TY - JOUR
T1 - PCSK9 in metabolism and diseases
AU - Ajoolabady, Amir
AU - Pratico, Domenico
AU - Mazidi, Mohsen
AU - Davies, Ian G.
AU - Lip, Gregory Y.H.
AU - Seidah, Nabil
AU - Libby, Peter
AU - Kroemer, Guido
AU - Ren, Jun
N1 - Publisher Copyright:
© 2024 Elsevier Inc.
PY - 2025/2/1
Y1 - 2025/2/1
N2 - PCSK9 is a serine protease that regulates plasma levels of low-density lipoprotein (LDL) and cholesterol by mediating the endolysosomal degradation of LDL receptor (LDLR) in the liver. When PCSK9 functions unchecked, it leads to increased degradation of LDLR, resulting in elevated circulatory levels of LDL and cholesterol. This dysregulation contributes to lipid and cholesterol metabolism abnormalities, foam cell formation, and the development of various diseases, including cardiovascular disease (CVD), viral infections, cancer, and sepsis. Emerging clinical and experimental evidence highlights an imperative role for PCSK9 in metabolic anomalies such as hypercholesterolemia and hyperlipidemia, as well as inflammation, and disturbances in mitochondrial homeostasis. Moreover, metabolic hormones – including insulin, glucagon, adipokines, natriuretic peptides, and sex steroids - regulate the expression and circulatory levels of PCSK9, thus influencing cardiovascular and metabolic functions. In this comprehensive review, we aim to elucidate the regulatory role of PCSK9 in lipid and cholesterol metabolism, pathophysiology of diseases such as CVD, infections, cancer, and sepsis, as well as its pharmaceutical and non-pharmaceutical targeting for therapeutic management of these conditions.
AB - PCSK9 is a serine protease that regulates plasma levels of low-density lipoprotein (LDL) and cholesterol by mediating the endolysosomal degradation of LDL receptor (LDLR) in the liver. When PCSK9 functions unchecked, it leads to increased degradation of LDLR, resulting in elevated circulatory levels of LDL and cholesterol. This dysregulation contributes to lipid and cholesterol metabolism abnormalities, foam cell formation, and the development of various diseases, including cardiovascular disease (CVD), viral infections, cancer, and sepsis. Emerging clinical and experimental evidence highlights an imperative role for PCSK9 in metabolic anomalies such as hypercholesterolemia and hyperlipidemia, as well as inflammation, and disturbances in mitochondrial homeostasis. Moreover, metabolic hormones – including insulin, glucagon, adipokines, natriuretic peptides, and sex steroids - regulate the expression and circulatory levels of PCSK9, thus influencing cardiovascular and metabolic functions. In this comprehensive review, we aim to elucidate the regulatory role of PCSK9 in lipid and cholesterol metabolism, pathophysiology of diseases such as CVD, infections, cancer, and sepsis, as well as its pharmaceutical and non-pharmaceutical targeting for therapeutic management of these conditions.
KW - Atherosclerosis
KW - Cardiovascular disease (CVD)
KW - Clinical trials
KW - Inflammation
KW - Lipid and cholesterol metabolism
KW - Metabolic hormones
KW - PCSK9
UR - http://www.scopus.com/inward/record.url?scp=85211731395&partnerID=8YFLogxK
U2 - 10.1016/j.metabol.2024.156064
DO - 10.1016/j.metabol.2024.156064
M3 - Review article
C2 - 39547595
AN - SCOPUS:85211731395
SN - 0026-0495
VL - 163
JO - Metabolism: Clinical and Experimental
JF - Metabolism: Clinical and Experimental
M1 - 156064
ER -