Deubiquitinases Maintain Protein Homeostasis and Survival of Cancer Cells upon Glutathione Depletion. Academic Article uri icon

Overview

abstract

  • 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

  • Harris, Isaac S
  • Endress, Jennifer
  • Coloff, Jonathan L
  • Selfors, Laura M
  • McBrayer, Samuel K
  • Rosenbluth, Jennifer M
  • Takahashi, Nobuaki
  • Dhakal, Sabin
  • Koduri, Vidyasagar
  • Oser, Matthew G
  • Schauer, Nathan J
  • Doherty, Laura M
  • Hong, Andrew L
  • Kang, Yun Pyo
  • Younger, Scott T
  • Doench, John G
  • Hahn, William C
  • Buhrlage, Sara J
  • DeNicola, Gina M
  • Kaelin, William G
  • Brugge, Joan S

publication date

  • February 21, 2019

Research

keywords

  • Antioxidants
  • Cell Survival
  • Deubiquitinating Enzymes
  • Glutathione
  • Proteostasis

Identity

PubMed Central ID

  • PMC6506399

Scopus Document Identifier

  • 85064946215

Digital Object Identifier (DOI)

  • 10.1016/j.cmet.2019.01.020

PubMed ID

  • 30799286

Additional Document Info

volume

  • 29

issue

  • 5