Manenti G, De Gregorio L, Gariboldi M, Falvella F S, Zanesi N, Pierotti M A, Dragani T A
Division of Experimental Oncology A, Istituto Nazionale Tumori, Milan, Italy.
Recent Results Cancer Res. 1998;154:292-7. doi: 10.1007/978-3-642-46870-4_20.
Genetic linkage experiments using crosses between mouse inbred strains with an inherited predisposition and resistance to lung cancer make it possible to investigate the genetics of the complex inheritance of susceptibility and resistance to lung cancer. We have previously mapped a major locus (pulmonary adenoma susceptibility 1, Pas1) affecting inherited predisposition to lung cancer in mice onto chromosome 6, near Kras2. Appropriate crosses that include Pas1/+ mice provide a model system for identifying loci that can modify the lung cancer predisposition phenotype caused by Pas1. Using this approach, we mapped the pulmonary adenoma resistance 1 (Par1) locus on to mouse chromosome 11; this locus selectively inhibits lung tumor development in Pas1/+ animals and therefore behaves like a modulator gene of Pas1. More recently, we have mapped lung tumor modifier loci specifically affecting the initiation and progression of lung cancer. Thus experimental models provide an essential tool for the mapping of lung cancer susceptibility/resistance genes and for the subsequent cloning of candidate genes.
利用具有遗传性肺癌易感性和抗性的近交系小鼠品系之间的杂交进行的遗传连锁实验,使得研究肺癌易感性和抗性复杂遗传的遗传学成为可能。我们之前已将影响小鼠遗传性肺癌易感性的一个主要基因座(肺腺瘤易感性1,Pas1)定位到6号染色体上靠近Kras2的位置。包含Pas1/+小鼠的合适杂交提供了一个模型系统,用于鉴定可改变由Pas1引起的肺癌易感性表型的基因座。使用这种方法,我们将肺腺瘤抗性1(Par1)基因座定位到小鼠11号染色体上;该基因座选择性抑制Pas1/+动物的肺肿瘤发展,因此其行为类似于Pas1的调节基因。最近,我们已经定位了特异性影响肺癌起始和进展的肺肿瘤修饰基因座。因此,实验模型为肺癌易感性/抗性基因的定位以及随后候选基因的克隆提供了重要工具。