Double <i>PIK3CA</i> mutations in cis increase oncogenicity and sensitivity to PI3Kα inhibitors

Neil Vasan(Memorial Sloan Kettering Cancer Center), Pedram Razavi(Memorial Sloan Kettering Cancer Center), Jared L. Johnson(Cornell University), Hong Shao(Memorial Sloan Kettering Cancer Center), Hardik Shah(Icahn School of Medicine at Mount Sinai), Alesia Antoine(Icahn School of Medicine at Mount Sinai), Erik Ladewig(Memorial Sloan Kettering Cancer Center), Alexander N. Gorelick(Memorial Sloan Kettering Cancer Center), Ting-Yu Lin(Cornell University), Eneda Toska(Memorial Sloan Kettering Cancer Center), Guotai Xu(Memorial Sloan Kettering Cancer Center), Abiha Kazmi(Memorial Sloan Kettering Cancer Center), Matthew T. Chang, Barry S. Taylor(Memorial Sloan Kettering Cancer Center), Maura N. Dickler(Memorial Sloan Kettering Cancer Center), Komal Jhaveri(Memorial Sloan Kettering Cancer Center), Sarat Chandarlapaty(Memorial Sloan Kettering Cancer Center), Raúl Rabadán(Columbia University), Ed Reznik(Memorial Sloan Kettering Cancer Center), Melissa Smith(Icahn School of Medicine at Mount Sinai), Robert Sebra(Sema4 (United States)), Frauke Schimmöller, Timothy R. Wilson, Lori S. Friedman(Sunesis (United States)), Lewis C. Cantley(Cornell University), Maurizio Scaltriti(Memorial Sloan Kettering Cancer Center), José Baselga(Memorial Sloan Kettering Cancer Center)
Science
November 7, 2019
Cited by 295Open Access
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Abstract

Seeing double can be a good thing Many human breast cancers harbor activating mutations in PIK3CA , the gene coding for the catalytic subunit of phosphoinositide 3-kinase (PI3K). Clinical trials are underway to evaluate the efficacy of PI3K inhibitors in cancer patients. Vasan et al. found unexpectedly that a subset of breast cancers harbor not one—but two— PIK3CA mutations, and the mutations occur on the same allele (see the Perspective by Toker). In model systems, the double mutations hyperactivate PI3K signaling and enhance tumor growth. Preliminary analysis of clinical trial data suggests that breast cancers with double mutations are more responsive to PI3K inhibitors than those with a single mutation. PIK3CA mutational status could help identify the breast cancer patients most likely to benefit from these drugs. Science , this issue p. 714 ; see also p. 685


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