Mutations of the PIK3CA gene in hereditary colorectal cancers
Article first published online: 1 JUN 2007
Copyright © 2007 Wiley-Liss, Inc.
International Journal of Cancer
Volume 121, Issue 7, pages 1627–1630, 1 October 2007
How to Cite
Miyaki, M., Iijima, T., Yamaguchi, T., Takahashi, K., Matsumoto, H., Yasutome, M., Funata, N. and Mori, T. (2007), Mutations of the PIK3CA gene in hereditary colorectal cancers. Int. J. Cancer, 121: 1627–1630. doi: 10.1002/ijc.22829
- Issue published online: 24 JUL 2007
- Article first published online: 1 JUN 2007
- Manuscript Accepted: 11 APR 2007
- Manuscript Received: 21 FEB 2007
- PIK3CA mutation;
- colorectal tumor;
Somatic mutations of the PIK3CA gene have recently been detected in various human cancers, including sporadic colorectal cancer. However, mutations of the PIK3CA gene in hereditary colorectal cancers have not been clarified. To elucidate the mutation status in familial adenomatous polyposis (FAP) and hereditary nonpolyposis colorectal cancer (HNPCC), which are the most common hereditary colorectal cancers, we investigated PIK3CA mutations in 163 colorectal tumors, including adenomas, intramucosal carcinomas and invasive carcinomas. For comparison, we also analyzed mutations of the same gene in 160 sporadic colorectal tumors at various histopathological stages. Analysis at exons 1, 7, 9 and 20 of the PIK3CA gene revealed somatic mutations in 21% (8 of 39) of FAP invasive carcinomas, 21% (7 of 34) of HNPCC invasive carcinomas, 15% (8 of 52) of sporadic invasive carcinomas, and 14% (7 of 50) of sporadic colorectal metastases in the liver. Mutations in FAP and HNPCC carcinomas predominantly occurred in the kinase domain (exon 20), while the majority of mutations in sporadic cases occurred in the helical domain (exon 9). Adenomas and intramucosal carcinomas from all patients exhibited no mutations (0 of 148). Our data suggest that PIK3CA mutations contribute to the invasion step from intramucosal carcinoma to invasive carcinoma in colorectal carcinogenesis in FAP and HNPCC patients at a similar extent to that seen in sporadic patients. © 2007 Wiley-Liss, Inc.