Evidence map›Paper›PMID 21748788›Full record

ArticleJournal of cellular biochemistry2011

Substance P signaling mediates BMP-dependent heterotopic ossification.

Lixin Kan, Vitali Y Lounev, Robert J Pignolo, Lishu Duan, Yijie Liu, Stuart R Stock, Tammy L McGuire, Bao Lu, Norma P Gerard, Eileen M Shore and 2 more

Open access · greenAbstract read
In one paragraph

Article in Journal of cellular biochemistry, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 69 papers.

0numbers the graph read from it
0cells of the map it votes in
69citing papers in PubMed
6.2field-weighted citation impact, top 3% 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

69 citing papers in PubMed, 110 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Article
  5. Review
  6. Article
  7. Review
  8. A microCT-based platform to quantify drug targeting.European radiology experimental · 2023
    Article
  9. Article
  10. Article
  11. Heterotopic mesenteric ossification: a report of two cases.Journal of pathology and translational medicine · 2022
    Article
  12. Review
  13. Review
  14. Review
  15. Review
  16. Article
  17. Do Interactions of Vitamin DCurrent osteoporosis reports · 2021
    Review
  18. Article
  19. Article
  20. Article

9 more citing papers are in PubMed but not listed here.

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

12 authors at 3 institutions in 1 country.

Lixin KanDepartment of Neurology, Northwestern University Feinberg Medical School, Chicago, Illinois 60611, USA. l-kan@northwestern.edu
Vitali Y Lounev
Robert J Pignolo
Lishu Duan
Yijie Liu
Stuart R Stock
Tammy L McGuire
Bao Lu
Norma P Gerard
Eileen M Shore
Frederick S Kaplan
John A Kessler
Northwestern University · USUniversity of Pennsylvania · USBoston Children's Hospital · US

Funding

Theranostic Magnetic Nanostructures for the Molecular Imaging of CancerU54CA151880 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI OMARY, REED A. · 2010 to 2014
$11.5M
REGULATION OF NEUROTRANSMITTER METABOLISMR01NS020778 · NINDS · YESHIVA UNIVERSITY · PI KESSLER, JOHN A · 1985 to 2014
$4.6M
MECHANISMS GOVERNING NEURONAL DEVELOPMENTR01NS020013 · NINDS · YESHIVA UNIVERSITY · PI KESSLER, JOHN A · 1985 to 2013
$4.1M
The Cellular and Molecular Basis of FOP LesionsR01AR041916 · NIAMS · UNIVERSITY OF PENNSYLVANIA · PI KAPLAN, FREDERICK SAMUEL, SHORE, EILEEN M · 1994 to 2014
$3.8M
NCI NIH HHS U54 CA151880NIAMS NIH HHS R01-AR041916NINDS NIH HHS NS20013NINDS NIH HHS NS20778NINDS NIH HHS R01 NS020013NINDS NIH HHS R01 NS020778
6 · The paper itself

Abstract

Heterotopic ossification (HO) is a disabling condition associated with neurologic injury, inflammation, and overactive bone morphogenetic protein (BMP) signaling. The inductive factors involved in lesion formation are unknown. We found that the expression of the neuro-inflammatory factor Substance P (SP) is dramatically increased in early lesional tissue in patients who have either fibrodysplasia ossificans progressiva (FOP) or acquired HO, and in three independent mouse models of HO. In Nse-BMP4, a mouse model of HO, robust HO forms in response to tissue injury; however, null mutations of the preprotachykinin (PPT) gene encoding SP prevent HO. Importantly, ablation of SP(+) sensory neurons, treatment with an antagonist of SP receptor NK1r, deletion of NK1r gene, or genetic down-regulation of NK1r-expressing mast cells also profoundly inhibit injury-induced HO. These observations establish a potent neuro-inflammatory induction and amplification circuit for BMP-dependent HO lesion formation, and identify novel molecular targets for prevention of HO.

Indexed as

AnimalsBone Morphogenetic Protein 4Bone Morphogenetic ProteinsFemaleHumansImmunohistochemistryIsoindolesMaleMiceMice, TransgenicMyositis OssificansNeurokinin-1 Receptor AntagonistsOssification, HeterotopicProtein PrecursorsReceptors, Neurokinin-1Sensory Receptor Cells7,7-diphenyl-2-(1-imino-2-(2-methoxyphenyl)ethyl)perhydroisoindol-4-oneBmp4 protein, mouseBone Morphogenetic Protein 4Bone Morphogenetic ProteinsIsoindolesNeurokinin-1 Receptor AntagonistspreprotachykininProtein PrecursorsReceptors, Neurokinin-1Substance PTachykinins

Identifiers

PMID21748788
PMCPMC3508732
OpenAlexW1974137634

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.