Insight into the Evolving Role of PCSK9

被引:36
作者
Maliglowka, Mateusz [1 ]
Kosowski, Michal [1 ]
Hachula, Marcin [1 ]
Cyrnek, Marcin [1 ]
Buldak, Lukasz [1 ]
Basiak, Marcin [1 ]
Boldys, Aleksandra [1 ]
Machnik, Grzegorz [1 ]
Buldak, Rafal Jakub [2 ]
Okopien, Boguslaw [1 ]
机构
[1] Med Univ Silesia, Sch Med Katowice, Dept Internal Med & Clin Pharmacol, PL-40007 Katowice, Poland
[2] Univ Opole, Inst Med Sci, PL-45040 Opole, Poland
关键词
PCSK9; cholesterol; anti-PCSK9; cardiovascular diseases; genetic; atherosclerosis; alirocumab; evolocumab; inclisiran; LOW-DENSITY-LIPOPROTEIN; SUBTILISIN/KEXIN TYPE 9; FAMILIAL HYPERCHOLESTEROLEMIA SUBJECTS; SMOOTH-MUSCLE-CELLS; CIRCULATING PCSK9; ENDOTHELIAL DYSFUNCTION; CARDIOVASCULAR-DISEASE; VENOUS THROMBOEMBOLISM; INFLAMMATORY PROFILE; INHIBITOR EVOLOCUMAB;
D O I
10.3390/metabo12030256
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Proprotein convertase subtilisin/kexin type 9 (PCSK9) is the last discovered member of the family of proprotein convertases (PCs), mainly synthetized in hepatic cells. This serine protease plays a pivotal role in the reduction of the number of low-density lipoprotein receptors (LDLRs) on the surface of hepatocytes, which leads to an increase in the level of cholesterol in the blood. This mechanism and the fact that gain of function (GOF) mutations in PCSK9 are responsible for causing familial hypercholesterolemia whereas loss-of-function (LOF) mutations are associated with hypocholesterolemia, prompted the invention of drugs that block PCSK9 action. The high efficiency of PCSK9 inhibitors (e.g., alirocumab, evolocumab) in decreasing cardiovascular risk, pleiotropic effects of other lipid-lowering drugs (e.g., statins) and the multifunctional character of other proprotein convertases, were the cause for proceeding studies on functions of PCSK9 beyond cholesterol metabolism. In this article, we summarize the current knowledge on the roles that PCSK9 plays in different tissues and perspectives for its clinical use.
引用
收藏
页数:25
相关论文
共 235 条
[1]   Mutations in PCSK9 cause autosomal dominant hypercholesterolemia [J].
Abifadel, M ;
Varret, M ;
Rabès, JP ;
Allard, D ;
Ouguerram, K ;
Devillers, M ;
Cruaud, C ;
Benjannet, S ;
Wickham, L ;
Erlich, D ;
Derré, A ;
Villéger, L ;
Farnier, M ;
Beucler, I ;
Bruckert, E ;
Chambaz, J ;
Chanu, B ;
Lecerf, JM ;
Luc, G ;
Moulin, P ;
Weissenbach, J ;
Prat, A ;
Krempf, M ;
Junien, C ;
Seidah, NG ;
Boileau, C .
NATURE GENETICS, 2003, 34 (02) :154-156
[2]   The Lipogenesis Pathway as a Cancer Target [J].
Abramson, Hanley N. .
JOURNAL OF MEDICINAL CHEMISTRY, 2011, 54 (16) :5615-5638
[3]   Inhibitory effect of PCSK9 on Abca1 protein expression and cholesterol efflux in macrophages [J].
Adorni, Maria Pia ;
Cipollari, Eleonora ;
Favari, Elda ;
Zanotti, Ilaria ;
Zimetti, Francesca ;
Corsini, Alberto ;
Ricci, Chiara ;
Bernini, Franco ;
Ferri, Nicola .
ATHEROSCLEROSIS, 2017, 256 :1-6
[4]   Role of low-density lipoprotein receptor in the hepatitis C virus life cycle [J].
Albecka, Anna ;
Belouzard, Sandrine ;
de Beeck, Anne Op ;
Descamps, Veronique ;
Goueslain, Lucie ;
Bertrand-Michel, Justine ;
Terce, Francois ;
Duverlie, Gilles ;
Rouille, Yves ;
Dubuisson, Jean .
HEPATOLOGY, 2012, 55 (04) :998-1007
[5]   Identification of PCSK9 as a novel serum biomarker for the prenatal diagnosis of neural tube defects using iTRAQ quantitative proteomics [J].
An, Dong ;
Wei, Xiaowei ;
Li, Hui ;
Gu, Hui ;
Huang, Tianchu ;
Zhao, Guifeng ;
Liu, Bo ;
Wang, Weilin ;
Chen, Lizhu ;
Ma, Wei ;
Zhang, Henan ;
Cao, Songying ;
Yuan, Zhengwei .
SCIENTIFIC REPORTS, 2015, 5
[6]   Malaria severity: Possible influence of the E670G PCSK9 polymorphism: A preliminary case-control study in Malian children [J].
Arama, Charles ;
Diarra, Issa ;
Kouriba, Bourema ;
Sirois, Francine ;
Fedoryak, Olesya ;
Thera, Mahamadou A. ;
Coulibaly, Drissa ;
Lyke, Kirsten E. ;
Plowe, Christopher V. ;
Chretien, Michel ;
Doumbo, Ogobara K. ;
Mbikay, Majambu .
PLOS ONE, 2018, 13 (02)
[7]   Extrahepatic Complications of Nonalcoholic Fatty Liver Disease [J].
Armstrong, Matthew J. ;
Adams, Leon A. ;
Canbay, Ali ;
Syn, Wing-Kin .
HEPATOLOGY, 2014, 59 (03) :1174-1197
[8]   Kidney-derived PCSK9-a new driver of hyperlipidemia in nephrotic syndrome? [J].
Artunc, Ferruh .
KIDNEY INTERNATIONAL, 2020, 98 (06) :1393-1395
[9]  
Athyros Vasilios G, 2011, Open Cardiovasc Med J, V5, P24, DOI 10.2174/1874192401105010024
[10]   Successful treatment of a patient with refractory nephrotic syndrome with PCSK9 inhibitors: a case report [J].
Awanami, Yuki ;
Fukuda, Makoto ;
Nonaka, Yasunori ;
Takashima, Tsuyoshi ;
Matsumoto, Keiichiro ;
Yamasaki, Masatora ;
Miyazono, Motoaki ;
Ikeda, Yuji .
BMC NEPHROLOGY, 2017, 18