Protein kinases as therapeutic targets in Alzheimer’s disease: challenges, insights, and new frontiers

IF 3.1 4区 医学 Q3 CHEMISTRY, MEDICINAL
Chanwool Tak, Swapnil P. Bhujbal, Jung-Mi Hah
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Abstract

Alzheimer’s disease (AD) remains the leading cause of dementia worldwide, imposing an enormous and growing societal burden with more than 55 million people affected globally. Despite decades of intensive investigation, existing therapeutic options provide only modest symptomatic relief and fail to prevent or slow disease progression, emphasizing the critical need for interventions that target the fundamental molecular mechanisms of neurodegeneration. Pathologically, Alzheimer’s disease is characterized by extracellular accumulation of amyloid-β plaques, intracellular neurofibrillary tangles formed by hyperphosphorylated tau, profound synaptic loss, chronic neuroinflammation, and extensive neuronal degeneration. Although amyloid-focused strategies have long dominated drug development, their limited clinical benefit and safety liabilities highlight the multifactorial nature of AD and the need to move beyond amyloid-centric paradigms. Protein kinases have emerged as key integrators of multiple pathogenic processes in AD, governing tau phosphorylation, amyloid precursor protein processing, synaptic signaling, and neuroimmune responses. Aberrant kinase signaling drives tau pathology and propagation, promotes amyloidogenic pathways, disrupts synaptic function, and perpetuates inflammatory cascades. While extensive work on kinases such as GSK-3β, CDK5, JNKs, and CSF1R has firmly established the relevance of kinase dysregulation in AD, no kinase-directed therapy has yet translated into clinical success. This review highlights emerging kinase targets beyond these classical pathways, including Fyn, Casein Kinase 1 Delta (CK1δ), Tau-Tubulin Kinase 1 (TTBK1), and Dual Leucine Zipper Kinase (DLK), which are supported by mechanistic insights and compelling preclinical evidence. Continued advances in brain-penetrant, isoform-selective, and mechanism-driven kinase inhibitor design may enable the development of next-generation disease-modifying therapies for Alzheimer’s disease.

The alternative text for this image may have been generated using AI.

Abstract Image

蛋白激酶作为阿尔茨海默病的治疗靶点:挑战、见解和新领域
阿尔茨海默病(AD)仍然是全世界痴呆症的主要原因,造成了巨大且日益加重的社会负担,全球有超过5500万人受到影响。尽管经过数十年的深入研究,现有的治疗方案仅提供适度的症状缓解,不能预防或减缓疾病进展,强调了针对神经退行性变基本分子机制的干预措施的迫切需要。在病理学上,阿尔茨海默病的特征是细胞外淀粉样蛋白-β斑块的积累,细胞内由过度磷酸化的tau形成的神经原纤维缠结,严重的突触丧失,慢性神经炎症和广泛的神经元变性。尽管以淀粉样蛋白为中心的策略长期以来主导着药物开发,但其有限的临床益处和安全性问题突出了阿尔茨海默病的多因子性质,以及超越淀粉样蛋白为中心的范式的必要性。蛋白激酶已成为阿尔茨海默病多个致病过程的关键整合者,控制tau磷酸化、淀粉样蛋白前体蛋白加工、突触信号传导和神经免疫反应。异常激酶信号驱动tau病理和繁殖,促进淀粉样蛋白生成途径,破坏突触功能,并延续炎症级联反应。虽然对激酶(如GSK-3β、CDK5、JNKs和CSF1R)的大量研究已经牢固地确立了AD中激酶失调的相关性,但尚未有激酶导向的治疗方法转化为临床成功。这篇综述强调了这些经典途径之外的新兴激酶靶点,包括Fyn、酪蛋白激酶1δ (CK1δ)、tau -微管蛋白激酶1 (TTBK1)和双亮氨酸拉链激酶(DLK),这些靶点得到了机制见解和令人信服的临床前证据的支持。脑渗透、异构体选择性和机制驱动的激酶抑制剂设计的持续进展可能使阿尔茨海默病的下一代疾病修饰疗法的发展成为可能。此图像的替代文本可能是使用AI生成的。
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来源期刊
Medicinal Chemistry Research
Medicinal Chemistry Research 医学-医药化学
CiteScore
4.70
自引率
3.80%
发文量
162
审稿时长
5.0 months
期刊介绍: Medicinal Chemistry Research (MCRE) publishes papers on a wide range of topics, favoring research with significant, new, and up-to-date information. Although the journal has a demanding peer review process, MCRE still boasts rapid publication, due in part, to the length of the submissions. The journal publishes significant research on various topics, many of which emphasize the structure-activity relationships of molecular biology.
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