Evidence map›Paper›PMID 36914001›Full record

ArticleThe Journal of investigative dermatology2023

Matrix Metalloproteinase-1 Expression in Fibroblasts Accelerates Dermal Aging and Promotes Papilloma Development in Mouse Skin.

Taihao Quan, Wei Xia, Tianyuan He, Kenneth Calderone, George Bou-Gharios, John J Voorhees, Andrzej A Dlugosz, Gary J Fisher

Open access · greenAbstract read
In one paragraph

Article in The Journal of investigative dermatology, 2023. 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
8.6field-weighted citation impact, top 2% 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, 30 citations in OpenAlex.

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  11. Journal of Taibah University Medical Sciences · 2025
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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

8 authors at 2 institutions in 2 countries.

Taihao QuanDepartment of Dermatology, University of Michigan Medical School, Ann Arbor, Michigan, USA.
Wei XiaDepartment of Dermatology, University of Michigan Medical School, Ann Arbor, Michigan, USA.
Tianyuan HeDepartment of Dermatology, University of Michigan Medical School, Ann Arbor, Michigan, USA.
Kenneth CalderoneDepartment of Dermatology, University of Michigan Medical School, Ann Arbor, Michigan, USA.
George Bou-GhariosInstitute of Ageing and Chronic Diseases, University of Liverpool, Liverpool United Kingdom.
John J VoorheesDepartment of Dermatology, University of Michigan Medical School, Ann Arbor, Michigan, USA.
Andrzej A DlugoszDepartment of Dermatology, University of Michigan Medical School, Ann Arbor, Michigan, USA.
Gary J FisherDepartment of Dermatology, University of Michigan Medical School, Ann Arbor, Michigan, USA. Electronic address: gjfisher@med.umich.edu.
University of Michigan · USUniversity of Liverpool · GB

Funding

University of Michigan Skin Biology and Diseases Resource-based CenterP30AR075043 · NIAMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Johann Eli Gudjonsson · 2019 to 2026
$6.6M
The impact of aged-related dermal microenvironment on the development of precancerous stroma and cancer initiationU01AG077924 · NIA · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI DLUGOSZ, ANDRZEJ A., FISHER, GARY J · 2021 to 2025
$2.3M
Role of dermal extracellular matrix microenvironment in skin agingR01AG051849 · NIA · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI FISHER, GARY J, QUAN, TAIHAO · 2016 to 2020
$1.6M
NIAMS NIH HHS P30 AR075043NIA NIH HHS R01 AG051849NIA NIH HHS U01 AG077924
6 · The paper itself

Abstract

Fragmentation, disorganization, and depletion of the collagen-rich dermal extracellular matrix are hallmarks of aged human skin. These deleterious alterations are thought to critically mediate many of the prominent clinical attributes of aged skin, including thinning, fragility, impaired wound healing, and a propensity for carcinoma. Matrix metalloproteinase-1 (MMP1) initiates the cleavage of collagen fibrils and is significantly increased in dermal fibroblasts in aged human skin. To investigate the role of elevated MMP1 in skin aging, we generated a conditional bitransgenic mouse (type I collagen alpha chain 2; human MMP1 [Col1a2;hMMP1]) that expresses full-length, catalytically active hMMP1 in dermal fibroblasts. hMMP1 expression is activated by a tamoxifen-inducible Cre recombinase that is driven by the Col1a2 promoter and upstream enhancer. Tamoxifen induced hMMP1 expression and activity throughout the dermis Col1a2:hMMP1 mice. At 6 months of age, Col1a2;hMMP1 mice displayed loss and fragmentation of dermal collagen fibrils, which was accompanied by many of the features of aged human skin, such as contracted fibroblast morphology, reduced collagen production, increased expression of multiple endogenous MMPs, and proinflammatory mediators. Interestingly, Col1a2;hMMP1 mice displayed substantially increased susceptibility to skin papilloma development. These data demonstrate that fibroblast expression of hMMP1 is a critical mediator of dermal aging and creates a dermal microenvironment that promotes keratinocyte tumor development.

Indexed as

PapillomaSkin AgingAgedAnimalsCells, CulturedCollagenCollagen Type IFibroblastsHumansMatrix Metalloproteinase 1MiceSkinTumor MicroenvironmentCollagenCollagen Type ICollagen Type I, alpha2 SubunitMatrix Metalloproteinase 1

Identifiers

PMID36914001
PMCPMC11577279
OpenAlexW4323922739

What OpenQuestion holds

Textmetadata
LicenceTDM
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.