Sekeris C E
Institute of Biological Research and Biotechnology, National Hellenic Research Foundation, Athens, Greece.
J Cancer Res Clin Oncol. 1991;117(2):96-101. doi: 10.1007/BF01613131.
Recent advances in the molecular action of steroid hormones and in the role of oncogenes in cell transformation are considered in defining, at the molecular level, the involvement of steroid hormones in tumour formation. In the context of the generally accepted three-stage model of carcinogenesis, it is proposed that the hormonal steroids act as tumour promoters by modulating oncogene expression. It is postulated that the hormonal steroids act on cells in which the initiating carcinogen has either induced mutations in protooncogenes normally hormonally regulated or has induced changes in gene architecture, aligning protooncogenes to hormone-responsive elements, thus placing these genes under non-physiological hormonal control. In contrast to the defined action of solitary carcinogens on the genetic material, tumour promoters appear to act by various molecular pathways, one of which, as hypothesized for hormonal steroids, could be a direct effect on oncogene expression.
在分子水平上定义类固醇激素参与肿瘤形成的过程中,人们考虑了类固醇激素分子作用以及癌基因在细胞转化中的作用的最新进展。在普遍接受的致癌作用三阶段模型的背景下,有人提出激素类固醇通过调节癌基因表达而作为肿瘤促进剂起作用。据推测,激素类固醇作用于这样的细胞,在这些细胞中,引发致癌物要么在通常受激素调节的原癌基因中诱导了突变,要么诱导了基因结构的变化,使原癌基因与激素反应元件对齐,从而使这些基因处于非生理性的激素控制之下。与单一致癌物对遗传物质的明确作用相反,肿瘤促进剂似乎通过各种分子途径起作用,其中之一,如对激素类固醇所假设的,可能是对癌基因表达的直接影响。