| Literature DB >> 24747911 |
Marie Schoumacher1, Kristen E Hurov1, Joseph Lehár1, Yan Yan-Neale1, Yuji Mishina1, Dmitriy Sonkin1, Joshua M Korn1, Daisy Flemming1, Michael D Jones1, Brandon Antonakos1, Vesselina G Cooke1, Janine Steiger1, Jebediah Ledell1, Mark D Stump1, William R Sellers1, Nika N Danial1, Wenlin Shao2.
Abstract
Tankyrases (TNKS) play roles in Wnt signaling, telomere homeostasis, and mitosis, offering attractive targets for anticancer treatment. Using unbiased combination screening in a large panel of cancer cell lines, we have identified a strong synergy between TNKS and MEK inhibitors (MEKi) in KRAS-mutant cancer cells. Our study uncovers a novel function of TNKS in the relief of a feedback loop induced by MEK inhibition on FGFR2 signaling pathway. Moreover, dual inhibition of TNKS and MEK leads to more robust apoptosis and antitumor activity both in vitro and in vivo than effects observed by previously reported MEKi combinations. Altogether, our results show how a novel combination of TNKS and MEK inhibitors can be highly effective in targeting KRAS-mutant cancers by suppressing a newly discovered resistance mechanism. ©2014 American Association for Cancer Research.Entities:
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Year: 2014 PMID: 24747911 DOI: 10.1158/0008-5472.CAN-14-0138-T
Source DB: PubMed Journal: Cancer Res ISSN: 0008-5472 Impact factor: 12.701