Evidence map›Paper›PMID 28837057›Full record

ArticleToxins2017

The Natural Fungal Metabolite Beauvericin Exerts Anticancer Activity In Vivo: A Pre-Clinical Pilot Study.

Daniela Heilos, Yelko Rodríguez-Carrasco, Bernhard Englinger, Gerald Timelthaler, Sushilla van Schoonhoven, Michael Sulyok, Simon Boecker, Roderich D Süssmuth, Petra Heffeter, Rosa Lemmens-Gruber and 2 more

Open access · goldAbstract read
In one paragraph

Article in Toxins, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
3.3field-weighted citation impact, top 9% 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

20 citing papers in PubMed, 40 citations in OpenAlex.

  1. Review
  2. The mycotoxin Beauvericin is an uncompetitive inhibitor of Cathepsin B.Protein science : a publication of the Protein Society · 2025
    Article
  3. Evaluation of Beauvericin's activity and mode of action against all life stages ofFrontiers in cellular and infection microbiology · 2025
    Article
  4. Journal of natural products · 2024
    Article
  5. Review
  6. Genotoxicity of beauvericin.EFSA journal. European Food Safety Authority · 2024
    Article
  7. Article
  8. Review
  9. Article
  10. Review
  11. Article
  12. Article
  13. Review
  14. Mycotoxins from Fusarium proliferatum: new inhibitors of papain-like cysteine proteases.Brazilian journal of microbiology : [publication of the Brazilian Society for Microbiology] · 2020
    Article
  15. Antimicrobial agents and chemotherapy · 2020
    Article
  16. Article
  17. Toxins · 2018
    Review
  18. Article
  19. Review
  20. Fungal biology and biotechnology · 2018
    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

12 authors at 5 institutions in 3 countries.

Daniela HeilosInstitute of Cancer Research, Department of Medicine I, Medical University of Vienna, and Comprehensive Cancer Center of the Medical University, Borschkegasse 8a, 1090 Vienna, Austria. daniela.heilos@univie.ac.at.
Yelko Rodríguez-CarrascoDepartment of Food Chemistry and Toxicology, Faculty of Pharmacy, University of Valencia, Av. Vicent A. Estellés s/n, 46100 Burjassot, Spain. yelko.rodriguez@uv.es.
Bernhard EnglingerInstitute of Cancer Research, Department of Medicine I, Medical University of Vienna, and Comprehensive Cancer Center of the Medical University, Borschkegasse 8a, 1090 Vienna, Austria. bernhard.englinger@meduniwien.ac.at.
Gerald TimelthalerInstitute of Cancer Research, Department of Medicine I, Medical University of Vienna, and Comprehensive Cancer Center of the Medical University, Borschkegasse 8a, 1090 Vienna, Austria. gerald.timelthaler@meduniwien.ac.at.
Sushilla van SchoonhovenInstitute of Cancer Research, Department of Medicine I, Medical University of Vienna, and Comprehensive Cancer Center of the Medical University, Borschkegasse 8a, 1090 Vienna, Austria. sushilla.vanschoonhoven@meduniwien.ac.at.
Michael SulyokDepartment of Agrobiotechnology (IFA-Tulln), University of Natural Resources and Life Sciences, Vienna (BOKU), Konrad Lorenz Str. 20, 3430 Tulln, Austria. michael.sulyok@boku.ac.at.
Simon BoeckerInstitut für Chemie, Technische Universität Berlin, Straße des 17. Juni 124, 10623 Berlin, Germany. simon.boecker@chem.tu-berlin.de.
Roderich D SüssmuthInstitut für Chemie, Technische Universität Berlin, Straße des 17. Juni 124, 10623 Berlin, Germany. suessmuth@chem.tu-berlin.de.
Petra HeffeterInstitute of Cancer Research, Department of Medicine I, Medical University of Vienna, and Comprehensive Cancer Center of the Medical University, Borschkegasse 8a, 1090 Vienna, Austria. petra.heffeter@meduniwien.ac.at.
Rosa Lemmens-GruberDepartment of Pharmacology and Toxicology, University of Vienna, Althanstr. 14, 1090 Vienna, Austria. rosa.lemmens@univie.ac.at.
Rita Dornetshuber-FleissInstitute of Cancer Research, Department of Medicine I, Medical University of Vienna, and Comprehensive Cancer Center of the Medical University, Borschkegasse 8a, 1090 Vienna, Austria. rita.dornetshuber@univie.ac.at.
Walter BergerInstitute of Cancer Research, Department of Medicine I, Medical University of Vienna, and Comprehensive Cancer Center of the Medical University, Borschkegasse 8a, 1090 Vienna, Austria. walter.berger@meduniwien.ac.at.
Comprehensive Cancer Center Vienna · ATUniversity of Vienna · ATTechnische Universität Berlin · DEBOKU University · ATUniversitat de València · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recently, in vitro anti-cancer properties of beauvericin, a fungal metabolite were shown in various cancer cell lines. In this study, we assessed the specificity of this effect by comparing beauvericin cytotoxicity in malignant versus non-malignant cells. Moreover, we tested in vivo anticancer effects of beauvericin by treating BALB/c and CB-17/SCID mice bearing murine CT-26 or human KB-3-1-grafted tumors, respectively. Tumor size and weight were measured and histological sections were evaluated by Ki-67 and H/E staining as well as TdT-mediated-dUTP-nick-end (TUNEL) labeling. Beauvericin levels were determined in various tissues and body fluids by LC-MS/MS. In addition to a more pronounced activity against malignant cells, we detected decreased tumor volumes and weights in beauvericin-treated mice compared to controls in both the allo- and the xenograft model without any adverse effects. No significant differences were detected concerning percentages of proliferating and mitotic cells in tumor sections from treated and untreated mice. However, a significant increase of necrotic areas within whole tumor sections of beauvericin-treated mice was found in both models corresponding to an enhanced number of TUNEL-positive, i.e., apoptotic, cells. Furthermore, moderate beauvericin accumulation was detected in tumor tissues. In conclusion, we suggest beauvericin as a promising novel natural compound for anticancer therapy.

Indexed as

Adipose TissueAlanine TransaminaseAnimalsAntineoplastic AgentsAspartate AminotransferasesCell Line, TumorCell SurvivalColonDepsipeptidesFecesHumansKidneyLiverMice, Inbred BALB CMice, SCIDNeoplasmsAlanine TransaminaseAntineoplastic AgentsAspartate AminotransferasesbeauvericinDepsipeptidesbeauvericincervix carcinomacolorectal carcinomacyclohexadepsipeptidetherapy

Identifiers

PMID28837057
PMCPMC5618191
OpenAlexW2746092198

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.