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原发性小细胞肺癌中频繁的微卫星不稳定性

Frequent microsatellite instability in primary small cell lung cancer.

作者信息

Merlo A, Mabry M, Gabrielson E, Vollmer R, Baylin S B, 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 Apr 15;54(8):2098-101.

PMID:8174113
Abstract

Alterations in microsatellite sequences characterize hereditary nonpolyposis colorectal cancer. This microsatellite instability is due in some kindreds to a germline mutation of the mismatch repair gene hMSH2 on chromosome 2p. Although microsatellite alterations have been reported in other hereditary nonpolyposis colorectal cancer-associated tumors including endometrial and gastric cancers, such changes were not detected in most other major neoplasms. We found that 15 of 33 (45%) primary small cell lung cancers, tumors not found in the hereditary nonpolyposis colorectal cancer syndrome, displayed alterations of microsatellite loci which consisted of deletions or expansions of (CA)n dinucleotide repeats. In 8 of these 15 neoplasms, microsatellite instability was detected in more than 10% of all tested alleles. However, small cell lung cancers that revealed instability contained widespread allelic loss and had a uniformly poor prognosis. These results expand considerably the known spectrum of tumors with microsatellite instability.

摘要

微卫星序列的改变是遗传性非息肉病性结直肠癌的特征。这种微卫星不稳定性在某些家族中是由于2号染色体上错配修复基因hMSH2的种系突变所致。尽管在包括子宫内膜癌和胃癌在内的其他遗传性非息肉病性结直肠癌相关肿瘤中已报道有微卫星改变,但在大多数其他主要肿瘤中未检测到此类变化。我们发现,33例原发性小细胞肺癌(遗传性非息肉病性结直肠癌综合征中未发现的肿瘤)中有15例(45%)显示微卫星位点改变,其由(CA)n二核苷酸重复序列的缺失或扩增组成。在这15例肿瘤中的8例中,在所有检测的等位基因中超过10%检测到微卫星不稳定性。然而,显示不稳定性的小细胞肺癌存在广泛的等位基因缺失,且预后均较差。这些结果大大扩展了已知的具有微卫星不稳定性的肿瘤谱。

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