| Literature DB >> 27659046 |
Thomas Horn1, Stéphane Ferretti2, Nicolas Ebel2, Angela Tam1, Samuel Ho3, Fred Harbinski4, Ali Farsidjani3, Matthew Zubrowski1, William R Sellers3, Robert Schlegel1, Dale Porter1, Erick Morris1, Jens Wuerthner2, Sébastien Jeay2, Joel Greshock1, Ensar Halilovic1, Levi A Garraway5, Giordano Caponigro6, Joseph Lehár6.
Abstract
Like classical chemotherapy regimens used to treat cancer, targeted therapies will also rely upon polypharmacology, but tools are still lacking to predict which combinations of molecularly targeted drugs may be most efficacious. In this study, we used image-based proliferation and apoptosis assays in colorectal cancer cell lines to systematically investigate the efficacy of combinations of two to six drugs that target critical oncogenic pathways. Drug pairs targeting key signaling pathways resulted in synergies across a broad spectrum of genetic backgrounds but often yielded only cytostatic responses. Enhanced cytotoxicity was observed when additional processes including apoptosis and cell cycle were targeted as part of the combination. In some cases, where cell lines were resistant to paired and tripled drugs, increased expression of antiapoptotic proteins was observed, requiring a fourth-order combination to induce cytotoxicity. Our results illustrate how high-order drug combinations are needed to kill drug-resistant cancer cells, and they also show how systematic drug combination screening together with a molecular understanding of drug responses may help define optimal cocktails to overcome aggressive cancers. Cancer Res; 76(23); 6950-63. ©2016 AACR. ©2016 American Association for Cancer Research.Entities:
Mesh:
Year: 2016 PMID: 27659046 DOI: 10.1158/0008-5472.CAN-15-3425
Source DB: PubMed Journal: Cancer Res ISSN: 0008-5472 Impact factor: 12.701