助于抑制肿瘤发生。p53也被认为是细胞衰老的关键调节因子。它可被包括端粒磨损、过度有丝分裂信号和基因毒性剂(如活性氧)在内的各种基因组应激激活,并介导细胞衰老。衰老细胞会出现生长停滞,并伴有基因谱改变。这些变化会引发慢性炎症和器官功能障碍,促进与年龄相关疾病的病理发展。在本综述中,我们阐述了p53诱导的细胞衰老在肥胖/糖尿病和心力衰竭等与年龄相关疾病中的作用。