Characterizing multi‐PIK3CA mutations across cancer types: Toward precision oncology

Author:

Nakamura Kohei12ORCID,Ishikawa Marin1,Kawano Ryutaro1,Aimono Eriko13,Mizuno Takaaki1,Nohara Sachio4,Tanishima Shigeki14,Hayashi Hideyuki1ORCID,Nishihara Hiroshi1,

Affiliation:

1. Genomics Unit, Keio Cancer Center Keio University School of Medicine Shinjuku‐ku, Tokyo Japan

2. Department of Obstetrics and Gynecology Kumagaya General Hospital Kumagaya Saitama Japan

3. Department of Cancer Pathology, Faculty of Medicine Hokkaido University Sapporo Hokkaido Japan

4. Department of Biomedical Informatics, Communication Engineering Center, Electronic Systems Business Group Mitsubishi Electric Software Co., Ltd. Amagasaki Hyogo Japan

Abstract

AbstractBackgroundPIK3CA mutations are implicated in various cancers, but the implications of multiple concurrent mutations and their orientations within the gene have not been fully explored.MethodsIn this study, we analyzed multi‐PIK3CA mutations across a diverse pan‐cancer cohort comprising 3564 tumors.ResultsMulti‐PIK3CA mutations were present in 10.3% of all PIK3CA‐mutant tumors, predominantly occurring in breast and gynecological cancers. Notably, mutations within the helical domain (E542:E545) exclusively occurred in the trans‐orientation, contrasting with mutations in the kinase ABD and C2 domains, which mainly appeared in the cis orientation.ConclusionsThe distinct pattern of mutation orientations in PIK3CA suggests variable oncogenic potential, with helical domain mutations in the trans‐orientation potentially being less oncogenic. These findings highlight the importance of mutation orientation in the PIK3CA gene as potential biomarkers for targeted therapy. This understanding is crucial for designing clinical trials that leverage PI3K inhibitors, aiming for more effective and precise cancer treatment.

Funder

Japan Society for the Promotion of Science

Japan Agency for Medical Research and Development

Publisher

Wiley

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