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Overexpression of long non-coding RNA RP11-396F22.1 correlates poor prognosis of patients with early-stage cervical cancer

机译:长非编码RNA RP11-396F22.1的过表达与早期宫颈癌患者的不良预后相关

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摘要

Objective: The expression level and clinical significances of long non-coding RNAs (LncRNAs) are presently unknown in the early-stage cervical cancer (CC). This study was aimed to explore the expression signatures of lncRNAs between normal and cervix carcinoma tissues and the prognostic value of LncRNAs in early-stage CC patients. Materials and Methods: The patients diagnosed with FIGO stage I-IIb CC of the First Affiliated Hospital of Sun Yat-sen University between January 1st 2006 and December 31st 2009 were retrospectively reviewed. Molecular microarray was conducted to identify differentially expression profiles of LncRNAs. In situ hybridization was applied for detection of candidate lncRNAs in cervical tissues. Results: A total of 2574 upregulated lncRNAs and 3270 downregulated lncRNAs with significantly differential expression (≥2.0-fold) were identified. Among the differentially expressed lncRNAs, RP11-396F22.1 expression was one of the most significantly overexpressed in the CC tissues compared to nomal cervical tissues (P<0.001). In situ hybridization confirmed RP11-396F22.1 expression was highly expressed in cancerous tissues. The results of Scratch and Transwell test showed that the migration ability decreased remarkably in transfected group (P<0.001). Moreover, the coding gene cpne8 was significantly upregulated by RP11-396F22.1 knockdown (P=0.035). Conclusions: These findings demonstrate that LncRNA RP11-396F22.1 might be a potent biomarker for CC progression.
机译:目的:目前尚不清楚早期宫颈癌(CC)中长非编码RNA(LncRNA)的表达水平和临床意义。这项研究的目的是探讨正常和子宫颈癌组织中lncRNA的表达特征以及LncRNA在早期CC患者中的预后价值。资料与方法:回顾性分析2006年1月1日至2009年12月31日在中山大学附属第一医院诊断为FIGO I-IIb CC期的患者。进行分子微阵列鉴定LncRNA的差异表达谱。原位杂交技术用于检测宫颈组织中的候选lncRNA。结果:共鉴定到2574个上调的lncRNA和3270个下调的lncRNA,它们的表达差异显着(≥2.0倍)。与正常宫颈组织相比,在差异表达的lncRNA中,RP11-396F22.1表达是CC组织中最显着的过表达之一(P <0.001)。原位杂交证实RP11-396F22.1表达在癌组织中高表达。 Scratch和Transwell试验的结果表明,转染组的迁移能力显着降低(P <0.001)。此外,编码基因cpne8被RP11-396F22.1敲低显着上调(P = 0.035)。结论:这些发现表明,LncRNA RP11-396F22.1可能是CC进展的有效生物标志物。

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