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Title: Oxidation resistance 1 is a novel senolytic target

Journal Article · · Aging Cell
DOI:https://doi.org/10.1111/acel.12780· OSTI ID:1559794
 [1];  [2];  [1];  [1];  [1];  [1];  [3];  [3];  [1];  [1];  [4];  [5];  [6];  [7];  [8]
  1. Univ. of Arkansas for Medical Sciences, Little Rock, AR (United States). Dept. of Pharmaceutical Sciences, College of Pharmacy
  2. Univ. of Arkansas for Medical Sciences, Little Rock, AR (United States). Dept. of Pharmaceutical Sciences, College of Pharmacy; Soochow University School of Medicine, Suzhou (China). Hematology Center of Cyrus Tang Medical Institute, Collaborative Innovation Center of Hematology
  3. Univ. of Arkansas for Medical Sciences, Little Rock, AR (United States). Dept. of Biochemistry and Molecular Biology, College of Medicine
  4. Unity Biotechnology, Brisbane, CA (United States)
  5. The Buck Institute for Research on Aging, Novato, CA (United States); Lawrence Berkeley National Lab. (LBNL), Berkeley, CA (United States)
  6. Hematology Center of Cyrus Tang Medical Institute, Collaborative Innovation Center of Hematology, Soochow University School of Medicine, Suzhou China
  7. Univ. of Arkansas for Medical Sciences, Little Rock, AR (United States). Dept. of Pharmaceutical Sciences, College of Pharmacy; Univ. of Florida, Gainesville, FL (United States). Dept. of Medicinal Chemistry, College of Pharmacy
  8. Univ. of Arkansas for Medical Sciences, Little Rock, AR (United States). Dept. of Pharmaceutical Sciences, College of Pharmacy; Univ. of Florida, Gainesville, FL (United States). Dept. of Pharmocodynamics, College of Pharmacy

The selective depletion of senescent cells (SCs) by small molecules, termed senolytic agents, is a promising therapeutic approach for treating age-related diseases and chemotherapy- and radiotherapy-induced side effects. Piperlongumine (PL) was recently identified as a novel senolytic agent. However, its mechanism of action and molecular targets in SCs was unknown and thus was investigated. Specifically, we used a PL-based chemical probe to pull-down PL-binding proteins from live cells and then mass spectrometry-based proteomic analysis to identify potential molecular targets of PL in SCs. One prominent target was oxidation resistance 1 (OXR1), an important antioxidant protein that regulates the expression of a variety of antioxidant enzymes. We found that OXR1 was upregulated in senescent human WI38 fibroblasts. PL bound to OXR1 directly and induced its degradation through the ubiquitin-proteasome system in an SC-specific manner. The knockdown of OXR1 expression by RNA interference significantly increased the production of reactive oxygen species in SCs in conjunction with the downregulation of antioxidant enzymes such as heme oxygenase 1, glutathione peroxidase 2, and catalase, but these effects were much less significant when OXR1 was knocked down in non-SCs. More importantly, knocking down OXR1 selectively induced apoptosis in SCs and sensitized the cells to oxidative stress caused by hydrogen peroxide. These findings provide new insights into the mechanism by which SCs are highly resistant to oxidative stress and suggest that OXR1 is a novel senolytic target that can be further exploited for the development of new senolytic agents.

Research Organization:
Lawrence Berkeley National Laboratory (LBNL), Berkeley, CA (United States)
Sponsoring Organization:
USDOE Office of Science (SC); National Institutes of Health (NIH); University of Arkansas for Medical Sciences Proteomics Core Facility
Grant/Contract Number:
AC02-05CH11231; P20GM109005; R01CA122023; R01CA219836; R56AG056372; P20GM103429; P20GM121293; S10OD018445
OSTI ID:
1559794
Journal Information:
Aging Cell, Vol. 17, Issue 4; ISSN 1474-9718
Publisher:
Anatomical Society - WileyCopyright Statement
Country of Publication:
United States
Language:
English
Citation Metrics:
Cited by: 67 works
Citation information provided by
Web of Science

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Cited By (4)

Proteome Oxidative Modifications and Impairment of Specific Metabolic Pathways During Cellular Senescence and Aging journal March 2020
The chemistry of senescence journal June 2019
Senescence-induced inflammation: an important player and key therapeutic target in atherosclerosis journal January 2020
Cellular senescence, geroscience, cancer and beyond journal September 2018