Disulfidptosis: a new target for metabolic cancer therapy

Peijie Zheng1, Chuntao Zhou1, Yuemin Ding1,2,3

  • 1Department of Clinical Medicine, School of Medicine, Hangzhou City University, Hangzhou, 310015, China.

Insights

Cancer metabolism fuels tumor growth but also offers treatment targets. A new regulated cell death (RCD) pathway, disulfidptosis, is induced by targeting glucose transporters (GLUTs), offering a promising strategy for cancer therapy.

Area of Science:

  • Oncology
  • Metabolic pathways
  • Cell death mechanisms

Background:

  • Altered cellular metabolism is a key characteristic of cancer, presenting a therapeutic vulnerability.
  • Regulated cell death (RCD) is critical in cancer metabolic therapy.
  • Disulfidptosis is a newly identified metabolic-related RCD pathway.

Approach:

  • This review summarizes the underlying mechanisms of disulfidptosis.
  • It outlines potential future research directions for disulfidptosis.
  • The review discusses challenges in the clinical translation of disulfidptosis.

Key Points:

  • Disulfidptosis is a novel form of regulated cell death linked to metabolic dysregulation in cancer.
  • Inhibiting glucose transporters (GLUTs) can induce disulfidptosis, leading to cancer cell death.
  • Preclinical studies demonstrate the potential of GLUT inhibitors in triggering disulfidptosis for cancer treatment.

Conclusions:

  • Disulfidptosis represents a new therapeutic target in oncology.
  • Targeting metabolic pathways through GLUT inhibitors offers a promising approach for cancer treatment.
  • Further research is needed to overcome challenges in the clinical application of disulfidptosis-based therapies.

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