Matsumoto S, Kasumi F, Sakamoto G, Onda M, Nakamura Y, Emi M
Department of Molecular Biology, Nippon Medical School, Kawasaki, Japan.
Genes Chromosomes Cancer. 1997 Nov;20(3):268-74.
Loss of heterozygosity (LOH) on 3p is frequent in human renal cell carcinomas, lung cancers, and breast cancers. To define the region(s) on 3p that harbor presumptive tumor suppressor gene(s) for breast cancer, we examined 196 primary breast tumors for their patterns of LOH at 22 microsatellite marker loci distributed along this chromosome arm. Allelic loss at one or more loci was observed in 101 (52%) of these tumors. Detailed deletion mapping identified two distinct commonly deleted regions; one was localized to a 2-cM interval flanked by D3S1547 and D3S1295 at 3p14.3-21.1, and the other to a 5-cM interval flanked by D3S1286 and D3S1585 at 3p24.3-25.1. The FHIT gene lies in the vicinity of the proximal commonly deleted region. Attempts to correlate LOH on 3p to clinicopathological parameters detected an association with the absence of the progesterone receptor (P = 0.0096). The results suggest that inactivation of unidentified tumor suppressor genes on 3p plays a role in the mechanism whereby hormone dependency is lost in the course of breast carcinogenesis.
3p杂合性缺失(LOH)在人类肾细胞癌、肺癌和乳腺癌中很常见。为了确定3p上携带乳腺癌推定肿瘤抑制基因的区域,我们检测了196例原发性乳腺肿瘤在沿该染色体臂分布的22个微卫星标记位点处的LOH模式。在这些肿瘤中的101例(52%)中观察到一个或多个位点的等位基因缺失。详细的缺失图谱确定了两个不同的常见缺失区域;一个定位于3p14.3 - 21.1处由D3S1547和D3S1295侧翼的2厘摩区间,另一个定位于3p24.3 - 25.1处由D3S1286和D3S1585侧翼的5厘摩区间。FHIT基因位于近端常见缺失区域附近。将3p上的LOH与临床病理参数进行关联的尝试发现其与孕激素受体缺失有关(P = 0.0096)。结果表明,3p上未鉴定的肿瘤抑制基因的失活在乳腺癌发生过程中激素依赖性丧失的机制中起作用。