Defining principles of combination drug mechanisms of action

Combination chemotherapies have been a mainstay in the treatment of disseminated malignancies for almost 60 y, yet even successful regimens fail to cure many patients. Although their single-drug components are well studied, the mechanisms by which drugs work together in clinical combination regimens are poorly understood. Here, we combine RNAi-based functional signatures with complementary informatics tools to examine drug combinations. This approach seeks to bring to combination therapy what the knowledge of biochemical targets has brought to single-drug therapy and creates a statistical and experimental definition of “combination drug mechanisms of action.” We show that certain synergistic drug combinations may act as a more potent version of a single drug. Conversely, unlike these highly synergistic combinations, most drugs average extant single-drug variations in therapeutic response. When combined to form multidrug regimens, averaging combinations form averaging regimens that homogenize genetic variation in mouse models of cancer and in clinical genomics datasets. We suggest surprisingly simple and predictable combination mechanisms of action that are independent of biochemical mechanism and have implications for biomarker discovery as well as for the development of regimens with defined genetic dependencies.National Institutes of Health (U.S.) (Grant R01-CA128803-04)Poitras Foundation (Fellowship for Biomedical Engineering)Virginia and Daniel K. Ludwig Graduate FellowshipNational Cancer Institute (U.S.). Integrative Cancer Biology Program (Grant U54-CA112967-0)National Cancer Institute (U.S.). Integrative Cancer Biology Program (Summer Research Fellowship