The Role of Non-coding RNAs in Alzheimer’s Disease: Pathogenesis, novel biomarkers, and potential therapeutic targets

Author:

Saleh Othman1ORCID,Albakri Khaled12,Altiti Abdalrahmn1ORCID,Abutair Iser1ORCID,Shalan Suhaib1ORCID,Mohd Omar Bassam1ORCID,Negida Ahmed2345,Mushtaq Gohar6,Kamal Mohammad A.78910

Affiliation:

1. Faculty of Medicine, The Hashemite University, Zarqa, Jordan

2. Medical Research Group of Egypt, Cairo, Egypt

3. Department of Global Health and Social Medicine, Harvard Medical School, 641 Huntington Ave, Boston, MA, 02115, USA

4. School of Pharmacy and Biomedical Sciences, University of Portsmouth, Portsmouth, UK

5. Faculty of Medicine, Zagazig University, Zagazig, Egypt

6. Center for Scientific Research, Faculty of Medicine, Idlib University, Idlib, Syria

7. Institutes for Systems Genetics, Frontiers Science Center for Disease-related Molecular Network, West China Hospital, Sichuan University, China

8. King Fahd Medical Research Center, King Abdulaziz University, Saudi Arabia

9. Department of Pharmacy, Daffodil International University, Bangladesh

10. Enzymoics, NSW 2770; Novel Global Community Educational Foundation, Australia

Abstract

Objective: Long non-coding RNAs (IncRNAs) are regulatory RNA transcripts that have recently been associated with the onset of many neurodegenerative illnesses, including Alzheimer's disease (AD). Several IncRNAs have been found to be associated with AD pathophysiology, each with a distinct mechanism. In this review, we focused on the role of IncRNAs in the pathogenesis of AD and their potential as novel biomarkers and therapeutic targets. Methods: Searching for relevant articles was done using the PubMed and Cochrane library databases. Studies had to be published in full text in English in order to be considered. Results: Some IncRNAs were found to be upregulated, while others were downregulated. Dysregulation of IncRNAs expression may contribute to AD pathogenesis. Their effects manifest as the synthesis of beta-amyloid (Aβ) plaques increases, thereby altering neuronal plasticity, inducing inflammation, and promoting apoptosis. Conclusion: Despite the need for more investigations, IncRNAs could potentially increase the sensitivity of early detection of AD. Until now, there has been no effective treatment for AD. Hence, InRNAs are promising molecules and may serve as potential therapeutic targets. Although several dysregulated AD-associated lncRNAs have been discovered, the functional characterization of most lncRNAs is still lacking.

Publisher

Bentham Science Publishers Ltd.

Subject

Pharmacology,General Neuroscience

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