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miR-140 通过靶向 Wnt1 抑制骨肉瘤细胞的增殖并增强药物敏感性。

MiR-140 targets Wnt1 to inhibit the proliferation and enhance drug sensitivity in osteosarcoma cells.

机构信息

Foot and Ankle Surgery Center, Beijing Tongren Hospital of Capital Medical University, Beijing 100005, China.

出版信息

Cell Mol Biol (Noisy-le-grand). 2022 May 22;68(1):140-146. doi: 10.14715/cmb/2022.68.1.18.

Abstract

MicroRNAs (miRNAs) have been documented to function differently in numerous human cancers. Our study planned to investigate the role of microRNA-140 (miR-140) and to identify its possible target in osteosarcoma (OS) to predict their mechanism in OS. The miR-140 was down-regulated in OS, and its high expression decreased MG63 cell proliferation. At the molecular level, Wnt1 was a target of miR-140, and its expression could be suppressed by miR-140. Besides, miR-140 overexpression decreased drug resistance in OS cells treated by doxorubicin. Collectively, overexpression of miR-140 may inhibit human OS cell proliferation and may enhance drug sensitivity by direct regulation of Wnt/β-catenin signaling.

摘要

微小 RNA(miRNAs)在许多人类癌症中发挥着不同的功能。我们的研究计划探讨 microRNA-140(miR-140)的作用,并确定其在骨肉瘤(OS)中的可能靶点,以预测其在 OS 中的机制。miR-140 在 OS 中下调,其高表达可降低 MG63 细胞的增殖。在分子水平上,Wnt1 是 miR-140 的靶标,其表达可被 miR-140 抑制。此外,miR-140 的过表达可降低阿霉素处理的 OS 细胞的耐药性。总之,miR-140 的过表达可能通过直接调节 Wnt/β-catenin 信号通路抑制人骨肉瘤细胞的增殖,并增强药物敏感性。

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