Evidence map›Paper›PMID 29255421›Full record

ArticleFrontiers in physiology2017

Comparative Analysis of Muscle Hypertrophy Models Reveals Divergent Gene Transcription Profiles and Points to Translational Regulation of Muscle Growth through Increased mTOR Signaling.

Marcelo G Pereira, Kenneth A Dyar, Leonardo Nogara, Francesca Solagna, Manuela Marabita, Martina Baraldo, Francesco Chemello, Elena Germinario, Vanina Romanello, Hendrik Nolte and 1 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in physiology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.1field-weighted citation impact, top 22% 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

15 citing papers in PubMed, 23 citations in OpenAlex.

  1. Trial
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  3. Dietary Fermentation withInternational journal of molecular sciences · 2025
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  10. Molecular Mechanisms of Skeletal Muscle Hypertrophy.Journal of neuromuscular diseases · 2021
    Review
  11. Article
  12. Article
  13. Skeletal muscle mTORC1 regulates neuromuscular junction stability.Journal of cachexia, sarcopenia and muscle · 2020
    Article
  14. Article
  15. 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

11 authors at 4 institutions in 2 countries.

Marcelo G PereiraVenetian Institute of Molecular Medicine, Padova, Italy.
Kenneth A DyarVenetian Institute of Molecular Medicine, Padova, Italy.
Leonardo NogaraVenetian Institute of Molecular Medicine, Padova, Italy.
Francesca SolagnaVenetian Institute of Molecular Medicine, Padova, Italy.
Manuela MarabitaVenetian Institute of Molecular Medicine, Padova, Italy.
Martina BaraldoVenetian Institute of Molecular Medicine, Padova, Italy.
Francesco ChemelloDepartment of Biology, University of Padova, Padova, Italy.
Elena GerminarioDepartment of Biomedical Sciences, University of Padova, Padova, Italy.
Vanina RomanelloVenetian Institute of Molecular Medicine, Padova, Italy.
Hendrik NolteInstitute for Genetics, Cologne Excellence Cluster on Cellular Stress Responses in Aging-Associated Diseases, University of Cologne, Cologne, Germany.
Bert BlaauwVenetian Institute of Molecular Medicine, Padova, Italy.
Veneto Institute of Molecular Medicine · ITUniversity of Padua · ITCologne Excellence Cluster on Cellular Stress Responses in Aging Associated Diseases · DEGerman Center for Diabetes Research · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Skeletal muscle mass is a result of the balance between protein breakdown and protein synthesis. It has been shown that multiple conditions of muscle atrophy are characterized by the common regulation of a specific set of genes, termed atrogenes. It is not known whether various models of muscle hypertrophy are similarly regulated by a common transcriptional program. Here, we characterized gene expression changes in three different conditions of muscle growth, examining each condition during acute and chronic phases. Specifically, we compared the transcriptome of Extensor Digitorum Longus (EDL) muscles collected (1) during the rapid phase of postnatal growth at 2 and 4 weeks of age, (2) 24 h or 3 weeks after constitutive activation of AKT, and (3) 24 h or 3 weeks after overload hypertrophy caused by tenotomy of the Tibialis Anterior muscle. We observed an important overlap between significantly regulated genes when comparing each single condition at the two different timepoints. Furthermore, examining the transcriptional changes occurring 24 h after a hypertrophic stimulus, we identify an important role for genes linked to a stress response, despite the absence of muscle damage in the AKT model. However, when we compared all different growth conditions, we did not find a common transcriptional fingerprint. On the other hand, all conditions showed a marked increase in mTORC1 signaling and increased ribosome biogenesis, suggesting that muscle growth is characterized more by translational, than transcriptional regulation.

Indexed as

Akthypertrophyimmediate early genesmTORC1overloadpostnatal growthribosome biogenesisskeletal muscle

Identifiers

PMID29255421
PMCPMC5723052
OpenAlexW2773927993

What OpenQuestion holds

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Registered trials

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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.