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Multi-target-directed therapeutic strategies for Alzheimer's disease: controlling amyloid-β aggregation, metal ion homeostasis, and enzyme inhibition

Jeasang Yoo, Jimin Lee, Byeongha Ahn, Jiyeon Han, Mi Hee Lim

2025Chemical Science48 citationsDOIOpen Access PDF

Abstract

illustrates their interrelationships, with a particular emphasis on the interplay among Aβ, metal ions, and AD-related enzymes, such as β-site amyloid precursor protein cleaving enzyme 1 (BACE1), matrix metalloproteinase 9 (MMP9), lysyl oxidase-like 2 (LOXL2), acetylcholinesterase (AChE), and monoamine oxidase B (MAOB). We further underscore the potential of therapeutic strategies that simultaneously inhibit Aβ aggregation and address other pathogenic mechanisms. These approaches offer a more comprehensive and effective method for combating AD, overcoming the limitations of conventional therapies.

Topics & Concepts

HomeostasisAmyloid (mycology)EnzymeAlzheimer's diseaseAmyloid βChemistryDiseaseNeuroscienceBiochemistryMedicineBiologyCell biologyInternal medicineInorganic chemistryAlzheimer's disease research and treatmentsCholinesterase and Neurodegenerative DiseasesMedicinal Plants and Neuroprotection
Multi-target-directed therapeutic strategies for Alzheimer's disease: controlling amyloid-β aggregation, metal ion homeostasis, and enzyme inhibition | Litcius