Academic Journal

Downregulation of PIK3CB Involved in Alzheimer’s Disease via Apoptosis, Axon Guidance, and FoxO Signaling Pathway

التفاصيل البيبلوغرافية
العنوان: Downregulation of PIK3CB Involved in Alzheimer’s Disease via Apoptosis, Axon Guidance, and FoxO Signaling Pathway
المؤلفون: Zhike Zhou, Jun Bai, Shanshan Zhong, Rongwei Zhang, Kexin Kang, Xiaoqian Zhang, Ying Xu, Chuansheng Zhao, Mei Zhao
المصدر: Oxidative Medicine and Cellular Longevity, Vol 2022 (2022)
بيانات النشر: Hindawi Limited
سنة النشر: 2022
المجموعة: Directory of Open Access Journals: DOAJ Articles
مصطلحات موضوعية: Cytology, QH573-671
الوصف: Objective. To investigate the molecular function of phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta (PIK3CB) underlying Alzheimer’s disease (AD). Methods. RNA sequencing data were used to filtrate differentially expressed genes (DEGs) in AD/nondementia control and PIK3CB-low/high groups. An unbiased coexpression network was established to evaluate module-trait relationships by using weight gene correlation network analysis (WGCNA). Global regulatory network was constructed to predict the protein-protein interaction. Further cross-talking pathways of PIK3CB were identified by functional enrichment analysis. Results. The mean expression of PIK3CB in AD patients was significantly lower than those in nondementia controls. We identified 2,385 DEGs from 16,790 background genes in AD/control and PIK3CB-low/high groups. Five coexpression modules were established using WGCNA, which participated in apoptosis, axon guidance, long-term potentiation (LTP), regulation of actin cytoskeleton, synaptic vesicle cycle, FoxO, mitogen-activated protein kinase (MAPK), and vascular endothelial growth factor (VEGF) signaling pathways. DEGs with strong relation to AD and low PIK3CB expression were extracted to construct a global regulatory network, in which cross-talking pathways of PIK3CB were identified, such as apoptosis, axon guidance, and FoxO signaling pathway. The occurrence of AD could be accurately predicted by low PIK3CB based on the area under the curve of 71.7%. Conclusions. These findings highlight downregulated PIK3CB as a potential causative factor of AD, possibly mediated via apoptosis, axon guidance, and FoxO signaling pathway.
نوع الوثيقة: article in journal/newspaper
اللغة: English
تدمد: 1942-0994
Relation: http://dx.doi.org/10.1155/2022/1260161; https://doaj.org/toc/1942-0994; https://doaj.org/article/28cb81011bec4bd3b720c3e106114b5f
DOI: 10.1155/2022/1260161
الاتاحة: https://doi.org/10.1155/2022/1260161
https://doaj.org/article/28cb81011bec4bd3b720c3e106114b5f
رقم الانضمام: edsbas.BCA8B7D7
قاعدة البيانات: BASE
الوصف
تدمد:19420994
DOI:10.1155/2022/1260161