Brandt-Rauf P W
Columbia University, New York, NY 10032.
J Occup Med. 1988 May;30(5):399-404. doi: 10.1097/00043764-198805000-00005.
Molecular epidemiology is making rapid strides in the area of biologic monitoring for occupational cancer. Approaches are being developed and applied at the level of internal dose indicators (eg, urinary mutagenicity), biologically effective dose indicators (eg, carcinogen adducts), and preclinical response indicators (eg, chromosomal alterations). However, significant questions remain to be answered before these markers can be applied on a wider basis. In particular, it remains unclear how these markers relate to the clinical outcome of significance, namely occupational cancer. Recent developments in the understanding of oncogenes and their protein products offer new opportunities for the molecular epidemiology of occupational cancer through the use of these markers which seem to be critically involved in the oncogenic process and closely related to disease outcome. Thus, for example, through the application of immunoblotting of urine or serum with monoclonal antibodies to various oncogene proteins in cohorts of workers with potential carcinogen exposure, it may be feasible to identify those individuals most at risk for the development of occupational cancer at a sufficiently early stage that the oncogenic process could be aborted.
分子流行病学在职业性癌症的生物监测领域正取得迅速进展。针对内剂量指标(如尿致突变性)、生物有效剂量指标(如致癌物加合物)和临床前反应指标(如染色体改变),相关方法正在研发并应用。然而,在这些标志物能够更广泛应用之前,仍有一些重大问题有待解答。尤其是,这些标志物与具有重要意义的临床结果,即职业性癌症之间的关系仍不明确。对癌基因及其蛋白质产物认识的最新进展,通过使用这些似乎在致癌过程中起关键作用且与疾病结果密切相关的标志物,为职业性癌症的分子流行病学提供了新机遇。例如,在有潜在致癌物暴露的工人群体中,通过用针对各种癌基因蛋白质的单克隆抗体对尿液或血清进行免疫印迹,在致癌过程能够被阻断的足够早期阶段识别出那些最易患职业性癌症的个体可能是可行的。