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Unravelling the functional significance of PCSK9.

机译:阐明PCSK9的功能意义。

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PURPOSE OF REVIEW: Proprotein convertase subtilisin kexin type 9 (PCSK9) has emerged as a potential target for lowering plasma LDL cholesterol levels. This review summarizes recent studies published in print or online before January 2007 which have investigated the functional significance of this intriguing protease. RECENT FINDINGS: Increasing interest in PCSK9 has given rise to landmark epidemiological studies, the generation of animal models, the discovery of new human mutations, as well as numerous in-vitro studies. These studies have helped to unravel the molecular functions of PCSK9. SUMMARY: Mutations of PCSK9 are associated either with hypercholesterolemia or with hypocholesterolemia. In the latter case, the incidence of coronary heart disease is reduced, thereby demonstrating that low LDL cholesterol levels from birth are highly beneficial. PCSK9 promotes the degradation of the LDL receptor in hepatocytes apparently both intracellularly and by being a secreted protein that can bind the LDL receptor and be internalized. By virtue of its role as a major inhibitor of the LDL receptor, PCSK9 is a promising therapeutic target. Specific PCSK9 pharmacological inhibitors may prove to be useful in amplifying the well documented benefits of statins.
机译:审查目的:前蛋白转化酶枯草杆菌蛋白酶kexin 9型(PCSK9)已成为降低血浆LDL胆固醇水平的潜在靶标。这篇综述总结了2007年1月之前以印刷或在线形式发表的最新研究,这些研究调查了这种有趣的蛋白酶的功能意义。最近的发现:人们对PCSK9的兴趣日益增加,引起了具有里程碑意义的流行病学研究,动物模型的产生,新人类突变的发现以及众多的体外研究。这些研究有助于揭示PCSK9的分子功能。摘要:PCSK9突变与高胆固醇血症或低胆固醇血症相关。在后一种情况下,降低了冠心病的发生率,从而证明出生时低的LDL胆固醇水平是高度有益的。 PCSK9显然是在细胞内以及通过是一种可以结合LDL受体并被内在化的分泌蛋白,促进肝细胞中LDL受体的降解。凭借其作为LDL受体的主要抑制剂的作用,PCSK9是有前途的治疗靶标。特定的PCSK9药理抑制剂可能被证明可用于扩大他汀类药物的文献资料。

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