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微小RNA-506通过靶向ROCK1抑制神经母细胞瘤转移。

miR-506 suppresses neuroblastoma metastasis by targeting ROCK1.

作者信息

Li Dianguo, Cao Yanhua, Li Jinliang, Xu Jialong, Liu Qian, Sun Xiaogang

机构信息

Department of Pediatric Surgery, Second Hospital of Shandong University, Jinan, Shandong 250033, P.R. China.

Department of Pediatrics, General Hospital of Jinan Command, Jinan, Shandong 250031, P.R. China.

出版信息

Oncol Lett. 2017 Jan;13(1):417-422. doi: 10.3892/ol.2016.5442. Epub 2016 Nov 29.

Abstract

Neuroblastoma is a complex form of cancer with highly heterogeneous clinical behavior that arises during childhood from precursor cells of the sympathetic nervous system. In patients with neuroblastoma, mortality often occurs as a result of metastasis. The disease predominantly spreads to bone marrow, with a survival rate of ~40%. The current study demonstrates that microRNA (miR)-506 directly targets and downregulates Rho-associated, coiled-coil containing protein kinase 1 (ROCK1) in transforming growth factor (TGF)-β non-canonical pathways. It may be concluded that ROCK1 contributes to the invasion and migration of neuroblastoma cells by directly downregulating miR-506; thus, leading to the upregulation of ROCK1, which promotes cell invasion and migration. The present results provide a novel understanding of how miR-506 directly regulates TGF-β non-canonical signaling.

摘要

神经母细胞瘤是一种复杂的癌症形式,具有高度异质性的临床行为,它在儿童期起源于交感神经系统的前体细胞。在神经母细胞瘤患者中,死亡通常是转移的结果。这种疾病主要扩散到骨髓,生存率约为40%。当前研究表明,微小RNA(miR)-506在转化生长因子(TGF)-β非经典途径中直接靶向并下调含 Rho 相关卷曲螺旋蛋白激酶 1(ROCK1)。可以得出结论,ROCK1 通过直接下调 miR-506 促进神经母细胞瘤细胞的侵袭和迁移;因此,导致 ROCK1 的上调,进而促进细胞侵袭和迁移。目前的结果为 miR-506 如何直接调节 TGF-β 非经典信号传导提供了新的认识。

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