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台湾地区胃癌中p53基因的突变

Mutations of p53 gene in gastric carcinoma in Taiwan.

作者信息

Wang J Y, Lin S R, Hsieh J S, Hsu C H, Huang Y S, Huang T J

机构信息

Department of Surgery, Kaohsiung Medical University Hospital, No. 100, Shih Chuan 1st Road, Kaohsiung 807, Taiwan.

出版信息

Anticancer Res. 2001 Jan-Feb;21(1B):513-20.

Abstract

BACKGROUND

p53 gene mutation and p53 protein accumulation is the most common event in human cancers. The present study was conducted to investigate the occurrence of p53 mutations in patients with gastric carcinoma in Taiwan.

MATERIALS AND METHODS

Tumor samples from 36 patients with primary gastric carcinoma undergoing radical gastrectomy were evaluated. The mutational status of the p53 (exons 5 to 8) was screened by polymerase chain reaction/single strand conformation polymorphism (PCR-SSCP) analysis followed by direct sequencing. These results were compared with p53 protein expression as assessed by immunohistochemical staining.

RESULTS

Of all 36 gastric carcinomas, mutations of the p53 gene were found in 7 cases (19.4%). These results from direct sequencing indicated that mutations consisted of five missence mutations, one silent mutation and one mutation within the splice donor site of intron 5. Mutations were found at codon 145 in exon 5 (1 case), intron 5 (1 case), codon 248 in exon 7 (1 case), codon 251 in exon 7 (2 cases), codon 285 in exon 8 (1 case) and codon 287 in exon 8 (1 case). The mutation hot spot at codon 251 in gastric cancer has not been observed previously. Over-expression of p53 oncoprotein was observed in 10 patients (27.8%) immunohistochemically.

CONCLUSIONS

p53 gene mutation might contribute to the pathogenesis of human gastric carcinoma. However, the suggestion awaits further investigation for confirmation.

摘要

背景

p53基因突变和p53蛋白积累是人类癌症中最常见的事件。本研究旨在调查台湾地区胃癌患者中p53突变的发生情况。

材料与方法

对36例行根治性胃切除术的原发性胃癌患者的肿瘤样本进行评估。通过聚合酶链反应/单链构象多态性(PCR-SSCP)分析,随后进行直接测序,筛选p53(第5至8外显子)的突变状态。将这些结果与通过免疫组织化学染色评估的p53蛋白表达进行比较。

结果

在所有36例胃癌中,发现7例(19.4%)存在p53基因突变。直接测序结果表明,突变包括五个错义突变、一个沉默突变和一个内含子5剪接供体位点内的突变。在第5外显子的密码子145(1例)、内含子5(1例)、第7外显子的密码子248(1例)、第7外显子的密码子251(2例)、第8外显子的密码子285(1例)和第8外显子的密码子287(1例)发现了突变。胃癌中密码子251的突变热点以前未被观察到。免疫组织化学检测发现10例患者(27.8%)存在p53癌蛋白过表达。

结论

p53基因突变可能参与人类胃癌的发病机制。然而,这一推测有待进一步研究证实。

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