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Potential role of lycopene in targeting proprotein convertase subtilisin/kexin type-9 to combat hypercholesterolemia

dc.contributor.authorAlvi, Sahir Sultan
dc.contributor.authorAnsari, Irfan A.
dc.contributor.authorKhan, IMRAN
dc.contributor.authorIqbal, Johar
dc.contributor.authorKhan, M. Salman
dc.contributor.institutionauthorKHAN, IMRAN
dc.date.accessioned2021-04-10T20:59:09Z
dc.date.available2021-04-10T20:59:09Z
dc.date.issued2017-07-01T00:00:00Z
dc.description.abstractProprotein convertase subtilisin/kexin type 9 (PCSK-9) is a serine protease of the proprotien convertase (PC) family that has profound effects on plasma low density lipoprotein cholesterol (LDL-C) levels, the major risk factor for coronary heart disease (CHD), through its ability to mediate LDL receptor (LDL-R) protein degradation and reduced recycling to the surface of hepatocytes. Thus, the current study was premeditated not only to evaluate the role of lycopene in targeting the inhibition of PCSK-9 via modulation of genes involved in cholesterol homeostasis in HFD rats but also to examine a correlation between HFD induced inflammatory cascades and subsequent regulation of PCSK-9 expression. Besides the effect of lycopene on hepatic PCSK-9 gene expression, PPI studies for PCSK-9-Lycopene complex and EGF-A of LDL-R were also performed via molecular informatics approach to assess the dual mode of action of lycopene in LDL-R recycling and increased removal of circulatory LDL-C. We for the first time deciphered that lycopene treatment significantly down-regulates the expression of hepatic PCSK-9 and HMGR, whereas, hepatic LDL-R expression was significantly up-regulated. Furthermore, lycopene ameliorated inflammation stimulated expression of PCSK-9 via suppressing the expression of inflammatory markers. The results from our molecular informatics studies confirmed that lycopene, while occupying the active site of PCSK-9 crystal structure, reduces the affinity of PCSK-9 to complex with EGF-A of LDL-R, whereas, atorvastatin makes PCSK-9-EGF-A complex formation more feasible than both of PCSK-9-EGF-A alone and Lycopene-PCSK-9-EGF-A complex. Based on above results, it can be concluded that lycopene exhibits potent hypolipidemic activities via molecular mechanisms that are either identical (HMGR inhibition) or distinct from that of statins (down-regulation of PCSK-9 mRNA synthesis). To the best of our knowledge, this is the first report that lycopene has this specific biological property. Being a natural, safer and alternative therapeutic agent, lycopene could be used as a complete regulator of cholesterol homeostasis and ASCVD.
dc.identifier.citationAlvi S. S. , Ansari I. A. , Khan I., Iqbal J., Khan M. S. , -Potential role of lycopene in targeting proprotein convertase subtilisin/kexin type-9 to combat hypercholesterolemia-, FREE RADICAL BIOLOGY AND MEDICINE, cilt.108, ss.394-403, 2017
dc.identifier.doi10.1016/j.freeradbiomed.2017.04.012
dc.identifier.scopus85017535559
dc.identifier.urihttp://hdl.handle.net/20.500.12645/28723
dc.identifier.wosWOS:000403463500036
dc.titlePotential role of lycopene in targeting proprotein convertase subtilisin/kexin type-9 to combat hypercholesterolemia
dc.typeArticle
dspace.entity.typePublication
local.avesis.id86e8fd4f-6426-4617-abd6-e5c5ecdad66a
local.indexed.atWOS
local.indexed.atScopus
local.publication.isinternational1
relation.isAuthorOfPublication096be806-cf26-4766-b5b4-26f30c593af2
relation.isAuthorOfPublication.latestForDiscovery096be806-cf26-4766-b5b4-26f30c593af2

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