Evidence map›Paper›PMID 28384648›Full record

ArticlePloS one2017

Regulation of the JMJD3 (KDM6B) histone demethylase in glioblastoma stem cells by STAT3.

Maureen M Sherry-Lynes, Sejuti Sengupta, Shreya Kulkarni, Brent H Cochran

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
2.1field-weighted citation impact, top 12% 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

36 citing papers in PubMed, 54 citations in OpenAlex.

  1. Article
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  8. Article
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  10. Article
  11. Review
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  14. JMJD family proteins in cancer and inflammation.Signal transduction and targeted therapy · 2022
    Review
  15. JMJD3 PromotesDNA and cell biology · 2022
    Article
  16. Emerging roles of JMJD3 in cancer.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2022
    Review
  17. Review
  18. Article
  19. Sex determination without sex chromosomes.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2021
    Review
  20. JMJD3: a critical epigenetic regulator in stem cell fate.Cell communication and signaling : CCS · 2021
    Review
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.

Maureen M Sherry-LynesGraduate Program in Cell and Molecular Physiology, Sackler School of Graduate Biomedical Sciences and Dept. of Developmental,Molecular, and Chemical Biology Tufts University School of Medicine Boston, MA, United States of America.
Sejuti SenguptaGraduate Program in Cell and Molecular Physiology, Sackler School of Graduate Biomedical Sciences and Dept. of Developmental,Molecular, and Chemical Biology Tufts University School of Medicine Boston, MA, United States of America.
Shreya KulkarniGraduate Program in Cell and Molecular Physiology, Sackler School of Graduate Biomedical Sciences and Dept. of Developmental,Molecular, and Chemical Biology Tufts University School of Medicine Boston, MA, United States of America.ORCID http://orcid.org/0000-0002-1781-1542
Brent H CochranGraduate Program in Cell and Molecular Physiology, Sackler School of Graduate Biomedical Sciences and Dept. of Developmental,Molecular, and Chemical Biology Tufts University School of Medicine Boston, MA, United States of America.ORCID http://orcid.org/0000-0002-7598-5604
Tufts University · US

Funding

TUSM/T-NEMC CENTER FOR NEUROSCIENCE RESEARCH - Imaging CoreP30NS047243 · NINDS · TUFTS UNIVERSITY BOSTON · PI JACKSON, F ROB · 2003 to 2017
$10.0M
RNAi screen of the glioblastoma stem cell kinome under hypoxia and normoxiaR01NS072414 · NINDS · TUFTS UNIVERSITY BOSTON · PI COCHRAN, BRENT H. · 2011 to 2015
$1.8M
NINDS NIH HHS P30 NS047243NINDS NIH HHS R01 NS072414
6 · The paper itself

Abstract

The growth factor and cytokine regulated transcription factor STAT3 is required for the self-renewal of several stem cell types including tumor stem cells from glioblastoma. Here we show that STAT3 inhibition leads to the upregulation of the histone H3K27me2/3 demethylase Jmjd3 (KDM6B), which can reverse polycomb complex-mediated repression of tissue specific genes. STAT3 binds to the Jmjd3 promoter, suggesting that Jmjd3 is a direct target of STAT3. Overexpression of Jmjd3 slows glioblastoma stem cell growth and neurosphere formation, whereas knockdown of Jmjd3 rescues the STAT3 inhibitor-induced neurosphere formation defect. Consistent with this observation, STAT3 inhibition leads to histone H3K27 demethylation of neural differentiation genes, such as Myt1, FGF21, and GDF15. These results demonstrate that the regulation of Jmjd3 by STAT3 maintains repression of differentiation specific genes and is therefore important for the maintenance of self-renewal of normal neural and glioblastoma stem cells.

Indexed as

Brain NeoplasmsCell Line, TumorCell ProliferationChromatin ImmunoprecipitationDNA-Binding ProteinsGene Expression Regulation, NeoplasticGlioblastomaHumansJumonji Domain-Containing Histone DemethylasesNeoplastic Stem CellsPromoter Regions, GeneticSTAT3 Transcription FactorTranscription FactorsDNA-Binding ProteinsJumonji Domain-Containing Histone DemethylasesKDM6B protein, humanMYT1 protein, humanSTAT3 protein, humanSTAT3 Transcription FactorTranscription Factors

Identifiers

PMID28384648
PMCPMC5383422
OpenAlexW2950857505

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.