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Magnetically responsive nanoplatform targeting circRNA circ_0058051 inhibits hepatocellular carcinoma progression
Circular RNAs (circRNAs) are a class of highly stable and closed-loop noncoding RNA that are involved in the occurrence and development of hepatocellular carcinoma (HCC). However, little is known about the therapeutic role of circRNAs in HCC. We found that high circ_0058051 expression was negatively...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9892167/ https://www.ncbi.nlm.nih.gov/pubmed/36114310 http://dx.doi.org/10.1007/s13346-022-01237-z |
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author | You, Song Luo, Zijin Cheng, Niangmei Wu, Ming Lai, Yongping Wang, Fei Zheng, Xiaoyuan Wang, Yingchao Liu, Xiaolong Liu, Jingfeng Zhao, Bixing |
author_facet | You, Song Luo, Zijin Cheng, Niangmei Wu, Ming Lai, Yongping Wang, Fei Zheng, Xiaoyuan Wang, Yingchao Liu, Xiaolong Liu, Jingfeng Zhao, Bixing |
author_sort | You, Song |
collection | PubMed |
description | Circular RNAs (circRNAs) are a class of highly stable and closed-loop noncoding RNA that are involved in the occurrence and development of hepatocellular carcinoma (HCC). However, little is known about the therapeutic role of circRNAs in HCC. We found that high circ_0058051 expression was negatively correlated with the prognosis of HCC patients. Circ_0058051 knockdown attenuated the proliferation and colony formation, meanwhile inhibited migration of HCC cells. Circ_0058051 may be used as a target for HCC gene therapy. We synthesized a novel small interfering RNA (siRNA) delivery system, PEG-PCL-PEI-C14-SPIONs (PPPCSs), based on superparamagnetic iron oxide nanoparticles (SPIONs). PPPCSs protected the siRNA of circ_0058051 from degradation in serum and effectively delivered siRNA into SMMC-7721 cells. Meanwhile, intravenous injection of the PPPCSs/siRNA complex could inhibit tumor growth in the subcutaneous tumor model. In addition, the nanocomposite is not toxic to the organs of nude mice. The above results show that PPPCSs/si-circ_0058051 complex may provide a novel and promising method of HCC treatment. GRAPHICAL ABSTRACT: [Image: see text] |
format | Online Article Text |
id | pubmed-9892167 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-98921672023-02-03 Magnetically responsive nanoplatform targeting circRNA circ_0058051 inhibits hepatocellular carcinoma progression You, Song Luo, Zijin Cheng, Niangmei Wu, Ming Lai, Yongping Wang, Fei Zheng, Xiaoyuan Wang, Yingchao Liu, Xiaolong Liu, Jingfeng Zhao, Bixing Drug Deliv Transl Res Original Article Circular RNAs (circRNAs) are a class of highly stable and closed-loop noncoding RNA that are involved in the occurrence and development of hepatocellular carcinoma (HCC). However, little is known about the therapeutic role of circRNAs in HCC. We found that high circ_0058051 expression was negatively correlated with the prognosis of HCC patients. Circ_0058051 knockdown attenuated the proliferation and colony formation, meanwhile inhibited migration of HCC cells. Circ_0058051 may be used as a target for HCC gene therapy. We synthesized a novel small interfering RNA (siRNA) delivery system, PEG-PCL-PEI-C14-SPIONs (PPPCSs), based on superparamagnetic iron oxide nanoparticles (SPIONs). PPPCSs protected the siRNA of circ_0058051 from degradation in serum and effectively delivered siRNA into SMMC-7721 cells. Meanwhile, intravenous injection of the PPPCSs/siRNA complex could inhibit tumor growth in the subcutaneous tumor model. In addition, the nanocomposite is not toxic to the organs of nude mice. The above results show that PPPCSs/si-circ_0058051 complex may provide a novel and promising method of HCC treatment. GRAPHICAL ABSTRACT: [Image: see text] Springer US 2022-09-16 2023 /pmc/articles/PMC9892167/ /pubmed/36114310 http://dx.doi.org/10.1007/s13346-022-01237-z Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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/) . |
spellingShingle | Original Article You, Song Luo, Zijin Cheng, Niangmei Wu, Ming Lai, Yongping Wang, Fei Zheng, Xiaoyuan Wang, Yingchao Liu, Xiaolong Liu, Jingfeng Zhao, Bixing Magnetically responsive nanoplatform targeting circRNA circ_0058051 inhibits hepatocellular carcinoma progression |
title | Magnetically responsive nanoplatform targeting circRNA circ_0058051 inhibits hepatocellular carcinoma progression |
title_full | Magnetically responsive nanoplatform targeting circRNA circ_0058051 inhibits hepatocellular carcinoma progression |
title_fullStr | Magnetically responsive nanoplatform targeting circRNA circ_0058051 inhibits hepatocellular carcinoma progression |
title_full_unstemmed | Magnetically responsive nanoplatform targeting circRNA circ_0058051 inhibits hepatocellular carcinoma progression |
title_short | Magnetically responsive nanoplatform targeting circRNA circ_0058051 inhibits hepatocellular carcinoma progression |
title_sort | magnetically responsive nanoplatform targeting circrna circ_0058051 inhibits hepatocellular carcinoma progression |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9892167/ https://www.ncbi.nlm.nih.gov/pubmed/36114310 http://dx.doi.org/10.1007/s13346-022-01237-z |
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