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Updated: May 29, 2026

Differentiation of Mouse Breast Epithelial HC11 and EpH4 Cells
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HDAC3 at the fulcrum of an epithelial-mesenchymal balance
Sendurai A Mani1, Michelle Craig Barton
1Department of Molecular Pathology, The Center for Stem Cell and Developmental Biology, University of Texas MD Anderson Cancer Center, 1515 Holcombe Boulevard, Houston, TX 77030, USA. smani@mdanderson.org
Abstract:
In this issue of Molecular Cell, Wu et al. (2011) reveal an essential role for a chromatin modifier, histone deacetylase 3 (HDAC3), in hypoxia-induced epithelial-mesenchymal transition (EMT); HIF-activated HDAC3 integrates with WDR5 to impose chromatin modifications that culminate in EMT.
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