Evidence map›Paper›PMID 23015777›Full record

ArticleMarine drugs2012

Pardaxin, a fish antimicrobial peptide, exhibits antitumor activity toward murine fibrosarcoma in vitro and in vivo.

Shu-Ping Wu, Tsui-Chin Huang, Ching-Chun Lin, Cho-Fat Hui, Cheng-Hui Lin, Jyh-Yih Chen

Open access · goldAbstract read
In one paragraph

Article in Marine drugs, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
3.4field-weighted citation impact, top 8% 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

21 citing papers in PubMed, 48 citations in OpenAlex.

  1. Review
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  4. Review
  5. Short Fragmented Peptides fromCurrent drug discovery technologies · 2024
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  15. Anticancer drugs for the modulation of endoplasmic reticulum stress and oxidative stress.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2015
    Review
  16. Article
  17. Article
  18. Antimicrobial peptides from fish.Pharmaceuticals (Basel, Switzerland) · 2014
    Article
  19. Article
  20. 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

6 authors at 2 institutions in 1 country.

Shu-Ping WuDepartment of Aquaculture, National Taiwan Ocean University, Keelung 202, Taiwan.
Tsui-Chin HuangMarine Research Station, Institute of Cellular and Organismic Biology, Academia Sinica, 23-10 Dahuen Rd., Jiaushi, Ilan 262, Taiwan.
Ching-Chun LinInstitute of Cellular and Organismic Biology, Academia Sinica, Taipei 115, Taiwan.
Cho-Fat HuiInstitute of Cellular and Organismic Biology, Academia Sinica, Taipei 115, Taiwan.
Cheng-Hui LinDepartment of Aquaculture, National Taiwan Ocean University, Keelung 202, Taiwan.
Jyh-Yih ChenMarine Research Station, Institute of Cellular and Organismic Biology, Academia Sinica, 23-10 Dahuen Rd., Jiaushi, Ilan 262, Taiwan.
Institute of Cellular and Organismic Biology, Academia Sinica · TWNational Taiwan Ocean University · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The antitumor activity of pardaxin, a fish antimicrobial peptide, has not been previously examined in in vitro and in vivo systems for treating murine fibrosarcoma. In this study, the antitumor activity of synthetic pardaxin was tested using murine MN-11 tumor cells as the study model. We show that pardaxin inhibits the proliferation of MN-11 cells and reduces colony formation in a soft agar assay. Transmission electron microscopy (TEM) showed that pardaxin altered the membrane structure similar to what a lytic peptide does, and also produced apoptotic features, such as hollow mitochondria, nuclear condensation, and disrupted cell membranes. A qRT-PCR and ELISA showed that pardaxin induced apoptosis, activated caspase-7 and interleukin (IL)-7r, and downregulated caspase-9, ATF 3, SOCS3, STAT3, cathelicidin, p65, and interferon (IFN)-γ suggesting that pardaxin induces apoptosis through the death receptor/nuclear factor (NF)-κB signaling pathway after 14 days of treatment in tumor-bearing mice. An antitumor effect was observed when pardaxin (25 mg/kg; 0.5 mg/day) was used to treat mice for 14 days, which caused significant inhibition of MN-11 cell growth in mice. Overall, these results indicate that pardaxin has the potential to be a novel therapeutic agent to treat fibrosarcomas.

Indexed as

AnimalsAntineoplastic AgentsApoptosisCell MembraneCell ProliferationDose-Response Relationship, DrugEnzyme-Linked Immunosorbent AssayFemaleFibrosarcomaFish VenomsMaleMiceMice, Inbred C57BLMicroscopy, Electron, TransmissionNF-kappa BReverse Transcriptase Polymerase Chain ReactionAntineoplastic AgentsFish VenomsNF-kappa Bpardaxinantitumorfibrosarcomapardaxin

Identifiers

PMID23015777
PMCPMC3447341
OpenAlexW2025408279

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.