共 117 条
Strategies for proprotein convertase subtilisin kexin 9 modulation: a perspective on recent patents
被引:28
作者:

Abifadel, Marianne
论文数: 0 引用数: 0
h-index: 0
机构:
Hop Bichat Claude Bernard, INSERM, UMR698, F-75877 Paris 18, France
Univ St Joseph, Fac Pharm, Dept Biochem, Beirut 5076, Lebanon Hop Bichat Claude Bernard, INSERM, UMR698, F-75877 Paris 18, France

Pakradouni, Jihane
论文数: 0 引用数: 0
h-index: 0
机构:
Univ St Joseph, Fac Pharm, Dept Biochem, Beirut 5076, Lebanon Hop Bichat Claude Bernard, INSERM, UMR698, F-75877 Paris 18, France

Collin, Matthieu
论文数: 0 引用数: 0
h-index: 0
机构:
Inserm Transfert, F-75010 Paris, France Hop Bichat Claude Bernard, INSERM, UMR698, F-75877 Paris 18, France

Samson-Bouma, Marie-Elisabeth
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h-index: 0
机构:
Hop Bichat Claude Bernard, INSERM, UMR698, F-75877 Paris 18, France Hop Bichat Claude Bernard, INSERM, UMR698, F-75877 Paris 18, France

Varret, Mathilde
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h-index: 0
机构:
Hop Bichat Claude Bernard, INSERM, UMR698, F-75877 Paris 18, France Hop Bichat Claude Bernard, INSERM, UMR698, F-75877 Paris 18, France

Rabes, Jean-Pierre
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h-index: 0
机构:
Hop Bichat Claude Bernard, INSERM, UMR698, F-75877 Paris 18, France
Hop Ambroise Pare, AP HP, Serv Biochim & Genet Mol, F-92104 Boulogne, France
Univ Versailles St Quentin En Yvelines, UFR Med Paris Ile de France Ouest, F-78280 Guyancourt, France Hop Bichat Claude Bernard, INSERM, UMR698, F-75877 Paris 18, France

Boileau, Catherine
论文数: 0 引用数: 0
h-index: 0
机构:
Hop Bichat Claude Bernard, INSERM, UMR698, F-75877 Paris 18, France
Hop Ambroise Pare, AP HP, Serv Biochim & Genet Mol, F-92104 Boulogne, France
Univ Versailles St Quentin En Yvelines, UFR Med Paris Ile de France Ouest, F-78280 Guyancourt, France Hop Bichat Claude Bernard, INSERM, UMR698, F-75877 Paris 18, France
机构:
[1] Hop Bichat Claude Bernard, INSERM, UMR698, F-75877 Paris 18, France
[2] Univ St Joseph, Fac Pharm, Dept Biochem, Beirut 5076, Lebanon
[3] Inserm Transfert, F-75010 Paris, France
[4] Hop Ambroise Pare, AP HP, Serv Biochim & Genet Mol, F-92104 Boulogne, France
[5] Univ Versailles St Quentin En Yvelines, UFR Med Paris Ile de France Ouest, F-78280 Guyancourt, France
关键词:
antibody;
familial hypercholesterolemia;
patent;
PCSK9;
RNAi;
DENSITY-LIPOPROTEIN-RECEPTOR;
AUTOSOMAL-DOMINANT HYPERCHOLESTEROLEMIA;
C VIRUS-INFECTION;
FAMILIAL HYPERCHOLESTEROLEMIA;
PCSK9;
GENE;
SECRETED PCSK9;
PLASMA-CHOLESTEROL;
NONHUMAN-PRIMATES;
LDL-CHOLESTEROL;
HEPG2;
CELLS;
D O I:
10.1517/13543776.2010.518615
中图分类号:
R914 [药物化学];
学科分类号:
100701 ;
摘要:
Importance of the field: Proprotein convertase subtilisin kexin 9 (PCSK9) is a new actor discovered in 2003 that is implicated in autosomal dominant hyper-cholesterolemia, cholesterol homeostasis and coronary heart disease. It has been shown to degrade the low-density lipoprotein (LDL) receptor independently of its catalytic activity. Several pharmacological strategies to reduce PCSK9 are being thoroughly investigated. Areas covered in this review: This article reviews all different strategies that are presently pursued to modulate the functional activity of PCSK9 which is a prime target for controlling LDL-cholesterol. It also provides a briefing of all the patents up to July 2010 from various organizations including pharmaceutical companies and academic institutions that have been submitted and/or approved. What the reader will gain: This review is addressed to researchers from academia and pharmaceutical companies who are engaged in PCSK9 research/cholesterol regulation and in the development of cholesterol lowering drugs. Readers will gain an up-to-date overview of the different strategies that have been investigated to reduce PCSK9 including antisense technology and specific antibodies. Take home message: Clinical trials have been launched using RNA interference approaches to reduce PCSK9 expression or specific antibodies targeting and inhibiting PCSK9 interaction with the LDL receptor. They constitute very promising approaches to reducing cholesterol levels and coronary heart disease.
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收藏
页码:1547 / 1571
页数:25
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Rockefeller Univ, Biochem Genet & Metab Lab, New York, NY 10021 USA Rockefeller Univ, Biochem Genet & Metab Lab, New York, NY 10021 USA

Duncan, EM
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Rockefeller Univ, Biochem Genet & Metab Lab, New York, NY 10021 USA Rockefeller Univ, Biochem Genet & Metab Lab, New York, NY 10021 USA

Schayek, E
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Rockefeller Univ, Biochem Genet & Metab Lab, New York, NY 10021 USA Rockefeller Univ, Biochem Genet & Metab Lab, New York, NY 10021 USA

Breslow, JL
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Rockefeller Univ, Biochem Genet & Metab Lab, New York, NY 10021 USA Rockefeller Univ, Biochem Genet & Metab Lab, New York, NY 10021 USA
[70]
Annexin A2 Is a C-terminal PCSK9-binding Protein That Regulates Endogenous Low Density Lipoprotein Receptor Levels
[J].
Mayer, Gaetan
;
Poirier, Steve
;
Seidah, Nabil G.
.
JOURNAL OF BIOLOGICAL CHEMISTRY,
2008, 283 (46)
:31791-31801

Mayer, Gaetan
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Clin Res Inst Montreal, Biochem Neuroendocrinol Lab, Montreal, PQ H2W 1R7, Canada Clin Res Inst Montreal, Biochem Neuroendocrinol Lab, Montreal, PQ H2W 1R7, Canada

Poirier, Steve
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Clin Res Inst Montreal, Biochem Neuroendocrinol Lab, Montreal, PQ H2W 1R7, Canada Clin Res Inst Montreal, Biochem Neuroendocrinol Lab, Montreal, PQ H2W 1R7, Canada

Seidah, Nabil G.
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Clin Res Inst Montreal, Biochem Neuroendocrinol Lab, Montreal, PQ H2W 1R7, Canada Clin Res Inst Montreal, Biochem Neuroendocrinol Lab, Montreal, PQ H2W 1R7, Canada