非放射性同位素SSCA鉴定胃肠道和胰腺癌中p53基因突变。

D R Lohmann, A Funk, H P Niedermeyer, S Häupel, H Höfler
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引用次数: 69

摘要

建立了一种基于单链DNA构象分析(SSCA)的非同位素筛选方法,用于鉴定组织样本中p53基因的改变。这种方法的敏感性通过检测先前通过直接测序确定的突变得到了验证。应用该方法筛选了40例福尔马林固定石蜡包埋肿瘤,其中胃肠道类癌33例,胰腺内分泌肿瘤7例。只有一个突变(密码子283,从CGC到CCC)在一个临床良性类直肠癌中被发现。这种突变发生在肿瘤的发展过程中,并伴随着野生型基因的缺失。我们的数据表明,与胃肠道癌相比,p53基因的改变在胃肠道和胰腺癌的发展中是罕见的事件。此外,没有证据表明p53参与类癌的恶性转移进展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Identification of p53 gene mutations in gastrointestinal and pancreatic carcinoids by nonradioisotopic SSCA.

A nonisotopic screening method based on single-strand DNA conformation analysis (SSCA) was established for the identification of p53 gene alterations in achieved tissue samples. The sensitivity of this approach was validated by testing mutations previously identified by direct sequencing. Applying this assay, 40 samples of formalin-fixed, paraffin-embedded tumors, including 33 gastrointestinal carcinoids and seven endocrine pancreatic tumors, were screened. Only one mutation (codon 283, CGC to CCC) was identified in a single clinically benign rectal carcinoid. This mutation occurred during the development of the tumor and was accompanied by loss of the wild-type gene. Our data indicate, that, in contrast to gastrointestinal carcinomas, alterations of the p53 gene are infrequent events in the development of gastrointestinal and pancreatic carcinoids. In addition, there was no evidence for the involvement of p53 in the malignant metastatic progression of carcinoids.

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