Han Nayoung, Song Yun-Kyoung, Burckart Gilbert J, Ji Eunhee, Kim In-Wha, Oh Jung Mi
College of Pharmacy and Research Institute of Pharmaceutical Sciences, Seoul National University, Seoul 08826, Republic of Korea.
Office of Clinical Pharmacology, Office of Translational Sciences, Food and Drug Administration, Silver Spring, Maryland 20993, USA.
Biomol Ther (Seoul). 2017 Sep 1;25(5):482-489. doi: 10.4062/biomolther.2017.122.
Individual differences in drug responses are associated with genetic and epigenetic variability of pharmacogene expression. We aimed to identify the relevant miRNAs which regulate pharmacogenes associated with drug responses. The miRNA and mRNA expression profiles derived from data for normal and solid tumor tissues in The Cancer Genome Atlas (TCGA) Research Network. Predicted miRNAs targeted to pharmacogenes were identified using publicly available databases. A total of 95 pharmacogenes were selected from cholangiocarcinoma and colon adenocarcinoma, as well as kidney renal clear cell, liver hepatocellular, and lung squamous cell carcinomas. Through the integration analyses of miRNA and mRNA, 35 miRNAs were found to negatively correlate with mRNA expression levels of 16 pharmacogenes in normal bile duct, liver, colon, and lung tissues (<0.05). Additionally, 36 miRNAs were related to differential expression of 32 pharmacogene mRNAs in those normal and tumorigenic tissues (<0.05). These results indicate that changes in expression levels of miRNAs targeted to pharmacogenes in normal and tumor tissues may play a role in determining individual variations in drug response.
药物反应的个体差异与药物基因表达的遗传和表观遗传变异性相关。我们旨在鉴定调控与药物反应相关的药物基因的相关微小RNA(miRNA)。miRNA和mRNA表达谱源自癌症基因组图谱(TCGA)研究网络中正常和实体瘤组织的数据。使用公开可用的数据库鉴定靶向药物基因的预测miRNA。从胆管癌、结肠腺癌以及肾透明细胞癌、肝细胞肝癌和肺鳞状细胞癌中总共选择了95个药物基因。通过miRNA和mRNA的整合分析,发现在正常胆管、肝脏、结肠和肺组织中,35个miRNA与16个药物基因的mRNA表达水平呈负相关(<0.05)。此外,在这些正常和致瘤组织中,36个miRNA与32个药物基因mRNA的差异表达相关(<0.05)。这些结果表明,正常和肿瘤组织中靶向药物基因的miRNA表达水平的变化可能在决定药物反应的个体差异中起作用。