Evidence map›Paper›PMID 23781099›Full record

ArticleThe journals of gerontology. Series A, Biological sciences and medical sciences2014

Sonic hedgehog therapy in a mouse model of age-associated impairment of skeletal muscle regeneration.

Andrea Piccioni, Eleonora Gaetani, Valentina Neri, Ilaria Gatto, Mariangela Palladino, Marcy Silver, Roy C Smith, Igor Giarretta, Enrico Pola, Lynn Hlatky and 1 more

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in The journals of gerontology. Series A, Biological sciences and medical sciences, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.0field-weighted citation impact, top 23% 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

22 citing papers in PubMed, 40 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Skeletal Muscle Regeneration in Cardiotoxin-Induced Muscle Injury Models.International journal of molecular sciences · 2022
    Review
  7. Article
  8. Article
  9. Article
  10. Review
  11. The Hedgehog Signaling Pathway in Ischemic Tissues.International journal of molecular sciences · 2019
    Review
  12. An Endogenous Anti-aging Factor, Sonic Hedgehog, Suppresses Endometrial Stem Cell Aging through SERPINB2.Molecular therapy : the journal of the American Society of Gene Therapy · 2019
    Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Review
  19. Article
  20. Gene and cell therapy for muscle regeneration.Current reviews in musculoskeletal medicine · 2015
    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

11 authors at 2 institutions in 2 countries.

Andrea PiccioniCenter of Cancer Systems Biology, CBR4, St. Elizabeth's Medical Center, Tufts University School of Medicine, 736 Cambridge Street, Boston, MA 02135. rob_pola@hotmail.com.
Eleonora Gaetani
Valentina Neri
Ilaria Gatto
Mariangela Palladino
Marcy Silver
Roy C Smith
Igor Giarretta
Enrico Pola
Lynn Hlatky
Roberto Pola
Agostino Gemelli University Polyclinic · ITSt. Elizabeth's Medical Center · US

Funding

Sonic Muscle RegenerationR21HL089684 · NHLBI · STEWARD ST. ELIZABETH'S MEDICAL CENTER · PI POLA, ROBERTO · 2008 to 2009
$440k
NHLBI NIH HHS 1R21HL089684
6 · The paper itself

Abstract

Sonic hedgehog (Shh) is a morphogen regulating muscle development during embryogenesis. We have shown that the Shh pathway is postnatally recapitulated after injury and during regeneration of the adult skeletal muscle and regulates angiogenesis and myogenesis after muscle injury. Here, we demonstrate that in 18-month-old mice, there is a significant impairment of the upregulation of the Shh pathway that physiologically occurs in the young skeletal muscle after injury. Such impairment is even more pronounced in 24-month-old mice. In old animals, intramuscular therapy with a plasmid encoding the human Shh gene increases the regenerative capacities of the injured muscle, in terms of Myf5-positive cells, regenerating myofibers, and fibrosis. At the molecular level, Shh treatment increases the upregulation of the prototypical growth factors, insulin-like growth factor-1 and vascular endothelial growth factor. These data demonstrate that Shh increases regeneration after injury in the muscle of 24-month-old mice and suggest that the manipulation of the Shh pathway may be useful for the treatment of muscular diseases associated with aging.

Indexed as

AgingAnimalsCardiotoxinsDisease Models, AnimalFibrosisGenetic TherapyHedgehog ProteinsHumansInsulin-Like Growth Factor IIntercellular Signaling Peptides and ProteinsKruppel-Like Transcription FactorsMaleMiceMice, Inbred C57BLMice, Inbred StrainsMuscle DevelopmentCardiotoxinsGli1 protein, mouseHedgehog ProteinsInsulin-Like Growth Factor IIntercellular Signaling Peptides and ProteinsKruppel-Like Transcription FactorsMyf5 protein, mouseMyogenic Regulatory Factor 5SHH protein, humanVascular Endothelial Growth Factor Avascular endothelial growth factor A, mouseZinc Finger Protein GLI1Aging.Skeletal muscle regenerationSonic hedgehog

Identifiers

PMID23781099
PMCPMC3976139
OpenAlexW2146335442

What OpenQuestion holds

Textmetadata
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.