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Angiopoietin-Like 3: From Discovery to Therapeutic Gene Editing

Hyperlipidemia is a major causal risk factor for atherosclerosis and coronary heart disease (CHD). Angiopoietin-like 3 (ANGPTL3) has emerged as a promising molecular target to reduce CHD risk due to its regulation of all 3 major lipid traits: low-density lipoprotein cholesterol, high-density lipopro...

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Detalles Bibliográficos
Autores principales: Wang, Xiao, Musunuru, Kiran
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6834959/
https://www.ncbi.nlm.nih.gov/pubmed/31709322
http://dx.doi.org/10.1016/j.jacbts.2019.05.008
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author Wang, Xiao
Musunuru, Kiran
author_facet Wang, Xiao
Musunuru, Kiran
author_sort Wang, Xiao
collection PubMed
description Hyperlipidemia is a major causal risk factor for atherosclerosis and coronary heart disease (CHD). Angiopoietin-like 3 (ANGPTL3) has emerged as a promising molecular target to reduce CHD risk due to its regulation of all 3 major lipid traits: low-density lipoprotein cholesterol, high-density lipoprotein cholesterol, and triglycerides. Here, the authors review the discovery of ANGPTL3, the role of ANGPTL3 in lipoprotein metabolism, and the genetic association between naturally occurring ANGPTL3 loss-of-function mutations and CHD. In light of the favorable consequences of ANGPTL3 deficiency, various therapeutic strategies to target ANGPTL3 are currently in development, including a monoclonal antibody, an antisense oligonucleotide, and gene editing.
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spelling pubmed-68349592019-11-08 Angiopoietin-Like 3: From Discovery to Therapeutic Gene Editing Wang, Xiao Musunuru, Kiran JACC Basic Transl Sci STATE-OF-THE-ART REVIEW Hyperlipidemia is a major causal risk factor for atherosclerosis and coronary heart disease (CHD). Angiopoietin-like 3 (ANGPTL3) has emerged as a promising molecular target to reduce CHD risk due to its regulation of all 3 major lipid traits: low-density lipoprotein cholesterol, high-density lipoprotein cholesterol, and triglycerides. Here, the authors review the discovery of ANGPTL3, the role of ANGPTL3 in lipoprotein metabolism, and the genetic association between naturally occurring ANGPTL3 loss-of-function mutations and CHD. In light of the favorable consequences of ANGPTL3 deficiency, various therapeutic strategies to target ANGPTL3 are currently in development, including a monoclonal antibody, an antisense oligonucleotide, and gene editing. Elsevier 2019-10-28 /pmc/articles/PMC6834959/ /pubmed/31709322 http://dx.doi.org/10.1016/j.jacbts.2019.05.008 Text en © 2019 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle STATE-OF-THE-ART REVIEW
Wang, Xiao
Musunuru, Kiran
Angiopoietin-Like 3: From Discovery to Therapeutic Gene Editing
title Angiopoietin-Like 3: From Discovery to Therapeutic Gene Editing
title_full Angiopoietin-Like 3: From Discovery to Therapeutic Gene Editing
title_fullStr Angiopoietin-Like 3: From Discovery to Therapeutic Gene Editing
title_full_unstemmed Angiopoietin-Like 3: From Discovery to Therapeutic Gene Editing
title_short Angiopoietin-Like 3: From Discovery to Therapeutic Gene Editing
title_sort angiopoietin-like 3: from discovery to therapeutic gene editing
topic STATE-OF-THE-ART REVIEW
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6834959/
https://www.ncbi.nlm.nih.gov/pubmed/31709322
http://dx.doi.org/10.1016/j.jacbts.2019.05.008
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