Cairns P, Tokino K, Eby Y, Sidransky D
Johns Hopkins University School of Medicine, Baltimore, Maryland 21205.
Cancer Res. 1994 Mar 15;54(6):1422-4.
Deletion mapping studies of primary bladder tumors have identified nonoverlapping areas of loss on each arm of chromosome 9, indicating that two distinct tumor suppressor loci are located on this chromosome. The deleted region on the p arm overlaps an area of 9p previously reported to be lost in a variety of neoplasms. Detailed loss of heterozygosity analysis of 9p in 112 primary bladder tumors using 12 microsatellite markers identified a minimal area of loss around the alpha-interferon locus at 9p21-22. Frequent homozygous deletions of the alpha-interferon locus were then identified in these tumors by a novel, comparative, multiplex polymerase chain reaction assay and were subsequently confirmed by Southern analysis. Based on these deletions, a putative tumor suppressor gene locus involved in bladder tumorigenesis was localized to a 10 cM region (flanked by D9S162 and D9S171), previously implicated in the progression of many neoplasms. Application of the multiplex polymerase chain reaction-based assay will allow rapid identification of homozygous deletions in many neoplasms and thus aid in mapping studies of critical suppressor genes.
原发性膀胱肿瘤的缺失图谱研究已确定9号染色体每条臂上存在不重叠的缺失区域,这表明该染色体上存在两个不同的肿瘤抑制基因座。p臂上的缺失区域与先前报道的在多种肿瘤中发生缺失的9p区域重叠。使用12个微卫星标记对112例原发性膀胱肿瘤的9p进行详细的杂合性缺失分析,确定了9p21 - 22处α - 干扰素基因座周围的最小缺失区域。通过一种新型的、比较性的多重聚合酶链反应检测方法,随后在这些肿瘤中发现了α - 干扰素基因座的频繁纯合缺失,并通过Southern分析得到证实。基于这些缺失,一个与膀胱肿瘤发生相关的假定肿瘤抑制基因座被定位到一个10 cM的区域(位于D9S162和D9S171之间),该区域先前与许多肿瘤的进展有关。基于多重聚合酶链反应的检测方法的应用将有助于快速鉴定许多肿瘤中的纯合缺失,从而有助于关键抑制基因的图谱研究。