Abstract
In this issue of Molecular Cell, Byun et al. (2020) find that the dual targeting of glutamine metabolism and the PD-L1 checkpoint inhibitor augments anti-tumor immunity. Mechanistically, decreased glutamine availability attenuated S-glutathionylation of SERCA, resulting in an increase in cytosolic calcium, enhanced NF-κB activity, and upregulation of programmed death-ligand 1.
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CITATION STYLE
APA
Matias, M. I., Dardalhon, V., & Taylor, N. (2020, November 19). Targeting Glutamine Metabolism and PD-L1: A Novel Anti-tumor Pas de Deux. Molecular Cell. Cell Press. https://doi.org/10.1016/j.molcel.2020.11.005
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