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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ivyspring International Publisher 2018
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.
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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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