Evidence map›Paper›PMID 23504324›Full record

Trial reportThe Journal of biological chemistry2013

Cysteine-rich protein 61 (CCN1) domain-specific stimulation of matrix metalloproteinase-1 expression through αVβ3 integrin in human skin fibroblasts.

Zhaoping Qin, Gary J Fisher, Taihao Quan

Open access · hybridAbstract readClinical Trial
In one paragraph

Trial report in The Journal of biological chemistry, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing 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

27 citing papers in PubMed, 39 citations in OpenAlex.

  1. Article
  2. Connective Tissue Growth Factor: Regulation, Diseases, and Drug Discovery.International journal of molecular sciences · 2024
    Review
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  18. Genomic copy number analysis of a spectrum of blue nevi identifies recurrent aberrations of entire chromosomal arms in melanoma ex blue nevus.Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc · 2016
    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

3 authors at 1 institution in 1 country.

Zhaoping QinDepartment of Dermatology, University of Michigan Medical School, Ann Arbor, Michigan 48109, USA.
Gary J Fisher
Taihao Quan
University of Michigan–Ann Arbor · US

Funding

Transforming Growth Factor-Beta (TGF-b) Signaling in Photoaged and ChronologicallR01AG019364 · NIA · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI FISHER, GARY J, QUAN, TAIHAO · 2002 to 2014
$3.0M
Collagenase degradation in extracellular matrix in agingR01AG025186 · NIA · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI FISHER, GARY J · 2006 to 2010
$1.8M
CYR61-a novel potential mediator of photoaged human skinR01ES014697 · NIEHS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI QUAN, TAIHAO · 2007 to 2010
$1.7M
NIA NIH HHS AG019364NIA NIH HHS AG025186NIA NIH HHS R01 AG019364NIA NIH HHS R01 AG025186NIEHS NIH HHS ES014697 30S1NIEHS NIH HHS R01 ES014697
6 · The paper itself

Abstract

Human skin largely comprises collagenous extracellular matrix. The hallmark of skin aging is fragmentation of collagen fibrils. Matrix metalloproteinases (MMPs) are largely responsible for collagen degradation. MMP-1, principally derived from dermal fibroblasts, is the major protease capable of initiating degradation of native fibrillar collagens. Presently, we report that CCN1, a secreted and extracellular matrix-associated protein, is elevated in aged human skin dermal fibroblasts in vivo and stimulates MMP-1 expression through functional interaction with αVβ3 integrin in human dermal fibroblasts. CCN1 contains four conserved structural domains. Our results indicate that the three N-terminal domains (IGFBP, VWC, and TSP1), but not the C-terminal CT domain, are required for CCN1 to stimulate MMP-1 expression. This stimulation is dependent on interaction between the active structural domains and αVβ3 integrin. The interaction of VWC domain with integrin αVβ3 is necessary and requires functional cooperation with adjacent IGFBP and TSP1 domains to stimulate MMP-1 expression. Finally, induction of MMP-1 expression in dermal fibroblasts by CCN1 N-terminal domains resulted in fragmentation of type I collagen fibrils in a three-dimensional collagen lattice model. These data suggest that domain-specific interactions of CCN1 with αVβ3 integrin contribute to human skin aging by stimulating MMP-1-mediated collagen fibril fragmentation.

Indexed as

AdultAgingCollagen Type ICysteine-Rich Protein 61DermisFemaleFibroblastsGene Expression Regulation, EnzymologicHumansIntegrin alphaVbeta3MaleMatrix Metalloproteinase 1Protein Structure, TertiaryProteolysisCCN1 protein, humanCollagen Type ICysteine-Rich Protein 61Integrin alphaVbeta3Matrix Metalloproteinase 1MMP1 protein, human

Identifiers

PMID23504324
PMCPMC3636922
OpenAlexW2040951702

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.