Androgen receptor promotes arachidonic acid metabolism and angiogenic microenvironment in AFP-negative hepatocellular carcinoma

Nat Commun. 2025 Jul 12;16(1):6451. doi: 10.1038/s41467-025-61448-z.

Abstract

Alpha-fetoprotein (AFP) is a classic biomarker for hepatocellular carcinoma (HCC). AFP-positive HCC (AFP+ HCC) has been intensively investigated; however, the genomic, transcriptomic and microenvironmental characteristics of AFP-negative HCC (AFP- HCC) remain to be deciphered. Here we show that tumors display mild differences in genetic alterations between AFP- HCC and AFP+ HCC patients, while AFP- HCC exhibits hyperactive arachidonic acid metabolism. Furthermore, the transcription activity of androgen receptor (AR) is significantly increased in AFP- HCC and plays a positive regulatory role in arachidonic acid metabolism and its metabolite 11,12-epoxyeicosatrienoic acid (11,12-EET). The tumor-derived 11,12-EET exhibits high affinity for EGFR that promotes the migration and tube formation of endothelial cells in vitro. Combination of lenvatinib and bicalutamide (an AR antagonist) enhances the therapeutic efficacy for AFP- HCC. Overall, we uncover the AR-mediated hyperactive arachidonic acid metabolism in AFP- HCC, and reveal AR-11,12-EET-EGFR axis-induced angiogenesis, providing a promising strategy of combined AR antagonist with lenvatinib for AFP- HCC treatment.

MeSH terms

  • Androgen Receptor Antagonists / pharmacology
  • Anilides / pharmacology
  • Animals
  • Arachidonic Acid* / metabolism
  • Carcinoma, Hepatocellular* / blood supply
  • Carcinoma, Hepatocellular* / drug therapy
  • Carcinoma, Hepatocellular* / genetics
  • Carcinoma, Hepatocellular* / metabolism
  • Carcinoma, Hepatocellular* / pathology
  • Cell Line, Tumor
  • ErbB Receptors / metabolism
  • Female
  • Gene Expression Regulation, Neoplastic
  • Humans
  • Liver Neoplasms* / blood supply
  • Liver Neoplasms* / drug therapy
  • Liver Neoplasms* / genetics
  • Liver Neoplasms* / metabolism
  • Liver Neoplasms* / pathology
  • Male
  • Mice
  • Mice, Nude
  • Neovascularization, Pathologic* / genetics
  • Neovascularization, Pathologic* / metabolism
  • Nitriles / pharmacology
  • Phenylurea Compounds / pharmacology
  • Phenylurea Compounds / therapeutic use
  • Quinolines / pharmacology
  • Receptors, Androgen* / genetics
  • Receptors, Androgen* / metabolism
  • Tosyl Compounds
  • Tumor Microenvironment / drug effects
  • alpha-Fetoproteins* / genetics
  • alpha-Fetoproteins* / metabolism

Substances

  • Arachidonic Acid
  • Receptors, Androgen
  • alpha-Fetoproteins
  • Phenylurea Compounds
  • Anilides
  • Quinolines
  • Nitriles
  • AR protein, human
  • bicalutamide
  • ErbB Receptors
  • EGFR protein, human
  • AFP protein, human
  • Androgen Receptor Antagonists
  • Tosyl Compounds