Dual inhibition of MDMX and MDM2 as a therapeutic strategy in leukemia

Author:

Carvajal Luis A.1ORCID,Neriah Daniela Ben1,Senecal Adrien2ORCID,Benard Lumie1ORCID,Thiruthuvanathan Victor1ORCID,Yatsenko Tatyana1ORCID,Narayanagari Swathi-Rao13ORCID,Wheat Justin C.1ORCID,Todorova Tihomira I.1ORCID,Mitchell Kelly1ORCID,Kenworthy Charles2,Guerlavais Vincent4,Annis D. Allen4,Bartholdy Boris1,Will Britta1356,Anampa Jesus D.5ORCID,Mantzaris Ioannis5,Aivado Manuel4,Singer Robert H.2ORCID,Coleman Robert A.2ORCID,Verma Amit356,Steidl Ulrich1356ORCID

Affiliation:

1. Department of Cell Biology, Albert Einstein College of Medicine, Bronx, NY 10461, USA.

2. Department of Anatomy and Structural Biology, Albert Einstein College of Medicine, Bronx, NY 10461, USA.

3. Ruth L. and David S. Gottesman Institute for Stem Cell Research and Regenerative Medicine, Albert Einstein College of Medicine, Bronx, NY 10461, USA.

4. Aileron Therapeutics, Cambridge, MA 02139, USA.

5. Division of Hemato-Oncology, Department of Medicine (Oncology), Albert Einstein College of Medicine, Bronx, NY 10461, USA.

6. Albert Einstein Cancer Center, Albert Einstein College of Medicine, Bronx, NY 10461, USA.

Abstract

Dual inhibition of MDMX and MDM2 by an α-helical p53-stapled peptide (ALRN-6924) results in robust antitumor activity in acute myeloid leukemia.

Funder

National Institutes of Health

Publisher

American Association for the Advancement of Science (AAAS)

Subject

General Medicine

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