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Advanced Nanotheranostics of CRISPR/Cas for Viral Hepatitis and Hepatocellular Carcinoma
Liver disease, particularly viral hepatitis and hepatocellular carcinoma (HCC), is a global healthcare burden and leads to more than 2 million deaths per year worldwide. Despite some success in diagnosis and vaccine development, there are still unmet needs to improve diagnostics and therapeutics for...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8693080/ https://www.ncbi.nlm.nih.gov/pubmed/34665528 http://dx.doi.org/10.1002/advs.202102051 |
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author | Kong, Huimin Ju, Enguo Yi, Ke Xu, Weiguo Lao, Yeh‐Hsing Cheng, Du Zhang, Qi Tao, Yu Li, Mingqiang Ding, Jianxun |
author_facet | Kong, Huimin Ju, Enguo Yi, Ke Xu, Weiguo Lao, Yeh‐Hsing Cheng, Du Zhang, Qi Tao, Yu Li, Mingqiang Ding, Jianxun |
author_sort | Kong, Huimin |
collection | PubMed |
description | Liver disease, particularly viral hepatitis and hepatocellular carcinoma (HCC), is a global healthcare burden and leads to more than 2 million deaths per year worldwide. Despite some success in diagnosis and vaccine development, there are still unmet needs to improve diagnostics and therapeutics for viral hepatitis and HCC. The emerging clustered regularly interspaced short palindromic repeat/associated proteins (CRISPR/Cas) technology may open up a unique avenue to tackle these two diseases at the genetic level in a precise manner. Especially, liver is a more accessible organ over others from the delivery point of view, and many advanced strategies applied for nanotheranostics can be adapted in CRISPR‐mediated diagnostics or liver gene editing. In this review, the focus is on these two aspects of viral hepatitis and HCC applications. An overview on CRISPR editor development and current progress in clinical trials is first given, followed by highlighting the recent advances integrating the merits of gene editing and nanotheranostics. The promising systems that are used in other applications but may hold potentials in liver gene editing are also discussed. This review concludes with the perspectives on rationally designing the next‐generation CRISPR approaches and improving the editing performance. |
format | Online Article Text |
id | pubmed-8693080 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-86930802022-01-03 Advanced Nanotheranostics of CRISPR/Cas for Viral Hepatitis and Hepatocellular Carcinoma Kong, Huimin Ju, Enguo Yi, Ke Xu, Weiguo Lao, Yeh‐Hsing Cheng, Du Zhang, Qi Tao, Yu Li, Mingqiang Ding, Jianxun Adv Sci (Weinh) Reviews Liver disease, particularly viral hepatitis and hepatocellular carcinoma (HCC), is a global healthcare burden and leads to more than 2 million deaths per year worldwide. Despite some success in diagnosis and vaccine development, there are still unmet needs to improve diagnostics and therapeutics for viral hepatitis and HCC. The emerging clustered regularly interspaced short palindromic repeat/associated proteins (CRISPR/Cas) technology may open up a unique avenue to tackle these two diseases at the genetic level in a precise manner. Especially, liver is a more accessible organ over others from the delivery point of view, and many advanced strategies applied for nanotheranostics can be adapted in CRISPR‐mediated diagnostics or liver gene editing. In this review, the focus is on these two aspects of viral hepatitis and HCC applications. An overview on CRISPR editor development and current progress in clinical trials is first given, followed by highlighting the recent advances integrating the merits of gene editing and nanotheranostics. The promising systems that are used in other applications but may hold potentials in liver gene editing are also discussed. This review concludes with the perspectives on rationally designing the next‐generation CRISPR approaches and improving the editing performance. John Wiley and Sons Inc. 2021-10-19 /pmc/articles/PMC8693080/ /pubmed/34665528 http://dx.doi.org/10.1002/advs.202102051 Text en © 2021 The Authors. Advanced Science published by Wiley‐VCH GmbH https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Reviews Kong, Huimin Ju, Enguo Yi, Ke Xu, Weiguo Lao, Yeh‐Hsing Cheng, Du Zhang, Qi Tao, Yu Li, Mingqiang Ding, Jianxun Advanced Nanotheranostics of CRISPR/Cas for Viral Hepatitis and Hepatocellular Carcinoma |
title | Advanced Nanotheranostics of CRISPR/Cas for Viral Hepatitis and Hepatocellular Carcinoma |
title_full | Advanced Nanotheranostics of CRISPR/Cas for Viral Hepatitis and Hepatocellular Carcinoma |
title_fullStr | Advanced Nanotheranostics of CRISPR/Cas for Viral Hepatitis and Hepatocellular Carcinoma |
title_full_unstemmed | Advanced Nanotheranostics of CRISPR/Cas for Viral Hepatitis and Hepatocellular Carcinoma |
title_short | Advanced Nanotheranostics of CRISPR/Cas for Viral Hepatitis and Hepatocellular Carcinoma |
title_sort | advanced nanotheranostics of crispr/cas for viral hepatitis and hepatocellular carcinoma |
topic | Reviews |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8693080/ https://www.ncbi.nlm.nih.gov/pubmed/34665528 http://dx.doi.org/10.1002/advs.202102051 |
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