Suppr超能文献

人类上皮性卵巢癌等位基因型

Human epithelial ovarian cancer allelotype.

作者信息

Cliby W, Ritland S, Hartmann L, Dodson M, Halling K C, Keeney G, Podratz K C, Jenkins R B

机构信息

Department of Gynecologic Oncology, Mayo Clinic and Foundation, Rochester, Minnesota 55905.

出版信息

Cancer Res. 1993 May 15;53(10 Suppl):2393-8.

PMID:8485726
Abstract

To determine which chromosomes and chromosomal regions contain putative tumor suppressor genes important for human epithelial ovarian cancer, we performed loss of heterozygosity (LOH) studies on 37 primary epithelial ovarian tumors. Using 70 polymorphic markers, we examined all chromosome arms (excluding acrocentric arms) on all specimens. Our findings show a high frequency of LOH for the following chromosome arms: 5q (43%); 6p (62%); 6q (57%); 7p (36%); 8p (40%); 9q (54%); 13q (56%); 14q (47%); 15q (36%); 17p (81%); 17q (76%); 18q (43%); 21q (36%); and 22q (71%). When separated into low and high grade tumors, there were statistically significant differences of LOH for the following chromosome arms: 6p (29% versus 70%); 13q (0% versus 72%); 17p (33% versus 90%); and 17q (29% versus 87%). No statistically significant difference was found between different histological subtypes. The average fractional allelic loss for low grade tumors was 0.17 versus 0.40 for high grade and 0.35 for all tumors. In an effort to more specifically localize common regions of molecular genetic deletion, we examined the following chromosomes in greater detail: chromosome 13 (5 markers); chromosome 17 (8 markers); and chromosome 6 (8 polymorphic markers). No tumor showed deletion of only a portion of chromosome 13. When any informative marker for chromosome 13 showed loss, all markers showed loss. Similarly, the tumors of most patients demonstrated LOH of all informative markers that map to chromosome 17; however, regional deletion of 17p markers was observed in 3 tumors. Twelve tumors demonstrated regional deletions of portions of chromosome 6. These tumors suggest that at least 2 regions of chromosome 6 are important for ovarian epithelial carcinogenesis. One region appears to be on distal 6q and a second region is near the centromere of chromosome 6 proximal to the HLA locus.

摘要

为了确定哪些染色体和染色体区域含有对人类上皮性卵巢癌重要的假定肿瘤抑制基因,我们对37例原发性上皮性卵巢肿瘤进行了杂合性缺失(LOH)研究。我们使用70个多态性标记,检测了所有标本上的所有染色体臂(不包括近端着丝粒染色体臂)。我们的研究结果显示,以下染色体臂存在高频率的LOH:5q(43%);6p(62%);6q(57%);7p(36%);8p(40%);9q(54%);13q(56%);14q(47%);15q(36%);17p(81%);17q(76%);18q(43%);21q(36%);以及22q(71%)。当分为低级别和高级别肿瘤时,以下染色体臂的LOH存在统计学显著差异:6p(29%对70%);13q(0%对72%);17p(33%对90%);以及17q(29%对87%)。在不同组织学亚型之间未发现统计学显著差异。低级别肿瘤的平均等位基因缺失分数为0.17,高级别肿瘤为0.40,所有肿瘤为0.35。为了更具体地定位分子遗传缺失的常见区域,我们对以下染色体进行了更详细的检测:13号染色体(5个标记);17号染色体(8个标记);以及6号染色体(8个多态性标记)。没有肿瘤仅显示13号染色体的一部分缺失。当任何13号染色体的信息性标记显示缺失时,所有标记均显示缺失。同样,大多数患者的肿瘤显示所有定位于17号染色体的信息性标记均存在LOH;然而,在3个肿瘤中观察到17p标记的区域缺失。12个肿瘤显示6号染色体部分区域的缺失。这些肿瘤提示,6号染色体至少有2个区域对卵巢上皮癌发生很重要。一个区域似乎位于6q远端,另一个区域靠近6号染色体着丝粒,在HLA基因座近端。

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