骨质疏松症中的 Wnt 通路抑制剂:作用机制和作为治疗靶点的潜力。

0 MEDICINE, RESEARCH & EXPERIMENTAL
Jiayi Song, Weirong Chang, Yujie Wang, Peng Gao, Jie Zhang, Zhipan Xiao, Fangyu An, Chunlu Yan
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引用次数: 0

摘要

Wnt 信号通路是维持细胞功能(如细胞增殖和分化)最重要和最关键的信号通路之一。越来越多的证据证实,Wnt 信号通路在骨质疏松症的骨形成调节中也发挥着重要作用。因此,该通路的抑制剂,如硬骨素、Dickkopf-1 (DKK1)、WNT 抑制因子 1 (WIF1) 和分泌型 frizzled 相关蛋白 (SFRPs),在骨形成中具有负向调节作用,可作为骨质疏松症的有效治疗靶点。本综述探讨了 Wnt 信号通路抑制剂在骨质疏松症中的作用机制、Wnt 通路与其抑制剂之间的关系以及治疗骨质疏松症的新分子靶点。总之,总结了 Wnt 通路抑制剂的调控机制,为治疗和预防骨质疏松症提供科学理论指导。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Inhibitors of the Wnt pathway in osteoporosis: A review of mechanisms of action and potential as therapeutic targets

The Wnt signaling pathway is one of the most important and critical signaling pathways for maintaining cellular functions, such as cell proliferation and differentiation. Increasing evidence substantiates that the Wnt signaling pathway also plays a significant role in the regulation of bone formation in osteoporosis. Accordingly, inhibitors of this pathway, such as sclerostin, Dickkopf-1 (DKK1), WNT inhibitory factor 1 (WIF1), and secreted frizzled-related proteins (SFRPs), have a negative regulatory role in bone formation and may serve as effective therapeutic targets for osteoporosis. This review examines the mechanisms of action of Wnt signaling pathway inhibitors in osteoporosis, the relationship between the Wnt pathway and its inhibitors, and new molecular targets for osteoporosis treatment. Overall, the regulatory mechanisms of Wnt pathway inhibitors are summarized to provide scientific and theoretical guidance for the treatment and prevention of osteoporosis.

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