Insights into the oncogenic effects of /PIK3CA/ mutations from the structure of p110[alpha]/p85[alpha]
- JHU
Phosphatidylinositide-3-kinases (PI3K) initiate a number of signaling pathways by recruiting other kinases, such as Akt, to the plasma membrane. One of the isoforms, PI3K{alpha}, is an oncogene frequently mutated in several cancer types. These mutations increase PI3K kinase activity, leading to increased cell survival, cell motility, cell metabolism, and cell cycle progression. The structure of the complex between the catalytic subunit of PI3K{alpha}, p110{alpha}, and a portion of its regulatory subunit, p85{alpha} reveals that the majority of the oncogenic mutations occur at the interfaces between p110 domains and between p110 and p85 domains. At these positions, mutations disrupt interactions resulting in changes in the kinase domain that may increase enzymatic activity. The structure also suggests that interaction with the membrane is mediated by one of the p85 domains (iSH2). These findings may provide novel structural loci for the design of new anti-cancer drugs.
- Research Organization:
- Argonne National Lab. (ANL), Argonne, IL (United States). Advanced Photon Source (APS)
- Sponsoring Organization:
- National Institutes of Health (NIH)
- OSTI ID:
- 1019131
- Journal Information:
- Cell Cycle, Vol. 7, Issue (9) ; 05, 2008
- Country of Publication:
- United States
- Language:
- ENGLISH
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The Structure of a Human p110{alpha}/p85{alpha} Complex Elucidates the Effects of Oncogenic PI3K{alpha} Mutations
A frequent kinase domain mutation that changes the interaction between PI3K[alpha] and the membrane