Mechanisms Underlying Metabolic Regulation by Marine Toxins

A special issue of Toxins (ISSN 2072-6651). This special issue belongs to the section "Marine and Freshwater Toxins".

Deadline for manuscript submissions: closed (31 March 2025) | Viewed by 1688

Special Issue Editor


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Guest Editor
Alfred-Wegner-Institut Helmholtz-Zentrum für Polar- und Meeresforschung (AWI), Am Handelshafen 12, 27570 Bremerhaven, Germany
Interests: chemical and molecular ecology of protists; genetics of toxin biosynthesis; toxinology and ecotoxicology of harmful microalgae; harmful algal blooms and marine food webs; marine phycotoxin dynamics and diversity; marine microbial biotechnology
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Special Issue Information

Dear Colleagues,

Marine toxins are broadly defined as natural products with potent deleterious bioactivity against molecular targets in a host of marine and terrestrial species. These compounds are synthesized by and/or accumulated in the marine food web, often manifesting as seafood toxins or causing morbidity and mortality to marine fauna. Typical marine toxins are small molecules (<3000 Daltons) that belong to diverse structural classes such as alkaloids, secondary amino acids or polyether polyketides, or comprise specialized peptide/proteinaceous molecules. Their potency as toxins is usually defined with respect to mammalian targets, and this may tend to obscure their ecological function in chemical communication, defense against predation, competition, and transitions in the marine environment. Marine toxins continue to be carefully scrutinized in the search for pharmaceuticals, e.g., as analgesics against acute and chronic pain, anti-microbials (e.g., bacteria, fungi, microeukaryotes, and viruses), anti-cancer/anti-proliferative agents, and as neuropharmaceuticals. These discoveries are dependent upon obtaining more detailed knowledge of their role as enzyme inhibitors, cell cycle blockers, membrane disruptors, and ion channel effectors. Most of the chemical structures are well defined, and in a few cases, the biosynthetic pathways have been elucidated. The knowledge of the molecular, genetic regulation of toxin biosynthesis in producing species and the metabolic response of the target cells, tissues, and whole organisms cannot define the functional role of putative toxins. This Special Issue will focus on these mechanisms in natural species interactions, cell and whole-animal assays, and electrophysiology studies. Contributions leading to further insights in metabolomics and subsequent molecular modelling of the mode(s) of action of marine toxins are particularly welcome.

Prof. Dr. Allan Cembella
Guest Editor

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Keywords

  • chemical ecology
  • marine toxin
  • ecotoxicology
  • phycotoxins
  • marine bioactives
  • toxin biosynthesis
  • metabolic regulation
  • toxin mode of action
  • toxin modelling
  • metabolomics

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Published Papers (1 paper)

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Research

26 pages, 5898 KiB  
Article
Untargeted Metabolomic Analysis and Cytotoxicity of Extracts of the Marine Dinoflagellate Amphidinium eilatiense Against Human Cancer Cell Lines
by María del Carmen Osorio-Ramírez, Alan Gerardo Hernández-Melgar, Allan D. Cembella, Benjamin H. Maskrey, Laura Janeth Díaz-Rubio, Iván Córdova-Guerrero, Johanna Bernáldez-Sarabia, Leticia González-Maya, Baldomero Esquivel-Rodríguez, Celia Bustos-Brito, Alexei F. Licea-Navarro and Lorena M. Durán-Riveroll
Toxins 2025, 17(4), 150; https://doi.org/10.3390/toxins17040150 - 21 Mar 2025
Viewed by 1245
Abstract
Members of the benthic marine dinoflagellate genus Amphidinium produce a variety of bioactive compounds, exhibiting potent cytotoxicity in cell assays. Crude methanolic extracts from three genetically distinct cultured strains of A. eilatiense J.J. Lee were screened for cytotoxicity against three human breast and [...] Read more.
Members of the benthic marine dinoflagellate genus Amphidinium produce a variety of bioactive compounds, exhibiting potent cytotoxicity in cell assays. Crude methanolic extracts from three genetically distinct cultured strains of A. eilatiense J.J. Lee were screened for cytotoxicity against three human breast and four lung cancer cell lines to evaluate potential applications in anticancer therapy. A standard tetrazolium cell viability assay demonstrated that the methanolic crude extract (100 µg mL−1) from strain AeSQ181 reduced cell viability by 20–35% in five cancer cell lines. Further bioassay-guided fractionation of these crude extracts yielded non-polar fractions (FNP-5 and FNP-6) with particularly high cytotoxic activity against lung (H1563) and breast (MDA-MB-231) adenocarcinoma cell lines. Untargeted metabolomic analysis of cytotoxic fractions by liquid chromatography coupled with high-resolution mass spectrometry (LC-HRMS) revealed a much richer chemical diversity profile than previous toxigenicity studies on Amphidinium that exclusively focused on linear and cyclic polyethers and their macrolide analogs as putative cytotoxins. This untargeted metabolomic study showed substantial differences in chemical composition between the biologically active and non-active fractions. Preliminary biological and chemical characterization of these A. eilatiense fractions confirms that this species is a rich source of bioactive natural products with potential applications such as anticancer therapeutics. Full article
(This article belongs to the Special Issue Mechanisms Underlying Metabolic Regulation by Marine Toxins)
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