Evidence map›Paper›PMID 30510991›Full record

ArticleCellular and molecular gastroenterology and hepatology2019

Disruption of FOXP3-EZH2 Interaction Represents a Pathobiological Mechanism in Intestinal Inflammation.

Adebowale O Bamidele, Phyllis A Svingen, Mary R Sagstetter, Olga F Sarmento, Michelle Gonzalez, Manuel B Braga Neto, Subra Kugathasan, Gwen Lomberk, Raul A Urrutia, William A Faubion

Open access · goldAbstract read
In one paragraph

Article in Cellular and molecular gastroenterology and hepatology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
1.2field-weighted citation impact, top 23% of its field
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

26 citing papers in PubMed, 35 citations in OpenAlex.

  1. Review
  2. Review
  3. Treg-specific IL-6R signaling: a novel role in the regulation of the intestinal epithelium.American journal of physiology. Gastrointestinal and liver physiology · 2025
    Article
  4. Review
  5. Article
  6. Article
  7. Review
  8. Review
  9. Review
  10. Article
  11. Epigenetics of Inflammatory Bowel Diseases.The Turkish journal of gastroenterology : the official journal of Turkish Society of Gastroenterology · 2023
    Article
  12. The Regulatory Roles ofInternational journal of molecular sciences · 2023
    Article
  13. Review
  14. Article
  15. Review
  16. Review
  17. The histone methyltransferase Ezh2 restrains macrophage inflammatory responses.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2021
    Article
  18. Article
  19. Peritoneal Modulators of EZH2-miR-155 Cross-Talk in Endometriosis.International journal of molecular sciences · 2021
    Article
  20. Article
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

10 authors at 3 institutions in 1 country.

Adebowale O BamideleEpigenetics and Chromatin Dynamics Laboratory, Division of Gastroenterology and Hepatology and Translational Epigenomic Program, Center for Individualized Medicine, Mayo Clinic, Rochester, Minnesota.
Phyllis A SvingenEpigenetics and Chromatin Dynamics Laboratory, Division of Gastroenterology and Hepatology and Translational Epigenomic Program, Center for Individualized Medicine, Mayo Clinic, Rochester, Minnesota.
Mary R SagstetterEpigenetics and Chromatin Dynamics Laboratory, Division of Gastroenterology and Hepatology and Translational Epigenomic Program, Center for Individualized Medicine, Mayo Clinic, Rochester, Minnesota.
Olga F SarmentoEpigenetics and Chromatin Dynamics Laboratory, Division of Gastroenterology and Hepatology and Translational Epigenomic Program, Center for Individualized Medicine, Mayo Clinic, Rochester, Minnesota.
Michelle GonzalezEpigenetics and Chromatin Dynamics Laboratory, Division of Gastroenterology and Hepatology and Translational Epigenomic Program, Center for Individualized Medicine, Mayo Clinic, Rochester, Minnesota.
Manuel B Braga NetoEpigenetics and Chromatin Dynamics Laboratory, Division of Gastroenterology and Hepatology and Translational Epigenomic Program, Center for Individualized Medicine, Mayo Clinic, Rochester, Minnesota.
Subra KugathasanDepartment of Pediatrics, Emory University, School of Medicine, Atlanta, Georgia.
Gwen LomberkDepartment of Surgery, Medical College of Wisconsin, Milwaukee, Wisconsin.
Raul A UrrutiaDepartment of Surgery, Medical College of Wisconsin, Milwaukee, Wisconsin.
William A FaubionEpigenetics and Chromatin Dynamics Laboratory, Division of Gastroenterology and Hepatology and Translational Epigenomic Program, Center for Individualized Medicine, Mayo Clinic, Rochester, Minnesota. Electronic address: Faubion.William@mayo.edu.
Mayo Clinic · USMedical College of Wisconsin · USEmory University · US

Funding

PILOT AND FEASIBILTY PROGRAMP30DK084567 · NIDDK · MAYO CLINIC ROCHESTER · PI Nicholas F. LaRusso · 2009 to 2026
$22.2M
MULTIDISCRIPLINARY TRAINING IN DIGESTIVE DISEASEST32DK007198 · NIDDK · MAYO CLINIC ROCHESTER · PI Harmeet Malhi · 1986 to 2026
$8.9M
ZINC FINGER GENES AND PANCREATIC CELL GROWTHR01DK052913 · NIDDK · MEDICAL COLLEGE OF WISCONSIN · PI LOMBERK, GWEN, URRUTIA, RAUL A. · 1998 to 2023
$7.0M
KLF10 regulates colitis through mediating TGFb induction of FOXP3 in Treg cells.R01AI089714 · NIAID · MAYO CLINIC ROCHESTER · PI FAUBION, WILLIAM A · 2011 to 2025
$6.3M
KLF10 regulates colitis through mediating TGFb induction of FOXP3 in Treg cells.R56AI089714 · NIAID · MAYO CLINIC ROCHESTER · PI FAUBION, WILLIAM A · 2010 to 2010
$394k
The Role of Zinc Finger Genes in Pancreatic Cell GrowthR56DK052913 · NIDDK · MAYO CLINIC ROCHESTER · PI URRUTIA, RAUL A. · 2008 to 2008
$291k
NIAID NIH HHS R01 AI089714NIAID NIH HHS R56 AI089714NIDDK NIH HHS P30 DK084567NIDDK NIH HHS R01 DK052913NIDDK NIH HHS R56 DK052913NIDDK NIH HHS T32 DK007198
6 · The paper itself

Abstract

Background & Aims: Forkhead box protein 3 (FOXP3) Methods: Human FOXP3 mutations clinically relevant to intestinal inflammation were generated by site-directed mutagenesis. T lymphocytes were isolated from mice, human blood, and lamina propria of Crohn's disease (CD) patients and non-CD controls. We performed proximity ligation or a co-immunoprecipitation assay in FOXP3-mutant Results: EZH2 binding was abrogated by inflammatory bowel disease-associated FOXP3 cysteine 232 (C232) mutation. The C232 mutant showed impaired repression of Conclusions: FOXP3-C232 mutation disrupts EZH2 recruitment and gene co-repressive function. The proinflammatory cytokine IL6 abrogates FOXP3-EZH2 interaction. Studies in lesion-derived CD4

Indexed as

AdultAnimalsCell NucleusCell SeparationCo-Repressor ProteinsEnhancer of Zeste Homolog 2 ProteinFemaleForkhead Transcription FactorsHumansInflammationInflammatory Bowel DiseasesInterleukin-6IntestinesJanus KinasesJurkat CellsMaleCo-Repressor ProteinsEnhancer of Zeste Homolog 2 ProteinForkhead Transcription FactorsFOXP3 protein, humanFoxp3 protein, mouseInterleukin-6Janus KinasesPhosphotyrosinePolycomb Repressive Complex 2STAT3 Transcription FactorC232, cysteine 232CD, Crohn’s diseaseChIP, chromatin-immunoprecipitationco-IP, co-immunoprecipitationCrohn’s DiseaseEED, embryonic ectoderm developmentEpigeneticsEZH2, enhancer of zeste homolog 2FCS, fetal calf serumFOXP3, forkhead domain-containing X-chromosome–encoded proteinH3K27me3, trimethylated histone H3 at lysine 27IBD, inflammatory bowel diseaseIL, interleukinIPEX, immune dysregulation, polyendocrinopathy, enteropathy, X-linkedJAK, Janus kinaseLZ, leucine zipperPBMC, peripheral blood mononuclear cellPBS, phosphate-buffered salinePLA, proximity ligation assayPMA, phorbol 12-myristate 13-acetatePRC2, polycomb repressive complex 2Proinflammatory CytokineRegulatory T CellsSTAT, signal transducer and activator of transcriptionSUZ12, suppressor of zesteTh, T helperTreg, regulatory T cellWT, wild-type

Identifiers

PMID30510991
PMCPMC6260395
OpenAlexW2891357116

What OpenQuestion holds

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LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.