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The inhibitor of cyclin-dependent kinases, olomoucine II, exhibits potent antiviral properties
J Holcakova, P Tomasec, JJ Bugert, EC Wang, GW Wilkinson, R Hrstka, V Krystof, M Strnad, B Vojtesek
Language English Country Great Britain
Document type Research Support, Non-U.S. Gov't
NLK
Free Medical Journals
from 1999 to 1 year ago
ProQuest Central
from 1990-02-01 to 2015-12-31
Health & Medicine (ProQuest)
from 1990-02-01 to 2015-12-31
ROAD: Directory of Open Access Scholarly Resources
from 1990 to 2023
- MeSH
- Antiviral Agents pharmacology MeSH
- Cyclin-Dependent Kinases antagonists & inhibitors MeSH
- Virus Physiological Phenomena drug effects MeSH
- Inhibitory Concentration 50 MeSH
- Protein Kinase Inhibitors pharmacology MeSH
- Humans MeSH
- Purines pharmacology MeSH
- Virus Replication drug effects MeSH
- Viruses enzymology growth & development MeSH
- Check Tag
- Humans MeSH
- Publication type
- Research Support, Non-U.S. Gov't MeSH
BACKGROUND: Olomoucine II, the most recent derivative of roscovitine, is an exceptionally potent pharmacological inhibitor of cyclin-dependent kinase activities. Here, we report that olomoucine II is also an effective antiviral agent. METHODS: Antiviral activities of olomoucine II were tested on a range of human viruses in in vitro assays that evaluated viral growth and replication. RESULTS: Olomoucine II inhibited replication of a broad range of wild-type human viruses, including herpes simplex virus, human adenovirus type-4 and human cytomegalovirus. Olomoucine II also inhibited replication of vaccinia virus and herpes simplex virus mutants resistant to conventional acyclovir treatment. This report is the first demonstration of a poxvirus being sensitive to a cyclin-dependent kinase inhibitor. The antiviral effects of olomoucine II could be observed at lower concentrations than with roscovitine, although both were short-term. A remarkable observation was that olomoucine II, when used in combination with the DNA polymerase inhibitor cidofovir, was able to almost completely eliminate the spread of infectious adenovirus type-4 progeny from infected cells. CONCLUSIONS: Our results show that when targeting two complementary antiviral mechanisms, strongly additive effects could be observed.
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- $a Holčáková, Jitka $7 xx0125776 $u Department of Oncological and Experimental Pathology, Masaryk Memorial Cancer Institute, Brno, Czech Republic.
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- $a The inhibitor of cyclin-dependent kinases, olomoucine II, exhibits potent antiviral properties / $c J Holcakova, P Tomasec, JJ Bugert, EC Wang, GW Wilkinson, R Hrstka, V Krystof, M Strnad, B Vojtesek
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- $a BACKGROUND: Olomoucine II, the most recent derivative of roscovitine, is an exceptionally potent pharmacological inhibitor of cyclin-dependent kinase activities. Here, we report that olomoucine II is also an effective antiviral agent. METHODS: Antiviral activities of olomoucine II were tested on a range of human viruses in in vitro assays that evaluated viral growth and replication. RESULTS: Olomoucine II inhibited replication of a broad range of wild-type human viruses, including herpes simplex virus, human adenovirus type-4 and human cytomegalovirus. Olomoucine II also inhibited replication of vaccinia virus and herpes simplex virus mutants resistant to conventional acyclovir treatment. This report is the first demonstration of a poxvirus being sensitive to a cyclin-dependent kinase inhibitor. The antiviral effects of olomoucine II could be observed at lower concentrations than with roscovitine, although both were short-term. A remarkable observation was that olomoucine II, when used in combination with the DNA polymerase inhibitor cidofovir, was able to almost completely eliminate the spread of infectious adenovirus type-4 progeny from infected cells. CONCLUSIONS: Our results show that when targeting two complementary antiviral mechanisms, strongly additive effects could be observed.
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- $c Grant Number: G0300180(65735) (United Kingdom Medical Research Council)
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- $c Grant Number: G0500617(74644) (United Kingdom Medical Research Council)
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- $c Grant Number: G0901119(91900) (United Kingdom Medical Research Council)
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- $c Grant Number: (United Kingdom Medical Research Council)
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- $c Grant Number: (United Kingdom Wellcome Trust)
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- $t Antiviral Chemistry & Chemotherapy $p Antivir Chem Chemother $g Roč. 20, č. 3 (2010), s. 133-142 $w MED00193671 $x 0956-3202
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