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MTSS1 gene regulated by miR-96 inhibits cell proliferation and metastasis in tongue squamous cellular carcinoma Tca8113 cell line

机译:miR-96调控的MTSS1基因抑制舌鳞状细胞癌Tca8113细胞株的增殖和转移

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摘要

Background: Metastasis suppressor-1 (MTSS1) is a novel potential metastasis suppressor gene in several types of human cancers. However, the exact function and regulatory mechanism of MTSS1 in Tongue squamous cellular carcinoma (TSCC) have not been elucidated. Material/Methods: We first confirmed the MTSS1 gene expression by using quantitative real time-PCR (qRT-PCR) and immunohistochemical staining. Then we detected the effect of MTSS1 gene on Tca8113 cells proliferation and invasion ability by using MTT, wound healing and invasion assay. Finally by using bioinformatics analysis, luciferase reporter assay and a serial method, we analyzed the targeting of miR-96 on MTSS1 and the ability of miR-96 on MTSS1 gene mediated biological alterations in Tca8113 cells. Results: Our findings showed that the expression of MTSS1 was down-regulated in both TSCC tissues and Tca8113 cells. Forced expression of MTSS1 led to inhibited cell proliferation ability, retarded wound closing and reduced trans-membrane cell numbers. MiR-96 is confirmed to be a direct target of MTSS1 gene and could regulate MTSS1 mediated Tca8113 cells proliferation and metastasis. But miR-96 could not completely restore the invasion ability of Tca8113 cells. Conclusions: MiR-96 targeting and promoting MTSS1 repression may precipitate in the TSCC tumorigenesis through bypassing cell proliferation and metastasis control.
机译:背景:转移抑制因子-1(MTSS1)是在几种类型的人类癌症中的新型潜在转移抑制基因。但是,尚未阐明MTSS1在舌鳞状细胞癌(TSCC)中的确切功能和调控机制。材料/方法:我们首先通过实时定量PCR(qRT-PCR)和免疫组化染色确认了MTSS1基因的表达。然后通过MTT,伤口愈合和侵袭试验检测MTSS1基因对Tca8113细胞增殖和侵袭能力的影响。最后,通过生物信息学分析,荧光素酶报告基因分析和一系列方法,我们分析了miR-96对MTSS1的靶向作用以及miR-96对MTca1基因介导的Tca8113细胞生物学改变的能力。结果:我们的发现表明,在TSCC组织和Tca8113细胞中MTSS1的表达均被下调。 MTSS1的强制表达导致抑制细胞增殖能力,延迟伤口闭合和减少跨膜细胞数量。证实MiR-96是MTSS1基因的直接靶标,并且可以调节MTSS1介导的Tca8113细胞的增殖和转移。但是miR-96不能完全恢复Tca8113细胞的侵袭能力。结论:靶向MiR-96并促进其抑制MTSS1可能通过绕过细胞增殖和转移控制而在TSCC肿瘤发生中沉淀。

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