Specific apoptosis induction by the dual PI3K/mTor inhibitor NVP-BEZ235 in HER2 amplified and PIK3CA mutant breast cancer cells

被引:250
作者
Brachmann, Saskia M. [1 ]
Hofmann, Irmgard [1 ]
Schnell, Christian [1 ]
Fritsch, Christine [1 ]
Wee, Susan [2 ]
Lane, Heidi [1 ]
Wang, Shaowen [2 ]
Garcia-Echeverria, Carlos [1 ]
Maira, Sauveur-Michel [1 ]
机构
[1] Novartis Inst Biomed Res, Oncol Dis Area, CH-4002 Basel, Switzerland
[2] Novartis Inst Biomed Res, Oncol Dis Area, Cambridge, MA 02139 USA
关键词
kinase inhibitor; small molecule; PI3K; breat cancer; mTOR; PHOSPHATIDYLINOSITOL 3-KINASE/MAMMALIAN TARGET; VIVO ANTITUMOR-ACTIVITY; RAPAMYCIN INHIBITOR; PI3K INHIBITOR; DNA-DAMAGE; PTEN; MEK; CASPASE-2; COMPLEX; GROWTH;
D O I
10.1073/pnas.0905152106
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
NVP-BEZ235 is a dual PI3K/mTOR inhibitor currently in phase I clinical trials. We profiled this compound against a panel of breast tumor cell lines to identify the patient populations that would benefit from such treatment. In this setting, NVP-BEZ235 selectively induced cell death in cell lines presenting either HER2 amplification and/or PIK3CA mutation, but not in cell lines with PTEN loss of function or KRAS mutations, for which resistance could be attributed, in part to ERK pathway activity. An in depth analysis of death markers revealed that the cell death observed upon NVP-BEZ235 treatment could be recapitulated with other PI3K inhibitors and that this event is linked to active PARP cleavage indicative of an apoptotic process. Moreover, the effect seemed to be partly independent of the caspase-9 executioner and mitochondrial activated caspases, suggesting an alternate route for apoptosis induction by PI3K inhibitors. Overall, this study will provide guidance for patient stratification for forthcoming breast cancer phase II trials for NVP-BEZ235.
引用
收藏
页码:22299 / 22304
页数:6
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