Evidence map›Paper›PMID 27887635›Full record

ArticleParasites & vectors2016

Anisakis pegreffii (Nematoda: Anisakidae) products modulate oxidative stress and apoptosis-related biomarkers in human cell lines.

Concetta Maria Messina, Federica Pizzo, Andrea Santulli, Ivana Bušelić, Mate Boban, Stjepan Orhanović, Ivona Mladineo

Open access · goldAbstract read
In one paragraph

Article in Parasites & vectors, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
9.6field-weighted citation impact, top 2% 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

25 citing papers in PubMed, 72 citations in OpenAlex.

  1. Anisakiasis: A Decade of Molecular and Diagnostic Advancements (2015-2026).International journal of molecular sciences · 2026
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  7. Inflammatory Response in Caco-2 Cells Stimulated withPathogens (Basel, Switzerland) · 2022
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  15. Article
  16. Honey Bee Pollen in Meagre (Animals : an open access journal from MDPI · 2020
    Article
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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 2 countries.

Concetta Maria MessinaDipartimento di Scienze della Terra e del Mare DiSTeM, Università degli Studi di Palermo, Laboratorio di Biochimica Marina ed Ecotossicologia, Via G. Barlotta 4, 91100, Trapani, Italy.
Federica PizzoDipartimento di Scienze della Terra e del Mare DiSTeM, Università degli Studi di Palermo, Laboratorio di Biochimica Marina ed Ecotossicologia, Via G. Barlotta 4, 91100, Trapani, Italy.
Andrea SantulliDipartimento di Scienze della Terra e del Mare DiSTeM, Università degli Studi di Palermo, Laboratorio di Biochimica Marina ed Ecotossicologia, Via G. Barlotta 4, 91100, Trapani, Italy.
Ivana BušelićInstitute of Oceanography and Fisheries, Laboratory of Aquaculture, POBox 500, 21000, Split, Croatia.
Mate BobanUniversity of Split, Faculty of Natural Sciences, Teslina 12, 21000, Split, Croatia.
Stjepan OrhanovićUniversity of Split, Faculty of Natural Sciences, Teslina 12, 21000, Split, Croatia.
Ivona MladineoInstitute of Oceanography and Fisheries, Laboratory of Aquaculture, POBox 500, 21000, Split, Croatia. mladineo@izor.hr.
University of Palermo · ITInstitute of Oceanography and Fisheries · HRUniversity of Split · HR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIn countries with elevated prevalence of zoonotic anisakiasis and high awareness of this parasitosis, a considerable number of cases that associate Anisakis sp. (Nematoda, Anisakidae) and different bowel carcinomas have been described. Although neoplasia and embedded larvae were observed sharing the common site affected by chronic inflammation, no association between the nematode and malignancy were directly proved. Similarly, no data are available about the effect of secretory and excretory products of infecting larvae at the host's cellular level, except in respect to allergenic interaction.

methodsTo test the mechanisms by which human non-immune cells respond to the larvae, we exposed the fibroblast cell line HS-68 to two Anisakis products (ES, excretory/secretory products; and EC, crude extract) and evaluated molecular markers related to stress response, oxidative stress, inflammation and apoptosis, such as p53, HSP70, TNF-α, c-jun and c-fos, employing cell viability assay, spectrophotometry, immunoblotting and qPCR.

resultsBoth Anisakis products led to increased production of reactive oxygen species (ROS), especially in EC-treated cells. While the ES treatment induces activation of kinases suggesting inflammation and cell proliferation (or inhibition of apoptosis), in EC-treated cells, other signaling pathways indicate the inhibition of apoptosis, marked by strong upregulation of Hsp70. Elevated induction of p53 in fibroblasts treated by both Anisakis products, suggests a significantly negative effect on the host DNA.

conclusionsThis study shows that in vitro cell response to Anisakis products can result in at least two different scenarios, which in both cases lead to inflammation and DNA damage. Although these preliminary results are far from proving a relationship between the parasite and cancer, they are the first to support the existence of conditions where such changes are feasible.

Indexed as

ApoptosisOxidative StressAnimalsAnisakisBiological ProductsBiomarkersCell LineCell SurvivalHumansInflammation MediatorsLarvaReactive Oxygen SpeciesBiological ProductsBiomarkersInflammation MediatorsReactive Oxygen SpeciesAnisakis pegreffiiApoptosisFibroblast cell lines HS-68InflammationOxidative stress

Identifiers

PMID27887635
PMCPMC5124272
OpenAlexW2550791203

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.