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Ferroptosis and the tumor microenvironment.

Kaisa Cui1,2, Kang Wang3, Zhaohui Huang4,5

  • 1Wuxi Cancer Institute, Affiliated Hospital of Jiangnan University, Huihe Road 200, Wuxi, Jiangsu, 214062, China.

Journal of Experimental & Clinical Cancer Research : CR
|November 29, 2024
PubMed
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Ferroptosis, an iron-dependent cell death, is crucial in cancer. Non-cancer cells in the tumor microenvironment (TME) regulate cancer progression and therapy resistance via ferroptosis-related crosstalk.

Keywords:
CD8+ T cellCancer-associated fibroblastFerroptosisImmunotherapyTumor microenvironmentTumor-associated macrophage

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Area of Science:

  • Oncology
  • Cell Biology
  • Cancer Research

Background:

  • Ferroptosis is a regulated cell death pathway defined by iron dependence and oxidative damage.
  • It plays significant roles in cancer initiation, spread, and treatment response.
  • The tumor microenvironment (TME) comprises various cellular and non-cellular components influencing cancer.

Purpose of the Study:

  • To systematically review the role of ferroptosis within the TME.
  • To explore how ferroptosis influences TME reprogramming, impacting cancer progression and therapeutic resistance.
  • To summarize ferroptosis-targeted therapeutic strategies for the TME.

Main Methods:

  • Literature review and synthesis of current research findings.
  • Analysis of the interplay between ferroptosis and TME components.
  • Identification of therapeutic strategies targeting ferroptosis in the TME.

Main Results:

  • Non-cancer cells within the TME, including immune and stromal cells, significantly impact tumor progression and resistance.
  • Crosstalk between cancer cells and non-cancer cells in the TME is partially mediated by ferroptosis.
  • Ferroptosis-mediated TME reprogramming affects cancer progression and therapeutic outcomes.

Conclusions:

  • Ferroptosis is a key regulator of the TME, influencing cancer progression and treatment efficacy.
  • Targeting ferroptosis within the TME offers promising therapeutic avenues for cancer treatment.
  • Understanding ferroptosis-TME interactions is critical for developing novel cancer therapies.