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Powerful anti-colon cancer effect of modified nanoparticle-mediated IL-15 immunogene therapy through activation of the host immune system
Rationale: Colorectal cancer (CRC) is the third most commonly diagnosed cancer around the world. Over the past several years, immunotherapy has demonstrated considerable clinical benefit in CRC therapy, and the number of immunologic therapies for cancer treatment continues to climb each year. Interl...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Ivyspring International Publisher
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6037032/ https://www.ncbi.nlm.nih.gov/pubmed/30026861 http://dx.doi.org/10.7150/thno.24157 |
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author | Liu, Xiaoxiao Li, Yanyan Sun, Xiaodong Muftuoglu, Yagmur Wang, Bilan Yu, Ting Hu, Yuzhu Ma, Lu Xiang, Mingli Guo, Gang You, Chao Gao, Xiang Wei, Yuquan |
author_facet | Liu, Xiaoxiao Li, Yanyan Sun, Xiaodong Muftuoglu, Yagmur Wang, Bilan Yu, Ting Hu, Yuzhu Ma, Lu Xiang, Mingli Guo, Gang You, Chao Gao, Xiang Wei, Yuquan |
author_sort | Liu, Xiaoxiao |
collection | PubMed |
description | Rationale: Colorectal cancer (CRC) is the third most commonly diagnosed cancer around the world. Over the past several years, immunotherapy has demonstrated considerable clinical benefit in CRC therapy, and the number of immunologic therapies for cancer treatment continues to climb each year. Interleukin-15 (IL15), a potent pro-inflammatory cytokine, has emerged as a candidate immunomodulator for the treatment of CRC. Methods: In this study, we developed a novel gene delivery system with a self-assembly method using DOTAP and MPEG-PLA (DMA) to carry pIL15, denoted as DMA-pIL15 which was used to treat tumor-bearing mice. Results: Supernatant from lymphocytes treated with supernatant derived from CT26 cells transfected with DMA-pIL15 inhibited the growth of CT26 cells and induced cell apoptosis in vitro. Treatment of tumor-bearing mice with DMA-pIL15 complex significantly inhibited tumor growth in both subcutaneous and peritoneal models in vivo by inhibiting angiogenesis, promoting apoptosis, and reducing proliferation through activation of the host immune system. Conclusion: The IL-15 plasmid and DMA complex showed promise for treating CRC clinically as an experimental new drug. |
format | Online Article Text |
id | pubmed-6037032 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Ivyspring International Publisher |
record_format | MEDLINE/PubMed |
spelling | pubmed-60370322018-07-19 Powerful anti-colon cancer effect of modified nanoparticle-mediated IL-15 immunogene therapy through activation of the host immune system Liu, Xiaoxiao Li, Yanyan Sun, Xiaodong Muftuoglu, Yagmur Wang, Bilan Yu, Ting Hu, Yuzhu Ma, Lu Xiang, Mingli Guo, Gang You, Chao Gao, Xiang Wei, Yuquan Theranostics Research Paper Rationale: Colorectal cancer (CRC) is the third most commonly diagnosed cancer around the world. Over the past several years, immunotherapy has demonstrated considerable clinical benefit in CRC therapy, and the number of immunologic therapies for cancer treatment continues to climb each year. Interleukin-15 (IL15), a potent pro-inflammatory cytokine, has emerged as a candidate immunomodulator for the treatment of CRC. Methods: In this study, we developed a novel gene delivery system with a self-assembly method using DOTAP and MPEG-PLA (DMA) to carry pIL15, denoted as DMA-pIL15 which was used to treat tumor-bearing mice. Results: Supernatant from lymphocytes treated with supernatant derived from CT26 cells transfected with DMA-pIL15 inhibited the growth of CT26 cells and induced cell apoptosis in vitro. Treatment of tumor-bearing mice with DMA-pIL15 complex significantly inhibited tumor growth in both subcutaneous and peritoneal models in vivo by inhibiting angiogenesis, promoting apoptosis, and reducing proliferation through activation of the host immune system. Conclusion: The IL-15 plasmid and DMA complex showed promise for treating CRC clinically as an experimental new drug. Ivyspring International Publisher 2018-06-06 /pmc/articles/PMC6037032/ /pubmed/30026861 http://dx.doi.org/10.7150/thno.24157 Text en © Ivyspring International Publisher This is an open access article distributed under the terms of the Creative Commons Attribution (CC BY-NC) license (https://creativecommons.org/licenses/by-nc/4.0/). See http://ivyspring.com/terms for full terms and conditions. |
spellingShingle | Research Paper Liu, Xiaoxiao Li, Yanyan Sun, Xiaodong Muftuoglu, Yagmur Wang, Bilan Yu, Ting Hu, Yuzhu Ma, Lu Xiang, Mingli Guo, Gang You, Chao Gao, Xiang Wei, Yuquan Powerful anti-colon cancer effect of modified nanoparticle-mediated IL-15 immunogene therapy through activation of the host immune system |
title | Powerful anti-colon cancer effect of modified nanoparticle-mediated IL-15 immunogene therapy through activation of the host immune system |
title_full | Powerful anti-colon cancer effect of modified nanoparticle-mediated IL-15 immunogene therapy through activation of the host immune system |
title_fullStr | Powerful anti-colon cancer effect of modified nanoparticle-mediated IL-15 immunogene therapy through activation of the host immune system |
title_full_unstemmed | Powerful anti-colon cancer effect of modified nanoparticle-mediated IL-15 immunogene therapy through activation of the host immune system |
title_short | Powerful anti-colon cancer effect of modified nanoparticle-mediated IL-15 immunogene therapy through activation of the host immune system |
title_sort | powerful anti-colon cancer effect of modified nanoparticle-mediated il-15 immunogene therapy through activation of the host immune system |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6037032/ https://www.ncbi.nlm.nih.gov/pubmed/30026861 http://dx.doi.org/10.7150/thno.24157 |
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