Nagata Hiroaki, Kozaki Ken-Ichi, Muramatsu Tomoki, Hiramoto Hidekazu, Tanimoto Kousuke, Fujiwara Naoto, Imoto Seiya, Ichikawa Daisuke, Otsuji Eigo, Miyano Satoru, Kawano Tatsuyuki, Inazawa Johji
Department of Molecular Cytogenetics, Graduate School, Tokyo Medical and Dental University, Tokyo, Japan.
Department of Digestive Surgery, Graduate School of Medical Science, Kyoto Prefectural University of Medicine, Kamigyo-ku, Kyoto, Japan.
Oncotarget. 2017 Jun 6;8(23):37740-37750. doi: 10.18632/oncotarget.17147.
Lymph node metastasis (LNM) of esophageal squamous cell carcinoma (ESCC) is well-known to be an early event associated with poor prognosis in patients with ESCC. Recently, tumor-specific aberrant DNA methylation of CpG islands around the promoter regions of tumor-related genes has been investigated as a possible biomarker for use in early diagnosis and prediction of prognosis. However, there are few DNA methylation markers able to predict the presence of LNM in ESCC. To identify DNA methylation markers associated with LNM of ESCC, we performed a genome-wide screening of DNA methylation status in a discovery cohort of 67 primary ESCC tissues and their paired normal esophageal tissues using the Illumina Infinium HumanMethylation450 BeadChip. In this screening, we focused on differentially methylated regions (DMRs) that were associated with LNM of ESCC, as prime candidates for DNA methylation markers. We extracted three genes, HOXB2, SLC15A3, and SEPT9, as candidates predicting LNM of ESCC, using pyrosequencing and several statistical analyses in the discovery cohort. We confirmed that HOXB2 and SEPT9 were highly methylated in LNM-positive tumors in 59 ESCC validation samples. These results suggested that HOXB2 and SEPT9 may be useful epigenetic biomarkers for the prediction of the presence of LNM in ESCC.
食管鳞状细胞癌(ESCC)的淋巴结转移(LNM)是众所周知的与ESCC患者预后不良相关的早期事件。最近,肿瘤相关基因启动子区域周围CpG岛的肿瘤特异性异常DNA甲基化已被研究作为一种可能用于早期诊断和预后预测的生物标志物。然而,很少有DNA甲基化标志物能够预测ESCC中LNM的存在。为了鉴定与ESCC的LNM相关的DNA甲基化标志物,我们使用Illumina Infinium HumanMethylation450 BeadChip对67例原发性ESCC组织及其配对的正常食管组织的发现队列进行了全基因组DNA甲基化状态筛选。在该筛选中,我们关注与ESCC的LNM相关的差异甲基化区域(DMR),将其作为DNA甲基化标志物的主要候选者。我们在发现队列中使用焦磷酸测序和几种统计分析,提取了三个基因HOXB2、SLC15A3和SEPT9作为预测ESCC的LNM的候选基因。我们在59例ESCC验证样本中证实,HOXB2和SEPT9在LNM阳性肿瘤中高度甲基化。这些结果表明,HOXB2和SEPT9可能是用于预测ESCC中LNM存在的有用表观遗传生物标志物。