Soussi T
Université Pierre & Marie Curie, Unité 301 INSERM Institut de Génétique Moléculaire, Paris, France.
Mol Med Today. 1996 Jan;2(1):32-7. doi: 10.1016/1357-4310(96)88756-9.
The gene encoding the tumour suppressor protein p53 is one of the most commonly mutated genes in human cancers. Analysis of the mutational events that target the p53 gene has revealed evidence for both exogenous and endogenous mutational mechanisms. For example, the p53 mutational spectrum reveals evidence for a direct causal effect of ultraviolet radiation in skin cancer, of aflatoxin B1 in liver cancer and of tobacco smoke in lung cancer. This novel field, molecular epidemiology of human cancer risk, has added a new dimension to classical associative epidemiology by providing a direct link between human cancer and carcinogen exposure.
编码肿瘤抑制蛋白p53的基因是人类癌症中最常发生突变的基因之一。对靶向p53基因的突变事件进行分析后发现了外源性和内源性突变机制的证据。例如,p53突变谱揭示了紫外线辐射在皮肤癌、黄曲霉毒素B1在肝癌以及烟草烟雾在肺癌中存在直接因果效应的证据。这个新领域,即人类癌症风险的分子流行病学,通过在人类癌症与致癌物暴露之间建立直接联系,为经典的关联流行病学增添了新的维度。