Research advances of microRNA involved in bone cancer pain

Shi-you Wei
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Abstract

At present, since the mechanism of occurrence and development of bone cancer pain (BCP) is sophisticated, it is still perplexing in the clinical practice. MicroRNA (miRNA), which plays a regulatory role at the post-transcriptional level, may be in-volved in the BCP process. Therefore, the search for unique miRNA and biomarkers involved in the occurrence and development of BCP will be helpful for the treatment, clinical detection and diagnosis. In this paper, we reviewed recent researches and described how miRNA regulate osteoclast activation, promoted bone resorption and led to the formation of BCP. We also described how miRNA regu-late different signaling pathways [chemokine C-X-C motif ligand 12 (CXCL12)/chemokine C-X-C motif receptor 4 (CXCR4) signaling pathway, protein kinase A/cAMP-response element binding protein (CREB) signaling pathway, et al] that involved in the formation and development of BCP and how miRNA plays a role in BCP regulation by regulating neuronal plasticity and changing the expression of neuronal ion channels. Subsequently, This review summarizes the occurrence and development mechanism of BCP and provides help for clinical transformation. Key words: MicroRNA; Bone cancer pain; Osteoclast
微小RNA参与骨癌症疼痛的研究进展
目前,由于骨癌症疼痛(BCP)的发生和发展机制复杂,在临床实践中仍然令人困惑。微小RNA(miRNA)在转录后水平发挥调节作用,可能参与BCP过程。因此,寻找参与BCP发生和发展的独特miRNA和生物标志物将有助于BCP的治疗、临床检测和诊断。在这篇论文中,我们回顾了最近的研究,并描述了miRNA如何调节破骨细胞的活化,促进骨吸收并导致BCP的形成。我们还描述了miRNA如何调节参与BCP形成和发展的不同信号通路[趋化因子C-X-C基序配体12(CXCL12)/趋化因子C-X-C基阵受体4(CXCR4)信号通路、蛋白激酶A/cAMP反应元件结合蛋白(CREB)信号通路等],以及miRNA如何通过调节神经元可塑性和改变神经元离子通道的表达。随后,本文综述了BCP的发生发展机制,为临床转化提供了帮助。关键词:微小核糖核酸;骨癌症疼痛;破骨细胞
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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