Simultaneous inhibition of deubiquitinating enzymes (DUBs) and autophagy synergistically kills breast cancer cells

• Published in: Oncotarget 2015-02, Vol.6 (6), p.4159-4170
• Main Authors: Vogel, Rachel Isaksson, Coughlin, Kathleen, Scotti, Alessandra, Iizuka, Yoshie, Anchoori, Ravi, Roden, Richard B S, Marastoni, Mauro, Bazzaro, Martina
• Format: Article
• Language: English
• Subjects: Antineoplastic Combined Chemotherapy Protocols - pharmacology; Apoptosis - drug effects; Autophagy - drug effects; Cell Line, Tumor; Chloroquine - administration & dosage; Chloroquine - pharmacology; Drug Synergism; Female; Humans; Hydroxamic Acids - administration & dosage; Hydroxamic Acids - pharmacology; MCF-7 Cells; Protease Inhibitors - administration & dosage; Protease Inhibitors - pharmacology; Proteasome Endopeptidase Complex - metabolism; Research Paper; Triple Negative Breast Neoplasms - drug therapy; Triple Negative Breast Neoplasms - enzymology; Triple Negative Breast Neoplasms - pathology; Ubiquitin-Specific Proteases - antagonists & inhibitors; Ubiquitin-Specific Proteases - metabolism
• ISSN: 1949-2553; 1949-2553
• DOI: 10.18632/oncotarget.2904

Breast cancer is one of the leading causes of cancer death among women in the United States. Patients expressing the estrogen and progesterone receptor (ER and PR) and human epidermal growth factor 2 (HER-2) tumor markers have favorable prognosis and efficacious therapeutic options. In contrast, tumors that are negative for these markers (triple-negative) have a disproportionate share of morbidity and mortality due to lack of a validated molecular target. Deubiquitinating enzymes (DUBs) are a critical component of ubiquitin-proteasome-system degradation and have been shown to be differentially expressed and activated in a number of cancers, including breast, with their aberrant activity linked to cancer prognosis and clinical outcome. We evaluated the effect of the DUB inhibitors b-AP15 and RA-9 alone and in combination with early- and late-stage lysosomal inhibitors on cell viability in a panel of triple negative breast cancer (TNBC) cell lines. Our results indicate small-molecule DUB inhibitors have a profound effect on TNBC viability and lead to activation of autophagy as a cellular mechanism to compensate for ubiquitin-proteasome-system stress. Treatment with sub-optimal doses of DUB and lysosome inhibitors synergistically kills TNBC cells. This supports the evaluation of DUB inhibition, in combination with lysosomal inhibition, as a therapeutic approach for the treatment of TNBC.