Document Detail


Involvement of the pleiotropic drug resistance response, protein kinase C signaling, and altered zinc homeostasis in resistance of Saccharomyces cerevisiae to diclofenac.
MedLine Citation:
PMID:  21724882     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Diclofenac is a widely used analgesic drug that can cause serious adverse drug reactions. We used Saccharomyces cerevisiae as a model eukaryote with which to elucidate the molecular mechanisms of diclofenac toxicity and resistance. Although most yeast cells died during the initial diclofenac treatment, some survived and started growing again. Microarray analysis of the adapted cells identified three major processes involved in diclofenac detoxification and tolerance. In particular, pleiotropic drug resistance (PDR) genes and genes under the control of Rlm1p, a transcription factor in the protein kinase C (PKC) pathway, were upregulated in diclofenac-adapted cells. We tested if these processes or pathways were directly involved in diclofenac toxicity or resistance. Of the pleiotropic drug resistance gene products, the multidrug transporter Pdr5p was crucially important for diclofenac tolerance. Furthermore, deletion of components of the cell wall stress-responsive PKC pathway increased diclofenac toxicity, whereas incubation of cells with the cell wall stressor calcofluor white before the addition of diclofenac decreased its toxicity. Also, diclofenac induced flocculation, which might trigger the cell wall alterations. Genes involved in ribosome biogenesis and rRNA processing were downregulated, as were zinc-responsive genes. Paradoxically, deletion of the zinc-responsive transcription factor Zap1p or addition of the zinc chelator 1,10-phenanthroline significantly increased diclofenac toxicity, establishing a regulatory role for zinc in diclofenac resistance. In conclusion, we have identified three new pathways involved in diclofenac tolerance in yeast, namely, Pdr5p as the main contributor to the PDR response, cell wall signaling via the PKC pathway, and zinc homeostasis, regulated by Zap1p.
Authors:
Jolanda S van Leeuwen; Nico P E Vermeulen; J Chris Vos
Publication Detail:
Type:  Journal Article     Date:  2011-07-01
Journal Detail:
Title:  Applied and environmental microbiology     Volume:  77     ISSN:  1098-5336     ISO Abbreviation:  Appl. Environ. Microbiol.     Publication Date:  2011 Sep 
Date Detail:
Created Date:  2011-08-25     Completed Date:  2011-12-13     Revised Date:  2013-06-28    
Medline Journal Info:
Nlm Unique ID:  7605801     Medline TA:  Appl Environ Microbiol     Country:  United States    
Other Details:
Languages:  eng     Pagination:  5973-80     Citation Subset:  IM    
Affiliation:
LACDR, Division of Molecular Toxicology, Department of Chemistry and Pharmaceutical Sciences, VU University Amsterdam, De Boelelaan 1083, 1081 HV Amsterdam, The Netherlands.
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MeSH Terms
Descriptor/Qualifier:
ATP-Binding Cassette Transporters / genetics,  metabolism
Antifungal Agents / metabolism*,  toxicity
Diclofenac / metabolism*,  toxicity
Drug Resistance, Fungal*
Gene Expression Profiling
Microarray Analysis
Microbial Viability / drug effects
Protein Kinase C / genetics,  metabolism*
Saccharomyces cerevisiae / drug effects*,  genetics
Saccharomyces cerevisiae Proteins / genetics,  metabolism*
Signal Transduction*
Transcription Factors / genetics,  metabolism
Zinc / metabolism*
Chemical
Reg. No./Substance:
0/Antifungal Agents; 0/PDR5 protein, S cerevisiae; 0/Saccharomyces cerevisiae Proteins; 0/Transcription Factors; 0/ZAP1 protein, S cerevisiae; 15307-86-5/Diclofenac; 7440-66-6/Zinc; EC 2.7.11.13/PKC1 protein, S cerevisiae; EC 2.7.11.13/Protein Kinase C
Comments/Corrections

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