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Nanomedicines reveal how PBOV1 promotes hepatocellular carcinoma for effective gene therapy
There exists an urgent medical demand at present to develop therapeutic strategies which can improve the treatment outcome of hepatocellular carcinoma (HCC). Here, we explore the biological functions and clinical significance of PBOV1 in HCC in order to push forward the diagnosis and treatment of HC...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6109108/ https://www.ncbi.nlm.nih.gov/pubmed/30143633 http://dx.doi.org/10.1038/s41467-018-05764-7 |
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author | Guo, Yu Wu, Zhiqiang Shen, Shunli Guo, Ruomi Wang, Jing Wang, Weiwei Zhao, Kun Kuang, Ming Shuai, Xintao |
author_facet | Guo, Yu Wu, Zhiqiang Shen, Shunli Guo, Ruomi Wang, Jing Wang, Weiwei Zhao, Kun Kuang, Ming Shuai, Xintao |
author_sort | Guo, Yu |
collection | PubMed |
description | There exists an urgent medical demand at present to develop therapeutic strategies which can improve the treatment outcome of hepatocellular carcinoma (HCC). Here, we explore the biological functions and clinical significance of PBOV1 in HCC in order to push forward the diagnosis and treatment of HCC. Using theranostical nanomedicines, PBOV1 is verified to be a key oncogene which greatly promotes HCC proliferation, epithelial-to-mesenchymal transition, and stemness by activating the Wnt/β-catenin signaling pathway. Therefore, single-chain antibody for epidermal growth factor receptor (scAb-EGFR)-targeted nanomedicine effectively silencing the PBOV1 gene exhibits potent anticancer effects. In vivo HCC-targeting siRNA delivery mediated by the theranostical nanomedicine remarkably inhibits the tumor growth and metastasis. In addition, the superparamagnetic iron oxide nanocrystals (SPION)-encapsulated nanomedicines possess high MRI detection sensitivity, which endows them with the potential for MRI diagnosis of HCC. This study shows that PBOV1 represents a prognostic biomarker and therapeutic target for HCC. |
format | Online Article Text |
id | pubmed-6109108 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-61091082018-08-27 Nanomedicines reveal how PBOV1 promotes hepatocellular carcinoma for effective gene therapy Guo, Yu Wu, Zhiqiang Shen, Shunli Guo, Ruomi Wang, Jing Wang, Weiwei Zhao, Kun Kuang, Ming Shuai, Xintao Nat Commun Article There exists an urgent medical demand at present to develop therapeutic strategies which can improve the treatment outcome of hepatocellular carcinoma (HCC). Here, we explore the biological functions and clinical significance of PBOV1 in HCC in order to push forward the diagnosis and treatment of HCC. Using theranostical nanomedicines, PBOV1 is verified to be a key oncogene which greatly promotes HCC proliferation, epithelial-to-mesenchymal transition, and stemness by activating the Wnt/β-catenin signaling pathway. Therefore, single-chain antibody for epidermal growth factor receptor (scAb-EGFR)-targeted nanomedicine effectively silencing the PBOV1 gene exhibits potent anticancer effects. In vivo HCC-targeting siRNA delivery mediated by the theranostical nanomedicine remarkably inhibits the tumor growth and metastasis. In addition, the superparamagnetic iron oxide nanocrystals (SPION)-encapsulated nanomedicines possess high MRI detection sensitivity, which endows them with the potential for MRI diagnosis of HCC. This study shows that PBOV1 represents a prognostic biomarker and therapeutic target for HCC. Nature Publishing Group UK 2018-08-24 /pmc/articles/PMC6109108/ /pubmed/30143633 http://dx.doi.org/10.1038/s41467-018-05764-7 Text en © The Author(s) 2018 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Guo, Yu Wu, Zhiqiang Shen, Shunli Guo, Ruomi Wang, Jing Wang, Weiwei Zhao, Kun Kuang, Ming Shuai, Xintao Nanomedicines reveal how PBOV1 promotes hepatocellular carcinoma for effective gene therapy |
title | Nanomedicines reveal how PBOV1 promotes hepatocellular carcinoma for effective gene therapy |
title_full | Nanomedicines reveal how PBOV1 promotes hepatocellular carcinoma for effective gene therapy |
title_fullStr | Nanomedicines reveal how PBOV1 promotes hepatocellular carcinoma for effective gene therapy |
title_full_unstemmed | Nanomedicines reveal how PBOV1 promotes hepatocellular carcinoma for effective gene therapy |
title_short | Nanomedicines reveal how PBOV1 promotes hepatocellular carcinoma for effective gene therapy |
title_sort | nanomedicines reveal how pbov1 promotes hepatocellular carcinoma for effective gene therapy |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6109108/ https://www.ncbi.nlm.nih.gov/pubmed/30143633 http://dx.doi.org/10.1038/s41467-018-05764-7 |
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