Kim Sung-Jin, Tae Chung Hyun, Hong Sung Noh, Min Byung-Hoon, Chang Dong Kyung, Rhee Poong-Lyul, Kim Jae J, Kim Hee Cheol, Kim Duk-Hwan, Kim Young-Ho
Samsung Biomedical Research Institute, Samsung Medical Center, Seoul, Korea.
Department of Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.
Mol Carcinog. 2015 Dec;54(12):1748-57. doi: 10.1002/mc.22247. Epub 2015 Jan 25.
A previous genome-wide methylation array for colorectal cancer (CRC) identified aberrant promoter methylation of eyes absent 4 (EYA4). However, the correlations between EYA4 methylation and gene expression, the role played by EYA4 protein in colorectal carcinogenesis, and results of the gene-enrichment and functional annotation analysis have not yet been established. We analyzed the EYA4 methylation status and found EYA4 promoter methylation in CRC cell lines (100%), CRC tissues (93.5%) and advanced adenoma tissues (50.7%), compared with normal mucosa (32.6%). There was a significant inverse correlation between EYA4 methylation and expression. EYA4 transfection led to inhibition of cell proliferation in colony assays and xenograft studies. On performing the gene-enrichment and functional annotation analysis, we observed that the differentially expressed genes have been associated with the Wnt and MAPK signaling pathways. Our results demonstrate that EYA4 is under epigenetic regulation in CRC. It is a candidate tumor suppressor gene that acts by inducing up-regulation of DKK1 and inhibiting the Wnt signaling pathway. In addition, EYA4 methylation may be identified in stool samples and it serves as a potential stool biomarker for detection of advanced adenoma and CRC.
先前一项针对结直肠癌(CRC)的全基因组甲基化阵列研究确定了无眼4(EYA4)基因启动子存在异常甲基化。然而,EYA4甲基化与基因表达之间的相关性、EYA4蛋白在结直肠癌发生过程中所起的作用,以及基因富集和功能注释分析的结果尚未明确。我们分析了EYA4的甲基化状态,发现与正常黏膜(32.6%)相比,CRC细胞系(100%)、CRC组织(93.5%)和进展期腺瘤组织(50.7%)中均存在EYA4启动子甲基化。EYA4甲基化与表达之间存在显著的负相关。在集落试验和异种移植研究中,EYA4转染导致细胞增殖受到抑制。在进行基因富集和功能注释分析时,我们观察到差异表达基因与Wnt和MAPK信号通路有关。我们的结果表明,EYA4在CRC中受到表观遗传调控。它是一个候选肿瘤抑制基因,通过诱导DKK1上调并抑制Wnt信号通路发挥作用。此外,在粪便样本中可能检测到EYA4甲基化,它可作为检测进展期腺瘤和CRC的潜在粪便生物标志物。