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

被引:118
作者
Harris, Isaac S. [1 ,2 ]
Endress, Jennifer E. [1 ,2 ]
Coloff, Jonathan L. [1 ,2 ]
Selfors, Laura M. [2 ]
McBrayer, Samuel K. [3 ]
Rosenbluth, Jennifer M. [1 ,2 ,3 ]
Takahashi, Nobuaki [1 ,2 ]
Dhakal, Sabin [2 ]
Koduri, Vidyasagar [3 ]
Oser, Matthew G. [3 ]
Schauer, Nathan J. [3 ]
Doherty, Laura M. [3 ]
Hong, Andrew L. [3 ,4 ,5 ]
Kang, Yun Pyo [6 ]
Younger, Scott T. [5 ]
Doench, John G. [5 ]
Hahn, William C. [3 ,5 ,7 ]
Buhrlage, Sara J. [2 ,3 ]
DeNicola, Gina M. [6 ]
Kaelin, William G., Jr. [3 ]
Brugge, Joan S. [1 ,2 ]
机构
[1] Ludwig Canc Ctr, Boston, MA 02115 USA
[2] Harvard Med Sch, Boston, MA 02115 USA
[3] Dana Farber Canc Inst, Boston, MA 02115 USA
[4] Boston Childrens Hosp, Boston, MA 02115 USA
[5] Brd Inst Harvard & MIT, 415 Main St, Cambridge, MA 02142 USA
[6] H Lee Moffitt Canc Ctr & Res Inst, Dept Canc Physiol, Tampa, FL 33612 USA
[7] Brigham & Womens Hosp, Boston, MA 02115 USA
基金
加拿大健康研究院;
关键词
BUTHIONINE SULFOXIMINE; MOLECULAR-MECHANISMS; DRUG-COMBINATIONS; OXIDATIVE STRESS; INHIBITOR; THERAPY; MTOR; ROS; SPECIFICITY; DISEASE;
D O I
10.1016/j.cmet.2019.01.020
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
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.
引用
收藏
页码:1166 / +
页数:22
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