Alzheimer's Disease-Related Proteins Targeted by Secondary Metabolite Compounds from Streptomyces: A Scoping Review

被引:0
|
作者
Zainuddin, Muhammad-Safuan [1 ]
Bhuvanendran, Saatheeyavaane [2 ]
Radhakrishnan, Ammu K. [2 ]
Azman, Adzzie-Shazleen [1 ]
机构
[1] Monash Univ Malaysia, Sch Sci, Bandar Sunway, Malaysia
[2] Monash Univ Malaysia, Jeffery Cheah Sch Med & Hlth Sci, Bandar Sunway, Malaysia
关键词
Alzheimer's disease; amyloid-beta; secondary metabolites; Streptomyces sp; NEUROPROTECTIVE COMPOUND; EXPRESSION; AUTOPHAGY; PATHOGENESIS; GENOTYPE; IL-10;
D O I
10.3233/ADR-230065
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Background: 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 Streptomyces genus has attracted attention given its pharmaceutically beneficial secondary metabolites to treat neurodegenerative diseases. Objective: To present secondary metabolites from Streptomyces sp. with regulatory effects on proteins and identified prospective target proteins for AD treatment. Methods: 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: A total of 20 target proteins were identified from the 12 shortlisted articles. Amyloid-beta, 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 Streptomyces sp., including rapamycin, alborixin, enterocin, bonnevillamides D and E, caniferolide A, anhydroexfoliamycin, rhizolutin, streptocyclinone A and B, were identified to exhibit considerable regulatory effects on these target proteins. Conclusions: The review highlights several prospective target proteins that can be regulated through treatments with Streptomyces sp. compounds to prevent AD's early stages and progression. Further identification of Streptomyces sp. compounds with potential anti-AD properties is recommended.
引用
收藏
页码:1335 / 1350
页数:16
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