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Synergistic effect of a drug loaded electrospun patch and systemic chemotherapy in pancreatic cancer xenograft
Pancreatic cancer has a high rate of local recurrence and poor prognosis even with adjuvant chemotherapy after curative resection. The aim of this study was to investigate if local drug delivery combined with low dose systemic chemotherapy can increase the therapeutic effect of chemotherapy while re...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5620083/ https://www.ncbi.nlm.nih.gov/pubmed/28959053 http://dx.doi.org/10.1038/s41598-017-12670-3 |
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author | Jun, Eunsung Kim, Song Cheol Lee, Chan Mi Oh, Juyun Lee, Song Shim, In Kyong |
author_facet | Jun, Eunsung Kim, Song Cheol Lee, Chan Mi Oh, Juyun Lee, Song Shim, In Kyong |
author_sort | Jun, Eunsung |
collection | PubMed |
description | Pancreatic cancer has a high rate of local recurrence and poor prognosis even with adjuvant chemotherapy after curative resection. The aim of this study was to investigate if local drug delivery combined with low dose systemic chemotherapy can increase the therapeutic effect of chemotherapy while reducing systemic toxicities. Poly-L-lactic acid-based 5-FU releasing patch was fabricated by electrospinning, and its tumour killing effects were first confirmed in vitro. The 5-FU patch directly adhered to the tumour in subcutaneous and orthotopic murine models, and induced a significant decrease in tumour size. Systemic gemcitabine treatment group, 5-FU drug releasing patch group, and systemic gemcitabine plus 5-FU patch group were compared by tumour size measurement, non-invasive bio-imaging, and histology in subcutaneous models. Combination of local drug patch and systemic chemotherapy led to increased tumour suppression effects that lasted longer, as well as increased survival rate. Histology revealed higher degree of apoptosis in the combined group. Systemic toxicity was recovered within 7 days after the treatment in all mice. Conclusively, local drug delivery using biocompatible polymer patch significantly inhibited tumour growth, and combination with systemic chemotherapy was more effective than single systemic chemotherapy. |
format | Online Article Text |
id | pubmed-5620083 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-56200832017-10-11 Synergistic effect of a drug loaded electrospun patch and systemic chemotherapy in pancreatic cancer xenograft Jun, Eunsung Kim, Song Cheol Lee, Chan Mi Oh, Juyun Lee, Song Shim, In Kyong Sci Rep Article Pancreatic cancer has a high rate of local recurrence and poor prognosis even with adjuvant chemotherapy after curative resection. The aim of this study was to investigate if local drug delivery combined with low dose systemic chemotherapy can increase the therapeutic effect of chemotherapy while reducing systemic toxicities. Poly-L-lactic acid-based 5-FU releasing patch was fabricated by electrospinning, and its tumour killing effects were first confirmed in vitro. The 5-FU patch directly adhered to the tumour in subcutaneous and orthotopic murine models, and induced a significant decrease in tumour size. Systemic gemcitabine treatment group, 5-FU drug releasing patch group, and systemic gemcitabine plus 5-FU patch group were compared by tumour size measurement, non-invasive bio-imaging, and histology in subcutaneous models. Combination of local drug patch and systemic chemotherapy led to increased tumour suppression effects that lasted longer, as well as increased survival rate. Histology revealed higher degree of apoptosis in the combined group. Systemic toxicity was recovered within 7 days after the treatment in all mice. Conclusively, local drug delivery using biocompatible polymer patch significantly inhibited tumour growth, and combination with systemic chemotherapy was more effective than single systemic chemotherapy. Nature Publishing Group UK 2017-09-28 /pmc/articles/PMC5620083/ /pubmed/28959053 http://dx.doi.org/10.1038/s41598-017-12670-3 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Jun, Eunsung Kim, Song Cheol Lee, Chan Mi Oh, Juyun Lee, Song Shim, In Kyong Synergistic effect of a drug loaded electrospun patch and systemic chemotherapy in pancreatic cancer xenograft |
title | Synergistic effect of a drug loaded electrospun patch and systemic chemotherapy in pancreatic cancer xenograft |
title_full | Synergistic effect of a drug loaded electrospun patch and systemic chemotherapy in pancreatic cancer xenograft |
title_fullStr | Synergistic effect of a drug loaded electrospun patch and systemic chemotherapy in pancreatic cancer xenograft |
title_full_unstemmed | Synergistic effect of a drug loaded electrospun patch and systemic chemotherapy in pancreatic cancer xenograft |
title_short | Synergistic effect of a drug loaded electrospun patch and systemic chemotherapy in pancreatic cancer xenograft |
title_sort | synergistic effect of a drug loaded electrospun patch and systemic chemotherapy in pancreatic cancer xenograft |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5620083/ https://www.ncbi.nlm.nih.gov/pubmed/28959053 http://dx.doi.org/10.1038/s41598-017-12670-3 |
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