Department of Surgical Sciences, Uppsala University, Uppsala University Hospital, SE-75185 Uppsala, Sweden.
Exp Mol Med. 2010 Jul 31;42(7):484-502. doi: 10.3858/emm.2010.42.7.050.
Epigenomic and genomic changes affect gene expression and contribute to tumor development. The histone modifications trimethylated histone H3 lysine 4 (H3K4me3) and lysine 27 (H3K27me3) are epigenetic regulators associated to active and silenced genes, respectively and alterations of these modifications have been observed in cancer. Furthermore, genomic aberrations such as DNA copy number changes are common events in tumors. Pheochromocytoma is a rare endocrine tumor of the adrenal gland that mostly occurs sporadic with unknown epigenetic/genetic cause. The majority of cases are benign. Here we aimed to combine the genome-wide profiling of H3K4me3 and H3K27me3, obtained by the ChIP-chip methodology, and DNA copy number data with global gene expression examination in a malignant pheochromocytoma sample. The integrated analysis of the tumor expression levels, in relation to normal adrenal medulla, indicated that either histone modifications or chromosomal alterations, or both, have great impact on the expression of a substantial fraction of the genes in the investigated sample. Candidate tumor suppressor genes identified with decreased expression, a H3K27me3 mark and/or in regions of deletion were for instance TGIF1, DSC3, TNFRSF10B, RASSF2, HOXA9, PTPRE and CDH11. More genes were found with increased expression, a H3K4me3 mark, and/or in regions of gain. Potential oncogenes detected among those were GNAS, INSM1, DOK5, ETV1, RET, NTRK1, IGF2, and the H3K27 trimethylase gene EZH2. Our approach to associate histone methylations and DNA copy number changes to gene expression revealed apparent impact on global gene transcription, and enabled the identification of candidate tumor genes for further exploration.
表观遗传和基因组变化会影响基因表达,从而促进肿瘤的发展。组蛋白修饰的三甲基化组蛋白 H3 赖氨酸 4(H3K4me3)和赖氨酸 27(H3K27me3)分别与活性基因和沉默基因相关,在癌症中观察到这些修饰的改变。此外,基因组异常如 DNA 拷贝数变化是肿瘤中的常见事件。嗜铬细胞瘤是一种罕见的肾上腺内分泌肿瘤,主要为散发性,其表观遗传/遗传原因未知。大多数病例为良性。在这里,我们旨在将通过 ChIP-chip 方法获得的 H3K4me3 和 H3K27me3 的全基因组图谱与 DNA 拷贝数数据以及恶性嗜铬细胞瘤样本中的全局基因表达检查相结合。与正常肾上腺髓质相关的肿瘤表达水平的综合分析表明,要么是组蛋白修饰,要么是染色体改变,或者两者都对研究样本中相当一部分基因的表达有很大影响。候选肿瘤抑制基因的鉴定与表达下调、H3K27me3 标记和/或缺失区域有关,例如 TGIF1、DSC3、TNFRSF10B、RASSF2、HOXA9、PTPRE 和 CDH11。更多的基因被发现表达增加,有 H3K4me3 标记,和/或在增益区域。在这些基因中检测到的潜在癌基因包括 GNAS、INSM1、DOK5、ETV1、RET、NTRK1、IGF2 和 H3K27 三甲基化酶基因 EZH2。我们将组蛋白甲基化和 DNA 拷贝数变化与基因表达相关联的方法揭示了对全局基因转录的明显影响,并能够鉴定候选肿瘤基因以进行进一步探索。