Pan Bo-Yi, Chen Chen-Sheng, Chen Fang-Yu, Shen Ming-Yi
Graduate Institute of Biomedical Sciences, China Medical University, Taichung 40402, Taiwan.
The Ph.D. Program for Cancer Biology and Drug Discovery, China Medical University and Academia Sinica, Taichung 40402, Taiwan.
Int J Mol Sci. 2024 Nov 27;25(23):12759. doi: 10.3390/ijms252312759.
Apolipoprotein C3 (APOC3) plays a critical role in regulating triglyceride levels and serves as a key predictor of cardiovascular disease (CVD) risk, particularly in patients with diabetes. While APOC3 is known to inhibit lipoprotein lipase, recent findings reveal its broader influence across lipoprotein metabolism, where it modulates the structure and function of various lipoproteins. Therefore, this review examines the complex metabolic cycle of APOC3, emphasizing the impact of APOC3-containing lipoproteins on human metabolism, particularly in patients with diabetes. Notably, APOC3 affects triglyceride-rich lipoproteins and causes structural changes in high-, very low-, intermediate-, and low-density lipoproteins, thereby increasing CVD risk. Evidence suggests that elevated APOC3 levels-above the proposed safe range of 10-15 mg/dL-correlate with clinically significant CVD outcomes. Recognizing APOC3 as a promising biomarker for CVD, this review underscores the urgent need for high-throughput, clinically feasible methods to further investigate its role in lipoprotein physiology in both animal models and human studies. Additionally, we analyze the relationship between APOC3-related genes and lipoproteins, reinforcing the value of large-population studies to understand the impact of APOC3 on metabolic diseases. Ultimately, this review supports the development of therapeutic strategies targeting APOC3 reduction as a preventive approach for diabetes-related CVD.
载脂蛋白C3(APOC3)在调节甘油三酯水平方面发挥着关键作用,并且是心血管疾病(CVD)风险的关键预测指标,尤其是在糖尿病患者中。虽然已知APOC3会抑制脂蛋白脂肪酶,但最近的研究结果揭示了其在脂蛋白代谢中的更广泛影响,它在其中调节各种脂蛋白的结构和功能。因此,本综述探讨了APOC3复杂的代谢循环,强调了含APOC3脂蛋白对人体代谢的影响,特别是在糖尿病患者中。值得注意的是,APOC3会影响富含甘油三酯的脂蛋白,并导致高密度、极低密度、中间密度和低密度脂蛋白的结构变化,从而增加CVD风险。有证据表明,APOC3水平升高——高于建议的安全范围10 - 15毫克/分升——与具有临床意义的CVD结局相关。认识到APOC3是一种有前景的CVD生物标志物,本综述强调迫切需要高通量、临床可行的方法,以进一步研究其在动物模型和人体研究中脂蛋白生理学中的作用。此外,我们分析了APOC3相关基因与脂蛋白之间的关系,强化了大规模人群研究对于理解APOC3对代谢疾病影响的价值。最终,本综述支持开发以降低APOC3为靶点的治疗策略,作为预防糖尿病相关CVD的一种方法