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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
Language English Country United States
Document type Journal Article, Research Support, Non-U.S. Gov't
NLK
Directory of Open Access Journals
from 2017
Free Medical Journals
from 2007 to 1 year ago
PubMed Central
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Europe PubMed Central
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ProQuest Central
from 2007-06-01
Wiley-Blackwell Open Access Titles
from 2007
- MeSH
- Disulfiram * chemistry pharmacology therapeutic use MeSH
- Cannabidiol * pharmacology therapeutic use MeSH
- Humans MeSH
- Copper chemistry pharmacology MeSH
- Metallothionein MeSH
- Cell Line, Tumor MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't 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.
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