Evidence map›Paper›PMID 20959825›Full record

ArticleBritish journal of cancer2010

Elastin-derived peptides enhance melanoma growth in vivo by upregulating the activation of Mcol-A (MMP-1) collagenase.

J Devy, L Duca, B Cantarelli, D Joseph-Pietras, A Scandolera, A Rusciani, L Parent, J Thevenard, S Brassart Pasco, M Tarpin and 2 more

Open access · hybridAbstract read
In one paragraph

Article in British journal of cancer, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
0.8field-weighted citation impact, top 23% 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

26 citing papers in PubMed, 50 citations in OpenAlex.

  1. Review
  2. Role of elastic fiber degradation in disease pathogenesis.Biochimica et biophysica acta. Molecular basis of disease · 2023
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  11. The role of collagen in cancer: from bench to bedside.Journal of translational medicine · 2019
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  20. Tendon extracellular matrix damage, degradation and inflammation in response to in vitro overload exercise.Journal of orthopaedic research : official publication of the Orthopaedic Research Society · 2015
    Article
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 2 countries.

J DevyUniversité de Reims Champagne Ardenne (URCA), Laboratoire SiRMa, UMR CNRS 6237, IFR 53 Interactions cellules microenvironment, UFR Sciences Exactes et Naturelles, Moulin de la Housse, BP 1039, 51687 Reims Cedex 2, France.
L Duca
B Cantarelli
D Joseph-Pietras
A Scandolera
A Rusciani
L Parent
J Thevenard
S Brassart Pasco
M Tarpin
L Martiny
L Debelle
Université de Reims Champagne-Ardenne · FRCentre National de la Recherche Scientifique · FRTenovus Cancer Care · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundElastin peptides possess several biological activities and in vitro data suggest they could be involved in the early phase of melanoma growth.

methodsUsing diverse in vitro and in vivo techniques (cell proliferation, invasion and migration assays, zymography, western blots, collagen degradation assay, reverse transcription PCR, melanoma allographs and immunohistochemistry), we analysed the effect of elastin-derived peptides (EDPs) on B16F1 melanoma growth and invasion, as well as on the proteolytic systems involved.

resultsWe found that EDPs dramatically promote in vivo tumour development of B16F1 melanoma, as well as their in vitro migration and invasion. The inhibition of serine proteases and matrix metalloproteinases (MMPs) activities, by aprotinin and galardin, respectively, demonstrated that these enzymes were involved in these processes. However, we found that EDPs did not increase urokinase-type plasminogen activator, tissue-type plasminogen activator or MMP-2 expression and/or activation, neither in vitro nor in vivo. Nevertheless, we observed a strong increase of pro-MMP-9 secretion in EDPs-treated tumours and, more importantly, an increase in the expression and activation of the murine counterpart of MMP-1, named murine collagenase-A (Mcol-A). Moreover, we show that plasminogen system inhibition decreases collagen degradation by this enzyme. Finally, the use of a specific blocking antibody against Mcol-A abolished EDP-induced B16F1 invasion in vitro, showing that this MMP was directly involved in this process.

conclusionOur data show that in vivo, EDPs are involved in melanoma growth and invasion and reinforced the concept of elastin fragmentation as a predictive factor.

Indexed as

AnimalsCattleCell DivisionCell MovementDNA PrimersElastinEnzyme ActivationFemaleLigamentsMatrix Metalloproteinase 1Matrix Metalloproteinase 9Melanoma, ExperimentalMiceMice, Inbred C57BLPeptidesReverse Transcriptase Polymerase Chain ReactionDNA PrimersElastinMatrix Metalloproteinase 1Matrix Metalloproteinase 9Peptides

Identifiers

PMID20959825
PMCPMC2990576
OpenAlexW2080769950

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.