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Ferroptosis and Its Potential Role in Human Diseases

  • Chu Han
  • , Yuanyuan Liu
  • , Rongji Dai
  • , Nafissa Ismail
  • , Weijun Su
  • , Bo Li*
  • *Corresponding author for this work
  • Beijing Institute of Technology
  • University of Ottawa
  • Nankai University

Research output: Contribution to journalReview articlepeer-review

Abstract

Ferroptosis is a novel regulated cell death pattern discovered when studying the mechanism of erastin-killing RAS mutant tumor cells in 2012. It is an iron-dependent programmed cell death pathway mainly caused by an increased redox imbalance but with distinct biological and morphology characteristics when compared to other known cell death patterns. Ferroptosis is associated with various diseases including acute kidney injury, cancer, and cardiovascular, neurodegenerative, and hepatic diseases. Moreover, activation or inhibition of ferroptosis using a variety of ferroptosis initiators and inhibitors can modulate disease progression in animal models. In this review, we provide a comprehensive analysis of the characteristics of ferroptosis, its initiators and inhibitors, and the potential role of its main metabolic pathways in the treatment and prevention of various diseased states. We end the review with the current knowledge gaps in this area to provide direction for future research on ferroptosis.

Original languageEnglish
Article number239
JournalFrontiers in Pharmacology
Volume11
DOIs
Publication statusPublished - 17 Mar 2020

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • degenerative diseases
  • ferroptosis
  • pharmacology design
  • reactive oxygen species
  • signaling pathways

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