Evidence map›Paper›PMID 17952617›Full record

ArticleClinical & experimental metastasis2008

A novel alpha(v)beta (3)-blocking disintegrin containing the RGD motive, DisBa-01, inhibits bFGF-induced angiogenesis and melanoma metastasis.

Oscar H P Ramos, Alexandre Kauskot, Márcia R Cominetti, Iga Bechyne, Carmen L Salla Pontes, Fabrice Chareyre, Jan Manent, Roger Vassy, Marco Giovannini, Chantal Legrand and 3 more

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Article in Clinical & experimental metastasis, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

40 citing papers in PubMed, 94 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Article
  6. Review
  7. Article
  8. Snake venom disintegrins update: insights about new findings.The journal of venomous animals and toxins including tropical diseases · 2023
    Review
  9. Article
  10. Article
  11. Review
  12. Cytotoxic and anticancer properties of the Malaysian mangrove pit viper (The journal of venomous animals and toxins including tropical diseases · 2020
    Article
  13. Recombinant RGD-disintegrin DisBa-01 blocks integrin αCell communication and signaling : CCS · 2019
    Article
  14. Review
  15. Review
  16. Review
  17. Article
  18. Article
  19. Article
  20. 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

13 authors at 5 institutions in 3 countries.

Oscar H P RamosDep. Ciências Fisiológicas, Universidade Federal de São Carlos, São Carlos, SP, Brasil.
Alexandre Kauskot
Márcia R Cominetti
Iga Bechyne
Carmen L Salla Pontes
Fabrice Chareyre
Jan Manent
Roger Vassy
Marco Giovannini
Chantal Legrand
Heloisa S Selistre-de-Araujo
Michel Crépin
Arnaud Bonnefoy
Inserm · FRUniversidade Federal de São Carlos · BRUniversité Sorbonne Paris Nord · FRInstitut Universitaire de France · FRUniversité de Montréal · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The integrin alpha(v)beta(3) is involved in multiple aspects of malignant cancer, including tumor angiogenesis and metastasis, which makes the receptor a key target for the development of anti-cancer therapies. We report here on the production, the characterization and the in vivo anti-angiogenic and anti-metastatic properties of a novel alpha(v)beta(3)-binding disintegrin, DisBa-01, isolated from a cDNA library made with RNAs from the venom gland of Bothrops alternatus. The 11,637 Da-recombinant monomeric form of DisBa-01 displayed an RGD motif and interacted with purified alpha(v)beta(3) integrin in surface plasmon resonance studies, in a dose-dependent and cation sensitive manner. A three-dimensional molecular model of DisBa-01 in complex with alpha(v)beta(3) predicted a large surface of contacts with the beta(3) subunit. DisBa-01 inhibited the adhesion of alpha(v)beta(3)-expressing human microvascular endothelial cell line-1 (HMEC-1) and murine melanoma cell line B16F10 to vitronectin (IC(50) = 555 nM and 225 nM, respectively), and transiently inhibited their proliferation without direct cell toxicity, but did not affect the binding nor the proliferation of a human breast cancer-derived cell line (MDA-MB-231) not expressing alpha(v)beta(3). In vivo, DisBa-01 dose-dependently decreased bFGF-induced angiogenesis in a matrigel plug assay in athymic nude mice (IC(50) = 83 nM). When injected intravenously to C57BL/6 mice together with B16F10 melanoma cells, DisBa-01 time- and dose-dependently inhibited lung metastasis monitored by bioluminescent imaging. We conclude that DisBa-01 is a potent new inhibitor of alpha(v)beta(3)-dependent adherence mechanisms involved in neo-vascularization and tumor metastasis processes.

Indexed as

Amino Acid MotifsAmino Acid SequenceAnimalsAntineoplastic AgentsBase SequenceBothropsCell AdhesionCloning, MolecularCrotalid VenomsDisintegrinsFibroblast Growth FactorsHumansIntegrin alphaVbeta3Melanoma, ExperimentalMiceMolecular Sequence DataAntineoplastic AgentsCrotalid VenomsDisintegrinsFibroblast Growth FactorsIntegrin alphaVbeta3Recombinant Proteins

Identifiers

PMID17952617
OpenAlexW2120941547

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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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.