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人肺鳞状细胞癌中视网膜母细胞瘤基因位点的DNA畸变。

DNA aberrations at the retinoblastoma gene locus in human squamous cell carcinomas of the lung.

作者信息

Sachse R, Murakami Y, Shiraishi M, Hayashi K, Sekiya T

机构信息

Oncogene Division, National Cancer Center Research Institute, Tokyo, Japan.

出版信息

Oncogene. 1994 Jan;9(1):39-47.

PMID:8302602
Abstract

We detected DNA aberrations at the RB locus in surgical specimens of human primary non-small cell lung carcinoma by single-strand conformation polymorphism analysis of polymerase chain reaction products amplified from regions of exons 2 to 27 including parts of the flanking intron sequences. Detection of nucleotide sequence polymorphism revealed loss of heterozygosity in six of eight informative cases among 13 squamous cell carcinomas analysed. In two of the six cases, mutations in the remaining allele were detected. In 25 adenocarcinomas analysed, no loss of heterozygosity was observed in 16 informative cases and a point mutation was detected in one of the uninformative cases. In one of three adenosquamous carcinomas analysed, a point mutation was detected and one adenoid cystic carcinoma analysed showed allelic loss of the RB gene. Our results indicated that loss of heterozygosity at the RB locus is frequent in squamous cell carcinomas of the lung, but not in adenocarcinomas. In the squamous cell carcinomas with allelic loss, mutations of the RB gene in the remaining alleles were found in one third of the tumors.

摘要

我们通过对从外显子2至27区域(包括部分侧翼内含子序列)扩增的聚合酶链反应产物进行单链构象多态性分析,检测了人类原发性非小细胞肺癌手术标本中RB基因座的DNA畸变。核苷酸序列多态性检测显示,在分析的13例鳞状细胞癌中的8例信息丰富的病例中,有6例出现杂合性缺失。在这6例中的2例中,检测到其余等位基因发生突变。在分析的25例腺癌中,16例信息丰富的病例未观察到杂合性缺失,在1例信息不丰富的病例中检测到一个点突变。在分析的3例腺鳞癌中的1例中检测到一个点突变,分析的1例腺样囊性癌显示RB基因的等位基因缺失。我们的结果表明,RB基因座的杂合性缺失在肺鳞状细胞癌中很常见,但在腺癌中不常见。在有等位基因缺失的鳞状细胞癌中,三分之一的肿瘤在其余等位基因中发现了RB基因的突变。

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