Evidence map›Paper›PMID 29763387›Full record

ArticleExperimental biology and medicine (Maywood, N.J.)2018

Spider peptide toxin lycosin-I induces apoptosis and inhibits migration of prostate cancer cells.

Hongwei Shen, Yuan Xie, Senlin Ye, Kancheng He, Lu Yi, Rongrong Cui

Open access · greenAbstract read
In one paragraph

Article in Experimental biology and medicine (Maywood, N.J.), 2018. 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
0.9field-weighted citation impact, top 28% 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, 22 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Cancer-Targeting Applications of Cell-Penetrating Peptides.International journal of molecular sciences · 2024
    Review
  6. Review
  7. Article
  8. Article
  9. Review
  10. Review
  11. Review
  12. Antimicrobial Peptides with Anti-International journal of molecular sciences · 2022
    Review
  13. Anti-Biomedicines · 2021
    Article
  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

6 authors at 2 institutions in 1 country.

Hongwei Shen1 Centralab of the Second Xiangya Hospital of Central South University, Changsha 410011, China.
Yuan Xie2 Xiangya School of Medicine, Central South University, Changsha 410200, Hunan, China.
Senlin Ye3 Department of Urology, The Second Xiangya Hospital of Central South University, Changsha 410011, China.
Kancheng He3 Department of Urology, The Second Xiangya Hospital of Central South University, Changsha 410011, China.
Lu Yi3 Department of Urology, The Second Xiangya Hospital of Central South University, Changsha 410011, China.
Rongrong Cui4 Institute of Metabolism and Endocrinology, The Second XiangYa Hospital of Central South University, Changsha 410011, China.
Central South University · CNSecond Xiangya Hospital of Central South University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Spider toxins are molecularly diverse and some display not only a strong antibacterial effect but also exhibit significant inhibition of tumor growth and promote tumor cell apoptosis. The aim of the present investigation was to explore different antitumor effects of the spider peptide toxin lycosin-I through different pathways at different concentrations. It was found that by inactivating STAT3 pathway, high concentrations of lycosin-I induce apoptosis in prostate cancer cells and low concentrations of lycosin-I inhibit the migration of prostate cancer cells. This finding provides favorable evidence for further study of the molecular diversity of spider toxins. Impact statement The spider peptide toxin has become an important research topic. These toxins are molecularly diverse and some display not only a strong antibacterial effect but also exhibit significant inhibition of tumor growth and promote tumor cell apoptosis. Inspired by previous studies, the present study aims to investigate the effects of different concentrations of lycosin-I on the invasiveness and apoptosis of human prostate cancer cells. The findings provide favorable evidence for further study of the molecular diversity of spider toxins.

Indexed as

Antimicrobial Cationic PeptidesAntineoplastic AgentsApoptosisCell Line, TumorCell MovementHumansMaleModels, BiologicalProstatic NeoplasmsSpider VenomsAntimicrobial Cationic PeptidesAntineoplastic Agentslycosin-I, Lycosa singorensisSpider VenomsapoptosisMMP9prostate cancerSpider peptide toxin lycosin-ISTAT3tumor

Identifiers

PMID29763387
PMCPMC6378508
OpenAlexW2803229636

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.