Gene editing therapy ready for cardiovascular diseases: opportunities, challenges, and perspectives
Gene editing nucleases (GENs), represented by CRISPR/Cas9, have become major tools in biomedical research and offer potential cures for many human diseases. Gene editing therapy (GETx) studies in animal models targeting genes such as proprotein convertase subtilisin/kexin type 9 (PCSK9), apolipoprot...
Main Authors: | , , , , |
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Format: | Article |
Language: | English |
Published: |
De Gruyter
2021-10-01
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Series: | Medical Review |
Subjects: | |
Online Access: | https://doi.org/10.1515/mr-2021-0010 |
Summary: | Gene editing nucleases (GENs), represented by CRISPR/Cas9, have become major tools in biomedical research and offer potential cures for many human diseases. Gene editing therapy (GETx) studies in animal models targeting genes such as proprotein convertase subtilisin/kexin type 9 (PCSK9), apolipoprotein C3 (APOC3), angiopoietin Like 3 (ANGPTL3) and inducible degrader of the low-density lipoprotein receptor (IDOL) have demonstrated the benefits and advantages of GETx in managing atherosclerosis. Here we present our views on this brand new therapeutic option for cardiovascular diseases (CVD). |
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ISSN: | 2749-9642 |