Evidence map›Paper›PMID 27069480›Full record

ReviewStem cells international2016

Vascular Remodelling and Mesenchymal Transition in Systemic Sclerosis.

Pier Andrea Nicolosi, Enrico Tombetti, Norma Maugeri, Patrizia Rovere-Querini, Silvia Brunelli, Angelo A Manfredi

Open access · goldAbstract readReview
In one paragraph

Review in Stem cells international, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
4.9field-weighted citation impact, top 5% 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

20 citing papers in PubMed, 38 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Review
  6. Endothelial-to-mesenchymal transition in systemic sclerosis.Clinical and experimental immunology · 2021
    Review
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  8. Review
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  10. Article
  11. Article
  12. Review
  13. Review
  14. Article
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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

6 authors at 2 institutions in 1 country.

Pier Andrea NicolosiSchool of Medicine and Surgery, University of Milano-Bicocca, 20900 Monza, Italy.
Enrico TombettiUnit of Medicine and Division of Immunology, Transplantation and Infectious Diseases, San Raffaele Scientific Institute and Vita-Salute San Raffaele University, 20132 Milano, Italy.
Norma MaugeriUnit of Medicine and Division of Immunology, Transplantation and Infectious Diseases, San Raffaele Scientific Institute and Vita-Salute San Raffaele University, 20132 Milano, Italy.
Patrizia Rovere-QueriniUnit of Medicine and Division of Immunology, Transplantation and Infectious Diseases, San Raffaele Scientific Institute and Vita-Salute San Raffaele University, 20132 Milano, Italy.
Silvia BrunelliSchool of Medicine and Surgery, University of Milano-Bicocca, 20900 Monza, Italy.
Angelo A ManfrediUnit of Medicine and Division of Immunology, Transplantation and Infectious Diseases, San Raffaele Scientific Institute and Vita-Salute San Raffaele University, 20132 Milano, Italy.
Vita-Salute San Raffaele University · ITUniversity of Milano-Bicocca · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Fibrosis of the skin and of internal organs, autoimmunity, and vascular inflammation are hallmarks of Systemic Sclerosis (SSc). The injury and activation of endothelial cells, with hyperplasia of the intima and eventual obliteration of the vascular lumen, are early features of SSc. Reduced capillary blood flow coupled with deficient angiogenesis leads to chronic hypoxia and tissue ischemia, enforcing a positive feed-forward loop sustaining vascular remodelling, further exacerbated by extracellular matrix accumulation due to fibrosis. Despite numerous developments and a growing number of controlled clinical trials no treatment has been shown so far to alter SSc natural history, outlining the need of further investigation in the molecular pathways involved in the pathogenesis of the disease. We review some processes potentially involved in SSc vasculopathy, with attention to the possible effect of sustained vascular inflammation on the plasticity of vascular cells. Specifically we focus on mesenchymal transition, a key phenomenon in the cardiac and vascular development as well as in the remodelling of injured vessels. Recent work supports the role of transforming growth factor-beta, Wnt, and Notch signaling in these processes. Importantly, endothelial-mesenchymal transition may be reversible, possibly offering novel cues for treatment.

Identifiers

PMID27069480
PMCPMC4812480
OpenAlexW2301510790

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.