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Updated: May 24, 2026

Assessing Autophagic Flux by Measuring LC3, p62, and LAMP1 Co-localization Using Multispectral Imaging Flow Cytometry
Published on: July 21, 2017
Autophagy prolongs survival after NFκB inhibition in B-cell lymphomas
Thomas G Sommermann1, Hildegard I D Mack, Ellen Cahir-McFarland
1Department of Medicine, Division of Infectious Diseases, Brigham and Women's Hospital, Boston, MA, USA.
Abstract:
Autophagy allows cells to survive under conditions of nutrient deprivation. We have demonstrated that autophagy inhibitors are synthetically lethal with NFκB inhibitors in B-cell lymphomas because the NFκB pathway promotes survival by increasing glucose import. When NFκB is inhibited in B-cell lymphoma, glucose import decreases and cells become sensitive to perturbations in mitochondrial metabolism and autophagy. Thus, combined inhibition of autophagy and NFκB drives cells into metabolic crisis accelerating cell death.
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