Cornelis R S, Devilee P, van Vliet M, Kuipers-Dijkshoorn N, Kersenmaeker A, Bardoel A, Khan P M, Cornelisse C J
Department of Human Genetics, University of Leiden, Medical Faculty, The Netherlands.
Oncogene. 1993 Mar;8(3):781-5.
Loss of heterozygosity (LOH) of markers for chromosome 17 is the most frequent genetic change observed in breast cancer to date. To assess whether the location of several candidate target genes is compatible with patterns of allele losses in the individual tumors, we examined the LOH status of chromosome 17 in 109 primary breast tumors with 15 polymorphic DNA markers (three for 17p and 12 for 17q). Allelic imbalance (AI) at 17q was observed in 44 of the 97 informative cases. A significant correlation was found between AI at the long arm and AI at the short arm of chromosome 17. The patterns of AI on 17q in the tumors differed and were highly complex in some cases. A number of tumors showed AI distal to the growth hormone locus, whereas others showed AI exclusively proximal of this marker. These results indicate that there are at least two different regions of allele loss on 17q.
17号染色体标记的杂合性缺失(LOH)是迄今为止在乳腺癌中观察到的最常见的基因变化。为了评估几个候选靶基因的位置是否与个体肿瘤中的等位基因缺失模式相符,我们用15个多态性DNA标记(17p的3个和17q的12个)检测了109例原发性乳腺肿瘤中17号染色体的LOH状态。在97例信息充分的病例中,有44例观察到17q存在等位基因不平衡(AI)。发现17号染色体长臂的AI与短臂的AI之间存在显著相关性。肿瘤中17q的AI模式各不相同,在某些情况下非常复杂。许多肿瘤在生长激素基因座远端显示AI,而其他肿瘤仅在该标记近端显示AI。这些结果表明,17q上至少有两个不同的等位基因缺失区域。