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DOI 10.1111/ejn.70156

Медицинская библиотека · The European journal of neuroscience · 2025

The Role of Kinases in Neurodegenerative Diseases: From Pathogenesis to Treatment.

Naim Alkusha, Farooqui Azhar Mahmood, Badruddeen, Khan Mohammad Irfan, Akhtar Juber, Ahmad Asad, Islam Anas

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Аннотация

Neurodegenerative diseases are characterized by progressive neuronal loss and dysfunction, with protein kinases playing crucial roles in their pathogenesis. This article explores the involvement of protein kinases in these disorders, focusing on their contributions to disease mechanisms, potential as therapeutic targets and challenges in developing effective treatments. In Alzheimer's disease, kinases such as CDK5, GSK3β and MARK4 are implicated in tau hyperphosphorylation and the formation of neurofibrillary tangles. Kinases also regulate amyloid-β processing and plaque formation. In Parkinson's disease, LRRK2, PINK1 and other kinases contribute to α-synuclein pathology, mitochondrial dysfunction and neuroinflammation. LRRK2 inhibitors and PROTACs have shown promise in preclinical models. Huntington's disease involves altered kinase activity, with CK2, GSK3 and MAPK pathways influencing mutant huntingtin toxicity and aggregation. Kinases are also implicated in less common neurodegenerative diseases, such as ALS and spinocerebellar ataxias. Despite the therapeutic potential of targeting kinases, challenges remain, including the complexity of kinase networks, blood-brain barrier permeability and the lack of robust biomarkers. Emerging technologies, such as covalent inhibitors, targeted protein degradation and combination therapies, offer new avenues for addressing these challenges and developing more effective treatments for neurodegenerative diseases.

Для цитирования: Naim Alkusha, Farooqui Azhar Mahmood, Badruddeen, Khan Mohammad Irfan, Akhtar Juber, Ahmad Asad, Islam Anas. The Role of Kinases in Neurodegenerative Diseases: From Pathogenesis to Treatment.. The European journal of neuroscience. 2025. DOI: 10.1111/ejn.70156.

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