Mutation analysis of PIK3CA and PIK3CB in esophageal cancer and Barrett's esophagus

被引:65
|
作者
Phillips, WA
Russell, SE
Ciavarella, ML
Choong, DYH
Montgomery, KG
Smith, K
Pearson, RB
Thomas, RJS
Campbell, IG
机构
[1] Peter MacCallum Canc Ctr, Ctr Canc Genom & Prevent Med, Surg Oncol Lab, Melbourne, Vic 8006, Australia
[2] Univ Melbourne, St Vincents Hosp, Dept Surg, Parkville, Vic 3052, Australia
[3] Peter MacCallum Canc Ctr, VBCRC Canc Genet Lab, Melbourne, Vic, Australia
[4] Peter MacCallum Canc Ctr, Prot Chem Lab, Melbourne, Vic, Australia
[5] Univ Melbourne, Dept Biochem & Mol Biol, Parkville, Vic 3052, Australia
[6] Monash Univ, Dept Biochem & Mol Biol, Clayton, Vic 3168, Australia
关键词
phosphatidylinositide 3 '-kinase; mutation; oncogene; esophageal cancer; Barrett's esophagus;
D O I
10.1002/ijc.21706
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Mutation of PIK3CA, the gene coding for the p110 alpha catalytic subunit of phosphoinositide 3-kinase (PI3K), has been reported in a limited range of human tumors. We now report that PIK3CA is also mutated in esophageal tumors. Single-strand conformational polymorphism (SSCP) and denaturing high-performance liquid chromatography (DHPLC) were used to screen all 20 exons of PIK3CA in 101 samples from 95 individuals with esophageal cancer and/or Barrett's esophagus. Somatic mutation of PIK3CA was detected in 4 of 35 (11.8%) of esophageal squamous cell carcinomas (SCC) and 3 of 50 (6%) adenocarcinomas. No mutations were detected in any of 17 samples of Barrett's esophagus. For PIK3CB, we screened exons 11 and 22, which code for the regions corresponding to the exon 9 and 20 mutational 'hotspots'of PIK3CA. No somatic changes were detected in PIK3CB This study extends previous observations in other tumor types by demonstrating the presence of somatic PIK3CA mutations in both SCC and adenocarcinoma of the esophagus, thus implicating the PI3K pathway in the initiation and/or progression of esophageal cancers. (c) 2005 Wiley-Liss, Inc.
引用
收藏
页码:2644 / 2646
页数:3
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