Herzog C R, Wang Y, You M
Department of Pathology, Medical College of Ohio, Toledo 43699, USA.
Oncogene. 1995 Nov 2;11(9):1811-5.
Loss of heterozygosity (LOH) of distal chromosome 4 was studied to localize a putative tumor suppressor gene in mouse lung neoplasia. Previous studies have implicated this region and its homologue on human chromosome 1p36-34 as sites of potential tumor suppressor genes. One hundred adenocarcinomas and 38 adenomas of the mouse lung were examined for LOH using nine simple sequence length polymorphism markers in a polymerase chain reaction-based approach. Forty-four adenocarcinomas displayed allele loss, all of which included losses at marker D4MIT54, which defined a critical region of 3 centiMorgans as the likely location of a putative tumor suppressor gene. In 58% of the tumors displaying LOH, all markers used in this study incurred allele loss. In contrast, retention of heterozygosity was observed at all markers tested in each of the adenomas studied, which suggests that the inactivation of this tumor suppressor gene participates in mouse lung tumor progression.
为了在小鼠肺癌中定位一个假定的肿瘤抑制基因,对4号染色体远端的杂合性缺失(LOH)进行了研究。先前的研究表明,该区域及其在人类1号染色体1p36 - 34上的同源区域是潜在肿瘤抑制基因的位点。使用基于聚合酶链反应的方法,利用9个简单序列长度多态性标记物,对100例小鼠肺腺癌和38例腺瘤进行了LOH检测。44例腺癌出现等位基因缺失,所有这些缺失都包括标记物D4MIT54处的缺失,该标记物确定了一个3厘摩的关键区域,作为假定肿瘤抑制基因的可能位置。在58%显示LOH的肿瘤中,本研究中使用的所有标记物都出现了等位基因缺失。相比之下,在所研究的每个腺瘤中,所有测试标记物均观察到杂合性保留,这表明该肿瘤抑制基因的失活参与了小鼠肺癌的进展。