Targeting proprotein convertase subtilisin/kexin type 9 (PCSK9): from bench to bedside

dc.contributor.author

Bao, Xuhui

dc.contributor.author

Liang, Yongjun

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Chang, Hanman

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Cai, Tianji

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Feng, Baijie

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Gordon, Konstantin

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Zhu, Yuekun

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Shi, Hailian

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He, Yundong

dc.contributor.author

Xie, Liyi

dc.date.accessioned

2024-01-08T06:00:26Z

dc.date.available

2024-01-08T06:00:26Z

dc.description.abstract

<jats:title>Abstract</jats:title><jats:p>Proprotein convertase subtilisin/kexin type 9 (PCSK9) has evolved as a pivotal enzyme in lipid metabolism and a revolutionary therapeutic target for hypercholesterolemia and its related cardiovascular diseases (CVD). This comprehensive review delineates the intricate roles and wide-ranging implications of PCSK9, extending beyond CVD to emphasize its significance in diverse physiological and pathological states, including liver diseases, infectious diseases, autoimmune disorders, and notably, cancer. Our exploration offers insights into the interaction between PCSK9 and low-density lipoprotein receptors (LDLRs), elucidating its substantial impact on cholesterol homeostasis and cardiovascular health. It also details the evolution of PCSK9-targeted therapies, translating foundational bench discoveries into bedside applications for optimized patient care. The advent and clinical approval of innovative PCSK9 inhibitory therapies (PCSK9-iTs), including three monoclonal antibodies (Evolocumab, Alirocumab, and Tafolecimab) and one small interfering RNA (siRNA, Inclisiran), have marked a significant breakthrough in cardiovascular medicine. These therapies have demonstrated unparalleled efficacy in mitigating hypercholesterolemia, reducing cardiovascular risks, and have showcased profound value in clinical applications, offering novel therapeutic avenues and a promising future in personalized medicine for cardiovascular disorders. Furthermore, emerging research, inclusive of our findings, unveils PCSK9’s potential role as a pivotal indicator for cancer prognosis and its prospective application as a transformative target for cancer treatment. This review also highlights PCSK9’s aberrant expression in various cancer forms, its association with cancer prognosis, and its crucial roles in carcinogenesis and cancer immunity. In conclusion, this synthesized review integrates existing knowledge and novel insights on PCSK9, providing a holistic perspective on its transformative impact in reshaping therapeutic paradigms across various disorders. It emphasizes the clinical value and effect of PCSK9-iT, underscoring its potential in advancing the landscape of biomedical research and its capabilities in heralding new eras in personalized medicine.</jats:p>

dc.identifier.issn

2059-3635

dc.identifier.uri

https://hdl.handle.net/10161/29666

dc.language

en

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Springer Science and Business Media LLC

dc.relation.ispartof

Signal Transduction and Targeted Therapy

dc.relation.isversionof

10.1038/s41392-023-01690-3

dc.rights.uri

https://creativecommons.org/licenses/by-nc/4.0

dc.title

Targeting proprotein convertase subtilisin/kexin type 9 (PCSK9): from bench to bedside

dc.type

Journal article

duke.contributor.orcid

Bao, Xuhui|0000-0003-4653-0288

pubs.issue

1

pubs.organisational-group

Duke

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School of Medicine

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Clinical Science Departments

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Pathology

pubs.publication-status

Published online

pubs.volume

9

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