Myc-induced SUMOylation is a therapeutic vulnerability for B-cell lymphoma

Author:

Hoellein Alexander1,Fallahi Mohammad2,Schoeffmann Stephanie1,Steidle Sabine1,Schaub Franz X.2,Rudelius Martina3,Laitinen Iina4,Nilsson Lisa5,Goga Andrei6,Peschel Christian17,Nilsson Jonas A.5,Cleveland John L.2,Keller Ulrich17

Affiliation:

1. III. Medical Department, Technische Universität München, Munich, Germany;

2. Department of Cancer Biology, The Scripps Research Institute, Scripps Florida, Jupiter, FL;

3. Institute of Pathology and Clinical Cancer Center Mainfranken, Universität Würzburg, Würzburg, Germany;

4. Department of Nuclear Medicine, Technische Universität München, Munich, Germany;

5. Department of Surgery, Sahlgrenska Cancer Center, Institute of Clinical Sciences, University of Gothenburg, Gothenburg, Sweden;

6. Department of Cell/Tissue Biology, University of California, San Francisco, San Francisco, CA; and

7. German Cancer Consortium (DKTK) and German Cancer Research Center (DKFZ), Heidelberg, Germany

Abstract

Key Points The Myc oncoprotein targets central regulators of the SUMOylation machinery, resulting in a hyper-SUMOylation state in Myc-induced lymphoma. Targeting SUMOylation by genetic or pharmacologic means represents a novel therapeutic option for lymphomas with MYC involvement.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

Reference61 articles.

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