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Intelligent Photosensitive Mesenchymal Stem Cells and Cell-Derived Microvesicles for Photothermal Therapy of Prostate Cancer

Targeted delivery of nanomedicines into the tumor site and improving the intratumoral distribution remain challenging in cancer treatment. Here, we report an effective transportation system utilizing both of mesenchymal stem cells (MSCs) and their secreted microvesicles containing assembled gold nan...

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Autores principales: Huang, Liqun, Xu, Chang, Xu, Peng, Qin, Yu, Chen, Mengwei, Feng, Qishuai, Pan, Jing, Cheng, Qian, Liang, Feng, Wen, Xiaofei, Wang, Ying, Shi, Yufang, Cheng, Yu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ivyspring International Publisher 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6328305/
https://www.ncbi.nlm.nih.gov/pubmed/30662822
http://dx.doi.org/10.7150/ntno.28450
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author Huang, Liqun
Xu, Chang
Xu, Peng
Qin, Yu
Chen, Mengwei
Feng, Qishuai
Pan, Jing
Cheng, Qian
Liang, Feng
Wen, Xiaofei
Wang, Ying
Shi, Yufang
Cheng, Yu
author_facet Huang, Liqun
Xu, Chang
Xu, Peng
Qin, Yu
Chen, Mengwei
Feng, Qishuai
Pan, Jing
Cheng, Qian
Liang, Feng
Wen, Xiaofei
Wang, Ying
Shi, Yufang
Cheng, Yu
author_sort Huang, Liqun
collection PubMed
description Targeted delivery of nanomedicines into the tumor site and improving the intratumoral distribution remain challenging in cancer treatment. Here, we report an effective transportation system utilizing both of mesenchymal stem cells (MSCs) and their secreted microvesicles containing assembled gold nanostars (GNS) for targeted photothermal therapy of prostate cancer. The stem cells act as a cell carrier to actively load and assemble GNS into the lysosomes. Accumulation of GNS in the lysosomes facilitates the close interaction of nanoparticles, which could result in a 20 nm red-shift of surface plasmon resonance of GNS with a broad absorption in the near infrared region. Moreover, the MSCs can behave like an engineering factory to pack and release the GNS clusters into microvesicles. The secretion of GNS can be stimulated via light irradiation, providing an external trigger-assisted approach to encapsulate nanoparticles into cell derived microvesicles. In vivo studies demonstrate that GNS-loaded MSCs have an extensive intratumoral distribution, as monitored via photoacoustic imaging, and efficient antitumor effect under light exposure in a prostate-cancer subcutaneous model by intratumoral and intravenous injection. Our work presents a light-responsive transportation approach for GNS in combination of MSCs and their extracellular microvesicles and holds the promise as an effective strategy for targeted cancer therapy including prostate cancer.
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spelling pubmed-63283052019-01-18 Intelligent Photosensitive Mesenchymal Stem Cells and Cell-Derived Microvesicles for Photothermal Therapy of Prostate Cancer Huang, Liqun Xu, Chang Xu, Peng Qin, Yu Chen, Mengwei Feng, Qishuai Pan, Jing Cheng, Qian Liang, Feng Wen, Xiaofei Wang, Ying Shi, Yufang Cheng, Yu Nanotheranostics Research Paper Targeted delivery of nanomedicines into the tumor site and improving the intratumoral distribution remain challenging in cancer treatment. Here, we report an effective transportation system utilizing both of mesenchymal stem cells (MSCs) and their secreted microvesicles containing assembled gold nanostars (GNS) for targeted photothermal therapy of prostate cancer. The stem cells act as a cell carrier to actively load and assemble GNS into the lysosomes. Accumulation of GNS in the lysosomes facilitates the close interaction of nanoparticles, which could result in a 20 nm red-shift of surface plasmon resonance of GNS with a broad absorption in the near infrared region. Moreover, the MSCs can behave like an engineering factory to pack and release the GNS clusters into microvesicles. The secretion of GNS can be stimulated via light irradiation, providing an external trigger-assisted approach to encapsulate nanoparticles into cell derived microvesicles. In vivo studies demonstrate that GNS-loaded MSCs have an extensive intratumoral distribution, as monitored via photoacoustic imaging, and efficient antitumor effect under light exposure in a prostate-cancer subcutaneous model by intratumoral and intravenous injection. Our work presents a light-responsive transportation approach for GNS in combination of MSCs and their extracellular microvesicles and holds the promise as an effective strategy for targeted cancer therapy including prostate cancer. Ivyspring International Publisher 2019-01-01 /pmc/articles/PMC6328305/ /pubmed/30662822 http://dx.doi.org/10.7150/ntno.28450 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
Huang, Liqun
Xu, Chang
Xu, Peng
Qin, Yu
Chen, Mengwei
Feng, Qishuai
Pan, Jing
Cheng, Qian
Liang, Feng
Wen, Xiaofei
Wang, Ying
Shi, Yufang
Cheng, Yu
Intelligent Photosensitive Mesenchymal Stem Cells and Cell-Derived Microvesicles for Photothermal Therapy of Prostate Cancer
title Intelligent Photosensitive Mesenchymal Stem Cells and Cell-Derived Microvesicles for Photothermal Therapy of Prostate Cancer
title_full Intelligent Photosensitive Mesenchymal Stem Cells and Cell-Derived Microvesicles for Photothermal Therapy of Prostate Cancer
title_fullStr Intelligent Photosensitive Mesenchymal Stem Cells and Cell-Derived Microvesicles for Photothermal Therapy of Prostate Cancer
title_full_unstemmed Intelligent Photosensitive Mesenchymal Stem Cells and Cell-Derived Microvesicles for Photothermal Therapy of Prostate Cancer
title_short Intelligent Photosensitive Mesenchymal Stem Cells and Cell-Derived Microvesicles for Photothermal Therapy of Prostate Cancer
title_sort intelligent photosensitive mesenchymal stem cells and cell-derived microvesicles for photothermal therapy of prostate cancer
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6328305/
https://www.ncbi.nlm.nih.gov/pubmed/30662822
http://dx.doi.org/10.7150/ntno.28450
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