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Gene Therapy for Pancreatic Cancer: Specificity, Issues and Hopes
A recent death projection has placed pancreatic ductal adenocarcinoma as the second cause of death by cancer in 2030. The prognosis for pancreatic cancer is very poor and there is a great need for new treatments that can change this poor outcome. Developments of therapeutic innovations in combinatio...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5486054/ https://www.ncbi.nlm.nih.gov/pubmed/28594388 http://dx.doi.org/10.3390/ijms18061231 |
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author | Rouanet, Marie Lebrin, Marine Gross, Fabian Bournet, Barbara Cordelier, Pierre Buscail, Louis |
author_facet | Rouanet, Marie Lebrin, Marine Gross, Fabian Bournet, Barbara Cordelier, Pierre Buscail, Louis |
author_sort | Rouanet, Marie |
collection | PubMed |
description | A recent death projection has placed pancreatic ductal adenocarcinoma as the second cause of death by cancer in 2030. The prognosis for pancreatic cancer is very poor and there is a great need for new treatments that can change this poor outcome. Developments of therapeutic innovations in combination with conventional chemotherapy are needed urgently. Among innovative treatments the gene therapy offers a promising avenue. The present review gives an overview of the general strategy of gene therapy as well as the limitations and stakes of the different experimental in vivo models, expression vectors (synthetic and viral), molecular tools (interference RNA, genome editing) and therapeutic genes (tumor suppressor genes, antiangiogenic and pro-apoptotic genes, suicide genes). The latest developments in pancreatic carcinoma gene therapy are described including gene-based tumor cell sensitization to chemotherapy, vaccination and adoptive immunotherapy (chimeric antigen receptor T-cells strategy). Nowadays, there is a specific development of oncolytic virus therapies including oncolytic adenoviruses, herpes virus, parvovirus or reovirus. A summary of all published and on-going phase-1 trials is given. Most of them associate gene therapy and chemotherapy or radiochemotherapy. The first results are encouraging for most of the trials but remain to be confirmed in phase 2 trials. |
format | Online Article Text |
id | pubmed-5486054 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-54860542017-06-29 Gene Therapy for Pancreatic Cancer: Specificity, Issues and Hopes Rouanet, Marie Lebrin, Marine Gross, Fabian Bournet, Barbara Cordelier, Pierre Buscail, Louis Int J Mol Sci Review A recent death projection has placed pancreatic ductal adenocarcinoma as the second cause of death by cancer in 2030. The prognosis for pancreatic cancer is very poor and there is a great need for new treatments that can change this poor outcome. Developments of therapeutic innovations in combination with conventional chemotherapy are needed urgently. Among innovative treatments the gene therapy offers a promising avenue. The present review gives an overview of the general strategy of gene therapy as well as the limitations and stakes of the different experimental in vivo models, expression vectors (synthetic and viral), molecular tools (interference RNA, genome editing) and therapeutic genes (tumor suppressor genes, antiangiogenic and pro-apoptotic genes, suicide genes). The latest developments in pancreatic carcinoma gene therapy are described including gene-based tumor cell sensitization to chemotherapy, vaccination and adoptive immunotherapy (chimeric antigen receptor T-cells strategy). Nowadays, there is a specific development of oncolytic virus therapies including oncolytic adenoviruses, herpes virus, parvovirus or reovirus. A summary of all published and on-going phase-1 trials is given. Most of them associate gene therapy and chemotherapy or radiochemotherapy. The first results are encouraging for most of the trials but remain to be confirmed in phase 2 trials. MDPI 2017-06-08 /pmc/articles/PMC5486054/ /pubmed/28594388 http://dx.doi.org/10.3390/ijms18061231 Text en © 2017 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 | Review Rouanet, Marie Lebrin, Marine Gross, Fabian Bournet, Barbara Cordelier, Pierre Buscail, Louis Gene Therapy for Pancreatic Cancer: Specificity, Issues and Hopes |
title | Gene Therapy for Pancreatic Cancer: Specificity, Issues and Hopes |
title_full | Gene Therapy for Pancreatic Cancer: Specificity, Issues and Hopes |
title_fullStr | Gene Therapy for Pancreatic Cancer: Specificity, Issues and Hopes |
title_full_unstemmed | Gene Therapy for Pancreatic Cancer: Specificity, Issues and Hopes |
title_short | Gene Therapy for Pancreatic Cancer: Specificity, Issues and Hopes |
title_sort | gene therapy for pancreatic cancer: specificity, issues and hopes |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5486054/ https://www.ncbi.nlm.nih.gov/pubmed/28594388 http://dx.doi.org/10.3390/ijms18061231 |
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