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作 者:张小静[1] 黄伟玲[2] 高燕 黄勇[2] 张媛[2] 简千贺 冯先玲[1] 侯刚强 范新民[1] 金哲[1,4]
机构地区:[1]深圳大学医学院病理教研室,深圳天然小分子创新药物工程实验室,深圳市肿瘤转化医学重点实验室,广东深圳518060 [2]深圳大学医学院临床医学系,广东深圳518060 [3]深圳市第六人民医院(南山医院)放射科,广东深圳518060 [4]北京大学深圳研究生院化学基因组学重点实验室,广东深圳518060
出 处:《肿瘤》2014年第6期507-513,共7页Tumor
基 金:国家自然科学基金面上项目(编号:81172282);深圳市海外高层次人才创新创业专项资金项目(编号:KQCX20130621101141669);深圳市科技研发资金国家和省计划配套项目(编号:GJHS20120621142654087);深圳市战略新兴产业发展专项资金项目(编号:ZDSY20130329101130496)
摘 要:目的:筛选与胃癌转移相关的微小RNA(microRNA,miRNA,miR),并进行生物信息学分析。方法:应用miRNA芯片对胃癌低转移细胞株(RF-1和MKN28)和高转移细胞株(RF-48、NCI-N87和KATOⅢ)进行miRNA差异表达谱分析,筛选差异表达的miRNA;应用实时荧光定量-PCR法对差异表达的miR-192、miR-215和miR-194进行验证,应用miRfocus在线数据库对筛选获得的miR-192、miR-193a、miR-194和miR-215进行靶基因预测及其信号转导通路进行分析。结果:与低转移细胞株比较,高转移细胞株中miR-192、miR-193a、miR-194和miR-215的表达水平明显上调,miR-105、miR-767、miR-149、miR-205、miR-30a、miR-30d、miR-365、miR-193b、miR-326、miR-100、miR-30b、miR-125b和miR-584的表达水平明显下调。实时荧光定量-PCR法对miR-192、miR-215和miR-194的表达进行验证,结果显示与miRNA芯片检测结果一致;生物信息学分析结果显示,miR-192、miR-193a、miR-194和miR-215及其靶基因参与肿瘤的发生、转移、细胞周期及范可尼贫血等通路。结论:胃癌高转移细胞中miR-192、miR-193a、miR-194和miR-215的上调可能与胃癌的发生和转移等有关。Objective: To screen the microRNA (miRNA, miR) associated with metastasis of gastric cancer and to analyze its bioinformation. Methods: The differentially expressed miRNAs in gastric cancer cell lines with low metastatic potentials (RF-1 and MKN28) or high metastatic potentials (RF-48, NCI-N87 and KATO III) were analyzed and screened by miRNA microarrays. The differentially expressed miR-1 92, miR-21 5 and miR-194 were verified by real-time fluorescence quantitative-PCR. The targets prediction of miR-192, miR-193a, miR-194, miR-215 and signal pathway analysis were performed via miRfocus database. Results: As compared with the cells with low metastatic potentials, the expression levels of miR-192, miR-193a, miR-194 and miR-215 were up-regulated and the expression levels of miR-105, miR-767, miR-149, miR-205, miR-3Oa, miR-3Od, miR-365, miR-193b, miR-326, miR-lO0, miR-3Ob, miR-125b and miR-584 were down-regulated in highly metastatic cells. Up-regualtions of miR-192, miR-194 and miR-215 were validated by real-time fluorescence quantitative-PCR and the results were consistent with those of microRNA microarray. Bioinformatic analysis, functions of targets of miR-1 92, miR-193a, miR-194 and miR-215 were focused on the miRNA in cancer, pathway in cancer, cell cycle and Fanconi anemia pathway, etc. Conclusion= miR-192, miR-193a, miR-194 and miR-215 are overexpressed in highly metastatic gastric cancer cells, and they may be related to the progression and metastasis of gastric cancer.
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