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Regression of prostate tumors after intravenous administration of lactoferrin-bearing polypropylenimine dendriplexes encoding TNF-α, TRAIL, and interleukin-12
The possibility of using gene therapy for the treatment of prostate cancer is limited by the lack of intravenously administered delivery systems able to safely and selectively deliver therapeutic genes to tumors. Given that lactoferrin (Lf) receptors are overexpressed on prostate cancer cells, we hy...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6058574/ https://www.ncbi.nlm.nih.gov/pubmed/29493296 http://dx.doi.org/10.1080/10717544.2018.1440666 |
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author | Altwaijry, Najla Somani, Sukrut Parkinson, John A. Tate, Rothwelle J. Keating, Patricia Warzecha, Monika Mackenzie, Graeme R. Leung, Hing Y. Dufès, Christine |
author_facet | Altwaijry, Najla Somani, Sukrut Parkinson, John A. Tate, Rothwelle J. Keating, Patricia Warzecha, Monika Mackenzie, Graeme R. Leung, Hing Y. Dufès, Christine |
author_sort | Altwaijry, Najla |
collection | PubMed |
description | The possibility of using gene therapy for the treatment of prostate cancer is limited by the lack of intravenously administered delivery systems able to safely and selectively deliver therapeutic genes to tumors. Given that lactoferrin (Lf) receptors are overexpressed on prostate cancer cells, we hypothesized that the conjugation of Lf to generation 3-diaminobutyric polypropylenimine dendrimer would improve its transfection and therapeutic efficacy in prostate cancer cells. In this study, we demonstrated that the intravenous administration of Lf-bearing DAB dendriplexes encoding TNFα resulted in the complete suppression of 70% of PC-3 and 50% of DU145 tumors over one month. Treatment with DAB-Lf dendriplex encoding TRAIL led to tumor suppression of 40% of PC-3 tumors and 20% of DU145 tumors. The treatment was well tolerated by the animals. Lf-bearing generation 3-polypropylenimine dendrimer is therefore a highly promising delivery system for non-viral gene therapy of prostate cancer. |
format | Online Article Text |
id | pubmed-6058574 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-60585742018-08-17 Regression of prostate tumors after intravenous administration of lactoferrin-bearing polypropylenimine dendriplexes encoding TNF-α, TRAIL, and interleukin-12 Altwaijry, Najla Somani, Sukrut Parkinson, John A. Tate, Rothwelle J. Keating, Patricia Warzecha, Monika Mackenzie, Graeme R. Leung, Hing Y. Dufès, Christine Drug Deliv Research Article The possibility of using gene therapy for the treatment of prostate cancer is limited by the lack of intravenously administered delivery systems able to safely and selectively deliver therapeutic genes to tumors. Given that lactoferrin (Lf) receptors are overexpressed on prostate cancer cells, we hypothesized that the conjugation of Lf to generation 3-diaminobutyric polypropylenimine dendrimer would improve its transfection and therapeutic efficacy in prostate cancer cells. In this study, we demonstrated that the intravenous administration of Lf-bearing DAB dendriplexes encoding TNFα resulted in the complete suppression of 70% of PC-3 and 50% of DU145 tumors over one month. Treatment with DAB-Lf dendriplex encoding TRAIL led to tumor suppression of 40% of PC-3 tumors and 20% of DU145 tumors. The treatment was well tolerated by the animals. Lf-bearing generation 3-polypropylenimine dendrimer is therefore a highly promising delivery system for non-viral gene therapy of prostate cancer. Taylor & Francis 2018-03-01 /pmc/articles/PMC6058574/ /pubmed/29493296 http://dx.doi.org/10.1080/10717544.2018.1440666 Text en © 2018 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Altwaijry, Najla Somani, Sukrut Parkinson, John A. Tate, Rothwelle J. Keating, Patricia Warzecha, Monika Mackenzie, Graeme R. Leung, Hing Y. Dufès, Christine Regression of prostate tumors after intravenous administration of lactoferrin-bearing polypropylenimine dendriplexes encoding TNF-α, TRAIL, and interleukin-12 |
title | Regression of prostate tumors after intravenous administration of lactoferrin-bearing polypropylenimine dendriplexes encoding TNF-α, TRAIL, and interleukin-12 |
title_full | Regression of prostate tumors after intravenous administration of lactoferrin-bearing polypropylenimine dendriplexes encoding TNF-α, TRAIL, and interleukin-12 |
title_fullStr | Regression of prostate tumors after intravenous administration of lactoferrin-bearing polypropylenimine dendriplexes encoding TNF-α, TRAIL, and interleukin-12 |
title_full_unstemmed | Regression of prostate tumors after intravenous administration of lactoferrin-bearing polypropylenimine dendriplexes encoding TNF-α, TRAIL, and interleukin-12 |
title_short | Regression of prostate tumors after intravenous administration of lactoferrin-bearing polypropylenimine dendriplexes encoding TNF-α, TRAIL, and interleukin-12 |
title_sort | regression of prostate tumors after intravenous administration of lactoferrin-bearing polypropylenimine dendriplexes encoding tnf-α, trail, and interleukin-12 |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6058574/ https://www.ncbi.nlm.nih.gov/pubmed/29493296 http://dx.doi.org/10.1080/10717544.2018.1440666 |
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