Kaye F J, Kratzke R A, Gerster J L, Lin P S
NCI-Navy Medical Oncology Branch, Naval Hospital, Bethesda, MD 20817.
Am Rev Respir Dis. 1990 Dec;142(6 Pt 2):S44-7. doi: 10.1164/ajrccm/142.6_Pt_2.S44.
The observation that carcinogen exposure is strongly associated with the probability of developing pulmonary neoplasms has suggested for many years that acquired somatic mutations play a key role in the genesis of these environmentally induced cancers. With the advent of new techniques in cytogenetics and in the molecular analysis of DNA extracted from lung tumors, it has now become possible to test this hypothesis and to search for candidate genes that may be targeted by the chronic exposure of these environmental insults. Early work in this field, studying lung tumors of different histologic types, appears to implicate several distinct chromosomal loci (at chromosomes 3p, 13q, 17p, and others), suggesting that sequential genetic events occur during the initiation and progression pathways to pulmonary tumorigenesis. Identifying the candidate gene products and understanding the chronology and stringency of mutational events at these loci will be an essential goal to understanding the cellular basis of lung tumors and for developing strategies for the next generation of diagnostic and therapeutic studies.
多年来,致癌物暴露与发生肺部肿瘤的可能性密切相关这一观察结果表明,获得性体细胞突变在这些环境诱导癌症的发生中起关键作用。随着细胞遗传学和从肺肿瘤中提取的DNA分子分析新技术的出现,现在已能够检验这一假设,并寻找可能因这些环境损害的长期暴露而成为靶点的候选基因。该领域早期研究不同组织学类型的肺肿瘤,似乎涉及几个不同的染色体位点(位于3号染色体短臂、13号染色体长臂、17号染色体短臂等),这表明在肺部肿瘤发生的起始和进展途径中会发生一系列遗传事件。确定候选基因产物并了解这些位点突变事件的时间顺序和严格性,将是理解肺肿瘤细胞基础以及制定下一代诊断和治疗研究策略的一个重要目标。