Evidence map›Paper›PMID 27377409›Full record

ArticleArthritis research & therapy2016

miR-155 in the progression of lung fibrosis in systemic sclerosis.

Romy B Christmann, Alicia Wooten, Percival Sampaio-Barros, Claudia L Borges, Carlos R R Carvalho, Ronaldo A Kairalla, Carol Feghali-Bostwick, Jessica Ziemek, Yu Mei, Salma Goummih and 10 more

Open access · goldAbstract read
In one paragraph

Article in Arthritis research & therapy, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 68 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
68citing papers in PubMed, 2 pooled it
11.1field-weighted citation impact, top 1% 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

68 citing papers in PubMed, 2 syntheses or guidelines pooled it, 110 citations in OpenAlex.

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  11. CD45+/ Col I+ Fibrocytes: Major source of collagen in the fibrotic lung, but not in passaged fibroblast cultures.Matrix biology : journal of the International Society for Matrix Biology · 2025
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8 more citing papers are in PubMed but not listed here.

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

20 authors at 7 institutions in 2 countries.

Romy B ChristmannBoston University School of Medicine, E501, Arthritis Center, Medical Campus, 72 East Concord Street, Boston, MA, 02118-2526, USA. romy.souza@gmail.com.
Alicia WootenBoston University School of Medicine, E501, Arthritis Center, Medical Campus, 72 East Concord Street, Boston, MA, 02118-2526, USA.
Percival Sampaio-BarrosHospital das Clinicas da Faculdade de Medicina da Universidade de São Paulo, São Paulo, SP, Brazil.
Claudia L BorgesUniversidade CEUMA, São Luís do Maranhão, MA, Brazil.
Carlos R R CarvalhoHospital das Clinicas da Faculdade de Medicina da Universidade de São Paulo, São Paulo, SP, Brazil.
Ronaldo A KairallaHospital das Clinicas da Faculdade de Medicina da Universidade de São Paulo, São Paulo, SP, Brazil.
Carol Feghali-BostwickMedical University of South Carolina, Charleston, SC, USA.
Jessica ZiemekBoston University School of Medicine, E501, Arthritis Center, Medical Campus, 72 East Concord Street, Boston, MA, 02118-2526, USA.
Yu MeiBoston University School of Medicine, E501, Arthritis Center, Medical Campus, 72 East Concord Street, Boston, MA, 02118-2526, USA.
Salma GoummihBoston University School of Medicine, E501, Arthritis Center, Medical Campus, 72 East Concord Street, Boston, MA, 02118-2526, USA.
Jiangning TanUniversity of Pittsburgh, Division of Pulmonary, Allergy, and Critical Care Medicine, and the Dorothy P. and Richard P. Simmons Center for Interstitial Lung Disease, Pittsburgh, PA, USA.
Diana AlvarezUniversity of Pittsburgh, Division of Pulmonary, Allergy, and Critical Care Medicine, and the Dorothy P. and Richard P. Simmons Center for Interstitial Lung Disease, Pittsburgh, PA, USA.
Daniel J KassUniversity of Pittsburgh, Division of Pulmonary, Allergy, and Critical Care Medicine, and the Dorothy P. and Richard P. Simmons Center for Interstitial Lung Disease, Pittsburgh, PA, USA.
Mauricio RojasUniversity of Pittsburgh, Division of Pulmonary, Allergy, and Critical Care Medicine, and the Dorothy P. and Richard P. Simmons Center for Interstitial Lung Disease, Pittsburgh, PA, USA.
Thiago Lemos de MattosUniversidade do Estado do Amazonas, Manaus, AM, Brazil.
Edwin ParraHospital das Clinicas da Faculdade de Medicina da Universidade de São Paulo, São Paulo, SP, Brazil.
Giuseppina StifanoBoston University School of Medicine, E501, Arthritis Center, Medical Campus, 72 East Concord Street, Boston, MA, 02118-2526, USA.
Vera L CapelozziHospital das Clinicas da Faculdade de Medicina da Universidade de São Paulo, São Paulo, SP, Brazil.
Robert W SimmsBoston University School of Medicine, E501, Arthritis Center, Medical Campus, 72 East Concord Street, Boston, MA, 02118-2526, USA.
Robert LafyatisBoston University School of Medicine, E501, Arthritis Center, Medical Campus, 72 East Concord Street, Boston, MA, 02118-2526, USA.
Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo · BRUniversity of Pittsburgh · USBoston Medical Center · USBoston University · USCentro Universitário do Maranhão · BRMedical University of South Carolina · USUniversidade do Estado do Amazonas · BR

Funding

Translational studies for identifying and targeting novel pathways in systemic sclerosis pathogenesisP50AR060780 · NIAMS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI LAFYATIS, ROBERT A. · 2011 to 2021
$14.9M
RESEARCH TRAINING IN IMMUNOLOGYT32AI007309 · NIAID · BOSTON UNIVERSITY MEDICAL CAMPUS · PI GUMMULURU, SURYARAM · 1988 to 2024
$7.4M
Boston University Clinical and Translational Science Institute - U ProgramU54TR001012 · NCATS · BOSTON UNIVERSITY MEDICAL CAMPUS · PI CENTER, DAVID M. · 2014 to 2014
$3.9M
Rheumatic Diseases Research Core CentersP30AR061271 · NIAMS · BOSTON UNIVERSITY MEDICAL CAMPUS · PI FEGHALI-BOSTWICK, CAROL A. · 2011 to 2015
$3.1M
Innate immunity in dermal fibrosis and systemic sclerosisR01AR051089 · NIAMS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI LAFYATIS, ROBERT A. · 2005 to 2015
$2.8M
Aging of Mesenchymal Stem Cells Missing Link in IPFR01HL123766 · NHLBI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI ROJAS, MAURICIO · 2015 to 2018
$1.9M
Twist1 subphenotypes and pulmonary fibrosisR01HL126990 · NHLBI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI KASS, DANIEL J · 2015 to 2019
$1.9M
TSLP profibrotic signaling and its interaction with TGF-betaK08AR065507 · NIAMS · BOSTON UNIVERSITY MEDICAL CAMPUS · PI CHRISTMANN, ROMY BEATRIZ · 2014 to 2016
$304k
NCATS NIH HHS U54 TR001012NHLBI NIH HHS R01 HL123766NHLBI NIH HHS R01 HL126990NIAID NIH HHS T32 AI007309NIAMS NIH HHS K08 AR065507NIAMS NIH HHS P30 AR061271NIAMS NIH HHS P50 AR060780NIAMS NIH HHS R01 AR051089
6 · The paper itself

Abstract

backgroundMicroRNA (miRNA) control key elements of mRNA stability and likely contribute to the dysregulated lung gene expression observed in systemic sclerosis associated interstitial lung disease (SSc-ILD). We analyzed the miRNA gene expression of tissue and cells from patients with SSc-ILD. A chronic lung fibrotic murine model was used.

methodsRNA was isolated from lung tissue of 12 patients with SSc-ILD and 5 controls. High-resolution computed tomography (HRCT) was performed at baseline and 2-3 years after treatment. Lung fibroblasts and peripheral blood mononuclear cells (PBMC) were isolated from healthy controls and patients with SSc-ILD. miRNA and mRNA were analyzed by microarray, quantitative polymerase chain reaction, and/or Nanostring; pathway analysis was performed by DNA Intelligent Analysis (DIANA)-miRPath v2.0 software. Wild-type and miR-155 deficient (miR-155ko) mice were exposed to bleomycin.

resultsLung miRNA microarray data distinguished patients with SSc-ILD from healthy controls with 185 miRNA differentially expressed (q < 0.25). DIANA-miRPath revealed 57 Kyoto Encyclopedia of Genes and Genomes pathways related to the most dysregulated miRNA. miR-155 and miR-143 were strongly correlated with progression of the HRCT score. Lung fibroblasts only mildly expressed miR-155/miR-21 after several stimuli. miR-155 PBMC expression strongly correlated with lung function tests in SSc-ILD. miR-155ko mice developed milder lung fibrosis, survived longer, and weaker lung induction of several genes after bleomycin exposure compared to wild-type mice.

conclusionsmiRNA are dysregulated in the lungs and PBMC of patients with SSc-ILD. Based on mRNA-miRNA interaction analysis and pathway tools, miRNA may play a role in the progression of the disease. Our findings suggest that targeting miR-155 might provide a novel therapeutic strategy for SSc-ILD.

Indexed as

AnimalsDisease Models, AnimalDisease ProgressionHigh-Throughput Nucleotide SequencingHumansLung Diseases, InterstitialMiceMice, Inbred C57BLMice, KnockoutMicroRNAsOligonucleotide Array Sequence AnalysisPulmonary FibrosisReal-Time Polymerase Chain ReactionScleroderma, SystemicMicroRNAsMIRN155 microRNA, humanBiomarkerBleomycinGene expressionLung fibrosismicroRNAmiR-155Systemic Sclerosis

Identifiers

PMID27377409
PMCPMC4932708
OpenAlexW2463213593

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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.