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Open Access Research article

Mutations of PIK3CA in gastric adenocarcinoma

Vivian Sze Wing Li1, Chi Wai Wong1, Tsun Leung Chan1, Agnes Sze Wah Chan1, Wei Zhao1, Kent-Man Chu2, Samuel So3, Xin Chen4, Siu Tsan Yuen1 and Suet Yi Leung1*

Author Affiliations

1 Department of Pathology, The University of Hong Kong, Queen Mary Hospital, Hong Kong

2 Department of Surgery, The University of Hong Kong, Queen Mary Hospital, Hong Kong

3 Department of Surgery, Stanford University School of Medicine, Stanford, CA 94305, USA

4 Department of Biopharmaceutical Sciences, University of California, San Francisco, USA

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BMC Cancer 2005, 5:29  doi:10.1186/1471-2407-5-29

Published: 23 March 2005

Abstract

Background

Activation of the phosphatidylinositol 3-kinase (PI3K) through mutational inactivation of PTEN tumour suppressor gene is common in diverse cancer types, but rarely reported in gastric cancer. Recently, mutations in PIK3CA, which encodes the p110α catalytic subunit of PI3K, have been identified in various human cancers, including 3 of 12 gastric cancers. Eighty percent of these reported mutations clustered within 2 regions involving the helical and kinase domains. In vitro study on one of the "hot-spot" mutants has demonstrated it as an activating mutation.

Methods

Based on these data, we initiated PIK3CA mutation screening in 94 human gastric cancers by direct sequencing of the gene regions in which 80% of all the known PIK3CA mutations were found. We also examined PIK3CA expression level by extracting data from the previous large-scale gene expression profiling study. Using Significance Analysis of Microarrays (SAM), we further searched for genes that show correlating expression with PIK3CA.

Results

We have identified PIK3CA mutations in 4 cases (4.3%), all involving the previously reported hotspots. Among these 4 cases, 3 tumours demonstrated microsatellite instability and 2 tumours harboured concurrent KRAS mutation. Data extracted from microarray studies showed an increased expression of PIK3CA in gastric cancers when compared with the non-neoplastic gastric mucosae (p < 0.001). SAM further identified 2910 genes whose expression levels were positively associated with that of PIK3CA.

Conclusion

Our data suggested that activation of the PI3K signalling pathway in gastric cancer may be achieved through up-regulation or mutation of PIK3CA, in which the latter may be a consequence of mismatch repair deficiency.