Evidence map›Paper›PMID 24802759›Full record

ArticleThe Journal of biological chemistry2014

Histone demethylase jumonji AT-rich interactive domain 1B (JARID1B) controls mammary gland development by regulating key developmental and lineage specification genes.

Mike Ran Zou, Jian Cao, Zongzhi Liu, Sung Jin Huh, Kornelia Polyak, Qin Yan

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

33 citing papers in PubMed, 60 citations in OpenAlex.

  1. Review
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  6. Review
  7. The Intellectual Disability Risk GeneThe Journal of neuroscience : the official journal of the Society for Neuroscience · 2024
    Article
  8. Lysine Demethylation in Pathogenesis.Advances in experimental medicine and biology · 2023
    Article
  9. Article
  10. Article
  11. Article
  12. Review
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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

6 authors at 3 institutions in 1 country.

Mike Ran ZouFrom the Department of Pathology, Yale School of Medicine, New Haven, Connecticut 06520.
Jian CaoFrom the Department of Pathology, Yale School of Medicine, New Haven, Connecticut 06520.
Zongzhi LiuFrom the Department of Pathology, Yale School of Medicine, New Haven, Connecticut 06520.
Sung Jin HuhDepartment of Medical Oncology, Dana-Farber Cancer Institute and Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts 02215, and.
Kornelia PolyakDepartment of Medical Oncology, Dana-Farber Cancer Institute and Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts 02215, and Harvard Stem Cell Institute, Cambridge, Massachusetts 02138.
Qin YanFrom the Department of Pathology, Yale School of Medicine, New Haven, Connecticut 06520, qin.yan@yale.edu.
Yale University · USBrigham and Women's Hospital · USHarvard University · US

Funding

Use of Organotypic and Mammary Gland Models to Investigate the Outcomes of ClonalP01CA080111 · NCI · WHITEHEAD INSTITUTE FOR BIOMEDICAL RES · PI WEINBERG, ROBERT A · 1999 to 2018
$36.0M
Yale University Clinical and Translational Science Award ProgramUL1TR000142 · NCATS · YALE UNIVERSITY · PI SHERWIN, ROBERT S · 2012 to 2015
$31.8M
The RBP2/JARID1A/KDM5A Histone Demethylase as a Potential Drug Target in CancerR01CA076120 · NCI · DANA-FARBER CANCER INSTITUTE · PI KAELIN, WILLIAM G. · 1998 to 2015
$3.6M
The Role of Immune Cells in Breast Development and CancerF32CA156991 · NCI · DANA-FARBER CANCER INST · PI HUH, SUNG JIN · 2011 to 2013
$161k
NCATS NIH HHS UL1 TR000142NCI NIH HHS F32 CA156991NCI NIH HHS P01 CA080111NCI NIH HHS R01 CA076120
6 · The paper itself

Abstract

The JmjC domain-containing H3K4 histone demethylase jumonji AT-rich interactive domain 1B (JARID1B) (also known as KDM5B and PLU1) is overexpressed in breast cancer and is a potential target for breast cancer treatment. To investigate the in vivo function of JARID1B, we developed Jarid1b(-/-) mice and characterized their phenotypes in detail. Unlike previously reported Jarid1b(-/-) strains, the majority of these Jarid1b(-/-) mice were viable beyond embryonic and neonatal stages. This allowed us to further examine phenotypes associated with the loss of JARID1B in pubertal development and pregnancy. These Jarid1b(-/-) mice exhibited decreased body weight, premature mortality, decreased female fertility, and delayed mammary gland development. Related to these phenotypes, JARID1B loss decreased serum estrogen level and reduced mammary epithelial cell proliferation in early puberty. In mammary epithelial cells, JARID1B loss diminished the expression of key regulators for mammary morphogenesis and luminal lineage specification, including FOXA1 and estrogen receptor α. Mechanistically, JARID1B was required for GATA3 recruitment to the Foxa1 promoter to activate Foxa1 expression. These results indicate that JARID1B positively regulates mammary ductal development through both extrinsic and cell-autonomous mechanisms.

Indexed as

AnimalsCell LineCell LineageCell ProliferationDNA-Binding ProteinsFemaleGATA3 Transcription FactorGene Expression Regulation, DevelopmentalHepatocyte Nuclear Factor 3-alphaJumonji Domain-Containing Histone DemethylasesMammary Glands, AnimalMiceMice, KnockoutOrganogenesisPregnancyDNA-Binding ProteinsFoxa1 protein, mouseGata3 protein, mouseGATA3 Transcription FactorHepatocyte Nuclear Factor 3-alphaJumonji Domain-Containing Histone DemethylasesKdm5b protein, mouseBreast CancerEpigeneticsEstrogenFOXA1GATA3Histone MethylationKDM5BLuminal LineageMammary Gland DevelopmentMouse Genetics

Identifiers

PMID24802759
PMCPMC4067197
OpenAlexW2054659582

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.