Evidence map›Paper›PMID 29993185›Full record

ArticleJournal of cellular and molecular medicine2018

Triggering of cancer cell cycle arrest by a novel scorpion venom-derived peptide-Gonearrestide.

Bin Li, Peng Lyu, Xinping Xi, Lilin Ge, Ravikiran Mahadevappa, Chris Shaw, Hang Fai Kwok

Open access · goldAbstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
4.2field-weighted citation impact, top 6% 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

30 citing papers in PubMed, 53 citations in OpenAlex.

  1. Review
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  8. Article
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  11. Biological Activity of Natural and Synthetic Peptides as Anticancer Agents.International journal of molecular sciences · 2024
    Review
  12. Review
  13. Article
  14. Article
  15. Bioactive Peptides and Proteins from Centipede Venoms.Molecules (Basel, Switzerland) · 2022
    Review
  16. Article
  17. Article
  18. Review
  19. Review
  20. Anti-inflammatory activities of arthropod peptides: a systematic review.The journal of venomous animals and toxins including tropical diseases · 2021
    Review
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

7 authors at 3 institutions in 3 countries.

Bin LiFaculty of Health Sciences, University of Macau, Taipa, Macau, Macao.
Peng LyuFaculty of Health Sciences, University of Macau, Taipa, Macau, Macao.
Xinping XiFaculty of Health Sciences, University of Macau, Taipa, Macau, Macao.
Lilin GeFaculty of Health Sciences, University of Macau, Taipa, Macau, Macao.
Ravikiran MahadevappaFaculty of Health Sciences, University of Macau, Taipa, Macau, Macao.
Chris ShawSchool of Pharmacy, Queen's University Belfast, Belfast, Northern Ireland, UK.
Hang Fai KwokFaculty of Health Sciences, University of Macau, Taipa, Macau, Macao.ORCID 0000-0002-6349-4517
University of Macau · MOQueen's University Belfast · GBNanjing University of Chinese Medicine · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In this study, a novel scorpion venom-derived peptide named Gonearrestide was identified in an in-house constructed scorpion venom library through a combination of high-throughput NGS transcriptome and MS/MS proteome platform. In total, 238 novel peptides were discovered from two scorpion species; and 22 peptides were selected for further study after a battery of functional prediction analysis. Following a series of bioinformatics analysis alongside with in vitro biological functional screenings, Gonearrestide was found to be a highly potent anticancer peptide which acts on a broad spectrum of human cancer cells while causing few if any observed cytotoxic effects on epithelial cells and erythrocytes. We further investigated the precise anticancer mechanism of Gonearrestide by focusing on its effects on the colorectal cancer cell line, HCT116. NGS RNA sequencing was employed to obtain full gene expression profiles in HCT116 cells, cultured in the presence and absence of Gonearrestide, to dissect signalling pathway differences. Taken together the in vitro, in vivo and ex vivo validation studies, it was proven that Gonearrestide could inhibit the growth of primary colon cancer cells and solid tumours by triggering cell cycle arrest in G1 phase through inhibition of cyclin-dependent kinases 4 (CDK4) and up-regulate the expression of cell cycle regulators/inhibitors-cyclin D3, p27, and p21. Furthermore, prediction of signalling pathways and potential binding sites used by Gonearrestide are also presented in this study.

Indexed as

Gene Expression Regulation, NeoplasticAnimalsAntineoplastic AgentsBinding SitesCell Line, TumorColonic NeoplasmsCyclin D3Cyclin-Dependent Kinase 4Cyclin-Dependent Kinase Inhibitor p21Cyclin-Dependent Kinase Inhibitor p27FemaleG1 PhaseHCT116 CellsHumansMice, NudePeptidesAntineoplastic AgentsCCND3 protein, humanCDK4 protein, humanCyclin D3Cyclin-Dependent Kinase 4Cyclin-Dependent Kinase Inhibitor p21Cyclin-Dependent Kinase Inhibitor p27PeptidesScorpion Venomsanticancer mechanismbinding sitesMS/MS proteomeNGS transcriptomesignalling pathwaysvenom library

Identifiers

PMID29993185
PMCPMC6111814
OpenAlexW2820019174

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.