Improving adenoviral vectors and strategies for prostate cancer gene therapy

Detalhes bibliográficos
Autor(a) principal: Tamura, Rodrigo Esaki
Data de Publicação: 2019
Outros Autores: Luna, Igor Vieira de, Lana, Marlous Gomes, Strauss, Bryan E.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Clinics
Texto Completo: https://www.revistas.usp.br/clinics/article/view/154756
Resumo: Gene therapy has been evaluated for the treatment of prostate cancer and includes the application of adenoviral vectors encoding a suicide gene or oncolytic adenoviruses that may be armed with a functional transgene. In parallel, versions of adenoviral vector expressing the p53 gene (Ad-p53) have been tested as treatments for head and neck squamous cell carcinoma and non-small cell lung cancer. Although Ad-p53 gene therapy has yielded some interesting results when applied to prostate cancer, it has not been widely explored, perhaps due to current limitations of the approach. To achieve better functionality, improvements in the gene transfer system and the therapeutic regimen may be required. We have developed adenoviral vectors whose transgene expression is controlled by a p53-responsive promoter, which creates a positive feedback mechanism when used to drive the expression of p53. Together with improvements that permit efficient transduction, this new approach was more effective than the use of traditional versions of Ad-p53 in killing prostate cancer cell lines and inhibiting tumor progression. Even so, gene therapy is not expected to replace traditional chemotherapy but should complement the standard of care. In fact, chemotherapy has been shown to assist in viral transduction and transgene expression. The cooperation between gene therapy and chemotherapy is expected to effectively kill tumor cells while permitting the use of reduced chemotherapy drug concentrations and, thus, lowering side effects. Therefore, the combination of gene therapy and chemotherapy may prove essential for the success of both approaches.
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spelling Improving adenoviral vectors and strategies for prostate cancer gene therapyProstate CancerAdenovirusp53ChemotherapyGene TherapyGene therapy has been evaluated for the treatment of prostate cancer and includes the application of adenoviral vectors encoding a suicide gene or oncolytic adenoviruses that may be armed with a functional transgene. In parallel, versions of adenoviral vector expressing the p53 gene (Ad-p53) have been tested as treatments for head and neck squamous cell carcinoma and non-small cell lung cancer. Although Ad-p53 gene therapy has yielded some interesting results when applied to prostate cancer, it has not been widely explored, perhaps due to current limitations of the approach. To achieve better functionality, improvements in the gene transfer system and the therapeutic regimen may be required. We have developed adenoviral vectors whose transgene expression is controlled by a p53-responsive promoter, which creates a positive feedback mechanism when used to drive the expression of p53. Together with improvements that permit efficient transduction, this new approach was more effective than the use of traditional versions of Ad-p53 in killing prostate cancer cell lines and inhibiting tumor progression. Even so, gene therapy is not expected to replace traditional chemotherapy but should complement the standard of care. In fact, chemotherapy has been shown to assist in viral transduction and transgene expression. The cooperation between gene therapy and chemotherapy is expected to effectively kill tumor cells while permitting the use of reduced chemotherapy drug concentrations and, thus, lowering side effects. Therefore, the combination of gene therapy and chemotherapy may prove essential for the success of both approaches.Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo2019-02-14info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://www.revistas.usp.br/clinics/article/view/15475610.6061/clinics/2018/e476sClinics; Vol. 73 No. Suppl. 1 (2018); e476sClinics; v. 73 n. Suppl. 1 (2018); e476sClinics; Vol. 73 Núm. Suppl. 1 (2018); e476s1980-53221807-5932reponame:Clinicsinstname:Universidade de São Paulo (USP)instacron:USPenghttps://www.revistas.usp.br/clinics/article/view/154756/150780Copyright (c) 2019 Clinicsinfo:eu-repo/semantics/openAccessTamura, Rodrigo EsakiLuna, Igor Vieira deLana, Marlous GomesStrauss, Bryan E.2019-05-14T11:48:25Zoai:revistas.usp.br:article/154756Revistahttps://www.revistas.usp.br/clinicsPUBhttps://www.revistas.usp.br/clinics/oai||clinics@hc.fm.usp.br1980-53221807-5932opendoar:2019-05-14T11:48:25Clinics - Universidade de São Paulo (USP)false
dc.title.none.fl_str_mv Improving adenoviral vectors and strategies for prostate cancer gene therapy
title Improving adenoviral vectors and strategies for prostate cancer gene therapy
spellingShingle Improving adenoviral vectors and strategies for prostate cancer gene therapy
Tamura, Rodrigo Esaki
Prostate Cancer
Adenovirus
p53
Chemotherapy
Gene Therapy
title_short Improving adenoviral vectors and strategies for prostate cancer gene therapy
title_full Improving adenoviral vectors and strategies for prostate cancer gene therapy
title_fullStr Improving adenoviral vectors and strategies for prostate cancer gene therapy
title_full_unstemmed Improving adenoviral vectors and strategies for prostate cancer gene therapy
title_sort Improving adenoviral vectors and strategies for prostate cancer gene therapy
author Tamura, Rodrigo Esaki
author_facet Tamura, Rodrigo Esaki
Luna, Igor Vieira de
Lana, Marlous Gomes
Strauss, Bryan E.
author_role author
author2 Luna, Igor Vieira de
Lana, Marlous Gomes
Strauss, Bryan E.
author2_role author
author
author
dc.contributor.author.fl_str_mv Tamura, Rodrigo Esaki
Luna, Igor Vieira de
Lana, Marlous Gomes
Strauss, Bryan E.
dc.subject.por.fl_str_mv Prostate Cancer
Adenovirus
p53
Chemotherapy
Gene Therapy
topic Prostate Cancer
Adenovirus
p53
Chemotherapy
Gene Therapy
description Gene therapy has been evaluated for the treatment of prostate cancer and includes the application of adenoviral vectors encoding a suicide gene or oncolytic adenoviruses that may be armed with a functional transgene. In parallel, versions of adenoviral vector expressing the p53 gene (Ad-p53) have been tested as treatments for head and neck squamous cell carcinoma and non-small cell lung cancer. Although Ad-p53 gene therapy has yielded some interesting results when applied to prostate cancer, it has not been widely explored, perhaps due to current limitations of the approach. To achieve better functionality, improvements in the gene transfer system and the therapeutic regimen may be required. We have developed adenoviral vectors whose transgene expression is controlled by a p53-responsive promoter, which creates a positive feedback mechanism when used to drive the expression of p53. Together with improvements that permit efficient transduction, this new approach was more effective than the use of traditional versions of Ad-p53 in killing prostate cancer cell lines and inhibiting tumor progression. Even so, gene therapy is not expected to replace traditional chemotherapy but should complement the standard of care. In fact, chemotherapy has been shown to assist in viral transduction and transgene expression. The cooperation between gene therapy and chemotherapy is expected to effectively kill tumor cells while permitting the use of reduced chemotherapy drug concentrations and, thus, lowering side effects. Therefore, the combination of gene therapy and chemotherapy may prove essential for the success of both approaches.
publishDate 2019
dc.date.none.fl_str_mv 2019-02-14
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv https://www.revistas.usp.br/clinics/article/view/154756
10.6061/clinics/2018/e476s
url https://www.revistas.usp.br/clinics/article/view/154756
identifier_str_mv 10.6061/clinics/2018/e476s
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv https://www.revistas.usp.br/clinics/article/view/154756/150780
dc.rights.driver.fl_str_mv Copyright (c) 2019 Clinics
info:eu-repo/semantics/openAccess
rights_invalid_str_mv Copyright (c) 2019 Clinics
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo
publisher.none.fl_str_mv Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo
dc.source.none.fl_str_mv Clinics; Vol. 73 No. Suppl. 1 (2018); e476s
Clinics; v. 73 n. Suppl. 1 (2018); e476s
Clinics; Vol. 73 Núm. Suppl. 1 (2018); e476s
1980-5322
1807-5932
reponame:Clinics
instname:Universidade de São Paulo (USP)
instacron:USP
instname_str Universidade de São Paulo (USP)
instacron_str USP
institution USP
reponame_str Clinics
collection Clinics
repository.name.fl_str_mv Clinics - Universidade de São Paulo (USP)
repository.mail.fl_str_mv ||clinics@hc.fm.usp.br
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