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miR-671-5p 通过阻断骨肉瘤细胞周期抑制肿瘤增殖。

miR-671-5p Inhibits Tumor Proliferation by Blocking Cell Cycle in Osteosarcoma.

机构信息

Department of Orthopedic Surgery, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan, China.

出版信息

DNA Cell Biol. 2019 Sep;38(9):996-1004. doi: 10.1089/dna.2019.4870. Epub 2019 Aug 8.

Abstract

Osteosarcoma (OS), a highly aggressive bone tumor, mainly occurs in young patients and always presents abnormalities in molecular biology, such as microRNAs (miRNAs). However, the characteristic and underlying mechanism of miR-671-5p in OS are still unclear. In this study, we certify that miR-671-5p is remarkably downregulated in OS tissues and cells. Overexpressed miR-671-5p can suppress OS cell proliferation and , by the way of arresting cell-cycle progression. The overexpression of cyclin D1 (CCND1) and CDC34 promotes cell proliferation and cell-cycle promotion, whose functions are contrary to miR-671-5p. miR-671-5p directly binds to CCND1 and CDC34, which are thought as the key factors in regulating cell cycle. Taken together, our results suggest that by targeting CCND1 and CDC34, miR-671-5p plays a tumor suppressor in OS to inhibit the development of OS, implicating it as a novel target for therapeutic intervention in OS.

摘要

骨肉瘤(OS)是一种高度侵袭性的骨肿瘤,主要发生在年轻患者中,其分子生物学经常表现出异常,如 microRNAs(miRNAs)。然而,miR-671-5p 在 OS 中的特征和潜在机制仍不清楚。在这项研究中,我们证实 miR-671-5p 在 OS 组织和细胞中显著下调。过表达 miR-671-5p 可以抑制 OS 细胞的增殖和,通过细胞周期进程的阻滞。细胞周期蛋白 D1(CCND1)和 CDC34 的过表达促进细胞增殖和细胞周期促进,其功能与 miR-671-5p 相反。miR-671-5p 可以直接结合 CCND1 和 CDC34,它们被认为是调节细胞周期的关键因素。总之,我们的研究结果表明,miR-671-5p 通过靶向 CCND1 和 CDC34 在 OS 中发挥肿瘤抑制作用,抑制 OS 的发展,提示它可能成为 OS 治疗干预的新靶点。

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