Alzheimer's Disease-Related Proteins Targeted by Secondary Metabolite Compounds from

Alzheimer’s disease Streptomyces sp amyloid-β secondary metabolites

Journal

Journal of Alzheimer's disease reports
ISSN: 2542-4823
Titre abrégé: J Alzheimers Dis Rep
Pays: Netherlands
ID NLM: 101705500

Informations de publication

Date de publication:
2023
Historique:
received: 12 07 2023
accepted: 16 10 2023
medline: 25 12 2023
pubmed: 25 12 2023
entrez: 25 12 2023
Statut: epublish

Résumé

Alzheimer's disease (AD) is a neurodegenerative disease that is characterized as rapid and progressive cognitive decline affecting 26 million people worldwide. Although immunotherapies are ideal, its clinical safety and effectiveness are controversial, hence, treatments are still reliant on symptomatic medications. Concurrently, the To present secondary metabolites from Research articles published between 2010 and 2021 were collected from five databases and 83 relevant research articles were identified. Post-screening, only 12 research articles on AD-related proteins were selected for further review. Bioinformatics analyses were performed through the Search Tool for the Retrieval of Interacting Genes/Proteins (STRING) network, PANTHER Go-Slim classification system (PANTHER17.0), and Kyoto Encyclopedia of Genes and Genomes (KEGG) Mapper. A total of 20 target proteins were identified from the 12 shortlisted articles. Amyloid-β, BACE1, Nrf-2, Beclin-1, and ATG5 were identified as the potential target proteins, given their role in initiating AD, mitigating neuroinflammation, and autophagy. Besides, 10 compounds from The review highlights several prospective target proteins that can be regulated through treatments with

Sections du résumé

Background UNASSIGNED
Alzheimer's disease (AD) is a neurodegenerative disease that is characterized as rapid and progressive cognitive decline affecting 26 million people worldwide. Although immunotherapies are ideal, its clinical safety and effectiveness are controversial, hence, treatments are still reliant on symptomatic medications. Concurrently, the
Objective UNASSIGNED
To present secondary metabolites from
Methods UNASSIGNED
Research articles published between 2010 and 2021 were collected from five databases and 83 relevant research articles were identified. Post-screening, only 12 research articles on AD-related proteins were selected for further review. Bioinformatics analyses were performed through the Search Tool for the Retrieval of Interacting Genes/Proteins (STRING) network, PANTHER Go-Slim classification system (PANTHER17.0), and Kyoto Encyclopedia of Genes and Genomes (KEGG) Mapper.
Results UNASSIGNED
A total of 20 target proteins were identified from the 12 shortlisted articles. Amyloid-β, BACE1, Nrf-2, Beclin-1, and ATG5 were identified as the potential target proteins, given their role in initiating AD, mitigating neuroinflammation, and autophagy. Besides, 10 compounds from
Conclusions UNASSIGNED
The review highlights several prospective target proteins that can be regulated through treatments with

Identifiants

pubmed: 38143777
doi: 10.3233/ADR-230065
pii: ADR230065
pmc: PMC10741902
doi:

Types de publication

Journal Article Review

Langues

eng

Pagination

1335-1350

Informations de copyright

© 2023 – The authors. Published by IOS Press.

Déclaration de conflit d'intérêts

The authors have no conflict of interest to report.

Auteurs

Muhammad-Safuan Zainuddin (MS)

School of Science, Monash University Malaysia, Bandar Sunway, Malaysia.

Saatheeyavaane Bhuvanendran (S)

Jeffery Cheah School of Medicine and Health Science, Monash University Malaysia, Bandar Sunway, Malaysia.

Ammu K Radhakrishnan (AK)

Jeffery Cheah School of Medicine and Health Science, Monash University Malaysia, Bandar Sunway, Malaysia.

Adzzie-Shazleen Azman (AS)

School of Science, Monash University Malaysia, Bandar Sunway, Malaysia.

Classifications MeSH