Evidence map›Paper›PMID 21866097›Full record

ReviewClinical pharmacology and therapeutics2011

Gene therapy targets in heart failure: the path to translation.

P W J Raake, H Tscheschner, J Reinkober, J Ritterhoff, H A Katus, W J Koch, P Most

Open access · greenAbstract readReview
In one paragraph

Review in Clinical pharmacology and therapeutics, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.7field-weighted citation impact, top 9% 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

11 citing papers in PubMed, 34 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Heart Failure: Diagnosis, Management and Utilization.Journal of clinical medicine · 2016
    Review
  5. Article
  6. Review
  7. Gene transfer for congestive heart failure: update 2013.Translational research : the journal of laboratory and clinical medicine · 2013
    Review
  8. Review
  9. Review
  10. Gene therapy for heart failure.Circulation research · 2012
    Review
  11. Article
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

7 authors at 2 institutions in 2 countries.

P W J RaakeDivision of Cardiology, Department of Internal Medicine III, University of Heidelberg, Heidelberg, Germany.
H Tscheschner
J Reinkober
J Ritterhoff
H A Katus
W J Koch
P Most
Heidelberg University · DEThomas Jefferson University · US

Funding

Regulation of Beta-Adrenergic Receptor Signaling by S-NitrosylationP01HL075443 · NHLBI · DUKE UNIVERSITY · PI STAMLER, JONATHAN S. · 2004 to 2019
$26.1M
Targeting GRK2 in the HeartR01HL061690 · NHLBI · THOMAS JEFFERSON UNIVERSITY · PI KOCH, WALTER J. · 1998 to 2022
$4.2M
Gene Transfer and Myocardial FunctionR01HL056205 · NHLBI · THOMAS JEFFERSON UNIVERSITY · PI KOCH, WALTER J. · 1998 to 2008
$2.6M
S100A1: A Novel Modulator of Myocardial Infarct Inflammation and RegenerationR01HL092130 · NHLBI · THOMAS JEFFERSON UNIVERSITY · PI PEPPEL, KARSTEN · 2008 to 2012
$2.2M
NHLBI NIH HHS P01 HL075443NHLBI NIH HHS R01 HL056205NHLBI NIH HHS R01 HL061690NHLBI NIH HHS R01 HL092130NHLBI NIH HHS R01 HL56205NHLBI NIH HHS R01 HL61690NHLBI NIH HHS R01 HL92130NHLBI NIH HHS R01 HL92130-02 S1
6 · The paper itself

Abstract

Heart failure (HF) is the common end point of cardiac diseases. Despite the optimization of therapeutic strategies and the consequent overall reduction in HF-related mortality, the key underlying intracellular signal transduction abnormalities have not been addressed directly. In this regard, the gaps in modern HF therapy include derangement of β-adrenergic receptor (β-AR) signaling, Ca(2+) disbalances, cardiac myocyte death, diastolic dysfunction, and monogenetic cardiomyopathies. In this review we discuss the potential of gene therapy to fill these gaps and rectify abnormalities in intracellular signaling. We also examine current vector technology and currently available vector-delivery strategies, and we delineate promising gene therapy structures. Finally, we analyze potential limitations related to the transfer of successful preclinical gene therapy approaches to HF treatment in the clinic, as well as impending strategies aimed at overcoming these limitations.

Indexed as

AnimalsClinical Trials as TopicGene TargetingGenetic TherapyHeart FailureHumansProtein BiosynthesisSignal Transduction

Identifiers

PMID21866097
PMCPMC4149909
OpenAlexW2009290143

What OpenQuestion holds

Textmetadata
LicenceTDM
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.