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Loss of Cyclin-Dependent Kinase Inhibitor Alters Oncolytic Adenovirus Replication and Promotes More Efficient Virus Production

We elucidate the role of p21/Waf-1, a cyclin-dependent kinase inhibitor, on the oncolytic infection and replication cycle of adenovirus by studying both mRNA and adenoviral proteins expression. We found that infection in the absence of p21 causes a significant increase in adenoviral genomes and late...

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Autores principales: Höti, Naseruddin, Johnson, Tamara Jane, Chowdhury, Wasim H., Rodriguez, Ronald
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6025342/
https://www.ncbi.nlm.nih.gov/pubmed/29914081
http://dx.doi.org/10.3390/cancers10060202
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author Höti, Naseruddin
Johnson, Tamara Jane
Chowdhury, Wasim H.
Rodriguez, Ronald
author_facet Höti, Naseruddin
Johnson, Tamara Jane
Chowdhury, Wasim H.
Rodriguez, Ronald
author_sort Höti, Naseruddin
collection PubMed
description We elucidate the role of p21/Waf-1, a cyclin-dependent kinase inhibitor, on the oncolytic infection and replication cycle of adenovirus by studying both mRNA and adenoviral proteins expression. We found that infection in the absence of p21 causes a significant increase in adenoviral genomes and late gene expression. Similarly, the oncolytic adenoviral infected p21(−/−) cells have earlier formation of replication foci and robust replication kinetics that were not observed in the wild type p21/Waf-1 intact cells. These findings suggest a culmination that the presence of intact p21 in host cells causes defects in the oncolytic viral life cycle which results in the production of immature and noninfectious particles.
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spelling pubmed-60253422018-07-09 Loss of Cyclin-Dependent Kinase Inhibitor Alters Oncolytic Adenovirus Replication and Promotes More Efficient Virus Production Höti, Naseruddin Johnson, Tamara Jane Chowdhury, Wasim H. Rodriguez, Ronald Cancers (Basel) Article We elucidate the role of p21/Waf-1, a cyclin-dependent kinase inhibitor, on the oncolytic infection and replication cycle of adenovirus by studying both mRNA and adenoviral proteins expression. We found that infection in the absence of p21 causes a significant increase in adenoviral genomes and late gene expression. Similarly, the oncolytic adenoviral infected p21(−/−) cells have earlier formation of replication foci and robust replication kinetics that were not observed in the wild type p21/Waf-1 intact cells. These findings suggest a culmination that the presence of intact p21 in host cells causes defects in the oncolytic viral life cycle which results in the production of immature and noninfectious particles. MDPI 2018-06-15 /pmc/articles/PMC6025342/ /pubmed/29914081 http://dx.doi.org/10.3390/cancers10060202 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Höti, Naseruddin
Johnson, Tamara Jane
Chowdhury, Wasim H.
Rodriguez, Ronald
Loss of Cyclin-Dependent Kinase Inhibitor Alters Oncolytic Adenovirus Replication and Promotes More Efficient Virus Production
title Loss of Cyclin-Dependent Kinase Inhibitor Alters Oncolytic Adenovirus Replication and Promotes More Efficient Virus Production
title_full Loss of Cyclin-Dependent Kinase Inhibitor Alters Oncolytic Adenovirus Replication and Promotes More Efficient Virus Production
title_fullStr Loss of Cyclin-Dependent Kinase Inhibitor Alters Oncolytic Adenovirus Replication and Promotes More Efficient Virus Production
title_full_unstemmed Loss of Cyclin-Dependent Kinase Inhibitor Alters Oncolytic Adenovirus Replication and Promotes More Efficient Virus Production
title_short Loss of Cyclin-Dependent Kinase Inhibitor Alters Oncolytic Adenovirus Replication and Promotes More Efficient Virus Production
title_sort loss of cyclin-dependent kinase inhibitor alters oncolytic adenovirus replication and promotes more efficient virus production
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6025342/
https://www.ncbi.nlm.nih.gov/pubmed/29914081
http://dx.doi.org/10.3390/cancers10060202
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