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APC基因突变很少见,但存在于人类肺癌中。

APC mutations are infrequent but present in human lung cancer.

作者信息

Ohgaki Hiroko, Kros Johan M, Okamoto Yoshikazu, Gaspert Ariana, Huang Hervé, Kurrer Michael O

机构信息

Unit of Molecular Pathology, International Agency for Research on Cancer, 150 cours Albert Thomas, Lyon 69372, France.

出版信息

Cancer Lett. 2004 Apr 30;207(2):197-203. doi: 10.1016/j.canlet.2003.10.020.

Abstract

Recent studies have revealed the presence of beta-catenin mutations in a small subset of human and rat lung carcinomas, suggesting the involvement of the Wnt pathway in pulmonary carcinogenesis. LOH on chromosome 5q (APC locus) is frequent in lung cancer, but previous studies have found no adenomatous polyposis coli (APC) mutations. In this study, we screened 114 human lung cancer specimens for alterations in the mutation cluster region of the APC gene and in exon 3 of the beta-catenin gene. SSCP followed by direct DNA sequencing revealed APC mutations in 2/44 (5%) squamous cell carcinomas, a 2-bp deletion in codon 1465 (AGT-->A), and a GAA-->CAA (Glu-->Gln) mutation at codon 1317. One of 32 (3%) small cell lung carcinomas contained a GAA-->AAA (Glu-->Lys) mutation at codon 1284. Two cases with an APC mutation showed focal nuclear beta-catenin staining. These results suggest that disruption of the Wnt pathway through APC mutations is infrequent, but may be involved in the pathogenesis of a small subset of human lung carcinomas.

摘要

最近的研究显示,在一小部分人类和大鼠肺癌中存在β-连环蛋白突变,提示Wnt信号通路参与了肺癌的发生。5号染色体长臂(APC基因座)的杂合性缺失在肺癌中很常见,但之前的研究未发现腺瘤性息肉病基因(APC)突变。在本研究中,我们筛查了114例人类肺癌标本,检测APC基因的突变簇区域和β-连环蛋白基因第3外显子的改变。采用单链构象多态性分析(SSCP)并直接进行DNA测序,结果显示在2/44例(5%)鳞状细胞癌中发现了APC突变,分别为密码子1465处2个碱基的缺失(AGT→A)以及密码子1317处GAA→CAA(Glu→Gln)突变。在32例(3%)小细胞肺癌中有1例在密码子1284处发生了GAA→AAA(Glu→Lys)突变。2例发生APC突变的病例显示β-连环蛋白呈局灶性核染色。这些结果提示,通过APC突变破坏Wnt信号通路的情况并不常见,但可能参与了一小部分人类肺癌的发病机制。

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