Zeiger M A, Gnarra J R, Zbar B, Linehan W M, Pass H I
Surgery Branch, National Cancer Institute, Bethesda, Maryland 20892.
Genes Chromosomes Cancer. 1994 Sep;11(1):15-20. doi: 10.1002/gcc.2870110104.
Cytogenetic analysis of mesothelioma cell lines and solid tumors has documented non-random chromosomal abnormalities on the short arm of chromosome 3 from 3p14 to 3p25. We therefore examined nine mesothelioma cell lines, their corresponding tumors, and 15 additional mesothelioma tumors for loss of heterozygosity on 3p from 3p13 to 3p25.5 by polymerase chain reaction and restriction fragment length polymorphism analysis at 8 loci: D3S3, D3S30, D3S6, D3S2, D3S32, D3F15S2, THRB, and VHL. Loss of heterozygosity was documented by loss of one of two alleles in the tumor DNA whose corresponding normal DNA was heterozygous and was documented in four of nine mesothelioma cell lines and six of 15 mesothelioma tumors or a total of 42% of the mesotheliomas evaluated. This study suggests the involvement of a gene on the short arm of chromosome 3 in the development of mesotheliomas.
间皮瘤细胞系和实体瘤的细胞遗传学分析已证明,在3号染色体短臂3p14至3p25区域存在非随机染色体异常。因此,我们通过聚合酶链反应和8个位点(D3S3、D3S30、D3S6、D3S2、D3S32、D3F15S2、THRB和VHL)的限制性片段长度多态性分析,检测了9个间皮瘤细胞系、其对应的肿瘤以及另外15个间皮瘤肿瘤在3p13至3p25.5区域的杂合性缺失情况。杂合性缺失通过肿瘤DNA中两个等位基因之一的缺失来记录,其对应的正常DNA为杂合型,在9个间皮瘤细胞系中的4个以及15个间皮瘤肿瘤中的6个检测到杂合性缺失,占评估的间皮瘤总数的42%。这项研究表明3号染色体短臂上的一个基因参与了间皮瘤的发生发展。