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) production via nicotinamide phosphoribosyltransferase (NAMPT) inhibition demonstrated that metabolic catastrophe drives the combination-induced cytotoxicity. This study provides a comprehensive single-agent and combinatorial drug screen for DMG and identifies concomitant HDAC and proteasome inhibition as a promising therapeutic strategy that underscores underrecognized metabolic vulnerabilities in DMG.
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Grant L. Lin
Kelli M. Wilson
Michele Ceribelli
Science Translational Medicine
Stanford University
Johns Hopkins University
National Institutes of Health
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Lin et al. (Wed,) studied this question.
www.synapsesocial.com/papers/6a09f0ef4db796859051ad2a — DOI: https://doi.org/10.1126/scitranslmed.aaw0064