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Screening target genes for the treatment of PCOS via analysis of single-cell sequencing data

BACKGROUND: Polycystic ovary syndrome (PCOS) is a condition of the female reproductive system and it remains imperative to identify target genes responsible for its pathogenesis and develop therapeutic drugs capable of effectively treating it. METHODS: We performed primary screening, staging, functi...

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Detalles Bibliográficos
Autores principales: Lu, Zhenzhen, Chen, Chunyan, Gao, Ying, Li, Yanhui, Zhao, Xiaojie, Zhang, Hanke, Wei, Qiongqiong, Zeng, Xinliu, Li, Yajie, Wan, Min
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9621251/
https://www.ncbi.nlm.nih.gov/pubmed/36286390
http://dx.doi.org/10.1080/07853890.2022.2136401
Descripción
Sumario:BACKGROUND: Polycystic ovary syndrome (PCOS) is a condition of the female reproductive system and it remains imperative to identify target genes responsible for its pathogenesis and develop therapeutic drugs capable of effectively treating it. METHODS: We performed primary screening, staging, functional analysis as well as screening of target genes and therapeutic drugs based on single cell sequencing data of 34 oocytes from the GEO database. RESULTS: Oxidative phosphorylation played a pivotal role in the development of oocytes, insulin resistance and ovulation disorders. At the cellular level, GV and MI phases were particularly critical for the biology of pregnancy. We screened PGR, SIRT1 and ADAMTS1 as hub differentially expressed genes (DEGs) and found relevant drugs using the Drug-Gene Interaction Database. In clinical study, oral contraceptives and insulin sensitisers were found to be effective in the treatment of PCOS. CONCLUSION: PGR, SIRT1 and ADAMTS1 KEY MESSAGES: Our study used a new bioinformatics approach to find target genes for the treatment of PCOS. Our study sought to identify target genes that affect human oocyte quality by analysing single-cell sequencing data from oocytes. We testified to our data by analysing a subset of clinical data.