Evidence map›Paper›PMID 22331469›Full record

ArticleMolecular and cellular biology2012

Mediator subunits MED1 and MED24 cooperatively contribute to pubertal mammary gland development and growth of breast carcinoma cells.

Natsumi Hasegawa, Akiko Sumitomo, Azusa Fujita, Nami Aritome, Shumpei Mizuta, Keiji Matsui, Ruri Ishino, Kana Inoue, Norinaga Urahama, Junko Nose and 4 more

Open access · bronzeAbstract read
In one paragraph

Article in Molecular and cellular biology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

31 citing papers in PubMed, 48 citations in OpenAlex.

  1. Article
  2. Article
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  4. Article
  5. Genetically Engineered Mice Unveil In Vivo Roles of the Mediator Complex.International journal of molecular sciences · 2023
    Review
  6. Upregulation of MED7 was associated with progression in hepatocellular carcinoma.Cancer biomarkers : section A of Disease markers · 2023
    Article
  7. Article
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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

14 authors at 3 institutions in 3 countries.

Natsumi HasegawaLaboratory of Hematology, Kobe University Graduate School of Health Sciences, Division of Oncology/Hematology, Department of Medicine, Kobe University Graduate School of Medicine, Kobe, Japan.
Akiko Sumitomo
Azusa Fujita
Nami Aritome
Shumpei Mizuta
Keiji Matsui
Ruri Ishino
Kana Inoue
Norinaga Urahama
Junko Nose
Toru Mukohara
Shingo Kamoshida
Robert G Roeder
Mitsuhiro Ito
RMIT University · AUKobe University · JPRockefeller University · US

Funding

Nuclear Receptor Coactivator Functions and MechanismsR01DK071900 · NIDDK · ROCKEFELLER UNIVERSITY · PI ROEDER, ROBERT G · 2005 to 2015
$5.9M
NIDDK NIH HHS DK071900NIDDK NIH HHS R01 DK071900
6 · The paper itself

Abstract

The Mediator subunit MED1 is essential for mammary gland development and lactation, whose contribution through direct interaction with estrogen receptors (ERs) is restricted to involvement in pubertal mammary gland development and luminal cell differentiation. Here, we provide evidence that the MED24-containing submodule of Mediator functionally communicates specifically with MED1 in pubertal mammary gland development. Mammary glands from MED1/MED24 double heterozygous knockout mice showed profound retardation in ductal branching during puberty, while single haploinsufficient glands developed normally. DNA synthesis of both luminal and basal cells were impaired in double mutant mice, and the expression of ER-targeted genes encoding E2F1 and cyclin D1, which promote progression through the G(1)/S phase of the cell cycle, was attenuated. Luciferase reporter assays employing double mutant mouse embryonic fibroblasts showed selective impairment in ER functions. Various breast carcinoma cell lines expressed abundant amounts of MED1, MED24, and MED30, and attenuated expression of MED1 and MED24 in breast carcinoma cells led to attenuated DNA synthesis and growth. These results indicate functional communications between the MED1 subunit and the MED24-containing submodule that mediate estrogen receptor functions and growth of both normal mammary epithelial cells and breast carcinoma cells.

Indexed as

Mammary Glands, AnimalAgingAnimalsBreast NeoplasmsCell Line, TumorCyclin D1E2F1 Transcription FactorFemaleG1 PhaseHumansMammary Neoplasms, AnimalMediator ComplexMediator Complex Subunit 1MiceS PhaseCyclin D1E2F1 Transcription FactorMED1 protein, humanMed1 protein, mouseMED24 protein, humanMed24 protein, mouseMediator ComplexMediator Complex Subunit 1

Identifiers

PMID22331469
PMCPMC3318591
OpenAlexW2118578251

What OpenQuestion holds

Textmetadata
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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.