| Literature DB >> 28574577 |
Farzad Khademi1, Amir Abbas Momtazi-Borojeni2,3, Željko Reiner4, Maciej Banach5,6, Khalid Al Al-Rasadi7, Amirhossein Sahebkar8,9.
Abstract
Elevated plasma low-density lipoprotein-cholesterol (LDL-C) concentration is the most important risk factor for atherosclerotic cardiovascular diseases (CVDs). Proprotein convertase subtilisin/kexin type 9 (PCSK9) is a ubiquitously expressed serine proteinase which plays a key role in cholesterol metabolism, but has been found to be implicated in some other lipid-independent physiological processes. In this review, the role of PCSK9 was evaluated not only concerning lipid metabolism but also hepatitis C virus (HCV) infection, bacterial infections/sepsis, and septic shock. Collected data from clinical trials revealed that treatment with PCSK9 inhibitors has beneficial effects in lowering LDL-C via inhibition of LDL-receptors (LDL-R), an antiviral effect on HCV infection via down-regulating the surface expression of LDL-R and CD81 on hepatic cells, and a positive association with increased inflammatory responses, as well as with septic shock by down-regulation of hepatocyte LDL-R. On the other hand, PCSK9 inhibition by therapeutic fully humanized antibodies has positive effects in reducing elevated LDL-C. However, their safety and tolerability is an important issue which has to be taken into consideration.Entities:
Keywords: LDL receptor; PCSK9; cholesterol; hepatitis C virus; infection
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Year: 2017 PMID: 28574577 DOI: 10.1002/jcp.26040
Source DB: PubMed Journal: J Cell Physiol ISSN: 0021-9541 Impact factor: 6.384