Cargando…
Targeting ANGPTL3 by GalNAc-conjugated siRNA ANGsiR10 lowers blood lipids with long-lasting and potent efficacy in mice and monkeys
Angiopoietin-like protein 3 (ANGPTL3) is an important regulator of lipoproteins by inhibiting both lipoprotein and endothelial lipases. It has been intensively investigated as a drug target for the treatment of dyslipidemia. In the present study, a modified small interfering RNA (siRNA) conjugated w...
Autores principales: | , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society of Gene & Cell Therapy
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9804015/ https://www.ncbi.nlm.nih.gov/pubmed/36618267 http://dx.doi.org/10.1016/j.omtn.2022.11.023 |
_version_ | 1784862008418500608 |
---|---|
author | Wang, Jue Zheng, Wen Zheng, Shuquan Yuan, Ye Wen, Wei Cui, Weiyi Xue, Lifang Sun, Xueting Shang, Haibao Zhang, Hongyan Xiao, Rui-Ping Gao, Shan Zhang, Xiuqin |
author_facet | Wang, Jue Zheng, Wen Zheng, Shuquan Yuan, Ye Wen, Wei Cui, Weiyi Xue, Lifang Sun, Xueting Shang, Haibao Zhang, Hongyan Xiao, Rui-Ping Gao, Shan Zhang, Xiuqin |
author_sort | Wang, Jue |
collection | PubMed |
description | Angiopoietin-like protein 3 (ANGPTL3) is an important regulator of lipoproteins by inhibiting both lipoprotein and endothelial lipases. It has been intensively investigated as a drug target for the treatment of dyslipidemia. In the present study, a modified small interfering RNA (siRNA) conjugated with GalNAc ANGsiR10 was characterized by in vivo and in vitro studies for its effect on ANGPTL3 silencing, the reduction of plasma triglycerides (TGs), and cholesterol levels in disease models. The results showed that ANGsiR10 displayed a significant and long-lasting efficacy in reducing blood TG and cholesterol levels in both mice and monkeys. Remarkably, the maximal reductions of plasma TG levels in the hApoC3-Tg mice, a model with high TG levels, and the spontaneous dyslipidemia model of rhesus monkey were 96.3% and 67.7%, respectively, after a single dose of ANGsiR10, with long-lasting effects up to 15 weeks. The cholesterol levels were also reduced in response to treatment, especially the non-HDL-c level, without altering the ApoA/ApoB ratio. This study showed that ANGsiR10 is effective in treating dyslipidemia and is worth further development. |
format | Online Article Text |
id | pubmed-9804015 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Society of Gene & Cell Therapy |
record_format | MEDLINE/PubMed |
spelling | pubmed-98040152023-01-05 Targeting ANGPTL3 by GalNAc-conjugated siRNA ANGsiR10 lowers blood lipids with long-lasting and potent efficacy in mice and monkeys Wang, Jue Zheng, Wen Zheng, Shuquan Yuan, Ye Wen, Wei Cui, Weiyi Xue, Lifang Sun, Xueting Shang, Haibao Zhang, Hongyan Xiao, Rui-Ping Gao, Shan Zhang, Xiuqin Mol Ther Nucleic Acids Original Article Angiopoietin-like protein 3 (ANGPTL3) is an important regulator of lipoproteins by inhibiting both lipoprotein and endothelial lipases. It has been intensively investigated as a drug target for the treatment of dyslipidemia. In the present study, a modified small interfering RNA (siRNA) conjugated with GalNAc ANGsiR10 was characterized by in vivo and in vitro studies for its effect on ANGPTL3 silencing, the reduction of plasma triglycerides (TGs), and cholesterol levels in disease models. The results showed that ANGsiR10 displayed a significant and long-lasting efficacy in reducing blood TG and cholesterol levels in both mice and monkeys. Remarkably, the maximal reductions of plasma TG levels in the hApoC3-Tg mice, a model with high TG levels, and the spontaneous dyslipidemia model of rhesus monkey were 96.3% and 67.7%, respectively, after a single dose of ANGsiR10, with long-lasting effects up to 15 weeks. The cholesterol levels were also reduced in response to treatment, especially the non-HDL-c level, without altering the ApoA/ApoB ratio. This study showed that ANGsiR10 is effective in treating dyslipidemia and is worth further development. American Society of Gene & Cell Therapy 2022-12-05 /pmc/articles/PMC9804015/ /pubmed/36618267 http://dx.doi.org/10.1016/j.omtn.2022.11.023 Text en © 2022 The Authors https://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 | Original Article Wang, Jue Zheng, Wen Zheng, Shuquan Yuan, Ye Wen, Wei Cui, Weiyi Xue, Lifang Sun, Xueting Shang, Haibao Zhang, Hongyan Xiao, Rui-Ping Gao, Shan Zhang, Xiuqin Targeting ANGPTL3 by GalNAc-conjugated siRNA ANGsiR10 lowers blood lipids with long-lasting and potent efficacy in mice and monkeys |
title | Targeting ANGPTL3 by GalNAc-conjugated siRNA ANGsiR10 lowers blood lipids with long-lasting and potent efficacy in mice and monkeys |
title_full | Targeting ANGPTL3 by GalNAc-conjugated siRNA ANGsiR10 lowers blood lipids with long-lasting and potent efficacy in mice and monkeys |
title_fullStr | Targeting ANGPTL3 by GalNAc-conjugated siRNA ANGsiR10 lowers blood lipids with long-lasting and potent efficacy in mice and monkeys |
title_full_unstemmed | Targeting ANGPTL3 by GalNAc-conjugated siRNA ANGsiR10 lowers blood lipids with long-lasting and potent efficacy in mice and monkeys |
title_short | Targeting ANGPTL3 by GalNAc-conjugated siRNA ANGsiR10 lowers blood lipids with long-lasting and potent efficacy in mice and monkeys |
title_sort | targeting angptl3 by galnac-conjugated sirna angsir10 lowers blood lipids with long-lasting and potent efficacy in mice and monkeys |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9804015/ https://www.ncbi.nlm.nih.gov/pubmed/36618267 http://dx.doi.org/10.1016/j.omtn.2022.11.023 |
work_keys_str_mv | AT wangjue targetingangptl3bygalnacconjugatedsirnaangsir10lowersbloodlipidswithlonglastingandpotentefficacyinmiceandmonkeys AT zhengwen targetingangptl3bygalnacconjugatedsirnaangsir10lowersbloodlipidswithlonglastingandpotentefficacyinmiceandmonkeys AT zhengshuquan targetingangptl3bygalnacconjugatedsirnaangsir10lowersbloodlipidswithlonglastingandpotentefficacyinmiceandmonkeys AT yuanye targetingangptl3bygalnacconjugatedsirnaangsir10lowersbloodlipidswithlonglastingandpotentefficacyinmiceandmonkeys AT wenwei targetingangptl3bygalnacconjugatedsirnaangsir10lowersbloodlipidswithlonglastingandpotentefficacyinmiceandmonkeys AT cuiweiyi targetingangptl3bygalnacconjugatedsirnaangsir10lowersbloodlipidswithlonglastingandpotentefficacyinmiceandmonkeys AT xuelifang targetingangptl3bygalnacconjugatedsirnaangsir10lowersbloodlipidswithlonglastingandpotentefficacyinmiceandmonkeys AT sunxueting targetingangptl3bygalnacconjugatedsirnaangsir10lowersbloodlipidswithlonglastingandpotentefficacyinmiceandmonkeys AT shanghaibao targetingangptl3bygalnacconjugatedsirnaangsir10lowersbloodlipidswithlonglastingandpotentefficacyinmiceandmonkeys AT zhanghongyan targetingangptl3bygalnacconjugatedsirnaangsir10lowersbloodlipidswithlonglastingandpotentefficacyinmiceandmonkeys AT xiaoruiping targetingangptl3bygalnacconjugatedsirnaangsir10lowersbloodlipidswithlonglastingandpotentefficacyinmiceandmonkeys AT gaoshan targetingangptl3bygalnacconjugatedsirnaangsir10lowersbloodlipidswithlonglastingandpotentefficacyinmiceandmonkeys AT zhangxiuqin targetingangptl3bygalnacconjugatedsirnaangsir10lowersbloodlipidswithlonglastingandpotentefficacyinmiceandmonkeys |