Evidence mapPaperPMID 42499502Full record

ArticleFrontiers in pharmacology2026

GUDCA drives colorectal cancer progression via ALKBH5-mediated m6A modification of ENO1 and glycolytic reprogramming.

Ruirong Lin, Shangkun Jin, Weijin Yang, Jiarong Zhang, Jiantao Jiang, Wenmin Xiao, Yun Xie, Changhua Zhuo, Xiaopeng Wang

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Article in Frontiers in pharmacology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

9 authors.

Ruirong Lin *Department of Thoracic Oncology Surgery, Clinical Oncology School of Fujian Medical University, Fujian Cancer Hospital, Fuzhou, China.
Shangkun Jin *Department of Colorectal Surgery, Clinical Oncology School of Fujian Medical University, Fujian Cancer Hospital, Fuzhou, China.
Weijin Yang *Department of Colorectal Surgery, Clinical Oncology School of Fujian Medical University, Fujian Cancer Hospital, Fuzhou, China.
Jiarong ZhangDepartment of Thoracic Oncology Surgery, Clinical Oncology School of Fujian Medical University, Fujian Cancer Hospital, Fuzhou, China.
Jiantao JiangDepartment of Colorectal Surgery, Clinical Oncology School of Fujian Medical University, Fujian Cancer Hospital, Fuzhou, China.
Wenmin XiaoCollege of Chemistry, Fuzhou University, Fuzhou, China.
Yun XieDepartment of Colorectal Surgery, Clinical Oncology School of Fujian Medical University, Fujian Cancer Hospital, Fuzhou, China.
Changhua ZhuoDepartment of Colorectal Surgery, Clinical Oncology School of Fujian Medical University, Fujian Cancer Hospital, Fuzhou, China.
Xiaopeng WangDepartment of Gastric Surgery Oncology, Clinical Oncology School of Fujian Medical University, Fujian Cancer Hospital, Fuzhou, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Colorectal cancer (CRC) is the third most diagnosed malignancy worldwide, yet the mechanisms by which bile acids drive metabolic reprogramming remain unclear. This study investigates whether glycoursodeoxycholic acid (GUDCA) promotes CRC progression through mA epitranscriptomic regulation. Methods: Serum bile acids were profiled in 106 CRC patients and 106 controls by UHPLC-MS/MS. Cellular phenotypes were assessed by CCK-8, colony formation, and xenograft models. mA modification was mapped by meRIP-seq and validated by meRIP-qPCR. Glycolytic function was measured by lactate production, glucose uptake, and ECAR. FXR binding to the ALKBH5 promoter was assessed by luciferase assay and ChIP-qPCR. Clinical correlations were analyzed in 25 CRC patients undergoing Results: GUDCA was the most significantly elevated bile acid in CRC patients and independently predicted poor survival (HR = 3.28, p < 0.001). GUDCA promoted CRC cell proliferation and xenograft tumor growth. Mechanistically, GUDCA antagonized FXR to suppress ALKBH5 transcription, elevating mA modification of ENO1 mRNA and enhancing its translation efficiency. ALKBH5 deficiency drove glycolytic reprogramming and mTORC1 activation. ENO1 silencing abolished GUDCA-induced glycolytic enhancement. Serum GUDCA positively correlated with Conclusion: GUDCA functions as an oncometabolite that drives CRC progression via the GUDCA-FXR-ALKBH5-ENO1 axis, establishing a feed-forward metabolic circuit linking bile acid signaling to mA-mediated glycolytic reprogramming. These findings identify GUDCA and ALKBH5 as potential therapeutic vulnerabilities in CRC.

Indexed as

ALKBH5colorectal cancerENO1glycolysisGUDCAm6A modification

Identifiers

PMID42499502
PMCPMC13395929

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.