Evidence map›Paper›PMID 16275757›Full record

ArticleThe Journal of cell biology2005

The matrix protein CCN1 (CYR61) induces apoptosis in fibroblasts.

Viktor Todorovic, Chih-Chiun Chen, Nissim Hay, Lester F Lau

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of cell biology, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 58 papers.

0numbers the graph read from it
0cells of the map it votes in
58citing papers in PubMed
3.3field-weighted citation impact, top 8% 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

58 citing papers in PubMed, 129 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Matricellular protein CCN1 promotes collagen alignment and scar integrity after myocardial infarction.Matrix biology : journal of the International Society for Matrix Biology · 2024
    Article
  5. Article
  6. Matricellular proteins in atherosclerosis development.Matrix biology : journal of the International Society for Matrix Biology · 2023
    Review
  7. Structural insights into regulation of CCN protein activities and functions.Journal of cell communication and signaling · 2023
    Review
  8. Article
  9. Article
  10. Article
  11. Review
  12. The Roles of CCN1/CYR61 in Pulmonary Diseases.International journal of molecular sciences · 2020
    Review
  13. Review
  14. Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. Cell surface receptors for CCN proteins.Journal of cell communication and signaling · 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

4 authors at 1 institution in 1 country.

Viktor TodorovicDepartment of Biochemistry and Molecular Genetics, University of Illinois at Chicago College of Medicine, Chicago, IL 60607, USA.
Chih-Chiun Chen
Nissim Hay
Lester F Lau
University of Illinois Chicago · US

Funding

The Role of Akt in Cell Survival and Cell GrowthR01AG016927 · NIA · UNIVERSITY OF ILLINOIS AT CHICAGO · PI HAY, NISSIM · 1998 to 2023
$9.0M
Structure and Function of the Matricellular Protein CCN1R01CA046565 · NCI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI LAU, LESTER F · 1988 to 2008
$3.0M
NCI NIH HHS CA46565NCI NIH HHS R01 CA046565NIA NIH HHS AG016927NIA NIH HHS R01 AG016927
6 · The paper itself

Abstract

Integrin-mediated cell adhesion to extracellular matrix proteins is known to promote cell survival, whereas detachment from the matrix can cause rapid apoptotic death in some cell types. Contrary to this paradigm, we show that fibroblast adhesion to the angiogenic matrix protein CCN1 (CYR61) induces apoptosis, whereas endothelial cell adhesion to CCN1 promotes cell survival. CCN1 induces fibroblast apoptosis through its adhesion receptors, integrin alpha6beta1 and the heparan sulfate proteoglycan (HSPG) syndecan-4, triggering the transcription-independent p53 activation of Bax to render cytochrome c release and activation of caspase-9 and -3. Neither caspase-8 activity nor de novo transcription or translation is required for this process. These results show that cellular interaction with a specific matrix protein can either induce or suppress apoptosis in a cell type-specific manner and that integrin alpha6beta1-HSPGs can function as receptors to induce p53-dependent apoptosis.

Indexed as

AnimalsApoptosisCaspasesCells, CulturedCell SurvivalCysteine-Rich Protein 61Endothelial CellsFibroblastsHumansImmediate-Early ProteinsIntegrin alpha6beta1Intercellular Signaling Peptides and ProteinsMembrane GlycoproteinsProtein BiosynthesisProteoglycansRatsCaspasesCCN1 protein, humanCysteine-Rich Protein 61Immediate-Early ProteinsIntegrin alpha6beta1Intercellular Signaling Peptides and ProteinsMembrane GlycoproteinsProteoglycansSDC4 protein, humanSdc4 protein, ratSyndecan-4Tumor Suppressor Protein p53

Identifiers

PMID16275757
PMCPMC1626352
OpenAlexW2100093802

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.