Salt-inducible kinase inhibition suppresses acute myeloid leukemia progression in vivo

Author:

Tarumoto Yusuke12ORCID,Lin Shan34,Wang Jinhua56,Milazzo Joseph P.1,Xu Yali1,Lu Bin1,Yang Zhaolin1ORCID,Wei Yiliang1ORCID,Polyanskaya Sofya17ORCID,Wunderlich Mark8ORCID,Gray Nathanael S.56ORCID,Stegmaier Kimberly34,Vakoc Christopher R.1ORCID

Affiliation:

1. Cold Spring Harbor Laboratory, Cold Spring Harbor, NY;

2. Institute for Frontier Life and Medical Sciences, Kyoto University, Kyoto, Japan;

3. Department of Pediatric Oncology, Dana-Farber Cancer Institute, Boston Children’s Hospital, Boston, MA;

4. Broad Institute of the Massachusetts Institute of Technology and Harvard University, Cambridge, MA;

5. Department of Cancer Biology, Dana-Farber Cancer Institute, Boston, MA;

6. Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Boston, MA;

7. Watson School of Biological Sciences, Cold Spring Harbor Laboratory, Cold Spring Harbor, NY; and

8. Division of Experimental Hematology and Cancer Biology, Cancer and Blood Disease Institute, Cincinnati Children’s Hospital Medical Center, Cincinnati, OH

Abstract

Transcription factors are important drivers in acute myeloid leukemia (AML), but they are notoriously difficult to target. The authors demonstrate that inhibition of salt-inducible kinase (SIK3) inhibits AML cell proliferation in cells dependent on the transcription factor MEF2C, identifying a small molecule that can disrupt a leukemogenic transcription factor pathway.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

Reference69 articles.

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