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人类结直肠癌1p32 - p36染色体区域的详细缺失图谱:三个常见等位基因缺失不同区域的鉴定。

Detailed deletion mapping on chromosome 1p32-p36 in human colorectal cancer: identification of three distinct regions of common allelic loss.

作者信息

Matsuzaki M, Nagase S, Abe T, Miura K, Shiiba K, Sunamura M, Horii A

机构信息

Department of Molecular Pathology, Tohoku University School of Medicine, Sendai 980-8575, Japan.

出版信息

Int J Oncol. 1998 Dec;13(6):1229-33. doi: 10.3892/ijo.13.6.1229.

Abstract

Recent studies have suggested the existence of one or several tumor-suppressor genes on chromosome arm 1p in colorectal tumors. To determine the localization of the putative tumor suppressor genes, we performed LOH analysis in 1p in colorectal tumors. A total of 48 paired normal and tumor DNAs of 46 colorectal tumor patients and 21 microsatellite markers on 1p32.1-p36.3 were used for PCR-LOH analysis. Three commonly deleted regions were found: i) 1p36.3 (10-cm); ii) 1p35.1-p36.3 (2-cm); and iii) 1p34.2-p35 (1-cm). These regions overlapped with those reported in several types of tumor. No significant associations were found between LOH and clinicopathologic features. The regions identified in the present study could harbor tumor suppressor genes that would also be associated with several types of human cancer.

摘要

近期研究表明,在结肠直肠肿瘤的1号染色体短臂上存在一个或多个肿瘤抑制基因。为了确定假定的肿瘤抑制基因的定位,我们对结肠直肠肿瘤的1号染色体短臂进行了杂合性缺失(LOH)分析。使用46例结肠直肠肿瘤患者的48对正常和肿瘤DNA以及1号染色体短臂32.1-36.3区域的21个微卫星标记进行聚合酶链反应-杂合性缺失(PCR-LOH)分析。发现了三个常见的缺失区域:i)1号染色体短臂36.3(10厘米);ii)1号染色体短臂35.1-36.3(2厘米);以及iii)1号染色体短臂34.2-35(1厘米)。这些区域与几种肿瘤类型中报道的区域重叠。未发现杂合性缺失与临床病理特征之间存在显著关联。本研究中确定的区域可能含有与多种人类癌症相关的肿瘤抑制基因。

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