Evidence map›Paper›PMID 41629953›Full record

ArticleJournal of translational medicine2026

Low-dose 5-hydroxymethylfurfural mitigates radiation -induced intestinal toxicity via HIF2α-driven IL22/STAT3 signaling enhancement.

Tao Zhang, Jingqin He, Jiang He, Cheng Xu, Yu Huang, Siting Huang, Haibing Jiang, Yingjie Fan, Li Liu, Hongli Li and 1 more

Abstract read
In one paragraph

Article in Journal of translational medicine, 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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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

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0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors.

Tao Zhang *College of Materials and New Energy, Chongqing University of Science and Technology, Chongqing, 401331, China. ztzuibang@126.com.
Jingqin He *College of Materials and New Energy, Chongqing University of Science and Technology, Chongqing, 401331, China.
Jiang He *College of Materials and New Energy, Chongqing University of Science and Technology, Chongqing, 401331, China.
Cheng XuCollege of Materials and New Energy, Chongqing University of Science and Technology, Chongqing, 401331, China.
Yu HuangCollege of Materials and New Energy, Chongqing University of Science and Technology, Chongqing, 401331, China.
Siting HuangCollege of Materials and New Energy, Chongqing University of Science and Technology, Chongqing, 401331, China.
Haibing JiangCollege of Materials and New Energy, Chongqing University of Science and Technology, Chongqing, 401331, China.
Yingjie FanCollege of New Energy Vehicles, Chongqing Technology and Business University, Chongqing, 401520, China.
Li LiuChongqing Industry Polytechnic College, Chongqing, 401120, China.
Hongli LiCollege of Medical Technology, Chongqing Medical and Pharmaceutical College, Chongqing, 401331, China. cqygzlhl@126.com.
Xianwen DongChongqing Academy of Animal Sciences, Chongqing, China. dxwcqxky@163.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIonizing radiation (IR)-induced intestinal injury limits the efficacy of radiotherapy for abdominal/pelvic malignancies, and there are few effective preventive measures. 5-Hydroxymethylfurfural (5-HMF), a bioactive compound abundant in heat-processed foods and herbal decoctions, has shown therapeutic benefits in inflammatory diseases, yet its role in IR-induced intestinal damage remains unclear.

methodsC57BL/6 male mice (n = 15~17/group) were administered intraperitoneal vehicle, low-dose (50 mg/kg/day), or high-dose (200 mg/kg/day) 5-HMF for 7 days prior to 8–10 Gy of whole-body irradiation (WBI) or total abdominal irradiation (TAI). Assessments included survival, weight recovery, intestinal permeability, crypt survival, as well as proliferation and apoptosis of intestinal stem cells (ISCs). Mechanistic investigations utilized RNA sequencing of crypts, organoid cultures, dual luciferase assays, and pharmacological hypoxia-inducible factor-2α (HIF-2α) inhibition (PT-2385) to explore the radioprotective mechanisms of 5-HMF.

resultsCompared with the control group or high-dose group, low-dose 5-HMF significantly improved survival, accelerated weight recovery, and enhanced crypt regeneration. It promoted ISCs proliferation while inhibiting apoptosis. Mechanistically, 5-HMF stabilized HIF-2α, which bound to hypoxia-response elements (HREs) in the Interleukin-22 receptor-1 (IL22R1) promoter, thereby upregulating IL22R1 expression and amplifying IL22-dependent signal transducer and activator of transcription 3 (STAT3) phosphorylation. Importantly, PT-2385-mediated HIF-2α inhibition abolished the effects of 5-HMF on IL22R1/STAT3 and its radioprotective role both in vivo and in organoids.

conclusionsLow-dose 5-HMF protects against IR-induced intestinal injury by stabilizing HIF-2α to enhance IL22/STAT3 signaling and drive ISC-mediated epithelial regeneration, identifying it as a promising dietary-derived radioprotectant for such damage.

Indexed as

Basic Helix-Loop-Helix ProteinsFuraldehydeInterleukinsIntestinesSignal TransductionSTAT3 Transcription FactorAnimalsApoptosisCell ProliferationEndothelial PAS Domain-Containing Protein 1Interleukin-22Intestinal Barrier FunctionMaleMiceMice, Inbred C57BLStem Cells5-hydroxymethylfurfuralBasic Helix-Loop-Helix ProteinsEndothelial PAS Domain-Containing Protein 1FuraldehydeInterleukin-22InterleukinsStat3 protein, mouseSTAT3 Transcription Factor5-HydroxymethylfurfuralHIF-2αIL22/STAT3Intestinal injuryIntestinal stem cells

Identifiers

PMID41629953
PMCPMC12955021

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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 OpenQuestion graph.