Benjamin Barwick
Atlanta
As seen in:
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Science Magazine,
BioRxiv,
Cell Press,
Genome Research,
The Journal of Immunology
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KDM6A Regulates Immune Response Genes in Multiple Myeloma
Abstract The histone H3K27 demethylase KDM6A is a tumor suppressor in multiple cancers, including multiple myeloma (MM). We created isogenic MM cells disrupted for KDM6A and tagged the endogenous protein to facilitate genome wide studies. KDM6A binds genes associated with immune recognition and cytokine signaling. Most importantly, KDM6A binds and activates NLRC5 and CIITA encoding regulators of Major Histocompatibility Complex (MHC) genes.
Genome-scale functional genomics identify genes preferentially essential for multiple myeloma cells compared to other neoplasias - Nature Cancer
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Abstract Clinical progress in multiple myeloma (MM), an incurable plasma cell (PC) neoplasia, has been driven by therapies that have limited applications beyond MM/PC neoplasias and do not target specific oncogenic mutations in MM. Instead, these agents target pathways critical for PC biology yet largely dispensable for malignant or normal cells of most other lineages.
By Benjamin Barwick, Vikas Gupta, Yiguo Hu, Jordan G Bryan, Andrew J. Aguirre, Benjamin Ebert, Christopher J. Ott, James E. Bradner, Jonathan Keats, Nathanael S. Gray, Aedín C. Culhane, James M McFarland, Joshua M. Dempster, Jonathan D. Licht, Lawrence Boise, William Hahn, Francisca Vazquez, Aviad Tsherniak
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Nature
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Chromatin Accessibility Identifies Regulatory Elements Predictive of Gene Expression and Disease Outcome in Multiple Myeloma
Translational Cancer Mechanisms and Therapy Benjamin G. Barwick, Vikas A. Gupta, Shannon M. Matulis, Jonathan C. Patton, Doris R. Powell, Yanyan Gu, David L. Jaye, Karen N. Conneely, Yin C. Lin, Craig C. Hofmeister, Ajay K. Nooka, Jonathan J. Keats, Sagar Lonial, Paula M. Vertino and Lawrence H. Boise DOI: 10.1158/1078-0432.CCR-20-2931 Published June 2021 This article requires a subscription to view the full text.
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