Strategies for proprotein convertase subtilisin kexin 9 modulation: a perspective on recent patents

被引:28
作者
Abifadel, Marianne [1 ,2 ]
Pakradouni, Jihane [2 ]
Collin, Matthieu [3 ]
Samson-Bouma, Marie-Elisabeth [1 ]
Varret, Mathilde [1 ]
Rabes, Jean-Pierre [1 ,4 ,5 ]
Boileau, Catherine [1 ,4 ,5 ]
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.
引用
收藏
页码:1547 / 1571
页数:25
相关论文
共 117 条
[61]   PCSK9 Impedes Hepatitis C Virus Infection In Vitro and Modulates Liver CD81 Expression [J].
Labonte, Patrick ;
Begley, Syntia ;
Guevin, Carl ;
Asselin, Marie-Claude ;
Nassoury, Nasha ;
Mayer, Gaetan ;
Prat, Annik ;
Seidah, Nabil G. .
HEPATOLOGY, 2009, 50 (01) :17-24
[62]   Secreted PCSK9 decreases the number of LDL receptors in hepatocytes and in livers of parabiotic mice [J].
Lagace, Thomas A. ;
Curtis, David E. ;
Garuti, Rita ;
McNutt, Markey C. ;
Park, Sahng Wook ;
Prather, Heidi B. ;
Anderson, Norma N. ;
Ho, Y. K. ;
Hammer, Robert E. ;
Horton, Jay D. .
JOURNAL OF CLINICAL INVESTIGATION, 2006, 116 (11) :2995-3005
[63]   Molecular basis of PCSK9 function [J].
Lambert, Gilles ;
Charlton, Francesca ;
Rye, Kerry-Anne ;
Piper, Derek E. .
ATHEROSCLEROSIS, 2009, 203 (01) :1-7
[64]   Therapeutic Silencing of MicroRNA-122 in Primates with Chronic Hepatitis C Virus Infection [J].
Lanford, Robert E. ;
Hildebrandt-Eriksen, Elisabeth S. ;
Petri, Andreas ;
Persson, Robert ;
Lindow, Morten ;
Munk, Martin E. ;
Kauppinen, Sakari ;
Orum, Henrik .
SCIENCE, 2010, 327 (5962) :198-201
[65]   Activation of the farnesoid X receptor represses PCSK9 expression in human hepatocytes [J].
Langhi, Cedric ;
Le May, Cedric ;
Kourimate, Sanae ;
Caron, Sandrine ;
Staels, Bart ;
Krempf, Michel ;
Costet, Philippe ;
Cariou, Bertrand .
FEBS LETTERS, 2008, 582 (06) :949-955
[66]   PCSK9 is expressed in pancreatic δ-cells and does not alter insulin secretion [J].
Langhi, Cedric ;
Le May, Cedric ;
Gmyr, Valery ;
Vandewalle, Brigitte ;
Kerr-Conte, Julie ;
Krempf, Michel ;
Pattou, Francois ;
Costet, Philippe ;
Cariou, Bertrand .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2009, 390 (04) :1288-1293
[67]   Hepatocyte Nuclear Factor 1α Plays a Critical Role in PCSK9 Gene Transcription and Regulation by the Natural Hypocholesterolemic Compound Berberine [J].
Li, Hai ;
Dong, Bin ;
Park, Sahng Wook ;
Lee, Hyun-Sook ;
Chen, Wei ;
Liu, Jingwen .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2009, 284 (42) :28885-28895
[68]   PCSK9 is not involved in the degradation of LDL receptors and BACE1 in the adult mouse brain [J].
Liu, Mali ;
Wu, Guoxin ;
Baysarowich, Jennifer ;
Kavana, Michael ;
Addona, George H. ;
Bierilo, Kathleen K. ;
Mudgett, John S. ;
Pavlovic, Guillaume ;
Sitlani, Ayesha ;
Renger, John J. ;
Hubbard, Brian K. ;
Fisher, Timothy S. ;
Zerbinatti, Celina V. .
JOURNAL OF LIPID RESEARCH, 2010, 51 (09) :2611-2618
[69]   Novel putative SREBP and LXR target genes identified by microarray analysis in liver of cholesterol-fed mice [J].
Maxwell, KN ;
Soccio, RE ;
Duncan, EM ;
Schayek, E ;
Breslow, JL .
JOURNAL OF LIPID RESEARCH, 2003, 44 (11) :2109-2119
[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