Bykov Vladimir J N, Wiman Klas G
Department of Oncology-Pathology, Cancer Center Karolinska, Karolinska Institute, Stockholm, Sweden.
Ann Med. 2003;35(7):458-65. doi: 10.1080/07853890310017152.
The p53 transcription factor prevents tumor development through induction of cell cycle arrest and cell death by apoptosis. As many as several hundred genes or more are regulated by p53. Around half of all human tumors carry p53 mutation, mostly point mutations that abrogate p53's specific DNA binding and transactivation activity. p53 mutation is associated with poor therapeutic response and prognosis. Tumors that carry wild type p53 often have other alterations in the p53 pathway that ablate the p53 response. Several strategies have been designed to restore p53 function in human tumors, including p53 gene therapy, reactivation of mutant p53, and activation of wild type p53 by inhibition of the p53 antagonist MDM2. In all cases, the aim is to eliminate the tumor through induction of massive apoptosis.
p53转录因子通过诱导细胞周期停滞和细胞凋亡导致的细胞死亡来预防肿瘤发展。多达数百个或更多基因受p53调控。所有人类肿瘤中约有一半携带p53突变,大多为点突变,这些突变会消除p53的特异性DNA结合和反式激活活性。p53突变与治疗反应不佳和预后不良相关。携带野生型p53的肿瘤在p53通路中常常有其他改变,从而消除p53反应。已经设计了几种策略来恢复人类肿瘤中的p53功能,包括p53基因治疗、突变型p53的重新激活以及通过抑制p53拮抗剂MDM2来激活野生型p53。在所有情况下,目标都是通过诱导大量细胞凋亡来消除肿瘤。