Evidence map›Paper›PMID 28164169›Full record

ArticleJACC. Basic to translational science2016

Adeno-associated Virus Serotype 9 - Driven Expression of BAG3 Improves Left Ventricular Function in Murine Hearts with Left Ventricular Dysfunction Secondary to a Myocardial Infarction.

Tijana Knezevic, Valerie D Myers, Feifei Su, JuFang Wang, Jianliang Song, Xue-Qian Zhang, Erhe Gao, Guofeng Gao, Madesh Muniswamy, Manish K Gupta and 8 more

Open access · goldAbstract read
In one paragraph

Article in JACC. Basic to translational science, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
3.1field-weighted citation impact, top 7% 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

32 citing papers in PubMed, 51 citations in OpenAlex.

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  6. Reply: Macrophage Activation in Systemic Sclerosis.JACC. Basic to translational science · 2025
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  11. Using Omics to Identify Novel Therapeutic Targets in Heart Failure.Circulation. Genomic and precision medicine · 2024
    Review
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  13. Cryptotanshinone Attenuated Pathological Cardiac RemodelingOxidative medicine and cellular longevity · 2023
    Article
  14. Review
  15. Review
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  20. Review
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

18 authors at 1 institution in 2 countries.

Tijana KnezevicDepartment of Biology, College of Science and Technology, Temple University, Philadelphia, Pennslyvnaia; Department of Neuroscience, the Lewis Katz School of Medicine at Temple University, Philadelphia, Pennsylvania.
Valerie D MyersDepartment of Medicine, the Lewis Katz School of Medicine at Temple University, Philadelphia, Pennsylvania.
Feifei SuDepartment of Medicine, the Lewis Katz School of Medicine at Temple University, Philadelphia, Pennsylvania; Department of Cardiology, TangDu Hospital, Fourth Military Medical University, Xi'an, China.
JuFang WangCenter for Translational Medicine, the Lewis Katz School of Medicine at Temple University, Philadelphia, Pennsylvania.
Jianliang SongCenter for Translational Medicine, the Lewis Katz School of Medicine at Temple University, Philadelphia, Pennsylvania.
Xue-Qian ZhangCenter for Translational Medicine, the Lewis Katz School of Medicine at Temple University, Philadelphia, Pennsylvania.
Erhe GaoCenter for Translational Medicine, the Lewis Katz School of Medicine at Temple University, Philadelphia, Pennsylvania.
Guofeng GaoDepartment of Medicine, the Lewis Katz School of Medicine at Temple University, Philadelphia, Pennsylvania.
Madesh MuniswamyCenter for Translational Medicine, the Lewis Katz School of Medicine at Temple University, Philadelphia, Pennsylvania.
Manish K GuptaDepartment of Neuroscience, the Lewis Katz School of Medicine at Temple University, Philadelphia, Pennsylvania.
Jennifer GordonDepartment of Neuroscience, the Lewis Katz School of Medicine at Temple University, Philadelphia, Pennsylvania.
Kristen N WeinerDepartment of Medicine, the Lewis Katz School of Medicine at Temple University, Philadelphia, Pennsylvania.
Joseph RabinowitzCenter for Translational Medicine, the Lewis Katz School of Medicine at Temple University, Philadelphia, Pennsylvania.
Frederick V RamseyDepartment of Biology, College of Science and Technology, Temple University, Philadelphia, Pennslyvnaia.
Douglas G TilleyCenter for Translational Medicine, the Lewis Katz School of Medicine at Temple University, Philadelphia, Pennsylvania.
Kamel KhaliliDepartment of Neuroscience, the Lewis Katz School of Medicine at Temple University, Philadelphia, Pennsylvania.
Joseph Y CheungDepartment of Medicine, the Lewis Katz School of Medicine at Temple University, Philadelphia, Pennsylvania; Center for Translational Medicine, the Lewis Katz School of Medicine at Temple University, Philadelphia, Pennsylvania.
Arthur M FeldmanDepartment of Medicine, the Lewis Katz School of Medicine at Temple University, Philadelphia, Pennsylvania.
Temple University · US

Funding

Targeted Cancer Therapeutics and Heart Failure: Mechanisms and Post-injury RepairP01HL091799 · NHLBI · THOMAS JEFFERSON UNIVERSITY · PI KOCH, WALTER J. · 2008 to 2018
$23.1M
Involvement of BAG3 in HIV-1 induced cardiomyopathyR01HL123093 · NHLBI · TEMPLE UNIV OF THE COMMONWEALTH · PI CHEUNG, JOSEPH Y, FELDMAN, ARTHUR M · 2014 to 2018
$3.7M
NHLBI NIH HHS P01 HL091799NHLBI NIH HHS R01 HL123093
6 · The paper itself

Abstract

objectivesThe present study was undertaken to test the hypothesis that gene delivery of BCL2-Associated Athanogene 3 (BAG3) to the heart of mice with left ventricular dysfunction secondary to a myocardial infarction could enhance cardiac performance.

backgroundBAG3 is a 575 amino acid protein that has pleotropic functions in the cell including pro-autophagy and anti-apoptosis. Mutations in BAG3 have been associated with both skeletal muscle dysfunction and familial dilated cardiomyopathy and BAG3 levels are diminished in non-familial heart failure.

methodsEight-week-old C57/BL6 mice underwent ligation of the left coronary artery (MI) or sham surgery (Sham). Eight weeks later, mice in both groups were randomly assigned to receive either a retro-orbital injection of rAAV9-BAG3 (MI-BAG3 or Sham-BAG3) or rAAV9-GFP (MI-GFP or Sham GFP). Mice were sacrificed at 3 weeks post-injection and myocytes were isolated from the left ventricle.

resultsMI-BAG3 mice demonstrated a significantly (p < 0.0001) higher left ventricular ejection fraction (LVEF) 9 days after rAAV9-BAG3 injection with further improvement in LVEF, fractional shortening and stroke volume at 3 weeks post-injection without changes in LV mass or LV volume. Injection of rAAV9-BAG3 had no effect on LVEF in Sham mice. The salutary benefits of rAAV9-BAG3 were also observed in myocytes isolated from MI hearts including improved cell shortening (p<0.05), increased systolic [Ca IMPLICATIONS: The results suggest that BAG3 gene therapy may provide a novel therapeutic option for the treatment of heart failure.

Identifiers

PMID28164169
PMCPMC5289821
OpenAlexW2562330537

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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 Socratic graph.