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LncRNA ITGB1 promotes the development of bladder cancer through regulating microRNA-10a expression

机译:LNCRNA ITGB1通过调节MicroRNA-10A表达来促进膀胱癌的发育

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OBJECTIVE: This study aims to investigate the expression level of lncRNA ITGB1 both in bladder cancer (BCa) tissue and cell lines, as well as to evaluate its function and potential mechanism in the progression of BCa. PATIENTS AND METHODS: The expressions of lncRNA ITGB1 in 36 BCa tissues samples (and corresponding adjacent normal ones) and cell lines were detected by quantitative real-time polymerase chain reaction (qRT-PCR). After transfection of sh-ITGB1 in BCa cell lines, the effect of ITGB1 on the proliferation of BCa cells was examined by cell counting kit-8 (CCK-8) assay and colony formation assay. Subsequently, qRT-PCR was used to examine microRNA-10a expression in BCa tissues and cells after ITGB1 was silenced. At the same time, the correlation between ITGB1 and microRNA-10a expression was analyzed. Finally, cell recovery experiment was applied for the in-depth study of the interaction between ITGB1 and microRNA-10a and its underlying mechanism. RESULTS: LncRNA ITGB1 was found upregulated in BCa tissues and cell lines. Knockdown of lncRNA ITGB1 remarkably inhibited cell proliferation. The expression levels of ITGB1 and microRNA-10a in BCa tissues were negatively correlated. ITGB1 downregulation was found to be able to enhance microRNA-10a expression, suggesting that microRNA-10a may be a potential target for ITGB1 in BCa. In addition, cell reverse experiment also verified that ITGB1 could regulate the expression of microRNA-10a, and their interaction affected the malignant progression of BCa. CONCLUSIONS: LncRNA ITGB1 level is upregulated in BCa tissues and associated with the pathological stage of BCa, which could be used as a new predictor of BCa patients’ prognosis. In addition, ITGB1 might promote BCa cell proliferation via regulating microRNA-10a expression.
机译:目的:本研究旨在探讨膀胱癌(BCA)组织和细胞系中LNCRNA ITGB1的表达水平,以及评估其在BCA进展中的功能和潜在机制。患者和方法:通过定量的实时聚合酶链反应(QRT-PCR)检测36bCA组织样品(和相应的相邻正常常规)和细胞系中LNCRNA ItGB1的表达。通过细胞计数试剂盒-8(CCK-8)测定和菌落形成测定,检查ITGB1对BCA细胞增殖的影响后的ITGB1对BCA细胞增殖的影响。随后,QRT-PCR用于检查BCA组织和细胞中的microRNA-10A表达,在ITGB1静音后。同时,分析ITGB1和MicroRNA-10A表达之间的相关性。最后,应用细胞回收实验用于对ITGB1和MicroRNA-10A的相互作用及其下面的机制进行深入研究。结果:在BCA组织和细胞系中发现LNCRNA ItGB1上调。 LNCRNA ITGB1的敲低显着抑制细胞增殖。 BCA组织中ITGB1和MicroRNA-10A的表达水平负相关。发现ITGB1下调能够增强MicroRNA-10A表达,表明MicroRNA-10A可以是BCA中ITGB1的潜在靶标。此外,细胞反向实验还核实ITGB1可以调节MicroRNA-10A的表达,它们的相互作用影响了BCA的恶性进展。结论:LNCRNA ITGB1水平在BCA组织中上调,与BCA的病理阶段相关,这可以用作BCA患者预后的新预测因子。此外,ITGB1可以通过调节MicroRNA-10A表达来促进BCA细胞增殖。

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