Targeting ferroptosis in renal cell carcinoma: Potential mechanisms and novel therapeutics

Lei Yang1, Yu Fan1, Qian Zhang1,2

  • 1Department of Urology, Peking University First Hospital, Institute of Urology, National Research Center for Genitourinary Oncology, Peking University, Beijing, China.

Heliyon
|August 9, 2023
PubMed

Insights

Renal cell carcinoma (RCC) is a growing cancer resistant to chemotherapy. Ferroptosis, an iron-dependent cell death, shows promise as a therapeutic target and clinical marker for RCC treatment.

Area of Science:

  • Oncology
  • Cell Biology
  • Biochemistry

Background:

  • Renal cell carcinoma (RCC) is a prevalent urologic malignancy with increasing incidence worldwide.
  • Advanced RCC exhibits resistance to conventional chemotherapy, necessitating novel therapeutic strategies.
  • Ferroptosis, a form of programmed cell death driven by iron-dependent lipid peroxidation, is implicated in tumor progression and drug resistance.

Purpose of the Study:

  • To review the regulatory mechanisms of ferroptosis concerning iron, amino acid, and lipid metabolism.
  • To elucidate the intricate relationship between ferroptosis and renal cell carcinoma (RCC).
  • To explore the potential of ferroptosis regulators as therapeutic targets and clinical markers for RCC.

Main Methods:

  • Literature review summarizing current research on ferroptosis and RCC.
  • Analysis of the roles of iron, amino acid, and lipid metabolism in ferroptosis.
  • Discussion of ferroptosis regulators' impact on RCC progression and chemoresistance.

Main Results:

  • Ferroptosis plays a significant role in RCC progression and chemoresistance.
  • Various ferroptosis regulators are dysregulated in RCC, exhibiting both tumor-suppressive and oncogenic effects.
  • These regulators present potential as clinical markers for RCC prognosis.

Conclusions:

  • Targeting ferroptosis regulators could offer novel therapeutic strategies for advanced RCC.
  • Ferroptosis-related biomarkers may aid in predicting RCC patient outcomes.
  • Further research into ferroptosis mechanisms in RCC is warranted for clinical translation.