PCSK9及其抑制剂在肝癌治疗中的研究进展
Research Progress of PCSK9 and Its Inhibitors in the Treatment of Hepatocellular Carcinoma
DOI: 10.12677/pi.2026.152014, PDF,    科研立项经费支持
作者: 刘亚峰, 杨 敏, 张 旋*:昆明医科大学药学院暨云南省天然药物药理重点实验室,云南省现代生物医药产业学院,云南 昆明
关键词: 前蛋白转化酶枯草溶菌素9脂质代谢肝癌免疫PCSK9 Lipid Metabolism Liver Cancer Immune
摘要: 前蛋白转化酶枯草溶菌素9 (PCSK9)是胆固醇代谢调控的关键分子,可以降解低密度脂蛋白受体(LDLR)维持胆固醇稳态。近年来研究显示,PCSK9在肝细胞癌(HCC)中异常高表达,并通过促进肿瘤增殖、侵袭、免疫逃逸及胆固醇代谢重编程等方式驱动肝癌进展,成为连接代谢异常与肝细胞癌的重要靶点。本文系统阐述了PCSK9的生物学功能及其在肝细胞癌发展中的作用机制,重点分析了PCSK9抑制剂在调节代谢、直接抑制肿瘤、重塑免疫微环境及协同增强治疗等方面的抗肿瘤潜力,同时总结了当前研究的局限,展望了未来研究方向,以期为PCSK9抑制剂在肝细胞癌个体化治疗中的临床应用提供理论支撑。
Abstract: Proprotein Convertase Subtilisin/Kexin type 9 (PCSK9) is a key molecule in the regulation of cholesterol metabolism, which can degrade Low-Density Lipoprotein Receptor (LDLR) to maintain cholesterol homeostasis. In recent years, studies have shown that PCSK9 is abnormally highly expressed in Hepatocellular Carcinoma (HCC) and drives liver cancer progression by promoting tumor proliferation, invasion, immune escape and cholesterol metabolic reprogramming, thus emerging as an important target linking metabolic disorders and hepatocellular carcinoma. This paper systematically elaborates the biological functions of PCSK9 and its mechanism of action in the development of hepatocellular carcinoma, with a focus on analyzing the anti-tumor potential of PCSK9 inhibitors in regulating metabolism, directly inhibiting tumors, remodeling the immune microenvironment and synergistically enhancing therapy. It summarizes the limitations of current research and prospects future research directions, aiming to provide theoretical support for the clinical application of PCSK9 inhibitors in the individualized treatment of hepatocellular carcinoma.
文章引用:刘亚峰, 杨敏, 张旋. PCSK9及其抑制剂在肝癌治疗中的研究进展[J]. 药物资讯, 2026, 15(2): 112-122. https://doi.org/10.12677/pi.2026.152014

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