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Downregulation of ARFGEF1 and CAMK2B by promoter hypermethylation in breast cancer cells

机译:通过乳腺癌细胞的启动子高甲基化下调Arfgef1和Camk2b

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To identify novel genes that are regulated by promoter methylation, a combinational approach involving in silico mining followed by molecular assay was performed. From the expression microarray data registered in the European bioinformatics institute (EBI), genes showing downregulation in breast cancer cells were initially screened and then selected by e-Northern analysis using the Unigene database. A series of these in silico methods identified CAMK2B and ARFGEF1 as candidates, and the two genes were revealed to be hypermethylated in breast cancer cell lines and hypomethylated in normal breast cell lines. Additionally, cancer cell lines showed downregulated expression of these genes. Furthermore, treatment of the cancer cell lines with a demethylation agent, 5-Aza-2'-deoxycytidine, recovered expression of CAMK2B and ARFGEF1, implying that hypermethyaltion silenced gene activity in cancer cells. Taken together, promoter methylations of CAMK2B and ARFGEF1 are novel epigenetic markers identified in breast cancer cell lines and can be utilized for the application to clinical cancer tissues.
机译:为了鉴定通过启动子甲基化调节的新基因,进行了涉及分子测定的硅挖掘的组合方法。从欧洲生物信息学研究所(EBI)中登记的表达微阵列数据,最初筛选出显示乳腺癌细胞下调的基因,然后使用Unigene数据库通过E-Northern分析选择。其中一系列这些在硅方法中鉴定Camk2b和Arfgef1作为候选物,并且两个基因被显示为在乳腺癌细胞系中以高甲基化,并在正常乳腺细胞系中使甲基化。另外,癌细胞系显示出这些基因的下调表达。此外,用去甲基化剂,5-AZA-2'-脱氧胞苷,回收CAMK2B和ARFGEF1的表达治疗癌细胞系,意味着癌细胞中的高甲基溴酸纤维沉默的基因活性。连同,Camk2b和Arfgef1的启动子甲基化是在乳腺癌细胞系中鉴定的新型表观遗传标记,并且可以用于临床癌组织的应用。

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