Fey M F, Hesketh C, Wainscoat J S, Gendler S, Thein S L
Department of Haematology, John Radcliffe Hospital, Headington, Oxford, UK.
Br J Cancer. 1989 May;59(5):750-4. doi: 10.1038/bjc.1989.157.
Using a panel of DNA probes for hypervariable DNA regions we screened 52 gastrointestinal carcinomas for clonal allele losses on chromosomes 1, 5, 7, 12, 16 and 17. A total of 24/35 informative cases of colorectal cancers showed loss of constitutional heterozygosity at a locus on chromosome 17p, while 9/31 cases informative for a locus on 5q showed allele loss. Loss of sequences at 5q was linked to allele loss at 17p with a single exception. In gastric cancers loss of heterozygosity most frequently occurred at 1q (5/10 tumours) and at 12q (6/11 tumours). Gastrointestinal tumours show consistent chromosomal losses and the loci involved are different in gastric and colorectal cancers.
我们使用一组针对高变DNA区域的DNA探针,对52例胃肠道癌进行筛查,以检测1号、5号、7号、12号、16号和17号染色体上的克隆性等位基因缺失情况。在35例信息充分的结直肠癌病例中,共有24例显示17号染色体短臂上某一位点的结构杂合性缺失,而在31例信息充分的5号染色体长臂上某一位点的病例中,有9例显示等位基因缺失。5号染色体长臂序列的缺失与17号染色体短臂的等位基因缺失相关联,仅有1例例外。在胃癌中,杂合性缺失最常发生于1号染色体长臂(10例肿瘤中有5例)和12号染色体长臂(11例肿瘤中有6例)。胃肠道肿瘤呈现出一致的染色体缺失情况,且胃癌和结直肠癌中涉及的位点有所不同。