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Baculoviruses as Vectors for Gene Therapy against Human Prostate Cancer

Current curative strategies for prostate cancer are restricted to the primary tumour, and the effect of treatments to control metastatic disease is not sustained. Therefore, the application of gene therapy to prostate cancer is an attractive alternative. Baculoviruses are highly restricted insect vi...

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Detalles Bibliográficos
Autores principales: Stanbridge, Lindsay J., Dussupt, Vincent, Maitland, Norman J.
Formato: Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2003
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC323953/
https://www.ncbi.nlm.nih.gov/pubmed/12721513
http://dx.doi.org/10.1155/S1110724303209049
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author Stanbridge, Lindsay J.
Dussupt, Vincent
Maitland, Norman J.
author_facet Stanbridge, Lindsay J.
Dussupt, Vincent
Maitland, Norman J.
author_sort Stanbridge, Lindsay J.
collection PubMed
description Current curative strategies for prostate cancer are restricted to the primary tumour, and the effect of treatments to control metastatic disease is not sustained. Therefore, the application of gene therapy to prostate cancer is an attractive alternative. Baculoviruses are highly restricted insect viruses, which can enter, but not replicate in mammalian cells. Baculoviruses can incorporate large amounts of extra genetic material, and will express transgenes in mammalian cells when under the control of a mammalian or strong viral promoter. Successful gene delivery has been achieved both in vitro and in vivo and into both dividing and nondividing cells, which is important since prostate cancers divide relatively slowly. In addition, the envelope protein gp64 is sufficiently mutable to allow targeted transduction of particular cell types. In this review, the advantages of using baculoviruses for prostate cancer gene therapy are explored, and the mechanisms of viral entry and transgene expression are described.
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spelling pubmed-3239532004-04-06 Baculoviruses as Vectors for Gene Therapy against Human Prostate Cancer Stanbridge, Lindsay J. Dussupt, Vincent Maitland, Norman J. J Biomed Biotechnol Review Article Current curative strategies for prostate cancer are restricted to the primary tumour, and the effect of treatments to control metastatic disease is not sustained. Therefore, the application of gene therapy to prostate cancer is an attractive alternative. Baculoviruses are highly restricted insect viruses, which can enter, but not replicate in mammalian cells. Baculoviruses can incorporate large amounts of extra genetic material, and will express transgenes in mammalian cells when under the control of a mammalian or strong viral promoter. Successful gene delivery has been achieved both in vitro and in vivo and into both dividing and nondividing cells, which is important since prostate cancers divide relatively slowly. In addition, the envelope protein gp64 is sufficiently mutable to allow targeted transduction of particular cell types. In this review, the advantages of using baculoviruses for prostate cancer gene therapy are explored, and the mechanisms of viral entry and transgene expression are described. Hindawi Publishing Corporation 2003-04-21 /pmc/articles/PMC323953/ /pubmed/12721513 http://dx.doi.org/10.1155/S1110724303209049 Text en Copyright © 2003, Hindawi Publishing Corporation
spellingShingle Review Article
Stanbridge, Lindsay J.
Dussupt, Vincent
Maitland, Norman J.
Baculoviruses as Vectors for Gene Therapy against Human Prostate Cancer
title Baculoviruses as Vectors for Gene Therapy against Human Prostate Cancer
title_full Baculoviruses as Vectors for Gene Therapy against Human Prostate Cancer
title_fullStr Baculoviruses as Vectors for Gene Therapy against Human Prostate Cancer
title_full_unstemmed Baculoviruses as Vectors for Gene Therapy against Human Prostate Cancer
title_short Baculoviruses as Vectors for Gene Therapy against Human Prostate Cancer
title_sort baculoviruses as vectors for gene therapy against human prostate cancer
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC323953/
https://www.ncbi.nlm.nih.gov/pubmed/12721513
http://dx.doi.org/10.1155/S1110724303209049
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