Evidence map›Paper›PMID 17316731›Full record

ArticleToxicon : official journal of the International Society on Toxinology2007

Inhibition of melanoma cell motility by the snake venom disintegrin eristostatin.

Jing Tian, Carrie Paquette-Straub, E Helene Sage, Sarah E Funk, Vivek Patel, Deni Galileo, Mary Ann McLane

Erratum issuedAbstract read
In one paragraph

Article in Toxicon : official journal of the International Society on Toxinology, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

14 citing papers in PubMed, 46 citations in OpenAlex.

  1. Article
  2. Snake venom disintegrins update: insights about new findings.The journal of venomous animals and toxins including tropical diseases · 2023
    Review
  3. Review
  4. Cell migration inhibition activity of a non-RGD disintegrin fromThe journal of venomous animals and toxins including tropical diseases · 2018
    Article
  5. Article
  6. Article
  7. Review
  8. Review
  9. Effect of the disintegrin eristostatin on melanoma-natural killer cell interactions.Toxicon : official journal of the International Society on Toxinology · 2013
    Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
4 · The record

Corrections and comments

  • Erratum issued
5 · Who and what money

Authors and funding

7 authors at 2 institutions in 1 country.

Jing TianDepartment of Medical Technology, University of Delaware, 305G Willard Hall, Education Building, Newark, DE 19716, USA.
Carrie Paquette-Straub
E Helene Sage
Sarah E Funk
Vivek Patel
Deni Galileo
Mary Ann McLane
University of Delaware · USBenaroya Research Institute

Funding

EXTRACELLULAR PROTEINS AS SIGNALS IN ENDOTHELIAL GROWTHR01GM040711 · NIGMS · UNIVERSITY OF WASHINGTON · PI SAGE, EMILY HELENE · 1988 to 2009
$2.7M
Melanoma Metastasis Inhibition by EristostatinR01CA098056 · NCI · UNIVERSITY OF DELAWARE · PI MCLANE, MARY ANN · 2003 to 2005
$705k
NCI NIH HHS CA098056NCI NIH HHS R01 CA098056NIGMS NIH HHS GM40711NIGMS NIH HHS R01 GM040711
6 · The paper itself

Abstract

Eristostatin, an RGD-containing disintegrin isolated from the venom of Eristicophis macmahoni, inhibits lung or liver colonization of melanoma cells in a mouse model. In this study, transwell migration and in vitro wound closure assays were used to determine the effect of eristostatin on the migration of melanoma cells. Eristostatin significantly impaired the migration of five human melanoma cell lines. Furthermore, it specifically inhibited cell migration on fibronectin in a concentration-dependent manner, but not that on collagen IV or laminin. In contrast, eristostatin was found to have no effect on cell proliferation or angiogenesis. These results indicate that the interaction between eristostatin and melanoma cells may involve fibronectin-binding integrins that mediate cell migration. Mutations to alanine of seven residues within the RGD loop of eristostatin and four residues outside the RGD loop of eristostatin resulted in significantly less potency in both platelet aggregation and wound closure assays. For six of the mutations, however, decreased activity was found only in the latter assay. We conclude that a different mechanism and/or integrin is involved in these two cell activities.

Indexed as

AlanineAnimalsAntineoplastic AgentsCell Line, TumorCell MovementCell ProliferationChorioallantoic MembraneHumansMelanomaMiceMutagenesis, Site-DirectedNeovascularization, PhysiologicPeptidesQuailViper VenomsAlanineAntineoplastic AgentseristostatinPeptidesViper Venoms

Identifiers

PMID17316731
PMCPMC1948081
OpenAlexW1999503216

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.