Evidence map›Paper›PMID 34831458›Full record

ArticleCells2021

Matrix Metalloproteinases Inhibition by Doxycycline Rescues Extracellular Matrix Organization and Partly Reverts Myofibroblast Differentiation in Hypermobile Ehlers-Danlos Syndrome Dermal Fibroblasts: A Potential Therapeutic Target?

Nicola Chiarelli, Nicoletta Zoppi, Marina Venturini, Daniele Capitanio, Cecilia Gelfi, Marco Ritelli, Marina Colombi

Open access · goldAbstract read
In one paragraph

Article in Cells, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.2field-weighted citation impact, top 19% 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

10 citing papers in PubMed, 14 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.

Nicola ChiarelliDivision of Biology and Genetics, Department of Molecular and Translational Medicine, University of Brescia, 25121 Brescia, Italy.ORCID 0000-0002-1760-5079
Nicoletta ZoppiDivision of Biology and Genetics, Department of Molecular and Translational Medicine, University of Brescia, 25121 Brescia, Italy.ORCID 0000-0003-0197-8927
Marina VenturiniDivision of Dermatology, Department of Clinical and Experimental Sciences, Spedali Civili University Hospital, 25121 Brescia, Italy.
Daniele CapitanioDepartment of Biomedical Sciences for Health, University of Milan, 20090 Milan, Italy.ORCID 0000-0001-7701-728X
Cecilia GelfiDepartment of Biomedical Sciences for Health, University of Milan, 20090 Milan, Italy.ORCID 0000-0002-2996-6912
Marco RitelliDivision of Biology and Genetics, Department of Molecular and Translational Medicine, University of Brescia, 25121 Brescia, Italy.ORCID 0000-0002-7025-2495
Marina ColombiDivision of Biology and Genetics, Department of Molecular and Translational Medicine, University of Brescia, 25121 Brescia, Italy.ORCID 0000-0002-3105-5990
University of Brescia · ITUniversity of Milan · ITAzienda Socio Sanitaria Territoriale degli Spedali Civili di Brescia · IT

Funding

The Ehlers-Danlos Society 2018.02c.LOI.26The Ehlers-Danlos Society Molecular Studies in hEDS and HSD $1 Million Grant
6 · The paper itself

Abstract

Hypermobile Ehlers-Danlos syndrome (hEDS) is the most frequent type of EDS and is characterized by generalized joint hypermobility and musculoskeletal manifestations which are associated with chronic pain, and mild skin involvement along with the presence of more than a few comorbid conditions. Despite numerous research efforts, no causative gene(s) or validated biomarkers have been identified and insights into the disease-causing mechanisms remain scarce. Variability in the spectrum and severity of symptoms and progression of hEDS patients' phenotype likely depend on a combination of age, gender, lifestyle, and the probable multitude of genes involved in hEDS. However, considering the clinical overlap with other EDS forms, which lead to abnormalities in extracellular matrix (ECM), it is plausible that the mechanisms underlying hEDS pathogenesis also affect the ECM to a certain extent. Herein, we performed a series of in vitro studies on the secretome of hEDS dermal fibroblasts that revealed a matrix metalloproteinases (MMPs) dysfunction as one of the major disease drivers by causing a detrimental feedback loop of excessive ECM degradation coupled with myofibroblast differentiation. We demonstrated that doxycycline-mediated inhibition of MMPs rescues in hEDS cells a control-like ECM organization and induces a partial reversal of their myofibroblast-like features, thus offering encouraging clues for translational studies confirming MMPs as a potential therapeutic target in hEDS with the expectation to improve patients' quality of life and alleviate their disabilities.

Indexed as

Cell DifferentiationCulture Media, ConditionedDermisDoxycyclineEhlers-Danlos SyndromeExtracellular MatrixFibroblastsGene OntologyHumansMatrix Metalloproteinase InhibitorsMolecular Targeted TherapyMyofibroblastsPhenotypeProtein Interaction MapsProteolysisProteomicsCulture Media, ConditionedDoxycyclineMatrix Metalloproteinase Inhibitorsdoxycyclineextracellular matrixhypermobile Ehlers-Danlos syndromematrix metalloproteinasesmyofibroblastssecretome

Identifiers

PMID34831458
PMCPMC8621259
OpenAlexW3217401674

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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.