Bellamy C O
Department of Pathology, University Medical School, Edinburgh, UK.
Br Med Bull. 1997;53(3):522-38. doi: 10.1093/oxfordjournals.bmb.a011628.
Loss of function of the p53 tumour suppressor gene is a frequent and important event in the genesis or progression of many human malignancies. Loss of p53 dependent apoptosis is believed to be critical to carcinogenesis in many of these cases, suggesting the possibility to therapeutically restore this pathway and directly eliminate malignant cells or increase or restore their sensitivity to chemotherapeutic agents. The regulation of p53-dependent responses is complex and variable between cell types, and whether a cell undergoes apoptosis after activation of p53 is highly sensitive to signal context, including environmental and cell intrinsic influences. This article focuses upon p53-dependent apoptosis, considering current understanding of the biochemical steps involved, the factors determining selection of apoptosis over other p53-dependent responses, the significance of p53-dependent apoptosis for the genesis, progression and drug resistance of human cancers, and finally the prospects for clinical manipulation of this pathway in cancer therapy.
p53肿瘤抑制基因功能的丧失在许多人类恶性肿瘤的发生或发展过程中是一个常见且重要的事件。在许多此类病例中,p53依赖的细胞凋亡丧失被认为对致癌作用至关重要,这表明有可能通过治疗手段恢复该途径,直接消除恶性细胞,或增强或恢复它们对化疗药物的敏感性。p53依赖反应的调控是复杂的,并且在不同细胞类型之间存在差异,而且细胞在p53激活后是否发生凋亡对信号背景高度敏感,包括环境和细胞内在影响。本文聚焦于p53依赖的细胞凋亡,探讨了对所涉及生化步骤的当前理解、决定选择细胞凋亡而非其他p53依赖反应的因素、p53依赖的细胞凋亡对人类癌症发生、发展和耐药性的意义,以及最后在癌症治疗中对该途径进行临床操控的前景。