Circ_KATNAL1通过miR-145-3p/WISP1通路调控前列腺癌细胞的生长和侵袭。

Yu Zheng, Chao-jiang Chen, Zhuoyuan Lin, Jianxin Li, Jie Liu, Fu-Jun Lin, Xing Zhou
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引用次数: 20

摘要

前列腺癌(PCa)是男性死亡的第二大原因,目前的研究表明环状rna (circRNAs)在其发生和发展中起着重要作用。检测PCa细胞中的circrna发现circ_KATNAL1下调,主要位于细胞质中,含有多个抗癌miRNA miR-145-3p的结合位点。抗ago2抗体RIP检测,生物素标记circ_KATNAL1探针或miR-145-3p模拟物RNA拉下实验,双荧光素酶报告基因实验证实circ_KATNAL1在细胞中直接结合miR-145-3p,而在许多肿瘤中高表达的WISP1是miR-145-3p的重要靶基因。Circ_KATNAL1和miR-145-3p相互促进表达,下调目的基因WISP1的表达。circ_KATNAL1和miR-145-3p均抑制细胞增殖、侵袭、迁移以及MMP-2和MMP-9的表达,促进细胞凋亡和Caspase-3、Caspase-8、Caspase-9和PARP的激活,而WISP1的作用相反,circ_KATNAL1的上述功能是通过miR-145-3p/WISP1通路实现的。因此,circ_KATNAL1通过miR-145-3p/WISP1通路在PCa细胞中发挥抗癌作用,可能是诊断和治疗PCa的重要靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Circ_KATNAL1 regulates prostate cancer cell growth and invasion through miR-145-3p/WISP1 pathway.
Prostate cancer (PCa) is the second leading cause of death in men, and current studies have shown that circular RNAs (circRNAs) play important roles in its occurrence and development. Detection of circRNAs in PCa cells found that circ_KATNAL1 was down-regulated, mainly located in the cytoplasm and contained multiple binding sites of miR-145-3p, an anti-cancer miRNA. RIP detection with anti-AGO2 antibody, RNA pull down assay with biotin-labeled circ_KATNAL1 probe or miR-145-3p mimics, and dual luciferase reporter gene assay confirmed that circ_KATNAL1 directly bound to miR-145-3p in cells, and WISP1, which was highly expressed in many tumors, was an important target gene of miR-145-3p. Circ_KATNAL1 and miR-145-3p promoted each other's expression, and down-regulated the expression of target gene WISP1. Both circ_KATNAL1 and miR-145-3p inhibited cell proliferation, invasion, migration and the expression of MMP-2 and MMP-9, promoted cell apoptosis and the activation of Caspase-3, Caspase-8, Caspase-9 and PARP, while WISP1 had the opposite effects, and the above functions of circ_KATNAL1 were performed through the miR-145-3p/WISP1 pathway. Therefore, circ_KATNAL1 plays an anti-cancer role in PCa cells through the miR-145-3p/WISP1 pathway, which may be an important target for the diagnosis and treatment of PCa.
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