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人类原发性非小细胞肺癌中9号染色体频繁缺失。

Frequent loss of chromosome 9 in human primary non-small cell lung cancer.

作者信息

Merlo A, Gabrielson E, Askin F, Sidransky D

机构信息

Department of Otolaryngology, Johns Hopkins University, School of Medicine, Baltimore, Maryland 21205.

出版信息

Cancer Res. 1994 Feb 1;54(3):640-2.

PMID:8306323
Abstract

We analyzed the pattern of allelic loss on chromosome 9 in 40 primary human non-small cell lung cancers including 16 squamous cell, 18 adeno-, and 6 large cell carcinomas. Using 24 polymorphic microsatellite markers spanning chromosome 9, we found that 27 of 40 (67.5%) of these neoplasms displayed loss of heterozygosity (LOH) on chromosome 9. Most tumors showed LOH for all informative markers on both chromosomal arms, whereas five tumors demonstrated partial LOH on chromosome 9. In four of these tumors, allelic loss was limited to the 9p arm, whereas in the remaining specimen, LOH extended from 9p21-22 to terminal 9q. These five tumors delineate a minimal area of loss at 9p21-22, which includes a previously defined tumor suppressor gene locus. We have identified a distinct region of loss on chromosome 9p commonly involved in non-small cell lung cancer tumorigenesis.

摘要

我们分析了40例原发性人类非小细胞肺癌(包括16例鳞状细胞癌、18例腺癌和6例大细胞癌)9号染色体上等位基因缺失的模式。使用跨越9号染色体的24个多态性微卫星标记,我们发现这些肿瘤中有27例(40例中的67.5%)在9号染色体上表现出杂合性缺失(LOH)。大多数肿瘤在两条染色体臂上所有信息性标记均显示LOH,而有5例肿瘤在9号染色体上表现为部分LOH。在其中4例肿瘤中,等位基因缺失仅限于9p臂,而在其余标本中,LOH从9p21 - 22延伸至9q末端。这5例肿瘤划定了9p21 - 22处的一个最小缺失区域,该区域包含一个先前定义的肿瘤抑制基因位点。我们已经确定了9号染色体p臂上一个在非小细胞肺癌肿瘤发生过程中常见的明显缺失区域。

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