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11号染色体p13区域的等位基因缺失定义了人非小细胞肺癌中过氧化氢酶基因和D11S935之间的一个肿瘤抑制区域。

Allelic deletion at chromosome 11p13 defines a tumour suppressor region between the catalase gene and D11S935 in human non-small cell lung carcinoma.

作者信息

Shipman R, Schraml P, Colombi M, Ludwig C U

机构信息

Visible Genetics Inc., 700 Bay Street, Suite 1000, Box 333, Toronto, Ontario M5G 1Z6, Canada.

出版信息

Int J Oncol. 1998 Jan;12(1):107-11.

PMID:9454893
Abstract

A previous study of 48 primary non-small cell lung carcinomas (NSCLC) for allelic loss at five polymorphic chromosome 11p loci indicated regions of allelic deletion for both 11p13 and 11p15. To further delineate the extent of this deletion 28 NSCLCs were examined by high resolution deletion mapping for allelic loss at 11p13.95% (18/28) of the informative cases displayed allelic loss at the catalase gene locus (CAT), 64% (18/28) at D11S935 and D11S941E, respectively, and 23% (6/26) at D11S907. The minimal region of deletion is bordered by CAT and D11S935 and spans about 3 cM. The relationship between allelic loss within this chromosomal region, the presence of a putative predisposition locus and the pathogenetics of NSCLC are discussed.

摘要

先前一项针对48例原发性非小细胞肺癌(NSCLC)在5个11号染色体p多态性位点的等位基因缺失研究表明,11p13和11p15均存在等位基因缺失区域。为进一步明确该缺失范围,通过高分辨率缺失图谱对28例NSCLC进行检测,以分析11p13的等位基因缺失情况。95%(18/28)的信息充分病例在过氧化氢酶基因位点(CAT)显示等位基因缺失,分别有64%(18/28)在D11S935和D11S941E显示等位基因缺失,23%(6/26)在D11S907显示等位基因缺失。最小缺失区域以CAT和D11S935为边界,跨度约为3厘摩。本文讨论了该染色体区域内等位基因缺失、假定的易感位点的存在与NSCLC发病机制之间的关系。

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