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March 29, 2026Frontiers in Immunology2 citationsOpen Access

Bile acids enrichment fuel tumor aerobic glycolysis and immune evasion via stabilizing FXR-RARα

HJHui JiangWXWenyan XiongYFYingna Feng

Key Points

  • This research investigates how bile acids contribute to tumor metabolism and immune evasion.
  • Used multiple mouse models including C57BL/6J and BALB/c.
  • Evaluated effects of bile acid depletion through a cholestyramine diet.
  • Analyzed bile acid profiles using UPLC-MS and immune cells via flow cytometry.
  • Measured oxygen consumption and extracellular acidification with Seahorse analyzers.
  • Bile acids were significantly enriched in melanoma and breast cancer tumor microenvironments.
  • Enrichment drives aerobic glycolysis and immune evasion by stabilizing the FXR-RARα complex.
  • Depletion of bile acids suppressed tumor progression and increased T cell infiltration.
  • Depletion led to upregulation of oxidative phosphorylation-related genes and reduced immune barriers.

Abstract

Introduction Fast-growing solid tumors exhibit aerobic glycolysis to meet metabolic demands and evade immune surveillance. While the tumor microenvironment (TME) plays a crucial role in supporting this glycolytic phenotype, the contribution of host metabolites remains incompletely understood. Methods The role of bile acids (BAs) in tumor progression was evaluated using multiple mouse models, including C57BL/6J mice injected with B16 melanoma cells, BALB/c mice inoculated with 4T1 breast cancer cells, and MMTV-PyMT mice with spontaneous tumor development. To assess the impact of BA depletion, subjects were fed a 2% cholestyramine diet compared to a regular diet. The study employed various analytical techniques, including UPLC-MS to evaluate BA profiles, flow cytometry for immune cell analysis, and Seahorse extracellular flux analyzers to measure oxygen consumption and extracellular acidification rates. Results Here, we demonstrate that multiple bile acids (BAs) are significantly enriched in the TMEs of melanoma and breast cancer. Mechanistically, this BA enrichment drives tumor aerobic glycolysis and promotes immune evasion by modulating the interaction between the farnesoid X receptor (FXR) and retinoic acid receptor alpha (RARa). Depletion of BAs in vivo suppressed tumor progression, enhanced T cell infiltration, and alleviated T cell exhaustion, accompanied by transcriptome-wide shifts towardincreased expression of genes involved in oxidative phosphorylation. Furtherinvestigations revealed that BAs activate and stabilize the FXR-RARa complex,thereby upregulating glycolytic pathways and impairing anti-tumor immunity. Conversely, BA depletion reduced FXR/RARa protein levels and disrupted tumorimmune barrier function. Discussion These findings unveil a mechanism by which bile acids promote tumor progression by modulating tumor metabolism and the immune microenvironment through FXR-RARa signaling. Targeting the BA-FXR-RARa axiscould offer promising strategies for cancer therapy and diagnosis.

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Cite This Study

Jiang et al. (2026) studied this question.

synapsesocial.com/papers/69c8c115de0f0f753b39b9fchttps://doi.org/10.3389/fimmu.2026.1750358
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