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Updated: Oct 21, 2025

Investigation of the Transcriptional Role of a RUNX1 Intronic Silencer by CRISPR/Cas9 Ribonucleoprotein in Acute Myeloid Leukemia Cells
Published on: September 1, 2019
Exploiting a key transcriptional dependency: ZMYND8 and IRF8 in AML
Samuel J Taylor1, Sriram Sundaravel1, Ulrich Steidl1
1Departments of Cell Biology, and of Medicine, Blood Cancer Institute, Albert Einstein Cancer Center; and Ruth L. and David S. Gottesman Institute for Stem Cell Research and Regenerative Medicine, Albert Einstein College of Medicine, Montefiore Medical Center, Bronx, NY, USA.
Abstract:
In this issue of Molecular Cell, Cao et al. (2021) report that AML cells are specifically addicted to an IRF8-MEF2D gene expression network. Furthermore, they identify a chromatin reader, ZMYND8, as the upstream regulator of the IRF8-MEF2D program whose activity is critical for AML cell survival.
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