| Literature DB >> 31221572 |
Angélique Sadlon1, Petros Takousis1, Panagiotis Alexopoulos2, Evangelos Evangelou3, Inga Prokopenko4, Robert Perneczky5.
Abstract
Despite the identification of several dozens of common genetic variants associated with Alzheimer's disease (AD) and Parkinson's disease (PD), most of the genetic risk remains uncharacterised. Therefore, it is important to understand the role of regulatory elements, such as miRNAs. Dysregulated miRNAs are implicated in AD and PD, with potential value in dissecting the shared pathophysiology between the two disorders. miRNAs relevant to both neurodegenerative diseases are related to axonal guidance, apoptosis, and inflammation, therefore, AD and PD likely arise from similar underlying biological pathway defects. Furthermore, pathways regulated by APP, L1CAM, and genes of the caspase family may represent promising therapeutic miRNA targets in AD and PD since they are targeted by dysregulated miRNAs in both disorders.Entities:
Keywords: biomarker; dementia; diagnosis; neurodegeneration; pathophysiology; therapy
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Year: 2019 PMID: 31221572 DOI: 10.1016/j.molmed.2019.05.006
Source DB: PubMed Journal: Trends Mol Med ISSN: 1471-4914 Impact factor: 11.951