Evidence map›Paper›PMID 22158614›Full record

ArticleThe Journal of biological chemistry2012

E74-like factor 3 (ELF3) impacts on matrix metalloproteinase 13 (MMP13) transcriptional control in articular chondrocytes under proinflammatory stress.

Miguel Otero, Darren A Plumb, Kaneyuki Tsuchimochi, Cecilia L Dragomir, Ko Hashimoto, Haibing Peng, Eleonora Olivotto, Michael Bevilacqua, Lujian Tan, Zhiyong Yang and 5 more

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 59 papers.

0numbers the graph read from it
0cells of the map it votes in
59citing papers in PubMed
3.7field-weighted citation impact, top 8% 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

59 citing papers in PubMed, 91 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

15 authors at 7 institutions in 2 countries.

Miguel OteroLaboratory for Cartilage Biology, Research Division, the Hospital for Special Surgery, Weill Cornell Medical College, New York, New York 10021, USA.
Darren A Plumb
Kaneyuki Tsuchimochi
Cecilia L Dragomir
Ko Hashimoto
Haibing Peng
Eleonora Olivotto
Michael Bevilacqua
Lujian Tan
Zhiyong Yang
Yumei Zhan
Peter Oettgen
Yefu Li
Kenneth B Marcu
Mary B Goldring
Hospital for Special Surgery · USHarvard University · USBeth Israel Deaconess Medical Center · USCornell University · USIstituto Ortopedico Rizzoli · ITPfizer (United States) · USStony Brook University · US

Funding

Defining Common Molecular Parameters For Onset and Progression of OsteoarthritisRC4AR060546 · NIAMS · HOSPITAL FOR SPECIAL SURGERY · PI GOLDRING, MARY B, LI, YEFU · 2010 to 2010
$4.1M
Role of ESE1 Regulation of Type II Collagen in CartilageR01AG022021 · NIA · HOSPITAL FOR SPECIAL SURGERY · PI GOLDRING, MARY B · 2002 to 2014
$3.4M
Epigenetic Regulation of MMP-13R21AR054887 · NIAMS · HOSPITAL FOR SPECIAL SURGERY · PI GOLDRING, MARY B · 2007 to 2008
$355k
NIAMS NIH HHS R21 AR054887NIAMS NIH HHS R21-AR054887NIAMS NIH HHS RC4 AR060546NIA NIH HHS R01 AG022021NIA NIH HHS R01-AG022021
6 · The paper itself

Abstract

Matrix metalloproteinase (MMP)-13 has a pivotal, rate-limiting function in cartilage remodeling and degradation due to its specificity for cleaving type II collagen. The proximal MMP13 promoter contains evolutionarily conserved E26 transformation-specific sequence binding sites that are closely flanked by AP-1 and Runx2 binding motifs, and interplay among these and other factors has been implicated in regulation by stress and inflammatory signals. Here we report that ELF3 directly controls MMP13 promoter activity by targeting an E26 transformation-specific sequence binding site at position -78 bp and by cooperating with AP-1. In addition, ELF3 binding to the proximal MMP13 promoter is enhanced by IL-1β stimulation in chondrocytes, and the IL-1β-induced MMP13 expression is inhibited in primary human chondrocytes by siRNA-ELF3 knockdown and in chondrocytes from Elf3(-/-) mice. Further, we found that MEK/ERK signaling enhances ELF3-driven MMP13 transactivation and is required for IL-1β-induced ELF3 binding to the MMP13 promoter, as assessed by chromatin immunoprecipitation. Finally, we show that enhanced levels of ELF3 co-localize with MMP13 protein and activity in human osteoarthritic cartilage. These studies define a novel role for ELF3 as a procatabolic factor that may contribute to cartilage remodeling and degradation by regulating MMP13 gene transcription.

Indexed as

Transcription, GeneticAnimalsCartilage, ArticularChondrocytesDNA-Binding ProteinsGene Expression Regulation, EnzymologicHumansInflammationInterleukin-1betaMatrix Metalloproteinase 13MiceMice, KnockoutOsteoarthritisProto-Oncogene ProteinsProto-Oncogene Proteins c-etsResponse ElementsDNA-Binding ProteinsELF3 protein, humanElf3 protein, mouseIL1B protein, humanInterleukin-1betaMatrix Metalloproteinase 13MMP13 protein, humanMmp13 protein, mouseProto-Oncogene ProteinsProto-Oncogene Proteins c-etsTranscription Factor AP-1Transcription Factors

Identifiers

PMID22158614
PMCPMC3271009
OpenAlexW1963744427

What Socratic 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 Socratic graph.