4.6 Review

Repurposing old drugs as new inhibitors of the ubiquitin-proteasome pathway for cancer treatment

Journal

SEMINARS IN CANCER BIOLOGY
Volume 68, Issue -, Pages 105-122

Publisher

ACADEMIC PRESS LTD- ELSEVIER SCIENCE LTD
DOI: 10.1016/j.semcancer.2019.12.013

Keywords

Drug reposition; Protein degradation; Post-translational modification; UPS inhibitors; Cancer therapies

Categories

Funding

  1. National Cancer Institute [R21CA184788]
  2. NCI [R01CA172480-01A1]
  3. National Institutes of Health [P30 CA022453]
  4. National Natural Science Foundation of China [81872439, 31700780, 81802405, 81670156, 81773213, 81772492, 81600147]

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The ubiquitin-proteasome system (UPS) is crucial in cellular protein degradation, and targeted protein degradation has been proven effective in cancer therapy. 20S proteasome inhibitors have been FDA-approved for multiple myeloma treatment, but face limitations like drug resistance. Repurposing old drugs with UPS-inhibitory properties as new anticancer agents is a strategy to improve current cancer treatment methods.
The ubiquitin-proteasome system (UPS) plays a central role in the degradation of cellular proteins. Targeting protein degradation has been validated as an effective strategy for cancer therapy since 2003. Several components of the UPS have been validated as potential anticancer targets, including 20S proteasomes, 19S proteasome-associated deubiquitinases (DUBs) and ubiquitin ligases (E3s). 20S proteasome inhibitors (such as bortezomib/BTZ and carfilzomib/CFZ) have been approved by the U.S. Food and Drug Administration (FDA) for the treatment of multiple myeloma (MM) and some other liquid tumors. Although survival of MM patients has been improved by the introduction of BTZ-based therapies, these clinical 20S proteasome inhibitors have several limitations, including emergence of resistance in MM patients, neuro-toxicities, and little efficacy in solid tumors. One of strategies to improve the current status of cancer treatment is to repurpose old drugs with UPS-inhibitory properties as new anticancer agents. Old drug reposition represents an attractive drug discovery approach compared to the traditional de novo drug discovery process which is time-consuming and costly. In this review, we summarize status of repurposed inhibitors of various UPS components, including 20S proteasomes, 19S -associated DUBs, and ubiquitin ligase E3s. The original and new mechanisms of action, molecular targets, and potential anticancer activities of these repurposed UPS inhibitors are reviewed, and their new uses including combinational therapies for cancer treatment are discussed.

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