Loss of ACSL1 fuels ferroptosis resistance in clear cell renal carcinoma

Cancer Biol Ther. 2025 Dec 31;26(1):2567815. doi: 10.1080/15384047.2025.2567815. Epub 2025 Oct 6.

Abstract

Background: Clear cell renal cell carcinoma (ccRCC), the most common kidney cancer subtype, is marked by lipid metabolism reprogramming and therapy resistance. Ferroptosis-an iron-dependent, lipid peroxidation-driven cell death-has gained attention as a therapeutic strategy. This study investigates the role of ACSL1, a key lipid metabolism enzyme, in ccRCC.

Methods: Using TCGA/GEO datasets, qPCR, immunohistochemistry, and immunofluorescence, ACSL1 expression and clinical significance were analyzed. Functional assays with ACSL1-overexpressing ccRCC cells and a xenograft mouse model evaluated its impact on tumor behavior. Transcriptomics and lipidomics, alongside ROS, ferroptosis, and p53 inhibitors, were applied to uncover mechanisms.

Results: ACSL1 is markedly downregulated in ccRCC and predicts poor prognosis. Overexpression suppressed proliferation and migration, induced cell death, and slowed tumor growth. Mechanistically, ACSL1 elevated ROS, activated p53, downregulated SLC7A11/GPX4, and triggered ferroptosis. Blocking ROS or p53 reversed these effects, confirming a ROS-p53-SLC7A11/GPX4 feedback loop.

Conclusion: ACSL1 functions as a tumor suppressor in ccRCC by inducing ferroptosis via the ROS-p53-SLC7A11/GPX4 axis. It holds promise as a prognostic biomarker and therapeutic target in ccRCC.

Keywords: ACSL1; ROS; ccRCC; ferroptosis; p53.

MeSH terms

  • Amino Acid Transport System y+
  • Animals
  • Carcinoma, Renal Cell* / genetics
  • Carcinoma, Renal Cell* / metabolism
  • Carcinoma, Renal Cell* / pathology
  • Cell Line, Tumor
  • Cell Proliferation
  • Coenzyme A Ligases* / genetics
  • Coenzyme A Ligases* / metabolism
  • Female
  • Ferroptosis* / genetics
  • Gene Expression Regulation, Neoplastic
  • Humans
  • Kidney Neoplasms* / genetics
  • Kidney Neoplasms* / metabolism
  • Kidney Neoplasms* / pathology
  • Long-Chain-Fatty-Acid-CoA Ligase
  • Male
  • Mice
  • Phospholipid Hydroperoxide Glutathione Peroxidase / metabolism
  • Prognosis
  • Reactive Oxygen Species / metabolism
  • Tumor Suppressor Protein p53 / metabolism
  • Xenograft Model Antitumor Assays

Substances

  • Coenzyme A Ligases
  • ACSL1 protein, human
  • Reactive Oxygen Species
  • Tumor Suppressor Protein p53
  • Long-Chain-Fatty-Acid-CoA Ligase
  • Phospholipid Hydroperoxide Glutathione Peroxidase
  • SLC7A11 protein, human
  • Amino Acid Transport System y+