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通过分析双膦酸盐治疗后破骨细胞的表达谱变化来寻找受干扰的生物途径和基因。

Searching for perturbed biological pathways and genes through analyzing the expression profile changes in osteoclasts after treatment by bisphosphonates.

作者信息

Zhao Long, Zhang Bin, Wu Feng, Chen Xuan-Huang

机构信息

Department of Orthopedics, The First Hospital of Lanzhou University, Lanzhou, Gansu 730000, P.R. China.

Department of Orthopedics, Chinese Medicine Hospital of Xi'an City, Xi'an, Shanxi 710021, P.R. China.

出版信息

Exp Ther Med. 2019 Apr;17(4):2541-2546. doi: 10.3892/etm.2019.7219. Epub 2019 Jan 30.

Abstract

Criticality pathways and genes related to osteoporosis were identified. We downloaded the expression data of osteoclasts treated with or without bisphosphonates and all human pathways from the public database. Gibbs sampling and Markov chain were performed to identify the disturbed pathways and the hub genes in the disturbed pathways. Pathways and genes with adjusted probability ( ) ≥0.75 were considered as the disturbed pathways and hub genes. We identified four disturbed pathways (Maturity onset diabetes of the young, Olfactory transduction, Cyanoamino acid metabolism, Taurine and hypotaurine metabolism) and two hub genes ( and ) with ≥0.75. The expression levels of these disturbed pathways and hub genes were downregulated in bisphosphonates group. In conclusion, four disturbed pathways and two hub genes related to osteoporosis were identified. These results give us a better understanding of the potential mechanism of bisphosphonate treatment and the pathogenesis of osteoporosis.

摘要

确定了与骨质疏松症相关的关键通路和基因。我们从公共数据库下载了用或不用双膦酸盐处理的破骨细胞的表达数据以及所有人类通路。进行吉布斯采样和马尔可夫链分析以识别受干扰的通路以及受干扰通路中的枢纽基因。调整概率()≥0.75的通路和基因被视为受干扰的通路和枢纽基因。我们确定了四个受干扰的通路(青少年成年型糖尿病、嗅觉转导、氰基氨基酸代谢、牛磺酸和次牛磺酸代谢)和两个调整概率≥0.75的枢纽基因(和)。这些受干扰的通路和枢纽基因的表达水平在双膦酸盐组中下调。总之,确定了与骨质疏松症相关的四个受干扰的通路和两个枢纽基因。这些结果使我们对双膦酸盐治疗的潜在机制和骨质疏松症的发病机制有了更好的理解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a7e/6425151/1779fcb1f916/etm-17-04-2541-g02.jpg

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