Pathway of PPAR-gamma coactivators in thermogenesis: a pivotal traditional Chinese medicine-associated target for individualized treatment of rheumatoid arthritis

被引:39
作者
Zhang, Yanqiong [1 ]
Mao, Xia [1 ]
Guo, Qiuyan [1 ]
Bai, Ming [2 ,3 ]
Zhang, Bo [2 ,3 ,4 ]
Liu, Chunfang [1 ]
Sun, Yanqun [1 ]
Li, Shao [2 ,3 ]
Lin, Na [1 ]
机构
[1] China Acad Chinese Med Sci, Inst Chinese Mat Med, Beijing 100700, Peoples R China
[2] Tsinghua Univ, Dept Automat, TNLIST, MOE Key Lab Bioinformat, Beijing 100084, Peoples R China
[3] Tsinghua Univ, Dept Automat, TNLIST, Bioinformat Div, Beijing 100084, Peoples R China
[4] Tianjin Int Joint Acad Biotechnol & Med, Tianjin 300457, Peoples R China
基金
中国国家自然科学基金;
关键词
rheumatoid arthritis; traditional Chinese medicine syndrome; network pharmacology; PPAR-gamma; individualized treatment; WU-TOU DECOCTION; IMBALANCED NETWORK; SYSTEMS;
D O I
10.18632/oncotarget.7419
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Traditional Chinese medicine (TCM) syndromes have been regarded as the crucial clinical manifestations for individualized diagnosis and treatment of complex diseases, including rheumatoid arthritis (RA) and cancer. Especially, RA patients are classified into cold and hot syndromes with different clinical manifestations, interventions and molecular mechanisms. Better effectiveness of a classic cold syndrome-specific herbal formula Wu-tou decoction (WTD) has been achieved. To explore molecular mechanisms of syndrome-specific formulae is of great clinical significance to improve the effectiveness and pertinence of treatment for the complex diseases with personalized conditions. However, the scientific basis of WTD treatment on RA with the cold syndrome remains unclear. Here, we predicted the putative targets for composite compounds contained in WTD using drugCIPHER-CS and constructed a WTD herbs-putative targets-RA related genes network. Next, a list of major WTD targets was identified based on their topological features, including the degree, node betweenness, closeness and k-coreness in the above pharmacological network. Importantly, pathway enrichment analysis revealed that these major WTD targets were significantly associated with the pathway of peroxisome proliferator-activated receptor (PPAR)-gamma (PPAR-gamma) coactivators in thermogenesis. These computational findings were subsequently verified by experiments on a rat model of collagen-induced arthritis (CIA) with cold or hot syndromes, and on human fibroblastlike synoviocytes-rheumatoid arthritis (HFLS-RA) cell line. In conclusion, the pathway of PPAR-. coactivators in thermogenesis might be one of the potential pharmacological targets of WTD to alleviate RA with the TCM cold syndrome. These findings may open new avenues for designing individualized treatment regimens for RA patients.
引用
收藏
页码:15885 / 15900
页数:16
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