Evidence map›Paper›PMID 26549358›Full record

ArticleJournal of molecular and cellular cardiology2015

Connective tissue growth factor regulates cardiac function and tissue remodeling in a mouse model of dilated cardiomyopathy.

Yevgeniya E Koshman, Mark D Sternlicht, Taehoon Kim, Christopher P O'Hara, Christopher A Koczor, William Lewis, Todd W Seeley, Kenneth E Lipson, Allen M Samarel

Open access · greenAbstract read
In one paragraph

Article in Journal of molecular and cellular cardiology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

19 citing papers in PubMed, 33 citations in OpenAlex.

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  7. NORAD lentivirus shRNA mitigates fibrosis and inflammatory responses in diabetic cardiomyopathy via the ceRNA network of NORAD/miR-125a-3p/Fyn.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2021
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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

9 authors at 3 institutions in 1 country.

Yevgeniya E KoshmanThe Cardiovascular Research Institute, Loyola University Chicago Stritch School of Medicine, Maywood, IL 60153, United States.
Mark D SternlichtFibroGen, Inc., San Francisco, CA 94158, United States.
Taehoon KimThe Cardiovascular Research Institute, Loyola University Chicago Stritch School of Medicine, Maywood, IL 60153, United States.
Christopher P O'HaraThe Cardiovascular Research Institute, Loyola University Chicago Stritch School of Medicine, Maywood, IL 60153, United States.
Christopher A KoczorDepartment of Pathology, Emory University School of Medicine, Atlanta, GA 30322, United States.
William LewisDepartment of Pathology, Emory University School of Medicine, Atlanta, GA 30322, United States.
Todd W SeeleyFibroGen, Inc., San Francisco, CA 94158, United States.
Kenneth E LipsonFibroGen, Inc., San Francisco, CA 94158, United States.
Allen M SamarelThe Cardiovascular Research Institute, Loyola University Chicago Stritch School of Medicine, Maywood, IL 60153, United States. Electronic address: asamare@luc.edu.
FibroGen (United States) · USLoyola University Chicago · USEmory University · US

Funding

Sarcomeric Modifications and Progressive Cardiac MaladaptationP01HL062426 · NHLBI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI DE TOMBE, PIETER P. · 2000 to 2020
$42.4M
Cocaine HIV/AIDS, and AntiretroviralsR01DA030996 · NIDA · EMORY UNIVERSITY · PI LEWIS, WILLIAM · 2010 to 2014
$4.4M
Novel Approaches in Treatment of Vascular Injury Following Balloon AngioplastyF32HL096143 · NHLBI · LOYOLA UNIVERSITY CHICAGO · PI KOSHMAN, YEVGENIYA EMRE · 2010 to 2013
$128k
NHLBI NIH HHS 1F32 HL096143NHLBI NIH HHS F32 HL096143NHLBI NIH HHS P01 HL062426NHLBI NIH HHS P01 HL62426NIDA NIH HHS R01 DA-030996NIDA NIH HHS R01 DA030996
6 · The paper itself

Abstract

Cardiac structural changes associated with dilated cardiomyopathy (DCM) include cardiomyocyte hypertrophy and myocardial fibrosis. Connective tissue growth factor (CTGF) has been associated with tissue remodeling and is highly expressed in failing hearts. Our aim was to test if inhibition of CTGF would alter the course of cardiac remodeling and preserve cardiac function in the protein kinase Cε (PKCε) mouse model of DCM. Transgenic mice expressing constitutively active PKCε in cardiomyocytes develop cardiac dysfunction that was evident by 3 months of age, and that progressed to cardiac fibrosis, heart failure, and increased mortality. Beginning at 3 months of age, PKCε mice were treated with a neutralizing monoclonal antibody to CTGF (FG-3149) for an additional 3 months. CTGF inhibition significantly improved left ventricular (LV) systolic and diastolic functions in PKCε mice, and slowed the progression of LV dilatation. Using gene arrays and quantitative PCR, the expression of many genes associated with tissue remodeling was elevated in PKCε mice, but significantly decreased by CTGF inhibition. However total collagen deposition was not attenuated. The observation of significantly improved LV function by CTGF inhibition in PKCε mice suggests that CTGF inhibition may benefit patients with DCM. Additional studies to explore this potential are warranted.

Indexed as

Ventricular Function, LeftVentricular RemodelingAgingAnimalsAntibodies, NeutralizingCardiomyopathy, DilatedCollagenConnective Tissue Growth FactorDiastoleDisease Models, AnimalDisease ProgressionExtracellular MatrixFibrosisGene Expression ProfilingMice, TransgenicMyocardiumAntibodies, NeutralizingCollagenConnective Tissue Growth FactorProtein Kinase C-epsilonGene arrayHeart failureQuantitative PCRRemodeling

Identifiers

PMID26549358
PMCPMC4689630
OpenAlexW2123706159

What OpenQuestion holds

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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.