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人类癌症中5号染色体上等位基因缺失图谱分析。

Allelic deletion mapping on chromosome 5 in human carcinomas.

作者信息

Wieland I, Böhm M, Arden K C, Ammermüller T, Bogatz S, Viars C S, Rajewsky M F

机构信息

Institute for Cell Biology, (Cancer Research), University of Essen Medical School, Germany.

出版信息

Oncogene. 1996 Jan 4;12(1):97-102.

PMID:8552404
Abstract

We analysed allelic deletions on chromosome 5 in microdissected human non-small cell lung cancers. Thirty-four primary squamous cell carcinomas, 15 primary adenocarcinomas and five regional lymph node metastases were investigated for loss of heterozygosity (LOH) in chromosomal region 5p15-q21. The sites analysed included the APC tumor suppressor gene at 5q21, five polymorphic microsatellite markers and the putative tumor suppressor locus del-27, that was assigned to chromosomal region 5p13-12 by fluorescence in situ hybridization (FISH) analysis. Allelic deletions encompassed larger genomic regions more often in squamous cell carcinomas than in adenocarcinomas. The del-27 amd APC regions were identified as two distinct regions with the highest LOH frequencies within 5p15-q21. In squamous cell carcinomas LOH frequencies were 73% at the del-27 and 70% at the APC locus. In adenocarcinomas LOH at the del-27 and APC loci occurred in 38% of the informative cases. Allelic deletion of the APC gene and at the del-27 locus was also detected in the metastases. The results suggest involvement of at least two tumor suppressor genes on chromosome 5 in lung tumorigenesis.

摘要

我们分析了显微切割的人类非小细胞肺癌中5号染色体上的等位基因缺失情况。对34例原发性鳞状细胞癌、15例原发性腺癌和5例区域淋巴结转移灶进行了5号染色体区域5p15-q21杂合性缺失(LOH)的研究。分析的位点包括5q21处的APC肿瘤抑制基因、5个多态性微卫星标记以及通过荧光原位杂交(FISH)分析定位于染色体区域5p13-12的假定肿瘤抑制位点del-27。与腺癌相比,鳞状细胞癌中等位基因缺失更常累及更大的基因组区域。del-27和APC区域被确定为5p15-q21内LOH频率最高的两个不同区域。在鳞状细胞癌中,del-27处的LOH频率为73%,APC位点处为70%。在腺癌中,38%的信息性病例在del-27和APC位点出现LOH。在转移灶中也检测到了APC基因和del-27位点的等位基因缺失。结果表明,5号染色体上至少有两个肿瘤抑制基因参与了肺癌的发生。

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