Department of Chemical Engineering, Villanova University, Villanova, PA 19085, USA.
Int J Environ Res Public Health. 2023 Jun 24;20(13):6217. doi: 10.3390/ijerph20136217.
Despite extensive research and seven approved drugs, the complex interplay of genes, proteins, and pathways in Alzheimer's disease remains a challenge. This implies the intricacies of the mechanism for Alzheimer's disease, which involves the interaction of hundreds of genes, proteins, and pathways. While the major hallmarks of Alzheimer's disease are the accumulation of amyloid plaques and tau protein tangles, excessive accumulation of cholesterol is reportedly correlated with Alzheimer's disease patients. In this work, protein-protein interaction analysis was conducted based upon the genes from a clinical database to identify the top protein targets with most data-indicated involvement in Alzheimer's disease, which include ABCA1, CYP46A1, BACE1, TREM2, GSK3B, and SREBP2. The reactions and pathways associated with these genes were thoroughly studied for their roles in regulating brain cholesterol biosynthesis, amyloid beta accumulation, and tau protein tangle formation. Existing clinical trials for each protein target were also investigated. The research indicated that the inhibition of SREBP2, BACE1, or GSK3B is beneficial to reduce cholesterol and amyloid beta accumulation, while the activation of ABCA1, CYP46A1, or TREM2 has similar effects. In this study, Sterol Regulatory Element-Binding Protein 2 (SREBP2) emerged as the primary protein target. SREBP2 serves a pivotal role in maintaining cholesterol balance, acting as a transcription factor that controls the expression of several enzymes pivotal for cholesterol biosynthesis. Novel studies suggest that SREBP2 performs a multifaceted role in Alzheimer's disease. The hyperactivity of SREBP2 may lead to heightened cholesterol biosynthesis, which suggested association with the pathogenesis of Alzheimer's disease. Lowering SREBP2 levels in an Alzheimer's disease mouse model results in reduced production of amyloid-beta, a major contributor to Alzheimer's disease progression. Moreover, its thoroughly analyzed crystal structure allows for computer-aided screening of potential inhibitors; SREBP2 is thus selected as a prospective drug target. While more protein targets can be added onto the list in the future, this work provides an overview of key proteins involved in the regulation of brain cholesterol biosynthesis that may be further investigated for Alzheimer's disease intervention.
尽管进行了广泛的研究并批准了七种药物,但阿尔茨海默病中基因、蛋白质和途径的复杂相互作用仍然是一个挑战。这意味着阿尔茨海默病的机制非常复杂,涉及数百个基因、蛋白质和途径的相互作用。虽然阿尔茨海默病的主要特征是淀粉样斑块和 tau 蛋白缠结的积累,但据报道,胆固醇的过度积累与阿尔茨海默病患者有关。在这项工作中,基于临床数据库中的基因进行了蛋白质-蛋白质相互作用分析,以确定与阿尔茨海默病最相关的数据表明参与的顶级蛋白质靶标,其中包括 ABCA1、CYP46A1、BACE1、TREM2、GSK3B 和 SREBP2。这些基因相关的反应和途径也进行了深入研究,以了解它们在调节大脑胆固醇生物合成、淀粉样β积累和 tau 蛋白缠结形成中的作用。还对每个蛋白质靶标的现有临床试验进行了调查。研究表明,抑制 SREBP2、BACE1 或 GSK3B 有利于减少胆固醇和淀粉样β的积累,而激活 ABCA1、CYP46A1 或 TREM2 则具有类似的效果。在这项研究中,固醇调节元件结合蛋白 2 (SREBP2) 成为主要的蛋白质靶标。SREBP2 在维持胆固醇平衡中起着至关重要的作用,作为一种转录因子,它控制着胆固醇生物合成的几个关键酶的表达。新的研究表明,SREBP2 在阿尔茨海默病中具有多方面的作用。SREBP2 的过度活跃可能导致胆固醇生物合成增加,这与阿尔茨海默病的发病机制有关。在阿尔茨海默病小鼠模型中降低 SREBP2 水平会导致淀粉样β的产生减少,淀粉样β是阿尔茨海默病进展的主要原因。此外,对其进行了深入分析的晶体结构允许进行潜在抑制剂的计算机辅助筛选;因此,SREBP2 被选为有前途的药物靶标。虽然将来可以在清单上添加更多的蛋白质靶标,但这项工作提供了一个涉及调节大脑胆固醇生物合成的关键蛋白质的概述,这些蛋白质可能会进一步研究用于阿尔茨海默病的干预。