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人类原发性膀胱癌4号染色体上等位基因缺失的不同区域。

Distinct regions of allelic loss on chromosome 4 in human primary bladder carcinoma.

作者信息

Polascik T J, Cairns P, Chang W Y, Schoenberg M P, Sidransky D

机构信息

James Buchanan Brady Urological Institute, Johns Hopkins Medical Institutions, Baltimore, Maryland 21287, USA.

出版信息

Cancer Res. 1995 Nov 15;55(22):5396-9.

PMID:7585608
Abstract

Accumulating evidence implicates the presence of putative tumor suppressor genes on human chromosome 4 that are potentially inactivated in the genesis of several different neoplasms. To accurately determine the frequency of allelic loss on both arms of human chromosome 4, we screened 282 fresh-frozen human bladder carcinomas for allelic loss. Loss of heterozygosity of at least one marker for chromosome 4 was identified in 129 tumors (45.7%). Fine mapping was accomplished using up to 15 polymorphic markers on the p arm and 19 markers on the q arm. We identified a 3-cM minimal area of loss on the p arm between microsatellite markers D4S1608 and D4S404 deleted in 82 tumors (29%). A total of 68 tumors (24%) targeted a 14-cM critical region identified on the distal q arm between markers D4S426 and D4S408. Loss of these two regions correlated with advanced stage and grade of the lesions. These data identify distinct regions of loss on chromosome 4 potentially involved in the late progression of bladder carcinoma.

摘要

越来越多的证据表明,人类4号染色体上存在假定的肿瘤抑制基因,这些基因在几种不同肿瘤的发生过程中可能会失活。为了准确确定人类4号染色体双臂上等位基因缺失的频率,我们对282例新鲜冷冻的人类膀胱癌进行了等位基因缺失筛查。在129例肿瘤(45.7%)中发现了4号染色体至少一个标记的杂合性缺失。使用p臂上多达15个多态性标记和q臂上19个标记完成了精细定位。我们在82例肿瘤(29%)中发现微卫星标记D4S1608和D4S404之间的p臂上有一个3厘摩的最小缺失区域。共有68例肿瘤(24%)靶向q臂远端标记D4S426和D4S408之间确定的一个14厘摩的关键区域。这两个区域的缺失与病变的晚期和分级相关。这些数据确定了4号染色体上不同的缺失区域,可能与膀胱癌的晚期进展有关。

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