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Polymeric nanoparticle‐based delivery of TRAIL DNA for cancer‐specific killing
Lack of specificity in cancer therapeutics severely limits the efficacy of many existing treatment modalities. The use of Tumor Necrosis Factor‐related Apoptosis‐Inducing Ligand (TRAIL) is of interest to the field due to this protein's ability to cause cell death specifically in cancer cells wi...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5365091/ https://www.ncbi.nlm.nih.gov/pubmed/28349127 http://dx.doi.org/10.1002/btm2.10019 |
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author | Tzeng, Stephany Y. Wilson, David R. Hansen, Sarah K. Quiñones‐Hinojosa, Alfredo Green, Jordan J. |
author_facet | Tzeng, Stephany Y. Wilson, David R. Hansen, Sarah K. Quiñones‐Hinojosa, Alfredo Green, Jordan J. |
author_sort | Tzeng, Stephany Y. |
collection | PubMed |
description | Lack of specificity in cancer therapeutics severely limits the efficacy of many existing treatment modalities. The use of Tumor Necrosis Factor‐related Apoptosis‐Inducing Ligand (TRAIL) is of interest to the field due to this protein's ability to cause cell death specifically in cancer cells without harming the surrounding healthy tissue. Here, we report that polymeric nanoparticles, based on synthetic poly(beta‐amino ester)s (PBAEs) and containing DNA, are able to selectively transfect cancer cells in vitro over healthy cells of the same tissue type. Moreover, PBAE‐based nanoparticles containing TRAIL DNA are able to transfect several human cancer cell cultures in vitro and cause cell death. While certain cell types, including human glioblastoma (GBM), showed resistance to TRAIL, we found that the expression of TRAIL‐binding surface proteins was predictive of each cell type's resistance to TRAIL therapy. We demonstrate a non‐viral nanomedicine approach to cancer gene therapy that can improve cancer specificity via both biomaterial selection and through the use of cancer‐targeting genetic cargo. |
format | Online Article Text |
id | pubmed-5365091 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-53650912017-06-01 Polymeric nanoparticle‐based delivery of TRAIL DNA for cancer‐specific killing Tzeng, Stephany Y. Wilson, David R. Hansen, Sarah K. Quiñones‐Hinojosa, Alfredo Green, Jordan J. Bioeng Transl Med Research Reports Lack of specificity in cancer therapeutics severely limits the efficacy of many existing treatment modalities. The use of Tumor Necrosis Factor‐related Apoptosis‐Inducing Ligand (TRAIL) is of interest to the field due to this protein's ability to cause cell death specifically in cancer cells without harming the surrounding healthy tissue. Here, we report that polymeric nanoparticles, based on synthetic poly(beta‐amino ester)s (PBAEs) and containing DNA, are able to selectively transfect cancer cells in vitro over healthy cells of the same tissue type. Moreover, PBAE‐based nanoparticles containing TRAIL DNA are able to transfect several human cancer cell cultures in vitro and cause cell death. While certain cell types, including human glioblastoma (GBM), showed resistance to TRAIL, we found that the expression of TRAIL‐binding surface proteins was predictive of each cell type's resistance to TRAIL therapy. We demonstrate a non‐viral nanomedicine approach to cancer gene therapy that can improve cancer specificity via both biomaterial selection and through the use of cancer‐targeting genetic cargo. John Wiley and Sons Inc. 2016-08-19 /pmc/articles/PMC5365091/ /pubmed/28349127 http://dx.doi.org/10.1002/btm2.10019 Text en © 2016 The Authors. Bioengineering & Translational Medicine is published by Wiley Periodicals, Inc. on behalf of The American Institute of Chemical Engineers. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Reports Tzeng, Stephany Y. Wilson, David R. Hansen, Sarah K. Quiñones‐Hinojosa, Alfredo Green, Jordan J. Polymeric nanoparticle‐based delivery of TRAIL DNA for cancer‐specific killing |
title | Polymeric nanoparticle‐based delivery of TRAIL DNA for cancer‐specific killing |
title_full | Polymeric nanoparticle‐based delivery of TRAIL DNA for cancer‐specific killing |
title_fullStr | Polymeric nanoparticle‐based delivery of TRAIL DNA for cancer‐specific killing |
title_full_unstemmed | Polymeric nanoparticle‐based delivery of TRAIL DNA for cancer‐specific killing |
title_short | Polymeric nanoparticle‐based delivery of TRAIL DNA for cancer‐specific killing |
title_sort | polymeric nanoparticle‐based delivery of trail dna for cancer‐specific killing |
topic | Research Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5365091/ https://www.ncbi.nlm.nih.gov/pubmed/28349127 http://dx.doi.org/10.1002/btm2.10019 |
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