Evidence map›Paper›PMID 24572787›Full record

ArticleGene therapy2014

Sonic hedgehog gene therapy increases the ability of the dystrophic skeletal muscle to regenerate after injury.

A Piccioni, E Gaetani, M Palladino, I Gatto, R C Smith, V Neri, M Marcantoni, I Giarretta, M Silver, S Straino and 3 more

Open access · bronzeAbstract read
PubMed Publisher
In one paragraph

Article in Gene therapy, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

14 citing papers in PubMed, 37 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Sonic hedgehog is expressed in human brain arteriovenous malformations and induces arteriovenous malformations in vivo.Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism · 2021
    Article
  7. Review
  8. Treatment of DystrophicBiomolecules · 2020
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. 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

13 authors at 4 institutions in 2 countries.

A Piccioni1] Department of Medicine, A. Gemelli University Hospital, Catholic University School of Medicine, Rome, Italy [2] Division of Cardiovascular Research, Steward St. Elizabeth's Medical Center, Tufts University School of Medicine, Boston, MA, USA.
E GaetaniDepartment of Medicine, A. Gemelli University Hospital, Catholic University School of Medicine, Rome, Italy.
M Palladino1] Department of Medicine, A. Gemelli University Hospital, Catholic University School of Medicine, Rome, Italy [2] Division of Cardiovascular Research, Steward St. Elizabeth's Medical Center, Tufts University School of Medicine, Boston, MA, USA.
I GattoDepartment of Medicine, A. Gemelli University Hospital, Catholic University School of Medicine, Rome, Italy.
R C SmithDivision of Cardiovascular Research, Steward St. Elizabeth's Medical Center, Tufts University School of Medicine, Boston, MA, USA.
V Neri1] Department of Medicine, A. Gemelli University Hospital, Catholic University School of Medicine, Rome, Italy [2] Division of Cardiovascular Research, Steward St. Elizabeth's Medical Center, Tufts University School of Medicine, Boston, MA, USA.
M MarcantoniDepartment of Medicine, A. Gemelli University Hospital, Catholic University School of Medicine, Rome, Italy.
I GiarrettaDepartment of Medicine, A. Gemelli University Hospital, Catholic University School of Medicine, Rome, Italy.
M SilverDivision of Cardiovascular Research, Steward St. Elizabeth's Medical Center, Tufts University School of Medicine, Boston, MA, USA.
S Straino1] Laboratory of Vascular Pathology, IDI IRCCS Research Institute, Rome, Italy [2] Explora Biotech, srl, Rome, Italy.
M CapogrossiLaboratory of Vascular Pathology, IDI IRCCS Research Institute, Rome, Italy.
R LandolfiDepartment of Medicine, A. Gemelli University Hospital, Catholic University School of Medicine, Rome, Italy.
R Pola1] Department of Medicine, A. Gemelli University Hospital, Catholic University School of Medicine, Rome, Italy [2] Division of Cardiovascular Research, Steward St. Elizabeth's Medical Center, Tufts University School of Medicine, Boston, MA, USA.
Agostino Gemelli University Polyclinic · ITIstituti di Ricovero e Cura a Carattere Scientifico · ITSt. Elizabeth's Medical Center · USTufts University · US

Funding

Sonic Muscle RegenerationR21HL089684 · NHLBI · STEWARD ST. ELIZABETH'S MEDICAL CENTER · PI POLA, ROBERTO · 2008 to 2009
$440k
NHLBI NIH HHS 1R21HL089684NHLBI NIH HHS R21 HL089684
6 · The paper itself

Abstract

The Hedgehog (Hh) pathway is a crucial regulator of muscle development during embryogenesis. We have previously demonstrated that Sonic hedgehog (Shh) regulates postnatal myogenesis in the adult skeletal muscle both directly, by acting on muscle satellite cells, and indirectly, by promoting the production of growth factors from interstitial fibroblasts. Here, we show that in mdx mice, the murine equivalent of Duchenne muscular dystrophy in humans, progression of the dystrophic pathology corresponds to progressive inhibition of the Hh signaling pathway in the skeletal muscle. We also show that the upregulation of the Hh pathway in response to injury and during regeneration is significantly impaired in mdx muscle. Shh treatment increases the proliferative potential of satellite cells isolated from the muscles of mdx mice. This treatment also increases the production of proregenerative factors, such as insulin-like growth factor-1 and vascular endothelial growth factor, from fibroblasts isolated from the muscle of mdx mice. In vivo, overexpression of the Hh pathway using a plasmid encoding the human Shh gene promotes successful regeneration after injury in terms of increased number of proliferating myogenic cells and newly formed myofibers, as well as enhanced vascularization and decreased fibrosis.

Indexed as

Genetic TherapyAnimalsHedgehog ProteinsHumansMiceMice, Inbred mdxMuscle DevelopmentMuscle, SkeletalMuscular Dystrophy, DuchenneMyoblastsRegenerationVascular Endothelial Growth Factor AHedgehog ProteinsVascular Endothelial Growth Factor A

Identifiers

PMID24572787
OpenAlexW2070731425

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.