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卵巢癌中杂合性缺失及p53基因过表达

Loss of heterozygosity and overexpression of the p53 gene in ovarian carcinoma.

作者信息

Frank T S, Bartos R E, Haefner H K, Roberts J A, Wilson M D, Hubbell G P

机构信息

Department of Pathology, University of Michigan Medical School, Ann Arbor.

出版信息

Mod Pathol. 1994 Jan;7(1):3-8.

PMID:7909153
Abstract

Mutation and allelic loss of the p53 gene have been demonstrated in a variety of human cancers. In this study, DNA was extracted from formalin-fixed paraffin sections of ovarian carcinoma from 33 patients informative for a restriction fragment length polymorphism (RFLP) for BstU 1 within the 4th exon of the p53 gene. Allelic loss of p53 as indicated by loss of heterozygosity for this RFLP was demonstrated in 16/33 cases (48%). Because immunoreactivity for p53 correlates closely with the presence of mutation in the p53 gene, we performed immunohistochemical staining with the monoclonal antibody PAb1801. Diffuse nuclear p53 immunoreactivity was observed in 16 of the 33 (48%) informative cases used for loss of heterozygosity analysis (37/80 (46%) cases of ovarian carcinoma overall). A significant correlation (Fisher's exact test, P = 0.04) was observed between p53 overexpression and allelic loss. We found no evidence of association of p53 allelic loss or overexpression with advanced stage or other clinical or pathologic prognostic parameters. We conclude that mutation and allelic loss of p53 are common and probably related events in the development of ovarian carcinoma. This study demonstrates the use of paraffin sections in the analysis of p53 alterations in neoplasia.

摘要

p53基因的突变和等位基因缺失已在多种人类癌症中得到证实。在本研究中,从33例卵巢癌患者的福尔马林固定石蜡切片中提取DNA,这些患者的p53基因第4外显子内的BstU 1限制性片段长度多态性(RFLP)信息明确。16/33例(48%)病例显示该RFLP杂合性缺失所提示的p53等位基因缺失。由于p53的免疫反应性与p53基因突变的存在密切相关,我们用单克隆抗体PAb1801进行了免疫组织化学染色。在用于杂合性缺失分析的33例信息明确的病例中有16例(48%)观察到弥漫性核p53免疫反应性(总体80例卵巢癌病例中有37例(46%))。p53过表达与等位基因缺失之间存在显著相关性(Fisher精确检验,P = 0.04)。我们未发现p53等位基因缺失或过表达与晚期或其他临床或病理预后参数相关的证据。我们得出结论,p53的突变和等位基因缺失在卵巢癌发生中很常见且可能是相关事件。本研究证明了石蜡切片在肿瘤p53改变分析中的应用。

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