Evidence map›Paper›PMID 23580199›Full record

ArticleDisease models & mechanisms2013

Raf-mediated cardiac hypertrophy in adult Drosophila.

Lin Yu, Joseph Daniels, Alex E Glaser, Matthew J Wolf

Open access · goldAbstract read
In one paragraph

Article in Disease models & mechanisms, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

29 citing papers in PubMed, 38 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. AlkCell communication and signaling : CCS · 2025
    Article
  5. Review
  6. Molecular mechanism on autophagy associated cardiovascular dysfunction inFrontiers in cell and developmental biology · 2025
    Review
  7. Attention LSTM U-Net model forBiomedical optics express · 2024
    Article
  8. Article
  9. The opportunities and challenges of usingFrontiers in physiology · 2023
    Article
  10. Article
  11. Article
  12. Review
  13. Analysis ofAmerican journal of physiology. Heart and circulatory physiology · 2022
    Article
  14. Article
  15. Communal living: the role of polyploidy and syncytia in tissue biology.Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology · 2021
    Review
  16. Article
  17. Review
  18. Article
  19. Aging and the clock: Perspective from flies to humans.The European journal of neuroscience · 2020
    Review
  20. As time flies by: Investigating cardiac aging in the short-lived Drosophila model.Biochimica et biophysica acta. Molecular basis of disease · 2019
    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

4 authors at 3 institutions in 1 country.

Lin YuDuke University Medical Center, 321 Sands Building, Research Drive, Durham, NC 27710, USA.
Joseph Daniels
Alex E Glaser
Matthew J Wolf
Duke University Hospital · USDuke Medical Center · USDuke University · US

Funding

Drosophila Transgenic RNAi Resource ProjectR01GM084947 · NIGMS · HARVARD MEDICAL SCHOOL · PI PERRIMON, NORBERT · 2008 to 2019
$9.8M
Novel pathways modulating Raf-mediated cardiac hypertrophyR01HL116581 · NHLBI · UNIVERSITY OF VIRGINIA · PI WOLF, MATTHEW J · 2013 to 2017
$2.0M
NHLBI NIH HHS R01 HL116581NHLBI NIH HHS R01HL116581NIGMS NIH HHS R01 GM084947
6 · The paper itself

Abstract

In response to stress and extracellular signals, the heart undergoes a process called cardiac hypertrophy during which cardiomyocytes increase in size. If untreated, cardiac hypertrophy can progress to overt heart failure that causes significant morbidity and mortality. The identification of molecular signals that cause or modify cardiomyopathies is necessary to understand how the normal heart progresses to cardiac hypertrophy and heart failure. Receptor tyrosine kinase (RTK) signaling is essential for normal human cardiac function, and the inhibition of RTKs can cause dilated cardiomyopathies. However, neither investigations of activated RTK signaling pathways nor the characterization of hypertrophic cardiomyopathy in the adult fly heart has been previously described. Therefore, we developed strategies using Drosophila as a model to circumvent some of the complexities associated with mammalian models of cardiovascular disease. Transgenes encoding activated EGFR(A887T), Ras85D(V12) and Ras85D(V12S35), which preferentially signal to Raf, or constitutively active human or fly Raf caused hypertrophic cardiomyopathy as determined by decreased end diastolic lumen dimensions, abnormal cardiomyocyte fiber morphology and increased heart wall thicknesses. There were no changes in cardiomyocyte cell numbers. Additionally, activated Raf also induced an increase in cardiomyocyte ploidy compared with control hearts. However, preventing increases in cardiomyocyte ploidy using fizzy-related (Fzr) RNAi did not rescue Raf-mediated cardiac hypertrophy, suggesting that Raf-mediated polyploidization is not required for cardiac hypertrophy. Similar to mammals, the cardiac-specific expression of RNAi directed against MEK or ERK rescued Raf-mediated cardiac hypertrophy. However, the cardiac-specific expression of activated ERK(D334N), which promotes hyperplasia in non-cardiac tissues, did not cause myocyte hypertrophy. These results suggest that ERK is necessary, but not sufficient, for Raf-mediated cardiac hypertrophy.

Indexed as

AgingAnimalsCardiomegalyDrosophila melanogasterDrosophila ProteinsErbB ReceptorsExtracellular Signal-Regulated MAP KinasesHumansMitogen-Activated Protein Kinase KinasesModels, BiologicalMutant ProteinsMyocytes, CardiacOrgan SpecificityPloidiesProto-Oncogene Proteins c-rafras ProteinsDrosophila ProteinsErbB ReceptorsExtracellular Signal-Regulated MAP KinasesMitogen-Activated Protein Kinase KinasesMutant ProteinsProto-Oncogene Proteins c-rafRaf protein, Drosophilaras Proteins

Identifiers

PMID23580199
PMCPMC3701216
OpenAlexW2141725769

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.