MEK inhibition induces MYOG and remodels super-enhancers in RAS-driven rhabdomyosarcoma

Author:

Yohe Marielle E.12ORCID,Gryder Berkley E.1ORCID,Shern Jack F.2,Song Young K.1,Chou Hsien-Chao1,Sindiri Sivasish1,Mendoza Arnulfo2,Patidar Rajesh1,Zhang Xiaohu3,Guha Rajarashi3ORCID,Butcher Donna4ORCID,Isanogle Kristine A.5,Robinson Christina M.5,Luo Xiaoling6,Chen Jin-Qiu6,Walton Ashley1,Awasthi Parirokh5ORCID,Edmondson Elijah F.4ORCID,Difilippantonio Simone5,Wei Jun S.1ORCID,Zhao Keji7,Ferrer Marc3,Thomas Craig J.3,Khan Javed1ORCID

Affiliation:

1. Oncogenomics Section, Genetics Branch, National Cancer Institute, National Institutes of Health (NIH), Bethesda, MD 20892, USA.

2. Pediatric Oncology Branch, National Cancer Institute, NIH, Bethesda, MD 20892, USA.

3. Division of Preclinical Innovation, National Center for Advancing Translational Sciences, NIH, Bethesda, MD 20892, USA.

4. Pathology/Histotechnology Laboratory, Leidos Biomedical Research Inc., Frederick National Laboratory for Cancer Research, NIH, Frederick, MD 21702, USA.

5. Laboratory Animal Sciences Program, Leidos Biomedical Research Inc., Frederick National Laboratory for Cancer Research, NIH, Frederick, MD 21701, USA.

6. Collaborative Protein Technology Resource, National Cancer Institute, NIH, Bethesda, MD 20892, USA.

7. Systems Biology Center, National Heart Lung and Blood Institute, NIH, Bethesda, MD 20892, USA.

Abstract

MEK inhibition decreases cell viability and induces differentiation in RAS-driven rhabdomyosarcoma via an epigenetic mechanism.

Funder

Alex’s Lemonade Stand Foundation for Childhood Cancer

Publisher

American Association for the Advancement of Science (AAAS)

Subject

General Medicine

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