The identification of dysfunctional crosstalk of pathways in Parkinson disease

被引:9
作者
Diao, Hongyu [1 ]
Li, Xinxing [1 ]
Hu, Sheng [2 ]
机构
[1] China Med Univ, Shengjing Hosp, Dept Neurosurg, Shenyang 110004, Peoples R China
[2] Second Peoples Hosp Chaoyang City, Dept Neurosurg, Chaoyang 122000, Peoples R China
关键词
Parkinson disease; Differentially expressed genes; Pathway crosstalk; LONG-TERM POTENTIATION; ALPHA-SYNUCLEIN; NERVOUS-SYSTEM; PROBE LEVEL; GENE; MUTATIONS; PROTEIN; MEMORY; SUSCEPTIBILITY; TRAFFICKING;
D O I
10.1016/j.gene.2012.11.003
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Parkinson disease (PD) is the second most common neurodegenerative disorder after Alzheimer's disease, affecting 1-2% of the population over the age of 65. Both genetic and environmental factors trigger risks of and protection from PD. However, the molecular mechanism of PD is far from being clear. In this study, we downloaded the gene expression profile of PD from Gene Expression Omnibus and identified differentially expressed genes (DEGs) and dysfunctional pathways in PD patients compared with controls. To further understand how these pathways act together to account for the initiation of PD, we constructed a pathway crosstalk network by calculating the Jaccard index among pathways. A total of 873 DEGs and 16 dysfunctional pathways between PD patients and controls were identified. Through constructing a network of pathways, the relationships among PD pathways were visually presented by their interactions. Our results demonstrate the existence of crosstalk between different pathways in PD pathogenesis. These results not only may explain the causes of PD, but could also open the door to new therapeutic approaches for this disease. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:159 / 162
页数:4
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