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MicroRNA-218 inhibits the migration epithelial-mesenchymal transition and cancer stem cell properties of prostate cancer cells

机译:MicroRNA-218抑制前列腺癌细胞的迁移上皮-间质转化和癌症干细胞特性

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摘要

MicroRNA (miRNA) is a class of non-coding single-stranded RNA, able to regulate tumor-associated genes via binding the 3′-UTR of the target gene mRNA. Previous publications have demonstrated that miRNA-218 (miR-218) acts as a tumor-suppressive miRNA in various types of human cancer, including prostate cancer (PCa). However, the role of miR-218 in regulating PCa cell stemness and epithelial-mesenchymal transition remains unknown and requires further research. In the present study, it is demonstrated that miR-218 was downregulated in 2 PCa cell lines and could suppress cell migration, EMT and the exhibition of cancer stem cell-like properties. The expression of GLI family zinc finger 1 (Gli1) was inhibited by miR-218 overexpression, suggesting miR-218-suppression of Gli1 as a potential mechanism for the tumor-suppressive effect of miR-218. Overall, the results indicate that miR-218 served a critical role in the inhibition of PCa development. This may provide new insight for elucidating the mechanisms of PCa oncogenesis and suggests that miR-218 may be a novel therapeutic target for PCa.
机译:MicroRNA(miRNA)是一类非编码单链RNA,能够通过结合靶基因mRNA的3'-UTR来调节肿瘤相关基因。先前的出版物已经证明,miRNA-218(miR-218)在包括前列腺癌(PCa)在内的各种类型的人类癌症中充当肿瘤抑制性miRNA。但是,miR-218在调节PCa细胞干性和上皮-间质转化中的作用仍然未知,需要进一步研究。在本研究中,已证明miR-218在2种PCa细胞系中被下调,并且可以抑制细胞迁移,EMT和癌症干细胞样特性的展示。 miR-218过表达抑制GLI家族锌指1(Gli1)的表达,提示miR-218抑制Gli1是miR-218抑癌作用的潜在机制。总体而言,结果表明,miR-218在抑制PCa发育中起关键作用。这可能为阐明PCa致癌机理提供新的见解,并表明miR-218可能是PCa的新型治疗靶标。

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