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首页> 外文期刊>Molecular and Cellular Biology >GATA-4 and GATA-5 Transcription Factor Genes and Potential Downstream Antitumor Target Genes Are Epigenetically Silenced in Colorectal and Gastric Cancer
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GATA-4 and GATA-5 Transcription Factor Genes and Potential Downstream Antitumor Target Genes Are Epigenetically Silenced in Colorectal and Gastric Cancer

机译:GATA-4和GATA-5转录因子基因和潜在的下游抗肿瘤靶基因在结直肠癌和胃癌中被表观遗传沉默。

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The GATA family of transcription factors participates in gastrointestinal (GI) development. Increases in GATA-4 and -5 expression occur in differentiation and GATA-6 expression in proliferation in embryonic and adult settings. We now show that in colorectal cancer (CRC) and gastric cancer promoter hypermethylation and transcriptional silencing are frequent for GATA-4 and -5 but are never seen for GATA-6. Potential antitumor target genes upregulated by GATA-4 and -5, the trefoil factors, inhibinα, and disabled-2 (Dab2) are also silenced, in GI cancers, with associated methylation of the promoters. Drug or genetically induced demethylation simultaneously leads to expression, in CRC cells, of all of the GATA-4, -5, and downstream genes. Expression of exogenous GATA-5 overrides methylation at the downstream promoters to activate the target genes. Selection for silencing of both upstream transcription factors and their target genes in GI cancers could indicate that epigenetic silencing of the involved genes provides a summated contribution to tumor progression.
机译:GATA转录因子家族参与胃肠道(GI)的发展。 GATA-4 -5 表达的增加发生在分化过程中,而 GATA-6 表达则在胚胎和成年环境中扩散。现在,我们显示在结直肠癌(CRC)和胃癌启动子中, GATA-4 -5 的甲基化和转录沉默水平较高,而 GATA从未见过-6 。 GATA-4和-5,三叶因子抑制素α disabled-2 Dab2 <在胃肠道癌症中,启动子的相关甲基化也被沉默。药物或遗传诱导的去甲基化同时导致所有 GATA-4 -5 和下游基因在CRC细胞中表达。外源 GATA-5 的表达优先于下游启动子的甲基化,从而激活靶基因。胃肠道癌症中上游转录因子及其靶基因的沉默选择可能表明所涉及基因的表观遗传沉默为肿瘤的发展提供了累加的贡献。

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