Wu Yenan, Kröller Lea, Miao Beiping, Boekhoff Henning, Bauer Andrea S, Büchler Markus W, Hackert Thilo, Giese Nathalia A, Taipale Jussi, Hoheisel Jörg D
Division of Functional Genome Analysis, German Cancer Research Center (DKFZ), Im Neuenheimer Feld 580, 69120 Heidelberg, Germany.
Faculty of Biosciences, Heidelberg University, Im Neuenheimer Feld, 69120 Heidelberg, Germany.
Cancers (Basel). 2021 Sep 11;13(18):4569. doi: 10.3390/cancers13184569.
Studies have indicated that some genes involved in carcinogenesis are highly methylated in their promoter regions but nevertheless strongly transcribed. It has been proposed that transcription factors could bind specifically to methylated promoters and trigger transcription. We looked at this rather comprehensively for pancreatic ductal adenocarcinoma (PDAC) and studied some cases in more detail. Some 2% of regulated genes in PDAC exhibited higher transcription coupled to promoter hypermethylation in comparison to healthy tissue. Screening 661 transcription factors, several were found to bind specifically to methylated promoters, in particular molecules of the NFAT family. One of them-NFATc1-was substantially more strongly expressed in PDAC than control tissue and exhibited a strong oncogenic role. Functional studies combined with computational analyses allowed determining affected genes. A prominent one was gene , which accelerates PDAC metastasis and correlates with a bad prognosis. Further studies confirmed the direct up-regulation of transcription by NFATc1 promoter binding in a methylation-dependent process, providing insights into the oncogenic role of transcription activation in PDAC that is promoted by DNA methylation.
研究表明,一些参与致癌过程的基因在其启动子区域高度甲基化,但仍能强烈转录。有人提出转录因子可以特异性结合甲基化启动子并触发转录。我们对胰腺导管腺癌(PDAC)进行了较为全面的研究,并对一些病例进行了更详细的分析。与健康组织相比,PDAC中约2%的调控基因表现出与启动子高甲基化相关的更高转录水平。在对661种转录因子进行筛选时,发现有几种转录因子能特异性结合甲基化启动子,特别是NFAT家族的分子。其中之一——NFATc1——在PDAC中的表达明显高于对照组织,并表现出强大的致癌作用。功能研究与计算分析相结合,确定了受影响的基因。一个突出的基因是 ,它加速了PDAC转移并与不良预后相关。进一步的研究证实,在一个依赖甲基化的过程中,NFATc1通过结合启动子直接上调 转录,这为DNA甲基化促进的转录激活在PDAC中的致癌作用提供了见解。