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Effect of miR-301a/PTEN pathway on the proliferation andapoptosis of cervical cancer

机译:miR-301a / PTEN途径对增殖和增殖的影响宫颈癌的细胞凋亡

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摘要

The aim of this study was to evaluate the effect of the miR-301a/PTENpathway in cervical cancer. miR-301a and PTEN expression were measuredby quantitative real-time PCR (qRT-PCR) in tissues samples and HeLacells. PTEN protein level was determined by Western blotting. Dualreporter luciferase assay was performed to validate as a direct target of miR-301a. The gain-and loss-of function assay was performed by miR-301a overexpressionand silencing. Cell proliferation was monitored by cell counting Kit-8(CCK-8). Cell apoptosis was quantitated by flow cytometry. SPSS wasused to analyze the significant difference in the treatments. miR-301ademonstrated a significantly higher expression in cervical carcinomatissues compared with the paired non-carcinoma tissues(  = 12), while PTEN expression was found to besignificantly lower in cervical carcinoma tissues than their pairednon-carcinoma tissues (  = 12). In addition, PTEN wasidentified as the direct target of miR-301a. Moreover, overexpressionof miR-301a significantly promoted HeLa cells proliferation andanti-apoptosis which had a reverse pattern after PTEN overexpression.Our results confirm as a direct target ofmiR-301a in HeLa cells and suggest that miR-301a/PTEN pathwaycontributes to the development and progression of cervical cancer.
机译:这项研究的目的是评估miR-301a / PTEN的作用子宫颈癌中的通路。测量miR-301a和PTEN表达通过实时定量PCR(qRT-PCR)对组织样本和HeLa细胞。通过蛋白质印迹测定PTEN蛋白水平。双进行报告荧光素酶测定以验证 作为miR-301a的直接靶标。增益-通过miR-301a过表达进行功能丧失测定和沉默。通过细胞计数试剂盒8监测细胞增殖(CCK-8)。通过流式细胞仪定量细胞凋亡。 SPSS原为用于分析治疗的显着差异。 miR-301a在宫颈癌中显示出明显更高的表达组织与配对的非癌组织相比(= 12),而发现PTEN表达为子宫颈癌组织明显低于配对癌组织非癌组织(= 12)。此外,PTEN是被确定为miR-301a的直接靶标。而且,过度表达miR-301a显着促进HeLa细胞增殖和PTEN过表达后具有相反模式的抗凋亡。我们的结果证实了直接目标HeLa细胞中的miR-301a,并提示miR-301a / PTEN途径有助于宫颈癌的发展和发展。

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