Glioblastoma stem cells reprogram chromatin in vivo to generate selective therapeutic dependencies on DPY30 and phosphodiesterases

Author:

Dixit Deobrat1ORCID,Prager Briana C.123ORCID,Gimple Ryan C.12ORCID,Miller Tyler E.4ORCID,Wu Qiulian15ORCID,Yomtoubian Shira1,Kidwell Reilly L.1ORCID,Lv Deguan15ORCID,Zhao Linjie15ORCID,Qiu Zhixin15ORCID,Zhang Guoxin1ORCID,Lee Derrick15,Park Donglim Esther1ORCID,Wechsler-Reya Robert J.6ORCID,Wang Xiuxing1ORCID,Bao Shideng37ORCID,Rich Jeremy N.15ORCID

Affiliation:

1. Division of Regenerative Medicine, Department of Medicine, University of California, San Diego, San Diego, CA 92037, USA.

2. Department of Pathology, Case Western Reserve University, Cleveland, OH 44106, USA.

3. Department of Molecular Medicine, Cleveland Clinic Lerner College of Medicine of Case Western Reserve University, Cleveland, OH 44106, USA.

4. Department of Pathology, Massachusetts General Hospital, Boston, MA 02114, USA.

5. University of Pittsburgh Medical Center Hillman Cancer Center, Pittsburgh, PA 15232, USA.

6. Tumor Initiation and Maintenance Program, NCI-Designated Cancer Center, Sanford Burnham Prebys Medical Discovery Institute, La Jolla, CA 92037, USA.

7. Department of Cancer Biology, Cleveland Clinic Lerner Research Institute, Cleveland, OH 44106, USA.

Abstract

DPY30 is an in vivo–specific dependency in glioblastoma that regulates phosphodiesterases and angiogenesis in the hypoxic tumor microenvironment.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

General Medicine

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