Evidence map›Paper›PMID 17130448›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2006

Angiopoietin-like 4 prevents metastasis through inhibition of vascular permeability and tumor cell motility and invasiveness.

Ariane Galaup, Aurelie Cazes, Sebastien Le Jan, Josette Philippe, Elisabeth Connault, Emmanuelle Le Coz, Halima Mekid, Lluis M Mir, Paule Opolon, Pierre Corvol and 2 more

Registry-linked trialOpen access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05214885 (Novel Biomarkers of Hypoxia and Metabolism in Clear Cell Renal Cell Carcinoma), which is not on this map. Cited by 138 papers.

0numbers the graph read from it
0cells of the map it votes in
138citing papers in PubMed
7.0field-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.

NCT05214885 recruitingnot on this mapstarted 2022, after this paper: background citation

Novel Biomarkers of Hypoxia and Metabolism in Clear Cell Renal Cell Carcinoma

TypeobservationalSponsorQianfoshan HospitalRan2022 to 2026Enrolled300ConditionsClear Cell Renal Cell CarcinomaArmsNo intervention was required for patients or control group in this study
3 · Its place in the literature

Who cites it

138 citing papers in PubMed, 250 citations in OpenAlex.

  1. Trial
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  11. Research (Washington, D.C.) · 2024
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  15. Primary tumor-derived systemic nANGPTL4 inhibits metastasis.The Journal of experimental medicine · 2023
    Article
  16. Article
  17. Article
  18. Review
  19. Review
  20. Article

78 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 4 institutions in 1 country.

Ariane GalaupInstitut National de la Santé et de la Recherche Médicale, Unit 36, 11 Place Marcelin Berthelot, 75005 Paris, France.
Aurelie Cazes
Sebastien Le Jan
Josette Philippe
Elisabeth Connault
Emmanuelle Le Coz
Halima Mekid
Lluis M Mir
Paule Opolon
Pierre Corvol
Catherine Monnot
Stephane Germain
Inserm · FRCentre National de la Recherche Scientifique · FRCollège de France · FRHôpital Européen Georges-Pompidou · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Angiopoietin-like 4 (ANGPTL4), a secreted protein of the angiopoietin-like family, is induced by hypoxia in both tumor and endothelial cells as well as in hypoxic perinecrotic areas of numerous cancers. Here, we investigated whether ANGPTL4 might affect tumor growth as well as metastasis. Metastatic 3LL cells were therefore xenografted into control mice and mice in which ANGPTL4 was expressed by using in vivo DNA electrotransfer. Whereas primary tumors grew at a similar rate in both groups, 3LL cells metastasized less efficiently to the lungs of mice that expressed ANGPTL4. Fewer 3LL emboli were observed in primary tumors, suggesting that intravasation of 3LL cells was inhibited by ANGPTL4. Furthermore, melanoma B16F0 cells injected into the retro-orbital sinus also metastasized less efficiently in mice expressing ANGPTL4. Although B16F0 cells were observed in lung vessels, they rarely invaded the parenchyma, suggesting that ANGPTL4 affects extravasation. In addition, recombinant B16F0 cells that overexpress ANGPTL4 were generated, showing a lower capacity for in vitro migration, invasion, and adhesion than control cells. Expression of ANGPTL4 induced reorganization of the actin cytoskeleton through inhibition of actin stress fiber formation and vinculin localization at focal contacts. Together, these results show that ANGPTL4, through its action on both vascular and tumor compartments, prevents the metastatic process by inhibiting vascular activity as well as tumor cell motility and invasiveness.

Indexed as

Angiopoietin-Like Protein 4AngiopoietinsAnimalsCapillary PermeabilityCarcinoma, Lewis LungCell Line, TumorCell MovementFemaleHumansIntercellular Signaling Peptides and ProteinsLung NeoplasmsLymphatic MetastasisLymph NodesLymphopoiesisMelanoma, ExperimentalMiceAngiopoietin-Like Protein 4AngiopoietinsANGPTL4 protein, humanIntercellular Signaling Peptides and Proteins

Identifiers

PMID17130448
PMCPMC1693729
OpenAlexW2066750311

What OpenQuestion holds

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Read underepoch 390

Registered trials

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.