Suppr超能文献

来自三个与BRCA1相关的家族性肿瘤中的杂合性缺失。

Loss of heterozygosity in familial tumors from three BRCA1-linked kindreds.

作者信息

Neuhausen S L, Marshall C J

机构信息

Department of Medical Informatics, University of Utah School of Medicine, Salt Lake City 84132.

出版信息

Cancer Res. 1994 Dec 1;54(23):6069-72.

PMID:7954448
Abstract

BRCA1, a breast-ovarian cancer susceptibility gene which has been localized to 17q21, appears to be a tumor suppressor gene based on evidence from loss of heterozygosity (LOH) studies. We analyzed 14 ovarian and breast tumors from BRCA1 carriers and 1 sporadic breast tumor from 3 kindreds for 17q21 LOH. Thirteen of the 14 tumors from gene carriers exhibited LOH of the wild-type allele. Tumors from one gene carrier and the sporadic breast case did not exhibit any LOH in the region. There was loss of the wild-type allele from both maternally and paternally derived chromosomes, therefore excluding the possibility of genomic imprinting and providing further evidence that BRCA1 is a tumor suppressor. Three tumors showed interstitial LOH in the region, and thus established the utility of familial tumors in refining a region surrounding a tumor suppressor gene in a manner analogous to using genetic recombinants.

摘要

BRCA1是一种已定位到17q21的乳腺癌-卵巢癌易感基因,基于杂合性缺失(LOH)研究的证据,它似乎是一种肿瘤抑制基因。我们分析了来自BRCA1携带者的14例卵巢和乳腺肿瘤以及来自3个家族的1例散发性乳腺肿瘤的17q21 LOH情况。基因携带者的14例肿瘤中有13例表现出野生型等位基因的LOH。来自一名基因携带者的肿瘤和散发性乳腺病例在该区域未表现出任何LOH。母源和父源染色体上的野生型等位基因均缺失,因此排除了基因组印记的可能性,并进一步证明BRCA1是一种肿瘤抑制基因。三个肿瘤在该区域表现出间质LOH,从而确立了家族性肿瘤在以类似于使用基因重组体的方式细化肿瘤抑制基因周围区域方面的实用性。

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