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多靶点:阿尔茨海默病的一种非常规药物研发策略

Multi-Targets: An Unconventional Drug Development Strategy for Alzheimer's Disease.

作者信息

Gong Cheng-Xin, Dai Chun-Ling, Liu Fei, Iqbal Khalid

机构信息

Department of Neurochemistry, Inge Grundke-Iqbal Research Floor, New York State Institute for Basic Research in Developmental Disabilities, New York, NY, United States.

出版信息

Front Aging Neurosci. 2022 Feb 9;14:837649. doi: 10.3389/fnagi.2022.837649. eCollection 2022.

Abstract

Alzheimer's disease (AD) is a progressive neurodegenerative disorder that eventually leads to dementia and death of the patient. Despite the enormous amounts of resources and efforts for AD drug development during the last three decades, no effective treatments have been developed that can slow or halt the progression of the disease. Currently available drugs for treating AD can only improve clinical symptoms temporarily with moderate efficacies. In recent years, the scientific community has realized these challenges and reconsidered the future directions of AD drug development. The most significant recent changes in AD drug development strategy include shifting from amyloid-based targets to other targets, such as tau, and efforts toward better designs for clinical trials. However, most AD drug development is still focused on a single mechanism or target, which is the conventional strategy for drug development. Although multifactorial mechanisms and, on this basis, multi-target strategies have been proposed in recent years, this approach has not been widely recognized and accepted by the mainstream of AD drug development. Here, we emphasize the multifactorial mechanisms of AD and discuss the urgent need for a paradigm shift in AD drug development from a single target to multiple targets, either with the multi-target-directed ligands approach or the combination therapy approach. We hope this article will increase the recognition of the multifactorial nature of AD and promote this paradigm shift. We believe that such a shift will facilitate successful development of effective AD therapies.

摘要

阿尔茨海默病(AD)是一种进行性神经退行性疾病,最终会导致患者痴呆和死亡。尽管在过去三十年里,为开发治疗AD的药物投入了大量资源并付出了巨大努力,但尚未开发出能够减缓或阻止该疾病进展的有效治疗方法。目前用于治疗AD的药物只能暂时改善临床症状,疗效一般。近年来,科学界已经认识到这些挑战,并重新考虑了AD药物开发的未来方向。AD药物开发策略中最近最显著的变化包括从基于淀粉样蛋白的靶点转向其他靶点,如tau蛋白,以及努力改进临床试验设计。然而,大多数AD药物开发仍集中在单一机制或靶点上,这是传统的药物开发策略。尽管近年来已经提出了多因素机制,并在此基础上提出了多靶点策略,但这种方法尚未得到AD药物开发主流的广泛认可和接受。在此,我们强调AD的多因素机制,并讨论AD药物开发从单一靶点向多个靶点转变的迫切需求,无论是采用多靶点导向配体方法还是联合治疗方法。我们希望本文能提高对AD多因素性质的认识,并推动这种范式转变。我们相信,这种转变将有助于成功开发有效的AD治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9bd/8864545/536c7060494d/fnagi-14-837649-g001.jpg

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