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Biodegradable FePS(3) nanoplatform for efficient treatment of osteosarcoma by combination of gene and NIR-II photothermal therapy

As a common tumor with high incidence, osteosarcoma possesses extremely poor prognosis and high mortality. Improving the survival of osteosarcoma patients is still a great challenge due to the precipice of advancement in treatment. In this study, a combination strategy of gene therapy and phototherm...

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Autores principales: Luo, Tingting, Jiang, Mingyang, Cheng, Ziqiang, Lin, Yuntao, Chen, Yuling, Zhang, Zhenyu, Zhou, Jian, Zhou, Wenhua, Yu, Xue-Feng, Li, Shuchun, Geng, Shengyong, Yang, Hongyu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10347837/
https://www.ncbi.nlm.nih.gov/pubmed/37443019
http://dx.doi.org/10.1186/s12951-023-01961-9
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author Luo, Tingting
Jiang, Mingyang
Cheng, Ziqiang
Lin, Yuntao
Chen, Yuling
Zhang, Zhenyu
Zhou, Jian
Zhou, Wenhua
Yu, Xue-Feng
Li, Shuchun
Geng, Shengyong
Yang, Hongyu
author_facet Luo, Tingting
Jiang, Mingyang
Cheng, Ziqiang
Lin, Yuntao
Chen, Yuling
Zhang, Zhenyu
Zhou, Jian
Zhou, Wenhua
Yu, Xue-Feng
Li, Shuchun
Geng, Shengyong
Yang, Hongyu
author_sort Luo, Tingting
collection PubMed
description As a common tumor with high incidence, osteosarcoma possesses extremely poor prognosis and high mortality. Improving the survival of osteosarcoma patients is still a great challenge due to the precipice of advancement in treatment. In this study, a combination strategy of gene therapy and photothermal therapy (PTT) is developed for efficient treatment of osteosarcoma. Two-dimensional (2D) FePS(3) nanosheets are synthesized and functionalized by poly-L-lysine-PEG-folic acid (PPF) to fabricate a multifunctional nanoplatform (FePS@PPF) for further loading microRNAs inhibitor, miR-19a inhibitor (anti-miR-19a). The photothermal conversion efficiency of FePS@PPF is up to 47.1% under irradiation by 1064 nm laser. In vitro study shows that anti-miR-19a can be efficiently internalized into osteosarcoma cells through the protection and delivery of FePS@PPF nanaocarrier, which induces up-regulation of PTEN protein and down-regulation p-AKT protein. After intravenous injection, the FePS@PPF nanoplatform specifically accumulates to tumor site of osteosarcoma-bearing mice. The in vitro and in vivo investigations reveal that the combined PTT-gene therapy displays most significant tumor ablation compared with monotherapy. More importantly, the good biodegradability promotes FePS@PPF to be cleared from body avoiding potential toxicity of long-term retention. Our work not only develops a combined strategy of NIR-II PTT and gene therapy mediated by anti-miR-19a/FePS@PPF but also provides insights into the design and applications of other nanotherapeutic platforms. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12951-023-01961-9.
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spelling pubmed-103478372023-07-15 Biodegradable FePS(3) nanoplatform for efficient treatment of osteosarcoma by combination of gene and NIR-II photothermal therapy Luo, Tingting Jiang, Mingyang Cheng, Ziqiang Lin, Yuntao Chen, Yuling Zhang, Zhenyu Zhou, Jian Zhou, Wenhua Yu, Xue-Feng Li, Shuchun Geng, Shengyong Yang, Hongyu J Nanobiotechnology Research As a common tumor with high incidence, osteosarcoma possesses extremely poor prognosis and high mortality. Improving the survival of osteosarcoma patients is still a great challenge due to the precipice of advancement in treatment. In this study, a combination strategy of gene therapy and photothermal therapy (PTT) is developed for efficient treatment of osteosarcoma. Two-dimensional (2D) FePS(3) nanosheets are synthesized and functionalized by poly-L-lysine-PEG-folic acid (PPF) to fabricate a multifunctional nanoplatform (FePS@PPF) for further loading microRNAs inhibitor, miR-19a inhibitor (anti-miR-19a). The photothermal conversion efficiency of FePS@PPF is up to 47.1% under irradiation by 1064 nm laser. In vitro study shows that anti-miR-19a can be efficiently internalized into osteosarcoma cells through the protection and delivery of FePS@PPF nanaocarrier, which induces up-regulation of PTEN protein and down-regulation p-AKT protein. After intravenous injection, the FePS@PPF nanoplatform specifically accumulates to tumor site of osteosarcoma-bearing mice. The in vitro and in vivo investigations reveal that the combined PTT-gene therapy displays most significant tumor ablation compared with monotherapy. More importantly, the good biodegradability promotes FePS@PPF to be cleared from body avoiding potential toxicity of long-term retention. Our work not only develops a combined strategy of NIR-II PTT and gene therapy mediated by anti-miR-19a/FePS@PPF but also provides insights into the design and applications of other nanotherapeutic platforms. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12951-023-01961-9. BioMed Central 2023-07-13 /pmc/articles/PMC10347837/ /pubmed/37443019 http://dx.doi.org/10.1186/s12951-023-01961-9 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Luo, Tingting
Jiang, Mingyang
Cheng, Ziqiang
Lin, Yuntao
Chen, Yuling
Zhang, Zhenyu
Zhou, Jian
Zhou, Wenhua
Yu, Xue-Feng
Li, Shuchun
Geng, Shengyong
Yang, Hongyu
Biodegradable FePS(3) nanoplatform for efficient treatment of osteosarcoma by combination of gene and NIR-II photothermal therapy
title Biodegradable FePS(3) nanoplatform for efficient treatment of osteosarcoma by combination of gene and NIR-II photothermal therapy
title_full Biodegradable FePS(3) nanoplatform for efficient treatment of osteosarcoma by combination of gene and NIR-II photothermal therapy
title_fullStr Biodegradable FePS(3) nanoplatform for efficient treatment of osteosarcoma by combination of gene and NIR-II photothermal therapy
title_full_unstemmed Biodegradable FePS(3) nanoplatform for efficient treatment of osteosarcoma by combination of gene and NIR-II photothermal therapy
title_short Biodegradable FePS(3) nanoplatform for efficient treatment of osteosarcoma by combination of gene and NIR-II photothermal therapy
title_sort biodegradable feps(3) nanoplatform for efficient treatment of osteosarcoma by combination of gene and nir-ii photothermal therapy
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10347837/
https://www.ncbi.nlm.nih.gov/pubmed/37443019
http://dx.doi.org/10.1186/s12951-023-01961-9
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