4.8 Article

Deubiquitinases Maintain Protein Homeostasis and Survival of Cancer Cells upon Glutathione Depletion

Journal

CELL METABOLISM
Volume 29, Issue 5, Pages 1166-+

Publisher

CELL PRESS
DOI: 10.1016/j.cmet.2019.01.020

Keywords

-

Funding

  1. Susan G. Komen for the Cure Foundation [SAC170002]
  2. Ludwig Center at Harvard
  3. Canadian Institutes of Health Research
  4. American Cancer Society [MRSG-18-202-01-TBG]
  5. Claudia Adams Barr Program
  6. NCI [U01CA176058]
  7. NIH [R37CA230042, R35CA210068-02]
  8. Howard Hughes Medical Institute

Ask authors/readers for more resources

Cells are subjected to oxidative stress during the initiation and progression of tumors, and this imposes selective pressure for cancer cells to adapt mechanisms to tolerate these conditions. Here, we examined the dependency of cancer cells on glutathione (GSH), the most abundant cellular antioxidant. While cancer cell lines displayed a broad range of sensitivities to inhibition of GSH synthesis, the majority were resistant to GSH depletion. To identify cellular pathways required for this resistance, we carried out genetic and pharmacologic screens. Both approaches revealed that inhibition of deubiquitinating enzymes (DUBs) sensitizes cancer cells to GSH depletion. Inhibition of GSH synthesis, in combination with DUB inhibition, led to an accumulation of polyubiquitinated proteins, induction of proteotoxic stress, and cell death. These results indicate that depletion of GSH renders cancer cells dependent on DUB activity to maintain protein homeostasis and cell viability and reveal a potentially exploitable vulnerability for cancer therapy.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.8
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available