Fu Zewei, Feng Baofeng, Akogo Herman Yao, Ma Jiajia, Liu Yukun, Quan Hezhi, Zhang Xiaohan, Hou Yu, Zhang Xuecong, Ma Jun, Cui Huixian
Hebei Medical University-Galway University Stem Cell Research Center, Hebei Medical University, Shijiazhuang, 050017, Hebei Province, China.
Hebei Research Center for Stem Cell Medical Translational Engineering, Shijiazhuang, 050017, Hebei Province, China.
Mol Neurobiol. 2025 May;62(5):6383-6396. doi: 10.1007/s12035-024-04681-9. Epub 2025 Jan 10.
This study utilises amyotrophic lateral sclerosis (ALS) and Parkinson's disease (PD) human brain samples from the GEO database and employs differential expression gene (DEG) analysis to identify genes that are pivotal in both neurodegenerative diseases. Through in depth GO and KEGG enrichment analyses, we elucidated the biological functions and potential pathways associated with these DEGs. Furthermore, by constructing protein‒protein interaction networks, we highlight the significance of shared DEGs in both cellular physiology and disease contexts. Analysis of drug‒gene associations revealed potential therapeutic compounds linked to ALS and PD treatment. Additionally, we explored the interactions between transcription factors, miRNAs, and common DEGs, revealing aspects of gene regulatory networks. This study provides insights into the molecular mechanisms of ALS and PD, offering valuable contributions to ongoing research and potential therapeutic avenues.
本研究利用来自基因表达综合数据库(GEO数据库)的肌萎缩侧索硬化症(ALS)和帕金森病(PD)人脑样本,并采用差异表达基因(DEG)分析来鉴定在这两种神经退行性疾病中起关键作用的基因。通过深入的基因本体(GO)和京都基因与基因组百科全书(KEGG)富集分析,我们阐明了与这些差异表达基因相关的生物学功能和潜在途径。此外,通过构建蛋白质-蛋白质相互作用网络,我们强调了共有差异表达基因在细胞生理学和疾病背景中的重要性。药物-基因关联分析揭示了与ALS和PD治疗相关的潜在治疗化合物。此外,我们探索了转录因子、微小RNA(miRNA)与共有差异表达基因之间的相互作用,揭示了基因调控网络的相关方面。本研究深入了解了ALS和PD的分子机制,为正在进行的研究和潜在的治疗途径提供了有价值的贡献。