Baffa R, Santoro R, Bullrich F, Mandes B, Ishii H, Croce C M
Kimmel Cancer Center, Jefferson Medical College, Philadelphia, Pennsylvania 19107, USA.
Clin Cancer Res. 2000 Apr;6(4):1372-7.
Loss of heterozygosity at several chromosomal loci is a common feature of the malignant progression of human tumors. These regions are thought to harbor one or more putative tumor suppressor gene(s) playing a role in tumor development. Allelic losses on the short arm of chromosome 8 (8p) have been reported as frequent events in several cancers, and three commonly deleted regions have been defined at 8p11.2-12, 8p21-22, and 8p23.1. To evaluate the possible involvement of these regions in gastric cancer, we used eight microsatellite markers to perform an extensive analysis of allele loss at 8p21-22 in 52 cases of primary gastric adenocarcinoma. We found that 44% of tumors showed allelic loss for at least one marker at 8p21-22. The critical region of loss was found to be between markers LPL and D8S258, which displayed loss of heterozygosity in 39% and 33% of cases, respectively. This region is centromeric to the LPL locus and centered on the D8S258 locus. We conclude that 8p22 deletion is a frequent event in gastric cancer and suggest the presence of a putative tumor suppressor gene near the D8S258 locus. Initial steps were taken toward the identification of this gene, which is likely to play an important role in the pathogenesis of gastric cancer and of other tumors as well.
多个染色体位点的杂合性缺失是人类肿瘤恶性进展的一个常见特征。这些区域被认为含有一个或多个在肿瘤发生中起作用的假定肿瘤抑制基因。据报道,8号染色体短臂(8p)上的等位基因缺失在几种癌症中是常见事件,并且在8p11.2 - 12、8p21 - 22和8p23.1处已确定了三个常见的缺失区域。为了评估这些区域在胃癌中的可能作用,我们使用八个微卫星标记对52例原发性胃腺癌中8p21 - 22处的等位基因缺失进行了广泛分析。我们发现44%的肿瘤在8p21 - 22处至少有一个标记显示等位基因缺失。发现缺失的关键区域在标记LPL和D8S258之间,分别在39%和33%的病例中显示杂合性缺失。该区域位于LPL基因座的着丝粒侧,以D8S258基因座为中心。我们得出结论,8p22缺失在胃癌中是常见事件,并提示在D8S258基因座附近存在一个假定的肿瘤抑制基因。已朝着鉴定该基因迈出了初步步骤,该基因可能在胃癌及其他肿瘤的发病机制中起重要作用。