Evidence map›Paper›PMID 26193001›Full record

ReviewThe international journal of biochemistry & cell biology2015

JMJD3 as an epigenetic regulator in development and disease.

Jana S Burchfield, Qingtian Li, Helen Y Wang, Rong-Fu Wang

Abstract readReview
In one paragraph

Review in The international journal of biochemistry & cell biology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 81 papers.

0numbers the graph read from it
0cells of the map it votes in
81citing papers in PubMed
5.6field-weighted citation impact, top 3% 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

81 citing papers in PubMed, 147 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Article
  6. Hemizygous mutation ofAmerican journal of physiology. Cell physiology · 2025
    Article
  7. Review
  8. Article
  9. Article
  10. Review
  11. Review
  12. Article
  13. Review
  14. Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article

21 more citing papers are in PubMed but not listed here.

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

4 authors at 2 institutions in 1 country.

Jana S BurchfieldCenter for Inflammation and Epigenetics, Houston Methodist Research Institute, Houston, TX 77030, USA.
Qingtian LiDepartment of Microbiology and Immunology, Weill Cornell Medical College, Cornell University, 1300 York Avenue, New York, NY 10065, USA.
Helen Y WangCenter for Inflammation and Epigenetics, Houston Methodist Research Institute, Houston, TX 77030, USA.
Rong-Fu WangCenter for Inflammation and Epigenetics, Houston Methodist Research Institute, Houston, TX 77030, USA; Department of Microbiology and Immunology, Weill Cornell Medical College, Cornell University, 1300 York Avenue, New York, NY 10065, USA. Electronic address: rwang3@tmhs.org.
Houston Methodist · USCornell University · US

Funding

Novel Strategies for Intervention of Inflammatory Diseases and Cancer - Research Supplement to R01-CA101795R01CA101795 · NCI · UNIVERSITY OF SOUTHERN CALIFORNIA · PI WANG, RONGFU · 2004 to 2022
$4.6M
The Role of CD4+ T Cells in Antitumor ImmunityR01CA090327 · NCI · METHODIST HOSPITAL RESEARCH INSTITUTE · PI WANG, RONGFU · 2002 to 2013
$3.0M
NCI NIH HHS R01 CA090327NCI NIH HHS R01CA090327NCI NIH HHS R01 CA101795NCI NIH HHS R01CA101795
6 · The paper itself

Abstract

Gene expression is epigenetically regulated through DNA methylation and covalent chromatin modifications, such as acetylation, phosphorylation, ubiquitination, sumoylation, and methylation of histones. Histone methylation state is dynamically regulated by different groups of histone methyltransferases and demethylases. The trimethylation of histone 3 (H3K4) at lysine 4 is usually associated with the activation of gene expression, whereas trimethylation of histone 3 at lysine 27 (H3K27) is associated with the repression of gene expression. The polycomb repressive complex contains the H3K27 methyltransferase Ezh2 and controls dimethylation and trimethylation of H3K27 (H3K27me2/3). The Jumonji domain containing-3 (Jmjd3, KDM6B) and ubiquitously transcribed X-chromosome tetratricopeptide repeat protein (UTX, KDM6A) have been identified as H3K27 demethylases that catalyze the demethylation of H3K27me2/3. The role and mechanisms of both JMJD3 and UTX have been extensively studied for their involvement in development, cell plasticity, immune system, neurodegenerative disease, and cancer. In this review, we will focus on recent progresses made on understanding JMJD3 in the regulation of gene expression in development and diseases. This article is part of a Directed Issue entitled: Epigenetics dynamics in development and disease.

Indexed as

Epigenesis, GeneticAnimalsChromatinEnhancer of Zeste Homolog 2 ProteinGene Expression Regulation, DevelopmentalGerm LayersHistone DemethylasesHistonesHumansImmunity, InnateJumonji Domain-Containing Histone DemethylasesLysineMiceNeoplasmsNeurodegenerative DiseasesNuclear ProteinsChromatinEnhancer of Zeste Homolog 2 ProteinEZH2 protein, humanHistone DemethylasesHistonesJumonji Domain-Containing Histone DemethylasesKDM6A protein, humanKDM6B protein, humanLysineNuclear ProteinsPolycomb Repressive Complex 2H3K27Histone demethylationJmjd3JumonjiUtx

Identifiers

PMID26193001
PMCPMC4564304
OpenAlexW2185909429

What OpenQuestion holds

Textmetadata
LicenceTDM
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.