Peroxiredoxin, Senescence, and Cancer

Cells. 2022 May 28;11(11):1772. doi: 10.3390/cells11111772.

Abstract

Peroxiredoxins are multifunctional enzymes that play a key role in protecting cells from stresses and maintaining the homeostasis of many cellular processes. Peroxiredoxins were firstly identified as antioxidant enzymes that can be found in all living organisms. Later studies demonstrated that peroxiredoxins also act as redox signaling regulators, chaperones, and proinflammatory factors and play important roles in oxidative defense, redox signaling, protein folding, cycle cell progression, DNA integrity, inflammation, and carcinogenesis. The versatility of peroxiredoxins is mainly based on their unique active center cysteine with a wide range of redox states and the ability to switch between low- and high-molecular-weight species for regulating their peroxidase and chaperone activities. Understanding the molecular mechanisms of peroxiredoxin in these processes will allow the development of new approaches to enhance longevity and to treat various cancers. In this article, we briefly review the history of peroxiredoxins, summarize recent advances in our understanding of peroxiredoxins in aging- and cancer-related biological processes, and discuss the future perspectives of using peroxiredoxins in disease diagnostics and treatments.

Keywords: DNA integrity; aging; cancer; carcinogenesis; chaperone; cycle cell progression; inflammation; oxidative defense system; peroxiredoxin; redox signaling.

Publication types

  • Review
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antioxidants / metabolism
  • Humans
  • Neoplasms* / metabolism
  • Oxidation-Reduction
  • Peroxidase / metabolism
  • Peroxiredoxins* / metabolism

Substances

  • Antioxidants
  • Peroxiredoxins
  • Peroxidase

Grants and funding

This research was funded by University Grants Committee, General Research Fund—grant number 15101520, and National Natural Science Foundation of China, General Programs—grant number 81870586. The APC was settled by the vouchers to C.-M.W. by reviewing manuscripts submitted to MDPI.