Beauvericin, A Fusarium Mycotoxin: Anticancer Activity, Mechanisms, and Human Exposure Risk Assessment
Language English Country Netherlands Media print
Document type Journal Article, Review
PubMed
30264680
DOI
10.2174/1389557518666180928161808
PII: MRMC-EPUB-93301
Knihovny.cz E-resources
- Keywords
- BEA, Beauvericin, anticancer, health risk, oxidative stress, signaling pathway.,
- MeSH
- Antineoplastic Agents pharmacology toxicity MeSH
- Depsipeptides pharmacology toxicity MeSH
- Fusarium chemistry MeSH
- Risk Assessment MeSH
- Humans MeSH
- Mycotoxins pharmacology toxicity MeSH
- Environmental Exposure adverse effects MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Review MeSH
- Names of Substances
- Antineoplastic Agents MeSH
- beauvericin MeSH Browser
- Depsipeptides MeSH
- Mycotoxins MeSH
Beauvericin (BEA) is a cyclic hexadepsipeptide, which derives from Cordyceps cicadae. It is also produced by Fusarium species, which are parasitic to maize, wheat, rice and other important commodities. BEA increases ion permeability in biological membranes by forming a complex with essential cations, which may affect ionic homeostasis. Its ion-complexing capability allows BEA to transport alkaline earth metal and alkali metal ions across cell membranes. Importantly, increasing lines of evidence show that BEA has an anticancer effect and can be potentially used in cancer therapeutics. Normally, BEA performs the anticancer effect due to the induced cancer cell apoptosis via a reactive oxygen species-dependent pathway. Moreover, BEA increases the intracellular Ca2+ levels and subsequently regulates the activity of a series of signalling pathways including MAPK, JAK/STAT, and NF-κB, and finally causes cancer cell apoptosis. In vivo studies further show that BEA reduces tumour volumes and weights. BEA especially targets differentiated and invasive cancer types. Currently, the anticancer activity of BEA is a hot topic; however, there is no review article to discuss the anticancer activity of BEA. Therefore, in this review, we have mainly summarized the anticancer activity of BEA and thoroughly discussed its underlying mechanisms. In addition, the human exposure risk assessment of BEA is also discussed. We hope that this review will provide further information for understanding the anticancer mechanisms of BEA.
Biomedical Research Centre University Hospital Hradec Kralove Czech Republic
College of Life Science Institute of Biomedicine Yangtze University Jingzhou 434025 China
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