Suppr超能文献

一个与高级别侵袭性上皮性卵巢癌相关的位于6号染色体6q25.1 - q25.2区域的新型4厘摩最小缺失单元。

A novel 4 cM minimal deletion unit on chromosome 6q25.1-q25.2 associated with high grade invasive epithelial ovarian carcinomas.

作者信息

Colitti C V, Rodabaugh K J, Welch W R, Berkowitz R S, Mok S C

机构信息

Department of Obstetrics, Gynecology and Reproductive Biology, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts 02115, USA.

出版信息

Oncogene. 1998 Jan 29;16(4):555-9. doi: 10.1038/sj.onc.1201523.

Abstract

Detailed deletion mapping of chromosome 6q has shown that the highest percentage of loss of heterozygosity (LOH) is located at 6q25-q27 and suggested that an ovarian cancer associated tumor suppressor gene may reside in this region. To further define the smallest region of common loss, we used 12 tandem repeat markers spanning a region no more than 18 cM, located between 6q25.1 and 6q26, to examine allelic loss in 54 fresh and paraffin embedded invasive ovarian epithelial tumor tissues. Loss of heterozygosity was observed more frequently at the loci defined by marker D6S473 (14 of 32 informative cases, 44%) and marker D6S448 (17 of 40 informative cases, 43%). Detailed mapping of chromosome 6q25-q26 in these tumor samples identified a 4 cM minimal region of LOH between markers D6S473 and D6S448 (6q25.1-q25.2). Loss of heterozygosity at D6S473 correlated significantly both with serous versus non-serous ovarian tumors (P=0.040) and with high grade versus low grade specimens (P=0.023). The results suggest that a 4 cM deletion unit located at 6q25.1-q25.2 may contain the putative tumor suppressor gene which may play a role in the development and progression of human invasive epithelial ovarian carcinomas (IEOC).

摘要

对6号染色体q臂的详细缺失图谱分析表明,杂合性缺失(LOH)比例最高的区域位于6q25 - q27,提示一个与卵巢癌相关的肿瘤抑制基因可能位于该区域。为了进一步确定共同缺失的最小区域,我们使用了12个串联重复标记,这些标记跨越不超过18 cM的区域,位于6q25.1和6q26之间,以检测54例新鲜和石蜡包埋的浸润性卵巢上皮肿瘤组织中的等位基因缺失情况。在由标记D6S473(32例信息性病例中的14例,44%)和标记D6S448(40例信息性病例中的17例,43%)定义的位点上,杂合性缺失更为频繁地被观察到。对这些肿瘤样本中6号染色体q25 - q26的详细图谱分析确定了在标记D6S473和D6S448(6q25.1 - q25.2)之间存在一个4 cM的最小杂合性缺失区域。D6S473处的杂合性缺失与浆液性与非浆液性卵巢肿瘤(P = 0.040)以及高级别与低级别标本(P = 0.023)均显著相关。结果表明,位于6q25.1 - q25.2的一个4 cM缺失单元可能包含推定的肿瘤抑制基因,该基因可能在人类浸润性上皮性卵巢癌(IEOC)的发生和发展中起作用。

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