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Cannabidiol-induced activation of the metallothionein pathway impedes anticancer effects of disulfiram and its metabolite CuET
T. Buchtova, Z. Skrott, K. Chroma, J. Rehulka, P. Dzubak, M. Hajduch, D. Lukac, S. Arampatzis, J. Bartek, M. Mistrik
Jazyk angličtina Země Spojené státy americké
Typ dokumentu časopisecké články, práce podpořená grantem
NLK
Directory of Open Access Journals
od 2017
Free Medical Journals
od 2007 do Před 1 rokem
PubMed Central
od 2007
Europe PubMed Central
od 2007
ProQuest Central
od 2007-06-01
Wiley-Blackwell Open Access Titles
od 2007
PubMed
34632694
DOI
10.1002/1878-0261.13114
Knihovny.cz E-zdroje
- MeSH
- disulfiram * chemie farmakologie terapeutické užití MeSH
- kanabidiol * farmakologie terapeutické užití MeSH
- lidé MeSH
- měď chemie farmakologie MeSH
- metalothionein MeSH
- nádorové buněčné linie MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
Disulfiram (DSF), an established alcohol-aversion drug, is a candidate for repurposing in cancer treatment. DSF's antitumor activity is supported by preclinical studies, case reports, and small clinical trials; however, ongoing clinical trials of advanced-stage cancer patients encounter variable results. Here, we show that one reason for the inconsistent clinical effects of DSF may reflect interference by other drugs. Using a high-throughput screening and automated microscopy, we identify cannabidiol, an abundant component of the marijuana plant used by cancer patients to mitigate side effects of chemotherapy, as a likely cause of resistance to DSF. Mechanistically, in cancer cells, cannabidiol triggers the expression of metallothioneins providing protective effects by binding heavy metal-based substances including the bis-diethyldithiocarbamate-copper complex (CuET). CuET is the documented anticancer metabolite of DSF, and we show here that the CuET's anticancer toxicity is effectively neutralized by metallothioneins. Overall, this work highlights an example of undesirable interference between cancer therapy and the concomitant usage of marijuana products. In contrast, we report that insufficiency of metallothioneins sensitizes cancer cells toward CuET, suggesting a potential predictive biomarker for DSF repurposing in oncology.
Citace poskytuje Crossref.org
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