Suppr超能文献

人类肺癌中16号染色体16q24.1-q24.2区域910 kb常见等位基因缺失的鉴定。

Identification of a 910-kb region of common allelic loss in chromosome bands 16q24.1-q24.2 in human lung cancer.

作者信息

Sato M, Mori Y, Sakurada A, Fukushige S, Ishikawa Y, Tsuchiya E, Saito Y, Nukiwa T, Fujimura S, Horii A

机构信息

Department of Molecular Pathology, Tohoku University School of Medicine, Sendai, Japan.

出版信息

Genes Chromosomes Cancer. 1998 May;22(1):1-8.

PMID:9591628
Abstract

To understand the molecular pathogenesis of human lung cancer, we analyzed allelic deletions on the long arm of chromosome 16 by PCR amplification of microsatellite markers. A total of 203 lung cancer specimens (78 squamous cell carcinomas and 125 adenocarcinomas) were analyzed. In both cell types, a common region of allelic loss was identified in 16q24.1-q24.2; it is flanked by the two markers D16S534 and D16S422 that spanned at most 910 kb. These results were confirmed by fluorescence in situ hybridization. There was no correlation between allelic loss and histopathologic diagnosis or clinical stage. These results suggest the existence of a tumor-suppressor gene that plays an important role in the course of carcinogenesis in both squamous cell carcinoma and adenocarcinoma of the lungs.

摘要

为了解人类肺癌的分子发病机制,我们通过微卫星标记的PCR扩增分析了16号染色体长臂上的等位基因缺失情况。共分析了203例肺癌标本(78例鳞状细胞癌和125例腺癌)。在两种细胞类型中,均在16q24.1-q24.2区域发现了一个常见的等位基因缺失区域;其两侧为两个标记D16S534和D16S422,跨度最大为910 kb。这些结果通过荧光原位杂交得到了证实。等位基因缺失与组织病理学诊断或临床分期之间无相关性。这些结果表明存在一种肿瘤抑制基因,该基因在肺鳞状细胞癌和腺癌的致癌过程中起重要作用。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验