Department of Surgery, Flinders University, Beford Park SA, Australia.
Oncol Rep. 2011 Oct;26(4):1011-7. doi: 10.3892/or.2011.1381. Epub 2011 Jul 4.
Neoadjuvant chemotherapy is often used in the treatment of advanced esophageal cancer. In this study, we determined the impact of chemotherapy on microRNA (miRNA) expression in esophageal cancer cells, and whether identified changes might have biological relevance. Two esophageal carcinoma cell lines (one adenocarcinoma and one squamous cell carcinoma) were treated with cisplatin or 5-fluorouracil for 24 or 72 h. RNA was extracted from cells following 24-h treatment, and used for microarray studies. Promising miRNA candidates were selected for RT-PCR validation. Target prediction using TargetScan, combined with bioinformatic analysis (Ingenuity Pathway Analysis, IPA), was performed to evaluate the implications of the altered miRNA expression. Thirteen miRNAs (miR-199a-5p, miR-302f, miR-320a, miR-342-3p, miR-425, miR-455-3p, miR-486-3p, miR-519c-5p, miR-548d-5p, miR-617, miR-758, miR-766, miR-1286) were deregulated after 24- and/or 72-h treatment in both cell lines, and most miRNAs presented similar expression changes after short- or long-term exposure. IPA revealed that the major networks which incorporate the predicted targets, include functions such as 'Cell death', 'Cell cycle', 'Cellular growth and proliferation', 'DNA replication, recombination, and repair' and 'Drug metabolism'. Cisplatin or 5-fluorouracil alter miRNA expression in esophageal cancer cells. IPA suggests that these miRNAs may target molecular pathways involved in cell survival after chemotherapy.
新辅助化疗常用于治疗晚期食管癌。本研究旨在确定化疗对食管癌细胞中 microRNA (miRNA) 表达的影响,以及鉴定出的变化是否具有生物学相关性。我们用顺铂或氟尿嘧啶处理两种食管癌细胞系(一种腺癌和一种鳞癌)24 或 72 小时。用顺铂处理 24 小时后,从细胞中提取 RNA,并用于微阵列研究。选择有前途的 miRNA 候选物进行 RT-PCR 验证。使用 TargetScan 进行靶预测,结合生物信息学分析(Ingenuity Pathway Analysis,IPA),评估改变的 miRNA 表达的影响。在两种细胞系中,13 种 miRNA(miR-199a-5p、miR-302f、miR-320a、miR-342-3p、miR-425、miR-455-3p、miR-486-3p、miR-519c-5p、miR-548d-5p、miR-617、miR-758、miR-766、miR-1286)在 24 小时和/或 72 小时处理后发生下调,并且大多数 miRNA 在短时间或长时间暴露后表现出相似的表达变化。IPA 显示,包含预测靶标的主要网络包括“细胞死亡”、“细胞周期”、“细胞生长和增殖”、“DNA 复制、重组和修复”和“药物代谢”等功能。顺铂或氟尿嘧啶改变食管癌细胞中的 miRNA 表达。IPA 表明,这些 miRNA 可能靶向化疗后细胞存活相关的分子途径。