Cancer discoveryJournal Article
02 Dec 2024
Combined EZH2 and RAS pathway inhibitors kill KRAS-mutant colorectal cancer cells and promote durable tumor regression in vivo.
These agents function by cooperatively suppressing the WNT pathway, driving differentiation, and epigenetically reprogramming cells to permit the induction of apoptotic signals, which then kill these more differentiated tumor cells.
P. Loi reports grants from the NIH/NCI during the conduct of the study. A.E. Schade reports grants from the American Cancer Society during the conduct of the study. M. Watanabe reports grants from Brigham and Women’s Hospital during the conduct of the study. O. Popow reports grants from Cancer Research UK and the Mark Foundation for Cancer Research during the conduct of the study. N. Gunduz reports grants from Cancer Grand Challenges during the conduct of the study. M. Giannakis reports grants from Janssen and personal fees from Nerviano Medical Sciences outside the submitted work. K. Ng reports nonfinancial support from Pharmavite, grants from Janssen, personal fees from Bayer, GlaxoSmithKline, Pfizer, CytomX, Jazz Pharmaceuticals, Revolution Medicines, AbbVie, Etiome, Seagen, CRICO, and JAMA outside the submitted work. S. Santagata reports being speaker honoraria for Novartis and Roche. K. Helin reports grants from the Cancer Research UK Grand Challenge and the Mark Foundation for Cancer Research to the SPECIFICANCER team during the conduct of the study. O.J. Sansom reports grants from AstraZeneca, Novartis, Boehringer Ingelheim, and Cancer Research Horizons outside the submitted work. K. Cichowski reports grants from Cancer Research UK and the Mark Foundation for Cancer Research during the conduct of the study, as well as other support from Erasca outside the submitted work. No disclosures were reported by the other authors.
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