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MiR-200c-3p inhibits cell migration and invasion of clear cell renal cell carcinoma via regulating SLC6A1

机译:MiR-200c-3p通过调节SLC6A1抑制细胞迁移和侵袭透明细胞肾细胞癌

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摘要

In this study, we investigated the mechanism of miR-200c-3p and SLC6A1 in regulating cell activity of clear cell renal cell carcinoma (CCRCC). The mRNA and miRNA expressions of tissue specimens were analyzed by CapitalBio Corporation (Beijing, China). The expression of SLC6A1 in CCRCC cells was examined through qRT-PCR and western blot. The migration and invasion ability of 786-O cells was testified by transwell assay after transfected. 786-O cell proliferation ability was detected by MTT assay. Dual luciferase reporter assay verified the association between SLC6A1 and miR-200c-3p. SLC6A1 was high expressed and miR-200c-3p was low expressed in CCRCC tissues and cells. Besides, lower SLC6A1 expression indicated longer survival time and higher survival rate. MiR-200c-3p could directly target at SLC6A1 and reduce its expression. MiR-200c-3p inhibited the proliferation, migration and invasion in 786-O cells by down-regulating SLC6A1 expression. The results suggested that the miR-200c-3p served as a suppressor for CCRCC via down-regulating SLC6A1.
机译:在这项研究中,我们研究了miR-200c-3p和SLC6A1调节透明细胞肾细胞癌(CCRCC)细胞活性的机制。由CapitalBio Corporation(中国北京)分析组织标本的mRNA和miRNA表达。通过qRT-PCR和western blot检测SLC6A1在CCRCC细胞中的表达。转染后,通过transwell法证实了786-O细胞的迁移和侵袭能力。通过MTT分析检测786-O细胞的增殖能力。双重荧光素酶报告基因分析证实了SLC6A1与miR-200c-3p之间的关联。在CCRCC组织和细胞中SLC6A1高表达而miR-200c-3p低表达。此外,较低的SLC6A1表达表明更长的存活时间和更高的存活率。 MiR-200c-3p可以直接靶向SLC6A1并降低其表达。 MiR-200c-3p通过下调SLC6A1表达来抑制786-O细胞的增殖,迁移和侵袭。结果表明,miR-200c-3p通过下调SLC6A1充当CCRCC的抑制剂。

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