Evidence map›Paper›PMID 21334359›Full record

ArticleToxicon : official journal of the International Society on Toxinology2011

Anti-metastatic activity of the recombinant disintegrin, r-mojastin 1, from the Mohave rattlesnake.

Sara Lucena, Elda E Sanchez, John C Perez

Abstract read
In one paragraph

Article in Toxicon : official journal of the International Society on Toxinology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.2field-weighted citation impact, top 20% 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, 39 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Protein structure of the venom in nine species of snake: from bio-compounds to possible healing agents.Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologica · 2020
    Article
  5. Article
  6. Review
  7. Review
  8. Article
  9. Article
  10. Article
  11. Review
  12. Anti-angiogenic activities of two recombinant disintegrins derived from the Mohave and Prairie rattlesnakes.Toxicon : official journal of the International Society on Toxinology · 2014
    Article
  13. Review
  14. 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

3 authors at 1 institution in 1 country.

Sara LucenaNational Natural Toxins Research Center, Biology Department, Texas A&M University-Kingsville, MSC 158, 975 West Avenue B, Kingsville, TX 78363, USA.
Elda E Sanchez
John C Perez
Texas A&M University – Kingsville · US

Funding

Viper Resource Center (VRC) at Texas A&M University-KingsvilleP40RR018300 · NCRR · TEXAS A&M UNIVERSITY-KINGSVILLE · PI PEREZ, JOHN CARLOS · 2003 to 2011
$4.5M
NCRR NIH HHS 5 P40 RR018300-07NCRR NIH HHS P40 RR018300
6 · The paper itself

Abstract

Cancer is the uncontrollable growth of cell, which may spread to other parts of the body. The interaction of cancer cells with extracellular matrix (ECM) is essential for metastasis, which is the principal cause of death in cancer patients. Disintegrins are naturally occurring low molecular weight peptides found in the venoms of many snakes. Disintegrins were first used to inhibit platelet aggregation, but more recently have been used to inhibit cancer cell growth, adhesion, migration, invasion and/or angiogenesis. The purpose of this study was to determine the anti-tumor properties of recombinant mojastin 1 (r-mojastin 1) and r-mojastin-GST, cloned from the venom glands of the Mohave rattlesnake (Crotalus scutulatus scutulatus). Human urinary bladder carcinoma (T24), human fibrosarcoma (HT-1080), human skin melanoma (SK-ML-28) and murine skin melanoma (B16F10) cell lines were used. r-Mojastin 1 inhibited SK-MEL-28 cell adhesion to fibronectin, but was not able to inhibit T24 cell adhesion to fibronectin. However, r-Mojastin-GST inhibited SK-MEL-28 and T24 cells adhesion to fibronectin. r-Mojastin-GST and r-mojastin 1 decreased the ability of SK-MEL-28 cells to migrate after 24 h of incubation but were not able to inhibit T24 cell migration. r-Mojastin 1 and r-mojastin-GST inhibited invasion of T24 and SK-MEL-28 cancer cells in vitro, and r-Mojastin 1 inhibited lung tumor colonization of B16F10 cells in mice in vivo. In conclusion, our studies suggest that r-mojastin could be a useful tool to develop novel anti-tumor agents by virtue of its ability to inhibit tumor cell adhesion, migration and invasion.

Indexed as

CrotalusAnimalsAntineoplastic AgentsCell AdhesionCell Line, TumorCell MovementCrotalid VenomsDisintegrinsFibronectinsHumansMiceNeoplasm InvasivenessNeoplasm MetastasisRecombinant ProteinsStatistics, NonparametricAntineoplastic AgentsCrotalid VenomsDisintegrinsFibronectinsmojastin protein, Crotalus scutulatusRecombinant Proteins

Identifiers

PMID21334359
PMCPMC3293478
OpenAlexW2052755274

What OpenQuestion holds

Textmetadata
LicenceTDM
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.