Integrated phosphoproteomics and transcriptional classifiers reveal hidden RAS signaling dynamics in multiple myeloma

Author:

Lin Yu-Hsiu T.1ORCID,Way Gregory P.2ORCID,Barwick Benjamin G.3ORCID,Mariano Margarette C.1,Marcoulis Makeba1,Ferguson Ian D.1ORCID,Driessen Christoph4,Boise Lawrence H.3,Greene Casey S.25ORCID,Wiita Arun P.1ORCID

Affiliation:

1. Department of Laboratory Medicine, University of California, San Francisco, San Francisco, CA;

2. Department of Systems Pharmacology and Translational Therapeutics, University of Pennsylvania, Philadelphia, PA;

3. Department of Hematology and Medical Oncology and Winship Cancer Institute, Emory University, Atlanta, GA;

4. Experimental Oncology and Hematology, Department of Oncology and Hematology, Kantonsspital St. Gallen, St. Gallen, Switzerland; and

5. Childhood Cancer Data Laboratory, Alex’s Lemonade Stand Foundation, Philadelphia, PA

Abstract

Key Points NRAS and KRAS mutations lead to different downstream transcriptional signatures and patient prognoses under current myeloma therapies. RAS genotype alone does not strongly predict degree of active MAPK signaling, suggesting alternate precision medicine approaches are needed.

Publisher

American Society of Hematology

Subject

Hematology

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