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Frequent hypomethylation in multiple promoter CpG islands is associated with global hypomethylation, but not with frequent promoter hypermethylation.

机译:在多个启动子CpG岛中频繁的低甲基化与整体的低甲基化有关,但与频繁的启动子高甲基化无关。

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摘要

Hypomethylation of the global genome, considered to be composed mainly of repetitive sequences, is consistently observed in cancers, and aberrant hypo- and hypermethylation of CpG islands (CGIs) in promoter regions are also observed. Since methylation alterations in unique promoter sequences and in other genomic regions have distinct consequences, we analyzed the relationship between the global hypomethylation and the hypomethylation of unique promoter CGIs using human gastric cancers. Seven of ten gastric cancer cell lines showed marked decreases in 5-methylcytosine content, which correlated with hypomethylation of the LINE1 repetitive sequence. Six of the seven cell lines showed hypomethylation in five or all of the six normally methylated CGIs in promoter regions of six genes, and this was associated with induction of aberrant expression. The remaining three cell lines without global hypomethylation showed promoter hypomethylation in one or none of the six CGIs. Frequent promoter hypomethylation, however, did not correlate with frequent promoter hypermethylation. In primary gastric cancers too, global hypomethylation was associated with hypomethylation of LINE1 repetitive sequence and promoter hypomethylation. Of 93 gastric cancers, 33 cancers with frequent promoter hypomethylation and 27 cancers with frequent promoter hypermethylation constituted different groups. These findings represent experimental evidence that frequent hypomethylation of normally methylated promoter CGIs is associated with global hypomethylation, and that these hypomethylations occur independently of frequent promoter CGI hypermethylation.
机译:在癌症中始终观察到被认为主要由重复序列组成的全球基因组的低甲基化,并且在启动子区域中也观察到了CpG岛(CGI)的异常甲基化和超甲基化。由于独特的启动子序列和其他基因组区域中的甲基化改变具有明显的后果,因此我们分析了人类胃癌的整体低甲基化与独特启动子CGI的低甲基化之间的关系。十个胃癌细胞系中有七个显示出5-甲基胞嘧啶含量显着下降,这与LINE1重复序列的低甲基化有关。七个细胞系中的六个在六个基因的启动子区域中的五个或全部六个正常甲基化的CGI中显示低甲基化,这与异常表达的诱导有关。其余三个没有总体低甲基化的细胞系在六个CGI中的一个或一个中均未显示启动子低甲基化。然而,频繁的启动子低甲基化与频繁的启动子高甲基化无关。在原发性胃癌中,整体的低甲基化也与LINE1重复序列的低甲基化和启动子的低甲基化有关。在93种胃癌中,有33个启动子低甲基化频繁的癌症和27个启动子高甲基化频繁的癌症组成了不同的组。这些发现代表实验证据,即正常甲基化的启动子CGI的频繁低甲基化与总体甲基化不足有关,并且这些低甲基化独立于频繁的启动子CGI过度甲基化而发生。

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