Evidence map›Paper›PMID 42198560›Full record

ArticleToxics2026

PIKfyve Deficiency Exacerbates Radiation-Induced Intestinal Toxicity.

Aoqiang Ji, Xing Shen, Chunan Zhao, Zhaopeng Weng, Xuewen Zhang, Kai-Kai Yu, Shuang Xing, Xinlong Yan, Zuyin Yu

Abstract read
In one paragraph

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

0numbers the graph read from it
0cells of the map it votes in
0citing papers 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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

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

9 authors.

Aoqiang JiAcademy of Military Medical Sciences, Academy of Military Science, Beijing 100850, China.ORCID 0009-0000-7109-8517
Xing ShenAcademy of Military Medical Sciences, Academy of Military Science, Beijing 100850, China.ORCID 0000-0003-2876-8743
Chunan ZhaoAcademy of Military Medical Sciences, Academy of Military Science, Beijing 100850, China.ORCID 0009-0002-6965-825X
Zhaopeng WengAcademy of Military Medical Sciences, Academy of Military Science, Beijing 100850, China.
Xuewen ZhangAcademy of Military Medical Sciences, Academy of Military Science, Beijing 100850, China.ORCID 0009-0003-1383-2236
Kai-Kai YuAcademy of Military Medical Sciences, Academy of Military Science, Beijing 100850, China.
Shuang XingAcademy of Military Medical Sciences, Academy of Military Science, Beijing 100850, China.ORCID 0000-0002-6155-5929
Xinlong YanBeijing Key Laboratory of Environmental and Viral Oncology, College of Chemistry and Life Science, Beijing University of Technology, Beijing 100124, China.
Zuyin YuAcademy of Military Medical Sciences, Academy of Military Science, Beijing 100850, China.ORCID 0000-0001-7037-4479

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIntestinal acute radiation syndrome (IARS) represents a life-threatening component of acute radiation syndrome with limited effective countermeasures. Understanding molecular determinants governing intestinal epithelial resilience to ionizing radiation is critical for developing radiation toxicity mitigation strategies.

objectivesThis study investigates the role of PIKfyve, a phosphoinositide kinase essential for endolysosomal homeostasis, in modulating radiation-induced intestinal toxicity.

methodsWe utilized an inducible intestinal epithelial-specific PIKfyve-knockout mouse model (PIKfyve cKO) subjected to 10 Gy abdominal irradiation. Intestinal toxicity was assessed through histopathology, barrier permeability (FD4 assay), apoptosis markers, and transcriptomic profiling. Small intestinal organoids were employed for mechanistic validation.

resultsPIKfyve deletion alone did not perturb normal gut architecture but precipitated severe post-irradiation toxicity, including villous atrophy, crypt hypoplasia, and massive crypt-cell apoptosis. Barrier dysfunction was evidenced by elevated serum FD4 and heightened systemic pro-inflammatory cytokines, culminating in markedly increased mortality. Transcriptomic analysis revealed potentiated DNA-damage signaling and amplified inflammatory cascades in PIKfyve-deficient intestines.

conclusionsThese findings identify PIKfyve as a critical guardian of intestinal epithelial integrity against radiation toxicity. Given emerging PIKfyve inhibitors in cancer therapy, our results raise important safety considerations for clinical radiotherapy and position PIKfyve as a potential target for radiation toxicity mitigation.

Indexed as

epithelial barrierintestinal acute radiation syndromePIKfyveradiation countermeasuresradiation toxicologytranslational radiobiology

Identifiers

PMID42198560
PMCPMC13211304

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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.