Evidence map›Paper›PMID 28667272›Full record

ArticleScientific reports2017

Adiponectin is an endogenous anti-fibrotic mediator and therapeutic target.

Roberta G Marangoni, Yuri Masui, Feng Fang, Benjamin Korman, Gabriel Lord, Junghwa Lee, Katja Lakota, Jun Wei, Philipp E Scherer, Laszlo Otvos and 7 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 54 papers.

0numbers the graph read from it
0cells of the map it votes in
54citing papers in PubMed
5.9field-weighted citation impact, top 3% 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

54 citing papers in PubMed, 88 citations in OpenAlex.

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  12. Adiponectin suppresses stiffness-dependent, profibrotic activation of lung fibroblasts.American journal of physiology. Lung cellular and molecular physiology · 2024
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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

17 authors at 6 institutions in 3 countries.

Roberta G MarangoniNorthwestern Scleroderma Program, Feinberg School of Medicine, Chicago, IL, 60611, USA. roberta.marangoni@northwestern.edu.
Yuri MasuiDepartment of Dermatology, University of Tokyo Graduate School of Medicine, Bunkyo-ku, Tokyo, 113-8655, Japan.
Feng FangNorthwestern Scleroderma Program, Feinberg School of Medicine, Chicago, IL, 60611, USA.
Benjamin KormanNorthwestern Scleroderma Program, Feinberg School of Medicine, Chicago, IL, 60611, USA.
Gabriel LordNorthwestern Scleroderma Program, Feinberg School of Medicine, Chicago, IL, 60611, USA.
Junghwa LeeDepartment of Preventive Medicine, Northwestern University Feinberg School of Medicine, Chicago, IL, 60611, USA.
Katja LakotaDepartment of Rheumatology, University Medical Centre Ljubljana, 1000, Ljubljana, Slovenia.
Jun WeiNorthwestern Scleroderma Program, Feinberg School of Medicine, Chicago, IL, 60611, USA.
Philipp E SchererTouchstone Diabetes Center, Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, TX, 75390, USA.ORCID 0000-0003-0680-3392
Laszlo OtvosDepartment of Biology, Temple University, Philadelphia, PA, 19140, USA.
Toshimasa YamauchiDepartment of Diabetes and Metabolic Diseases, University of Tokyo Graduate School of Medicine, Bunkyo-ku, Tokyo, 113-8655, Japan.
Naoto KubotaDepartment of Diabetes and Metabolic Diseases, University of Tokyo Graduate School of Medicine, Bunkyo-ku, Tokyo, 113-8655, Japan.
Takashi KadowakiDepartment of Diabetes and Metabolic Diseases, University of Tokyo Graduate School of Medicine, Bunkyo-ku, Tokyo, 113-8655, Japan.
Yoshihide AsanoDepartment of Dermatology, University of Tokyo Graduate School of Medicine, Bunkyo-ku, Tokyo, 113-8655, Japan.
Shinichi SatoDepartment of Dermatology, University of Tokyo Graduate School of Medicine, Bunkyo-ku, Tokyo, 113-8655, Japan.
Warren G TourtellotteDepartment of Pathology and Neurology, Northwestern University Feinberg School of Medicine, Chicago, IL, 60611, USA.
John VargaNorthwestern Scleroderma Program, Feinberg School of Medicine, Chicago, IL, 60611, USA. j-varga@northwestern.edu.
The University of Tokyo · JPNorthwestern University · USScleroderma Foundation · USLjubljana University Medical Centre · SITemple University · USThe University of Texas Southwestern Medical Center · US

Funding

Tumor Environment and Metastasis (TEAM) Research ProgramP30CA060553 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI Daniela E Matei · 1993 to 2026
$153.9M
Northwestern University Clinical and Translational Science Institute (NUCATS)UL1TR001422 · NCATS · NORTHWESTERN UNIVERSITY AT CHICAGO · PI D'AQUILA, RICHARD · 2015 to 2023
$56.8M
REGULATION OF COLLAGEN GENE EXPRESSION BY TGF-BETAR01AR042309 · NIAMS · UNIVERSITY OF ILLINOIS AT CHICAGO · PI VARGA, JOHN · 1994 to 2014
$4.4M
Fibroblast TGF-beta/Smad Signaling in SclerodermaR01AR049025 · NIAMS · UNIVERSITY OF ILLINOIS AT CHICAGO · PI VARGA, JOHN · 2002 to 2012
$3.7M
IMMEDIATE EARLY GENE REGULATED DEVELOPMENT/PLASTICITYK02NS046468 · NINDS · NORTHWESTERN UNIVERSITY AT CHICAGO · PI TOURTELLOTTE, WARREN G · 2005 to 2009
$785k
Aberrant TLR responses driving organ fibrosis in systemic sclerosisR56AR042309 · NIAMS · NORTHWESTERN UNIVERSITY AT CHICAGO · PI VARGA, JOHN · 2018 to 2018
$477k
Mentoring and Research in Mouse PathobiologyK26OD010945 · OD · NORTHWESTERN UNIVERSITY AT CHICAGO · PI TOURTELLOTTE, WARREN G · 2012 to 2014
$471k
Targeting Adiponectin Signaling: Novel Peptide Therapy for SclerodermaR21AR064925 · NIAMS · NORTHWESTERN UNIVERSITY AT CHICAGO · PI VARGA, JOHN · 2013 to 2014
$372k
Mentoring and Research in Mouse PathobiologyK26RR026099 · NCRR · NORTHWESTERN UNIVERSITY AT CHICAGO · PI TOURTELLOTTE, WARREN G · 2010 to 2011
$317k
Adipokine Modulation of Fibrosis: Novel Scleroderma PathwayR03AR066343 · NIAMS · NORTHWESTERN UNIVERSITY AT CHICAGO · PI GONCALVES MARANGONI, ROBERTA · 2015 to 2017
$232k
NCATS NIH HHS UL1 TR001422NCI NIH HHS P30 CA060553NCRR NIH HHS K26 RR026099NIAMS NIH HHS R01 AR042309NIAMS NIH HHS R01 AR049025NIAMS NIH HHS R03 AR066343NIAMS NIH HHS R21 AR064925NIAMS NIH HHS R56 AR042309NIH HHS K26 OD010945NINDS NIH HHS K02 NS046468
6 · The paper itself

Abstract

Skin fibrosis in systemic sclerosis (SSc) is accompanied by attrition of dermal white adipose tissue (dWAT) and reduced levels of circulating adiponectin. Since adiponectin has potent regulatory effects on fibroblasts, we sought to assess adiponectin signaling in SSc skin biopsies, and evaluate fibrosis in mice with adiponectin gain- and loss-of-function mutations. Furthermore, we investigated the effects and mechanism of action of agonist peptides targeting adiponectin receptors in vitro and in vivo. We found that adiponectin pathway activity was significantly reduced in a subset of SSc skin biopsies. Mice lacking adiponectin mounted an exaggerated dermal fibrotic response, while transgenic mice with constitutively elevated adiponectin showed selective dWAT expansion and protection from skin and peritoneal fibrosis. Adiponectin receptor agonists abrogated ex vivo fibrotic responses in explanted normal and SSc fibroblasts and in 3D human skin equivalents, in part by attenuating focal adhesion complex assembly, and prevented and reversed experimentally-induced organ fibrosis in mice. These results implicate aberrant adiponectin pathway activity in skin fibrosis, identifying a novel function for this pleiotropic adipokine in regulation of tissue remodeling. Restoring adiponectin signaling in SSc patients therefore might represent an innovative pharmacological strategy for intractable organ fibrosis.

Indexed as

AdiponectinAnimalsBiopsyDisease Models, AnimalFibroblastsFibrosisFluorescent Antibody TechniqueHumansMiceMice, KnockoutMice, TransgenicOligopeptidesReceptors, AdiponectinScleroderma, SystemicSignal TransductionSkinAdiponectinasparaginyl-isoleucyl-prolyl-norvalyl-leucyl-tyrosyl-seryl-phenylalanyl-alanyl-serinamideOligopeptidesReceptors, Adiponectin

Identifiers

PMID28667272
PMCPMC5493638
OpenAlexW2716775171

What OpenQuestion holds

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LicenceCC BY
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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.