Evidence map›Paper›PMID 25767098›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2015

STAT3-driven transcription depends upon the dimethylation of K49 by EZH2.

Maupali Dasgupta, Josephine Kam Tai Dermawan, Belinda Willard, George R Stark

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 87 papers.

0numbers the graph read from it
0cells of the map it votes in
87citing 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

87 citing papers in PubMed, 128 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Cellular signaling meets bacterial infection: the integrative role of STAT3.Frontiers in cellular and infection microbiology · 2026
    Review
  8. Article
  9. Fibroblasts-specific p16Clinical and translational medicine · 2025
    Article
  10. Article
  11. Review
  12. Review
  13. Review
  14. Article
  15. Lysine and arginine methylation of transcription factors.Cellular and molecular life sciences : CMLS · 2024
    Review
  16. Review
  17. Article
  18. Article
  19. Article
  20. Article

27 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 1 institution in 1 country.

Maupali DasguptaDepartment of Molecular Genetics and.
Josephine Kam Tai DermawanDepartment of Molecular Genetics and starkg@ccf.org.
Belinda WillardProteomics Core, Lerner Research Institute, Cleveland Clinic, Cleveland, OH 44195.
George R StarkDepartment of Molecular Genetics and starkg@ccf.org.
Cleveland Clinic Lerner College of Medicine · US

Funding

Clinical and Translational Science Collaborative of ClevelandUL1TR000439 · NCATS · CASE WESTERN RESERVE UNIVERSITY · PI KONSTAN, MICHAEL W. · 2012 to 2016
$50.0M
TELOMERASE INACTIVATION BY RNASE L SIGNALS CELL DEATHP01CA062220 · NCI · CLEVELAND CLINIC LERNER COM-CWRU · PI SEN, GANES C. · 1994 to 2020
$35.6M
LTQ-Orbitrap Velos instrumentS10RR031537 · NCRR · CLEVELAND CLINIC LERNER COM-CWRU · PI WILLARD, BELINDA BELLE · 2011 to 2011
$600k
NCATS NIH HHS UL1 TR000439NCI NIH HHS P01 CA062220NCRR NIH HHS 1S10RR031537-01NCRR NIH HHS S10 RR031537
6 · The paper itself

Abstract

Several transcription factors, including p53, NF-κB, and STAT3, are modified by the same enzymes that also modify histones, with important functional consequences. We have identified a previously unrecognized dimethylation of K49 of STAT3 that is crucial for the expression of many IL-6-dependent genes, catalyzed by the histone-modifying enzyme enhancer of zeste homolog 2 (EZH2). Loss of EZH2 is protumorigenic in leukemias, but its overexpression is protumorigenic in solid cancers. Connecting EZH2 to a functionally important methylation of STAT3, which is constitutively activated in many tumors, may help reveal the basis of the opposing roles of EZH2 in liquid and solid tumors and also may identify novel therapeutic opportunities.

Indexed as

Gene Expression Regulation, NeoplasticCell Line, TumorDNA MethylationEnhancer of Zeste Homolog 2 ProteinGene ExpressionHistone-Lysine N-MethyltransferaseHistone MethyltransferasesHistonesHumansInterleukin-6LysineMutationNeoplasmsPhosphorylationPolycomb Repressive Complex 2Promoter Regions, GeneticEnhancer of Zeste Homolog 2 ProteinEZH2 protein, humanHistone-Lysine N-MethyltransferaseHistone MethyltransferasesHistonesInterleukin-6LysinePolycomb Repressive Complex 2STAT3 protein, humanSTAT3 Transcription Factorgene expressionhistone methyltransferaseposttranslational modification

Identifiers

PMID25767098
PMCPMC4386339
OpenAlexW2005293755

What OpenQuestion holds

Textmetadata
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.