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SMYD3 links lysine methylation of MAP3K2 to Ras-driven cancer

Pawel K. Mazur, Nicolas Reynoird, Purvesh Khatri, Pascal W. T. C. Jansen, Alex W. Wilkinson, Shichong Liu, Olena Barbash, Glenn S. Van Aller, Michael Huddleston, Dashyant Dhanak, Peter J. Tummino, Ryan G. Kruger, Benjamin A. Garcia, Atul J. Butte, Michiel Vermeulen, Julien Sage () and Or Gozani ()
Additional contact information
Pawel K. Mazur: Stanford University School of Medicine
Nicolas Reynoird: Stanford University
Purvesh Khatri: Institute for Immunity, Transplantation and Infection, Stanford University School of Medicine
Pascal W. T. C. Jansen: University Medical Center Utrecht, 3508 AB Utrecht, The Netherlands
Alex W. Wilkinson: Stanford University
Shichong Liu: Perelman School of Medicine, University of Pennsylvania
Olena Barbash: Cancer Epigenetics DPU, Oncology R&D, GlaxoSmithKline, Collegeville
Glenn S. Van Aller: Cancer Epigenetics DPU, Oncology R&D, GlaxoSmithKline, Collegeville
Michael Huddleston: Cancer Epigenetics DPU, Oncology R&D, GlaxoSmithKline, Collegeville
Dashyant Dhanak: Cancer Epigenetics DPU, Oncology R&D, GlaxoSmithKline, Collegeville
Peter J. Tummino: Cancer Epigenetics DPU, Oncology R&D, GlaxoSmithKline, Collegeville
Ryan G. Kruger: Cancer Epigenetics DPU, Oncology R&D, GlaxoSmithKline, Collegeville
Benjamin A. Garcia: Perelman School of Medicine, University of Pennsylvania
Atul J. Butte: Stanford University School of Medicine
Michiel Vermeulen: University Medical Center Utrecht, 3508 AB Utrecht, The Netherlands
Julien Sage: Stanford University School of Medicine
Or Gozani: Stanford University

Nature, 2014, vol. 510, issue 7504, 283-287

Abstract: SMYD3 is a methyltransferase overexpressed in several human tumours; here methylation of the MAP3K2 kinase by SMYD3 is shown to be critical for Ras-induced tumour development in mouse models and human tumour cells, showing an unexpected role for methylation in a kinase signalling pathway and revealing a candidate therapeutic target.

Date: 2014
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DOI: 10.1038/nature13320

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