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Study Title: Modeling Epigenetic Lesions that Cause Gliomas
Publication: Cell, Tuesday, July 25, 2023, 11:00am ET (https://doi.org/10.1016/j.cell.2023.06.022)
Dana-Farber Cancer Institute Authors: Gilbert J. Rahme, PhD; Nauman M. Javed, MD, PhD; Kaitlyn L. Puorro; Volker Hovestadt, PhD; Sarah E. Johnstone, MD, PhD; Bradley E. Bernstein, MD, PhD
Summary:
While cancers often originate from mutations and other alterations of cells’ DNA, researchers in the Bernstein Laboratory at Dana-Farber and the Broad Institute of MIT and Harvard have found that gliomas – incurable brain tumors – can arise due to changes in the epigenome, the collection of compounds that are deposited on DNA and alter gene activity without changing the sequence of DNA itself. The researchers pinpointed two genes whose activity is epigenetically altered in human gliomas, including one cancer-causing oncogene and one cancer-preventing tumor suppressor gene. In animal models, they showed that changes to the epigenome that activate the oncogene and silence the tumor suppressor work in sync to spur brain tumor formation. The findings underscore the potential of therapies that seek to impede gliomas by targeting the epigenome.
Impact:
The discovery that glioma brain tumors can be driven by epigenetic changes – alterations in markings that control gene activity – suggests that new chemotherapy agents that target those changes may hold the key to stymying tumor growth.
Funding:
The research was supported by the National Cancer Institute, the National Institutes of Health, and the American Cancer Society.
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