Evidence map›Paper›PMID 27241177›Full record

ArticleJournal of cell communication and signaling2016

Emerging roles of CCN proteins in vascular development and pathology.

Philip A Klenotic, Chao Zhang, Zhiyong Lin

Open access · bronzeAbstract read
In one paragraph

Article in Journal of cell communication and signaling, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.7field-weighted citation impact, top 15% 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

17 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. CCN proteins: opportunities for clinical studies-a personal perspective.Journal of cell communication and signaling · 2023
    Review
  5. Article
  6. Matricellular proteins in atherosclerosis development.Matrix biology : journal of the International Society for Matrix Biology · 2023
    Review
  7. Article
  8. Expression of Cyr61 in ApoEScientific reports · 2021
    Article
  9. Article
  10. Article
  11. Article
  12. Observational
  13. Article
  14. CCN5/WISP2 and metabolic diseases.Journal of cell communication and signaling · 2018
    Review
  15. Article
  16. Review
  17. Extracellular Matrix, a Hard Player in Angiogenesis.International journal of molecular sciences · 2016
    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

3 authors at 3 institutions in 2 countries.

Philip A KlenoticCase Cardiovascular Research Institute, Case Western Reserve University School of Medicine, Harrington Heart and Vascular Institute, University Hospitals Case Medical Center, 2103 Cornell Road, Room 4-541, Cleveland, OH, 44106, USA.
Chao ZhangCase Cardiovascular Research Institute, Case Western Reserve University School of Medicine, Harrington Heart and Vascular Institute, University Hospitals Case Medical Center, 2103 Cornell Road, Room 4-541, Cleveland, OH, 44106, USA.
Zhiyong LinCase Cardiovascular Research Institute, Case Western Reserve University School of Medicine, Harrington Heart and Vascular Institute, University Hospitals Case Medical Center, 2103 Cornell Road, Room 4-541, Cleveland, OH, 44106, USA. Zhiyong.lin@case.edu.
Case Western Reserve University · USCornell University · USUniversity Hospitals Case Medical Center · US

Funding

CCN3 and Aortic AneurysmR01HL117759 · NHLBI · EMORY UNIVERSITY · PI LIN, ZHIYONG · 2013 to 2017
$1.9M
KLF15 and circadian regulation of alcohol-induced liver injuryR01AA021390 · NIAAA · EMORY UNIVERSITY · PI LIN, ZHIYONG · 2014 to 2018
$1.8M
NHLBI NIH HHS R01 HL117759NIAAA NIH HHS R01 AA021390
6 · The paper itself

Abstract

The CCN family of proteins consists of 6 members (CCN1-CCN6) that share conserved functional domains. These matricellular proteins interact with growth factors, extracellular matrix (ECM) proteins, cell surface integrins and other receptors to promote ECM-intracellular signaling. This signaling leads to propagation of a variety of cellular actions, including adhesion, invasion, migration and proliferation within several cell types, including epithelial, endothelial and smooth muscle cells. Though CCNs share significant homology, the function of each is unique due to distinct and cell specific expression patterns. Thus, their correct spatial and temporal expressions are critical during embryonic development, wound healing, angiogenesis and fibrosis. Disruption of these patterns leads to severe development disorders and contributes to the pathological progression of cancers, vascular diseases and chronic inflammatory diseases such as colitis, rheumatoid arthritis and atherosclerosis. While the effects of CCNs are diverse, this review will focus on the role of CCNs within the vasculature during development and in vascular diseases.

Indexed as

CCNVascular

Identifiers

PMID27241177
PMCPMC5055495
OpenAlexW2419428126

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.