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The shared KEGG pathways between icariin-targeted genes and osteoporosis

机译:甘草酸靶向基因与骨质疏松症之间共享的KEGG途径

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摘要

Osteoporosis is a common metabolic bone disease that affects about 40% of postmenopausal women. Treatment options for osteoporosis are limited, however. Icariin is an herbal substance that has been shown to improve bone mass, but the mechanisms are largely unknown. Using bioinformatics analysis, we have identified the hub genes and KEGG pathways shared between icariin-targeted genes and osteoporosis. The top five shared KEGG pathways were the Toll-like receptor signaling pathway, adipocytokine pathway, neurotrophin signaling pathway, NOD-like receptor signaling, and B cell receptor signaling pathway; the hub genes were RELA, NFKBIA, and IKBKB, belonging to the NF-κB family. The identified icariin-targeted genes are involved in inflammation, insulin resistance, apoptosis, and immune responses, and regulate the PI3K-Akt, NF-κB, MAPK, and JNK signaling pathways. Our data show that icariin inhibits apoptosis in human mesenchymal stem cells by suppressing JNK/c-Jun signaling pathway. Together, these findings indicate that icariin exerts its anti-osteoporotic function by inhibiting JNK/c-Jun signaling pathway, and suggest that icariin may be a promising treatment option for osteoporosis.
机译:骨质疏松症是一种常见的代谢性骨病,影响约40%的绝经后妇女。但是,骨质疏松症的治疗选择有限。伊卡瑞林是一种草药物质,已被证明可以改善骨骼质量,但其机理尚不清楚。使用生物信息学分析,我们已经确定了以菊黄素为靶标的基因与骨质疏松症之间共有的枢纽基因和KEGG通路。 KEGG共有5条最常见的信号通路是Toll样受体信号转导通路,脂肪细胞因子通路,神经营养蛋白信号通路,NOD样受体信号通路和B细胞受体信号通路。轮毂基因是RELA,NFKBIA和IKBKB,属于NF-κB家族。鉴定出的以大麻素为靶点的基因与炎症,胰岛素抵抗,细胞凋亡和免疫反应有关,并调节PI3K-Akt,NF-κB,MAPK和JNK信号通路。我们的数据表明,柠檬黄素通过抑制JNK / c-Jun信号通路抑制人间充质干细胞的凋亡。在一起,这些发现表明,蓖麻黄素通过抑制JNK / c-Jun信号传导途径发挥其抗骨质疏松功能,并表明其可能是骨质疏松症的有前途的治疗选择。

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