1. Academic Validation
  2. Functional characterization of an isoform-selective inhibitor of PI3K-p110β as a potential anticancer agent

Functional characterization of an isoform-selective inhibitor of PI3K-p110β as a potential anticancer agent

  • Cancer Discov. 2012 May;2(5):425-33. doi: 10.1158/2159-8290.CD-12-0003.
Jing Ni 1 Qingsong Liu Shaozhen Xie Coby Carlson Thanh Von Kurt Vogel Steve Riddle Cyril Benes Michael Eck Thomas Roberts Nathanael Gray Jean Zhao
Affiliations

Affiliation

  • 1 Department of Cancer Biology, Dana-Farber Cancer Institute, Harvard Medical School, Massachusetts General Hospital Cancer Center, Boston, Massachusetts 02115, USA.
Abstract

Genetic approaches have shown that the p110β isoform of class Ia phosphatidylinositol-3-kinase (PI3K) is essential for the growth of PTEN-null tumors. Thus, it is desirable to develop p110β-specific inhibitors for Cancer therapy. Using a panel of PI3K isoform-specific cellular assays, we screened a collection of compounds possessing activities against kinases in the PI3K superfamily and identified a potent and selective p110β inhibitor: KIN-193. We show that KIN-193 is efficacious specifically in blocking Akt signaling and tumor growth that are dependent on p110β activation or PTEN loss. Broad profiling across a panel of 422 human tumor cell lines shows that the PTEN mutation status of Cancer cells strongly correlates with their response to KIN-193. Together, our data provide the first pharmacologic evidence that PTEN-deficient tumors are dependent on p110β in Animals and suggest that KIN-193 can be pursued as a drug to treat tumors that are dependent on p110β while sparing other PI3K isoforms.

Significance: We report the first functional characterization of a p110β-selective inhibitor, KIN-193, that is efficacious as an antitumor agent in mice. We show that this class of inhibitor holds great promise as a pharmacologic agent that could be used to address the potential therapeutic benefit of treating p110β-dependent PTEN-deficient human tumors.

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