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Microarray profiling and co-expression network analysis of lncRNAs and mRNAs in ovarian cancer

机译:卵巢癌中lncRNA和mRNA的微阵列分析和共表达网络分析

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摘要

Dysregulated long noncoding RNAs (lncRNAs) are involved in the pathogenesis and development of human diseases, such as epithelial ovarian cancer (EOC). In this study, we identified EOC-related lncRNAs and performed lncRNA and mRNA microarray analyses using IOSE80, a normal ovary cell line, and two ovarian carcinoma cell lines (SKOV3 and SKOV3/DDP) to investigate the potential roles of lncRNAs in EOC. lncRNA-HEIH expression in EOC tissues and cell lines was measured by quantitative real-time polymerase chain reaction (qPCR). In addition, we generated a lncRNA–mRNA co-expression network in order to identify lncRNA-expression trends and potential lncRNA target genes. Cell viability, migration, and invasion were determined by Cell Counting Kit-8, transwell assay, and wound-healing assay, respectively, and apoptosis was analyzed by flow cytometry. We identified 3527 differentially expressed lncRNAs upon comparison of the lncRNA profiles from IOSE80 with those of SKOV3 cell lines, with 11 differentially expressed lncRNAs confirmed by qPCR. Both pathway and gene ontology analyses demonstrated the involvement of lncRNAs, especially HEIH and LINC-PINT, in multiple biological processes. Furthermore, in vitro knockdown experiments confirmed that suppression of HEIH expression inhibited EOC cell proliferation. Our findings provide a foundation for further research into the role of these lncRNAs in EOC carcinogenesis and progression.
机译:失调的长非编码RNA(lncRNA)异常参与人类疾病(例如上皮性卵巢癌(EOC))的发病和发展。在这项研究中,我们鉴定了与EOC相关的lncRNA,并使用正常卵巢细胞系IOSE80和两个卵巢癌细胞系(SKOV3和SKOV3 / DDP)进行了lncRNA和mRNA微阵列分析,以研究lncRNA在EOC中的潜在作用。通过定量实时聚合酶链反应(qPCR)测量EOC组织和细胞系中lncRNA-HEIH的表达。此外,我们生成了lncRNA–mRNA共表达网络,以鉴定lncRNA表达趋势和潜在的lncRNA靶基因。细胞活力,迁移和侵袭分别通过Cell Counting Kit-8,transwell测定法和伤口愈合测定法测定,并通过流式细胞术分析细胞凋亡。通过比较IOSE80和SKOV3细胞系的lncRNA图谱,我们鉴定了3527个差异表达的lncRNA,其中qPCR证实了11个差异表达的lncRNA。途径和基因本体分析均表明lncRNA,特别是HEIH和L​​INC-PINT,参与了多种生物过程。此外,体外敲除实验证实抑制HEIH表达可抑制EOC细胞增殖。我们的发现为进一步研究这些lncRNA在EOC癌变和发展中的作用提供了基础。

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