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MMP-2-Controlled Transforming Micelles for Heterogeneic Targeting and Programmable Cancer Therapy
Herein, through the active-peptide-functionalization, we developed a nanoscale micelles system (named HEKM) which consists of tumor microenvironment-regulated shape-changing with specific recognition abilities for enhanced cellular targeting, internalization and therapy of heterogeneic tumors. As a...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Ivyspring International Publisher
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6485184/ https://www.ncbi.nlm.nih.gov/pubmed/31037134 http://dx.doi.org/10.7150/thno.30915 |
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author | Wang, Zihua Wang, Yuehua Jia, Xiangqian Han, Qiuju Qian, Yixia Li, Qian Xiang, Junfeng Wang, Qian Hu, Zhiyuan Wang, Weizhi |
author_facet | Wang, Zihua Wang, Yuehua Jia, Xiangqian Han, Qiuju Qian, Yixia Li, Qian Xiang, Junfeng Wang, Qian Hu, Zhiyuan Wang, Weizhi |
author_sort | Wang, Zihua |
collection | PubMed |
description | Herein, through the active-peptide-functionalization, we developed a nanoscale micelles system (named HEKM) which consists of tumor microenvironment-regulated shape-changing with specific recognition abilities for enhanced cellular targeting, internalization and therapy of heterogeneic tumors. As a result, HEKMs could recognize and bind the tumor heterogeneity marker EGFR-HER2 complex, which led to an enhanced tumor targeting effect. In particular, HEKMs could self-assemble into nanorods under normal physiological conditions while transform into nanospheres in the tumor extracellular microenvironment by a sensitive response to matrix metalloproteinase-2 (MMP-2). The nanorods could prolong the blood circulation time while the nanospheres could accelerate tissue penetration in tumors. In vivo dual-modal targeted imaging was realized by FRET-fluorophore conjugation and gadolinium loading in HEKMs. Tumor cell apoptosis was achieved by proapoptotic element integration. The in vitro and in vivo studies both demonstrated that these rationally designed, shape-changing and targeting micelles could achieve maximized drug efficacy and minimum side effects. |
format | Online Article Text |
id | pubmed-6485184 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Ivyspring International Publisher |
record_format | MEDLINE/PubMed |
spelling | pubmed-64851842019-04-29 MMP-2-Controlled Transforming Micelles for Heterogeneic Targeting and Programmable Cancer Therapy Wang, Zihua Wang, Yuehua Jia, Xiangqian Han, Qiuju Qian, Yixia Li, Qian Xiang, Junfeng Wang, Qian Hu, Zhiyuan Wang, Weizhi Theranostics Research Paper Herein, through the active-peptide-functionalization, we developed a nanoscale micelles system (named HEKM) which consists of tumor microenvironment-regulated shape-changing with specific recognition abilities for enhanced cellular targeting, internalization and therapy of heterogeneic tumors. As a result, HEKMs could recognize and bind the tumor heterogeneity marker EGFR-HER2 complex, which led to an enhanced tumor targeting effect. In particular, HEKMs could self-assemble into nanorods under normal physiological conditions while transform into nanospheres in the tumor extracellular microenvironment by a sensitive response to matrix metalloproteinase-2 (MMP-2). The nanorods could prolong the blood circulation time while the nanospheres could accelerate tissue penetration in tumors. In vivo dual-modal targeted imaging was realized by FRET-fluorophore conjugation and gadolinium loading in HEKMs. Tumor cell apoptosis was achieved by proapoptotic element integration. The in vitro and in vivo studies both demonstrated that these rationally designed, shape-changing and targeting micelles could achieve maximized drug efficacy and minimum side effects. Ivyspring International Publisher 2019-02-28 /pmc/articles/PMC6485184/ /pubmed/31037134 http://dx.doi.org/10.7150/thno.30915 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 Wang, Zihua Wang, Yuehua Jia, Xiangqian Han, Qiuju Qian, Yixia Li, Qian Xiang, Junfeng Wang, Qian Hu, Zhiyuan Wang, Weizhi MMP-2-Controlled Transforming Micelles for Heterogeneic Targeting and Programmable Cancer Therapy |
title | MMP-2-Controlled Transforming Micelles for Heterogeneic Targeting and Programmable Cancer Therapy |
title_full | MMP-2-Controlled Transforming Micelles for Heterogeneic Targeting and Programmable Cancer Therapy |
title_fullStr | MMP-2-Controlled Transforming Micelles for Heterogeneic Targeting and Programmable Cancer Therapy |
title_full_unstemmed | MMP-2-Controlled Transforming Micelles for Heterogeneic Targeting and Programmable Cancer Therapy |
title_short | MMP-2-Controlled Transforming Micelles for Heterogeneic Targeting and Programmable Cancer Therapy |
title_sort | mmp-2-controlled transforming micelles for heterogeneic targeting and programmable cancer therapy |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6485184/ https://www.ncbi.nlm.nih.gov/pubmed/31037134 http://dx.doi.org/10.7150/thno.30915 |
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