Evidence map›Paper›PMID 26025306›Full record

ArticleArthritis research & therapy2015

Combined effect of genetic background and gender in a mouse model of bleomycin-induced skin fibrosis.

Nadira Ruzehaji, Jerome Avouac, Muriel Elhai, Maxime Frechet, Camelia Frantz, Barbara Ruiz, Joerg H Distler, Yannick Allanore

RetractedOpen access · goldAbstract readRetracted Publication
In one paragraph

Article in Arthritis research & therapy, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It has been retracted, and should not be counted. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
3.5field-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

12 citing papers in PubMed, 38 citations in OpenAlex.

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  10. Role of adipose tissue in facial aging.Clinical interventions in aging · 2017
    Review
  11. Interfacial Adipose Tissue in Systemic Sclerosis.Current rheumatology reports · 2017
    Review
  12. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 5 institutions in 2 countries.

Nadira RuzehajiINSERM U1016/UMR 8104, Cochin Institute, Paris, France. nadira.ruzehaji@inserm.fr.
Jerome AvouacINSERM U1016/UMR 8104, Cochin Institute, Paris, France. jerome.avouac@cch.aphp.fr.
Muriel ElhaiINSERM U1016/UMR 8104, Cochin Institute, Paris, France. muriel-elhai@hotmail.fr.
Maxime FrechetINSERM U1016/UMR 8104, Cochin Institute, Paris, France. maxime.frechet@gmail.com.
Camelia FrantzINSERM U1016/UMR 8104, Cochin Institute, Paris, France. camelia.frantz@gmail.com.
Barbara RuizINSERM U1016/UMR 8104, Cochin Institute, Paris, France. barbara.ruiz@inserm.fr.
Joerg H DistlerDepartment of Internal Medicine and Institute for Clinical Immunology, University of Erlangen-Nuremberg, Erlangen, Germany. Joerg.Distler@uk-erlangen.de.
Yannick AllanoreINSERM U1016/UMR 8104, Cochin Institute, Paris, France. yannick.allanore@inserm.fr.
Inserm · FRInstitut Cochin · FRDélégation Paris 5 · FRFriedrich-Alexander-Universität Erlangen-Nürnberg · DEUniversité Paris Cité · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionSystemic sclerosis (SSc) is a connective tissue disorder characterised by the development of skin fibrosis. Our current understanding of the disease pathogenesis is incomplete and the study of SSc is hindered, at least partially, by a lack of animal models that fully replicate the complex state of human disease. Murine model of bleomycin-induced dermal fibrosis encapsulates important events that take place early in the disease course.

methodsTo characterise the optimum in vivo parameters required for the successful induction of dermal fibrosis we subjected three commonly used mouse strains to repeated subcutaneous bleomycin injections. We aimed to identify the effects of genetic background and gender on the severity of skin fibrosis. We used male and female Balb/C, C57BL/6, and DBA/2 strains and assessed their susceptibility to bleomycin-induced fibrosis by measuring dermal thickness, hydroxyproline/collagen content and number of resident myofibroblasts, all of which are important indicators of the severity of skin fibrosis. All data are expressed as mean values ± SEM. The Mann-Whitney U test was used for statistical analysis with GraphPad Prism 6.04 software.

resultsDermal fibrosis was most severe in Balb/C mice compared to C57BL/6 and DBA/2 suggesting that Balb/C mice are more susceptible to bleomycin-induced fibrosis. Analysis of the effect of gender on the severity of fibrosis showed that male Balb/C, C57BL/6, DBA/2 mice had a tendency to develop more pronounced fibrosis phenotype than female mice. Of potential importance, male Balb/C mice developed the most severe fibrosis phenotype compared to male C57BL/6 and male DBA/2 as indicated by significantly increased number of dermal myofibroblasts.

conclusionOur study highlights the importance of genetic background and gender in the induction of murine dermal fibrosis. Robust and reproducible animal models of fibrosis are important research tools used in pharmacological studies which may lead to better understanding of the pathogenesis of fibrotic diseases and assist in identification of new drugs.

Indexed as

Genetic BackgroundAnimalsBiopsy, NeedleBleomycinCollagenDisease Models, AnimalFemaleFibrosisImmunohistochemistryInjections, SubcutaneousMaleMiceMice, Inbred BALB CMice, Inbred C57BLMice, Inbred DBARandom AllocationBleomycinCollagen

Identifiers

PMID26025306
PMCPMC4461998
OpenAlexW1562232435

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.