Lipsick Joseph
Departments of Pathology, Genetics, and Biology, Stanford University, Stanford, California 94305-5324, USA
Cold Spring Harb Perspect Med. 2025 Feb 3;15(2):a035931. doi: 10.1101/cshperspect.a035931.
The p53 tumor suppressor was first identified as a cellular protein that bound to the large T antigen in SV40-transformed cells. Initially thought to be the product of an oncogene, p53 turned out to be an anticancer protein whose loss or mutation could promote tumorigenesis. Subsequent work revealed it functions as a DNA-binding transcription factor central to the DNA damage response and cell cycle control. In this excerpt from his forthcoming book on the history of cancer research, Joe Lipsick looks back at the discovery of p53 and the groundbreaking work that revealed its role as "guardian of the genome."
p53肿瘤抑制蛋白最初被鉴定为一种细胞蛋白,它能与SV40转化细胞中的大T抗原结合。最初被认为是一种癌基因的产物,p53后来被证明是一种抗癌蛋白,其缺失或突变会促进肿瘤发生。随后的研究表明,它作为一种DNA结合转录因子,在DNA损伤反应和细胞周期控制中起着核心作用。在即将出版的关于癌症研究历史的书中的这段摘录中,乔·利普西克回顾了p53的发现以及揭示其作为“基因组守护者”作用的开创性工作。