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Specific oncolytic activity of herpesvirus saimiri in pancreatic cancer cells
The potential use of oncolytic viruses in the treatment of cancer has been investigated for some time. A variety of agents have been studied, including some which appear to be selectively replication-competent in cancer cell lines. In this study, we have investigated the ability of herpesvirus saimi...
Autores principales: | , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2000
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2374565/ https://www.ncbi.nlm.nih.gov/pubmed/10917547 http://dx.doi.org/10.1054/bjoc.2000.1346 |
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author | Stevenson, A J Giles, M S Hall, K T Goodwin, D J Calderwood, M A Markham, A F Whitehouse, A |
author_facet | Stevenson, A J Giles, M S Hall, K T Goodwin, D J Calderwood, M A Markham, A F Whitehouse, A |
author_sort | Stevenson, A J |
collection | PubMed |
description | The potential use of oncolytic viruses in the treatment of cancer has been investigated for some time. A variety of agents have been studied, including some which appear to be selectively replication-competent in cancer cell lines. In this study, we have investigated the ability of herpesvirus saimiri to specifically lyse selected human cancer cell lines. Upon infection with a replication-competent virus carrying the EGFP reporter gene and a neomycin resistance marker, the pancreatic cancer lines MIAPACA and PANC-1 exhibited definite cytopathic effects. In contrast, the colonic carcinoma cell lines SW480 and HCT116 were phenotypically unaltered. In addition, stable cell lines could not be generated from PANC-1 infected cultures, in marked contrast to cultures of cells from other human tissues. Virus recovery assays demonstrated that all of the cell lines produced a small amount of virus post-infection, but that virus replication was minimal after 1 week in culture. In addition, treatment with acyclovir inhibited virus replication but paradoxically increased cytopathic effect. These data suggest that herpesvirus saimiri may have potential as an oncolytic agent for the treatment of pancreatic cancer. © 2000 Cancer Research Campaign |
format | Text |
id | pubmed-2374565 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2000 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-23745652009-09-10 Specific oncolytic activity of herpesvirus saimiri in pancreatic cancer cells Stevenson, A J Giles, M S Hall, K T Goodwin, D J Calderwood, M A Markham, A F Whitehouse, A Br J Cancer Regular Article The potential use of oncolytic viruses in the treatment of cancer has been investigated for some time. A variety of agents have been studied, including some which appear to be selectively replication-competent in cancer cell lines. In this study, we have investigated the ability of herpesvirus saimiri to specifically lyse selected human cancer cell lines. Upon infection with a replication-competent virus carrying the EGFP reporter gene and a neomycin resistance marker, the pancreatic cancer lines MIAPACA and PANC-1 exhibited definite cytopathic effects. In contrast, the colonic carcinoma cell lines SW480 and HCT116 were phenotypically unaltered. In addition, stable cell lines could not be generated from PANC-1 infected cultures, in marked contrast to cultures of cells from other human tissues. Virus recovery assays demonstrated that all of the cell lines produced a small amount of virus post-infection, but that virus replication was minimal after 1 week in culture. In addition, treatment with acyclovir inhibited virus replication but paradoxically increased cytopathic effect. These data suggest that herpesvirus saimiri may have potential as an oncolytic agent for the treatment of pancreatic cancer. © 2000 Cancer Research Campaign Nature Publishing Group 2000-07 2000-07-03 /pmc/articles/PMC2374565/ /pubmed/10917547 http://dx.doi.org/10.1054/bjoc.2000.1346 Text en Copyright © 2000 Cancer Research Campaign https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material.If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Regular Article Stevenson, A J Giles, M S Hall, K T Goodwin, D J Calderwood, M A Markham, A F Whitehouse, A Specific oncolytic activity of herpesvirus saimiri in pancreatic cancer cells |
title | Specific oncolytic activity of herpesvirus saimiri in pancreatic cancer cells |
title_full | Specific oncolytic activity of herpesvirus saimiri in pancreatic cancer cells |
title_fullStr | Specific oncolytic activity of herpesvirus saimiri in pancreatic cancer cells |
title_full_unstemmed | Specific oncolytic activity of herpesvirus saimiri in pancreatic cancer cells |
title_short | Specific oncolytic activity of herpesvirus saimiri in pancreatic cancer cells |
title_sort | specific oncolytic activity of herpesvirus saimiri in pancreatic cancer cells |
topic | Regular Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2374565/ https://www.ncbi.nlm.nih.gov/pubmed/10917547 http://dx.doi.org/10.1054/bjoc.2000.1346 |
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