Evidence map›Paper›PMID 25791327›Full record

ArticleArchives of oral biology2015

Oestrogen receptor beta mediates decreased occlusal loading induced inhibition of chondrocyte maturation in female mice.

Ilona Polur, Yosuke Kamiya, Manshan Xu, Bianca S Cabri, Marwa Alshabeeb, Sunil Wadhwa, Jing Chen

Abstract read
In one paragraph

Article in Archives of oral biology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

4 citing papers in PubMed, 10 citations in OpenAlex.

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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

7 authors at 3 institutions in 1 country.

Ilona PolurDivision of Orthodontics, Columbia University College of Dental Medicine, New York, NY 10032, USA. Electronic address: ip2162@columbia.edu.
Yosuke KamiyaDivision of Orthodontics, Columbia University College of Dental Medicine, New York, NY 10032, USA. Electronic address: kamisuke816@gmail.com.
Manshan XuDivision of Orthodontics, Columbia University College of Dental Medicine, New York, NY 10032, USA. Electronic address: mx2137@cumc.columbia.edu.
Bianca S CabriColumbia University College of Dental Medicine, New York, NY 10032, USA. Electronic address: bsc2126@cumc.columbia.edu.
Marwa AlshabeebDivision of Orthodontics, Columbia University College of Dental Medicine, New York, NY 10032, USA. Electronic address: ma3315@columbia.edu.
Sunil WadhwaDivision of Orthodontics, Columbia University College of Dental Medicine, New York, NY 10032, USA. Electronic address: sw2680@cumc.columbia.edu.
Jing ChenDivision of Orthodontics, Columbia University College of Dental Medicine, New York, NY 10032, USA. Electronic address: jc3835@cumc.columbia.edu.
Columbia University Irving Medical Center · USColumbia University · USNew York University · US

Funding

Estrogen Receptor Beta Regulation of Mandibular Condylar GrowthR01DE020097 · NIDCR · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI WADHWA, SUNIL · 2010 to 2013
$1.5M
Role of Estrogen Receptor Alpha and Beta in Regulating Mandibular Condylar GrowthR56DE020097 · NIDCR · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI WADHWA, SUNIL · 2014 to 2014
$287k
NIDCR NIH HHS 1R01DE020097NIDCR NIH HHS R01 DE020097NIDCR NIH HHS R56 DE020097
6 · The paper itself

Abstract

objectiveTemporomandibular joint (TMJ) disorders predominantly afflict women, suggesting that estrogen may play a role in the disease process. Defects in mechanical loading-induced TMJ remodelling are believed to be a major etiological factor in TMJ degenerative disease. Previously, we found that, decreased occlusal loading caused a significant decrease in early chondrocyte maturation markers (Sox9 and Col 2) in female, but not male, C57BL/6 wild type mice (1). The goal of this study was to examine the role of Estrogen Receptor (ER) beta in mediating these effects.

design21-day-old male (n = 24) and female (n = 25) ER beta KO mice were exposed to decreased occlusal loading (soft diet administration and incisor trimming) for 4 weeks. At 49 days of age the mice were sacrificed. Proliferation, gene expression, Col 2 immunohistochemistry and micro-CT analysis were performed on the mandibular condyles.

resultsDecreased occlusal loading triggered similar effects in male and female ER beta KO mice; specifically, significant decreases in Col 10 expression, subchondral total volume, bone volume, and trabecular number.

conclusionDecreased occlusal loading induced inhibition of chondrocyte maturation markers (Sox9 and Col 2) did not occur in female ER beta deficient mice.

Indexed as

Bite ForceAnimalsCell DifferentiationCell ProliferationChondrocytesChondrogenesisDietDisease Models, AnimalEstrogen Receptor betaFemaleGene ExpressionImmunohistochemistryMaleMandibular CondyleMiceMice, Inbred C57BLEstrogen Receptor betaEstrogen receptor betaMechanical loadingMouseTemporomandibular joint

Identifiers

PMID25791327
PMCPMC4420665
OpenAlexW2121816586

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

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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.