Metabolic cell death in cancer: ferroptosis, cuproptosis, disulfidptosis, and beyond

  • Chao Mao 1 ,
  • Min Wang 2 ,
  • Li Zhuang 1 ,
  • Boyi Gan , 1,3
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  • 1. Department of Experimental Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA
  • 2. Department of Molecular and Cellular Biology, Baylor College of Medicine, Houston, TX 77030, USA
  • 3. The University of Texas MD Anderson UTHealth Graduate School of Biomedical Sciences, Houston, TX 77030, USA
bgan@mdanderson.org

Received date: 05 Jan 2024

Accepted date: 19 Feb 2024

Copyright

2024 The Author(s) 2024. Published by Oxford University Press on behalf of Higher Education Press.

Abstract

Cell death resistance represents a hallmark of cancer. Recent studies have identified metabolic cell death as unique forms of regulated cell death resulting from an imbalance in the cellular metabolism. This review discusses the mechanisms of metabolic cell death—ferroptosis, cuproptosis, disulfidptosis, lysozincrosis, and alkaliptosis—and explores their potential in cancer therapy. Our review underscores the complexity of the metabolic cell death pathways and offers insights into innovative therapeutic avenues for cancer treatment.

Cite this article

Chao Mao , Min Wang , Li Zhuang , Boyi Gan . Metabolic cell death in cancer: ferroptosis, cuproptosis, disulfidptosis, and beyond[J]. Protein & Cell, 2024 , 15(9) : 642 -660 . DOI: 10.1093/procel/pwae003

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