Suppr超能文献

2.4兆碱基9q33 - q34关键区域及DEC1在食管鳞状细胞癌中的肿瘤抑制作用

Tumor suppressive role of a 2.4 Mb 9q33-q34 critical region and DEC1 in esophageal squamous cell carcinoma.

作者信息

Yang Lichun, Leung Alfred C C, Ko Josephine M Y, Lo Paulisally H Y, Tang Johnny C O, Srivastava Gopesh, Oshimura Mitsuo, Stanbridge Eric J, Daigo Yataro, Nakamura Yusuke, Tang Cecilia M C, Lau Kwok W, Law Simon, Lung Maria L

机构信息

Department of Biology, Hong Kong University of Science and Technology, Hong Kong, China.

出版信息

Oncogene. 2005 Jan 20;24(4):697-705. doi: 10.1038/sj.onc.1208179.

Abstract

The key genes involved in the development of esophageal squamous cell carcinoma (ESCC) remain to be elucidated. Previous studies indicate extensive genomic alterations occur on chromosome 9 in ESCC. Using a monochromosome transfer approach, this study provides functional evidence and narrows down the critical region (CR) responsible for chromosome 9 tumor suppressing activity to a 2.4 Mb region mapping to 9q33-q34 between markers D9S1798 and D9S61. Interestingly, a high prevalence of allelic loss in this CR is also observed in primary ESCC tumors by microsatellite typing. Allelic loss is found in 30/34 (88%) tumors and the loss of heterozygosity (LOH) frequency ranges from 67 to 86%. Absent to low expression of a 9q32 candidate tumor suppressor gene (TSG), DEC1 (deleted in esophageal cancer 1), is detected in four Asian ESCC cell lines. Stably expressing DEC1 transfectants provide functional evidence for inhibition of tumor growth in nude mice and DEC1 expression is decreased in tumor segregants arising after long-term selection in vivo. There is 74% LOH in the DEC1 region of ESCC primary tumors. This study provides the first functional evidence for the presence of critical tumor suppressive regions on 9q33-q34. DEC1 is a candidate TSG that may be involved in ESCC development.

摘要

食管鳞状细胞癌(ESCC)发生发展过程中涉及的关键基因仍有待阐明。先前的研究表明,ESCC中9号染色体上发生了广泛的基因组改变。本研究采用单染色体转移方法,提供了功能证据,并将负责9号染色体肿瘤抑制活性的关键区域(CR)缩小至位于标记D9S1798和D9S61之间、定位于9q33 - q34的一个2.4 Mb区域。有趣的是,通过微卫星分型在原发性ESCC肿瘤中也观察到该CR中较高的等位基因缺失率。在34个肿瘤中有30个(88%)发现等位基因缺失,杂合性缺失(LOH)频率在67%至86%之间。在4个亚洲ESCC细胞系中检测到9q32候选肿瘤抑制基因(TSG)DEC1(食管癌1中缺失)表达缺失或低表达。稳定表达DEC1的转染子为抑制裸鼠肿瘤生长提供了功能证据,并且在体内长期选择后产生的肿瘤分离株中DEC1表达降低。ESCC原发性肿瘤的DEC1区域存在74%的LOH。本研究为9q33 - q34上存在关键肿瘤抑制区域提供了首个功能证据。DEC1是一个可能参与ESCC发生发展的候选TSG。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验