Jiang Yi-guo, Shen Yue-lan, Fu Juan, Zhou Lan-lan, Cao Hong
Institute for Chemical Carcinogenesis & Department of Preventive Medicine, Guangzhou Medical College, Guangzhou 510182, China.
Zhonghua Lao Dong Wei Sheng Zhi Ye Bing Za Zhi. 2008 Feb;26(2):81-5.
To screen microRNA (miRNA) profiles of malignantly transformed cells induced by anti-benzo-a-pyrene-trans-7, 8-dihydrodiol-9, 10-epoxide (BPDE) and to look for miRNAs which is expressed differently between malignantly transformed cells and normal human bronchial epithelial cells 16HBE.
Experimental group was the malignantly transformed 16HBE which was induced by cultured with final concentration 2.0 micromol/L of BPDE which was dissolved in dimethyl sulphoxide. The control group was 16HBE that was cultured with minimal essential medium including dimethyl sulphoxide. 327 miR-NAs were tested be-tween those two groups with miRNA microarray analysis. MiR-10a that was down expressed and miR-320 that was overexpressed were selected to be validated by miRNA specific quantitative real-time reverse transcriptase chain reaction (miR qRT-PCR).
327 human miRNAs were tested with miRNA microarray analysis. 55 miRNAs were found expressing differently between those two groups and of which 46 were overexpressed and 9 were down expressed. Some data were validated by quantitative RT-PCR.
miRNAs expressed significantly between malignantly transformed 16HBE and normal cells and this helps us look for unique miRNAs of malignantly transformed cells induced by BPDE, but there should have more sufficient evidences to prove their functions in malignant cells.
筛选抗苯并[a]芘-反式-7,8-二氢二醇-9,10-环氧化物(BPDE)诱导的恶性转化细胞的微小RNA(miRNA)谱,并寻找在恶性转化细胞与正常人支气管上皮细胞16HBE之间表达差异的miRNA。
实验组为用终浓度2.0 μmol/L溶解于二甲基亚砜的BPDE培养诱导的恶性转化16HBE。对照组为用含二甲基亚砜的最低必需培养基培养的16HBE。用miRNA芯片分析检测两组之间的327种miRNA。选择表达下调的miR-10a和表达上调的miR-320,通过miRNA特异性定量实时逆转录聚合酶链反应(miR qRT-PCR)进行验证。
用miRNA芯片分析检测了327种人类miRNA。发现两组之间有55种miRNA表达不同,其中46种上调,9种下调。一些数据通过定量RT-PCR得到验证。
恶性转化的16HBE与正常细胞之间miRNA表达有显著差异,这有助于我们寻找BPDE诱导的恶性转化细胞独特的miRNA,但需要有更充分的证据来证明它们在恶性细胞中的功能。