Institute of Basic Research in Clinical Medicine, China Academy of Chinese Medical Sciences, Dongzhimen, Beijing 100700, PR China.
Complement Ther Med. 2012 Feb-Apr;20(1-2):23-30. doi: 10.1016/j.ctim.2011.10.005. Epub 2011 Nov 3.
Rheumatoid arthritis (RA) is a heterogeneous disease, and traditional Chinese medicine (TCM) can be used to classify RA into different patterns such as cold and hot based on its clinical manifestations. The aim of this study was to investigate potential network-based biomarkers for RA with either a cold or a hot pattern.
Microarray technology was used to reveal gene expression profiles in CD4(+) T cells from 21 RA patients with cold pattern and 12 with hot pattern. A T-test was used to identify significant differences in gene expression among RA patients with either cold or hot pattern. Cytoscape software was used to search the existing literature and databases for protein-protein interaction information for genes of interest that were identified from this analysis. The IPCA algorithm was used to detect highly connected regions for inferring significant complexes or pathways in this protein-protein interaction network. Significant pathways and functions were extracted from these subnetworks by the Biological Network Gene Ontology tool.
Four genes were expressed at higher levels in RA patients with cold pattern than in patients with hot pattern, and 21 genes had lower levels of expression. Protein-protein interaction network analysis for these genes showed that there were four highly connected regions. The most relevant functions and pathways extracted from these subnetwork regions were involved in small G protein signaling pathways, oxidation-reduction in fatty acid metabolism and T cell proliferation.
Complicated network based pathways appear to play a role in the different pattern manifestations in patients with RA, and our results suggest that network-based pathways might be the scientific basis for TCM pattern classification.
类风湿关节炎(RA)是一种异质性疾病,中医(TCM)可以根据其临床表现将 RA 分为寒、热等不同证型。本研究旨在探讨具有寒证或热证表现的 RA 的潜在网络生物标志物。
采用微阵列技术揭示 21 例寒证 RA 患者和 12 例热证 RA 患者 CD4+T 细胞的基因表达谱。采用 T 检验比较 RA 寒证和热证患者基因表达的差异。采用 Cytoscape 软件搜索现有文献和数据库中感兴趣基因的蛋白-蛋白相互作用信息。采用 IPCA 算法检测蛋白-蛋白相互作用网络中的高度连接区域,以推断显著的复杂或通路。通过生物网络基因本体论工具从这些子网络中提取显著的通路和功能。
与热证 RA 患者相比,寒证 RA 患者中有 4 个基因表达水平较高,21 个基因表达水平较低。这些基因的蛋白-蛋白相互作用网络分析显示有 4 个高度连接区域。从这些子网区域中提取的最相关的功能和通路涉及小 G 蛋白信号通路、脂肪酸代谢中的氧化还原反应和 T 细胞增殖。
复杂的网络途径似乎在 RA 患者不同证型表现中发挥作用,我们的结果表明,网络途径可能是 TCM 证型分类的科学基础。