Division of Cancer Epigenomics, German Cancer Research Center (DKFZ), Im Neuenheimer Feld 280, 69120, Heidelberg, Germany.
Present Address: Division of Hematology Department of Internal Medicine, The Ohio State University, Columbus, OH, USA.
Clin Epigenetics. 2019 May 3;11(1):67. doi: 10.1186/s13148-019-0666-5.
Genetic aberrations in DNA repair genes are linked to cancer, but less is reported about epigenetic regulation of DNA repair and functional consequences. We investigated the intragenic methylation loss at the three prime repair exonuclease 2 (TREX2) locus in laryngeal (n = 256) and colorectal cancer cases (n = 95) and in pan-cancer data from The Cancer Genome Atlas (TCGA).
Significant methylation loss at an intragenic site of TREX2 was a frequent trait in both patient cohorts (p = 0.016 and < 0.001, respectively) and in 15 out of 22 TCGA studies. Methylation loss correlated with immunohistochemically staining for TREX2 (p < 0.0001) in laryngeal tumors and improved overall survival of laryngeal cancer patients (p = 0.045). Chromatin immunoprecipitation, demethylation experiments, and reporter gene assays revealed that the region of methylation loss can function as a CCAAT/enhancer binding protein alpha (CEBPA)-responsive enhancer element regulating TREX2 expression.
The data highlight a regulatory role of TREX2 DNA methylation for gene expression which might affect incidence and survival of laryngeal cancer. Altered TREX2 protein levels in tumors may affect drug-induced DNA damage repair and provide new tailored therapies.
DNA 修复基因的遗传异常与癌症有关,但关于 DNA 修复的表观遗传调控及其功能后果的报道较少。我们研究了三个头端修复外切酶 2(TREX2)基因座内基因的甲基化缺失在喉癌(n=256)和结直肠癌病例(n=95)中的情况,并在癌症基因组图谱(TCGA)的泛癌数据中进行了研究。
在两个患者队列中(分别为 p=0.016 和 <0.001)以及在 22 项 TCGA 研究中的 15 项中,TREX2 基因内位点的甲基化缺失是一个常见特征。甲基化缺失与喉肿瘤中 TREX2 的免疫组织化学染色相关(p<0.0001),并改善了喉癌患者的总体生存率(p=0.045)。染色质免疫沉淀、去甲基化实验和报告基因分析表明,甲基化缺失区域可以作为 CCAAT/增强子结合蛋白α(CEBPA)反应元件,调节 TREX2 的表达。
这些数据强调了 TREX2 DNA 甲基化对基因表达的调节作用,可能影响喉癌的发病和生存。肿瘤中 TREX2 蛋白水平的改变可能影响药物诱导的 DNA 损伤修复,并提供新的靶向治疗方法。