Zou Jing, Yin Fuqiang, Wang Qi, Zhang Wei, Li Li
Department of Gynecologic Oncology, Affiliated Tumor Hospital of Guangxi Medical University Nanning 530021, Guangxi, P.R. China.
Medical Scientific Research Centre, Guangxi Medical University Nanning 530021, Guangxi, P.R. China.
Int J Clin Exp Pathol. 2015 Jun 1;8(6):6847-58. eCollection 2015.
The aim of this study was to identify potential microRNAs and genes associated with drug resistance in ovarian cancer through web-available microarrays. The drug resistant-related microRNA microarray dataset GS54665 and mRNA dataset GSE33482, GSE28646, and GSE15372 were downloaded from the Gene Expression Omnibus database. Dysregulated microRNAs/genes were screened with GEO2R and were further identified in SKOV3 (SKOV3/DDP) and A2780 (A2780/DDP) cells by real-time quantitative PCR (qRT-PCR), and then their associations with drug resistance was analyzed by comprehensive bioinformatic analyses. Nine microRNAs (microRNA-199a-5p, microRNA-199a-3p, microRNA-199b-3p, microRNA-215, microRNA-335, microRNA-18b, microRNA-363, microRNA-645 and microRNA-141) and 38 genes were identified to be differentially expressed in drug-resistant ovarian cancer cells, with seven genes (NHSL1, EPHA3, USP51, ZSCAN4, EPHA7, SNCA and PI15) exhibited exactly the same expression trends in all three microarrays. Biological process annotation and pathway enrichment analysis of the 9 microRNAs and 38 genes identified several drug resistant-related signaling pathways, and the microRNA-mRNA interaction revealed the existence of a targeted regulatory relationship between the 9 microRNAs and most of the 38 genes. The expression of 9 microRNAs and the 7 genes by qRT-PCR in SKOV3/DDP and A2780/DDP cells indicating a consistent expression profile with the microarrays. Among those, the expression of EPHA7 and PI15 were negatively correlated with that of microRNA-141, and they were also identified as potential targets of this microRNA via microRNA-mRNA interaction. We thus concluded that microRNA-141, EPHA7, and PI15 might jointly participate in the regulation of drug resistance in ovarian cancer and serve as potential targets in targeted therapies.
本研究旨在通过可公开获取的微阵列来鉴定与卵巢癌耐药性相关的潜在微小RNA和基因。从基因表达综合数据库下载了耐药相关的微小RNA微阵列数据集GS54665以及mRNA数据集GSE33482、GSE28646和GSE15372。使用GEO2R筛选失调的微小RNA/基因,并通过实时定量PCR(qRT-PCR)在SKOV3(SKOV3/DDP)和A2780(A2780/DDP)细胞中进一步鉴定,然后通过综合生物信息学分析来分析它们与耐药性的关联。鉴定出9种微小RNA(微小RNA-199a-5p、微小RNA-199a-3p、微小RNA-199b-3p、微小RNA-215、微小RNA-335、微小RNA-18b、微小RNA-363、微小RNA-645和微小RNA-141)和38个基因在耐药性卵巢癌细胞中差异表达,其中7个基因(NHSL1、EPHA3、USP51、ZSCAN4、EPHA7、SNCA和PI15)在所有三个微阵列中呈现完全相同的表达趋势。对这9种微小RNA和38个基因进行生物学过程注释和通路富集分析,确定了几条与耐药性相关的信号通路,微小RNA-信使核糖核酸相互作用揭示了这9种微小RNA与38个基因中的大多数之间存在靶向调控关系。通过qRT-PCR检测SKOV3/DDP和A2780/DDP细胞中9种微小RNA和7个基因的表达,结果表明其表达谱与微阵列一致。其中,EPHA7和PI15的表达与微小RNA-141呈负相关,并且通过微小RNA-信使核糖核酸相互作用也将它们鉴定为该微小RNA的潜在靶标。因此,我们得出结论,微小RNA-141、EPHA7和PI15可能共同参与卵巢癌耐药性的调控,并作为靶向治疗的潜在靶点。