Department of Oncology, Jining No. 1 People's Hospital, Jining, Shandong 272051, P.R. China.
Oncol Rep. 2018 Aug;40(2):1165-1173. doi: 10.3892/or.2018.6494. Epub 2018 Jun 14.
NHERF1 is downregulated and has been identified as a new marker of colorectal cancer. However, the molecular mechanism of NHERF1 downregulation in colon cancer is not well understood. In the present study, we demonstrated that the NHERF1 mRNA level was downregulated and correlated with outcomes in colon cancer patients. NHERF1 expression was associated with EMT phenotype. High levels of promoter methylation of NHERF1 in colon cancer were observed. NHERF1 expression was restored by demethylation treatment. In addition, a negative correlation between methylation and mRNA expression of NHERF1 was observed in the TCGA dataset. Moreover, DNMT1 inhibited NHERF1 expression in vivo. DNMT1 expression was found to be negatively correlated with NHERF1 and NHERF1 expression was also restored by a DNMT1 inhibitor. DNMT1 and NHERF1 were regulated by the Wnt signaling pathway. In addition, among DNMT1 high expression patients, the Wnt signaling pathway was negatively correlated with NHERF1 expression. In contrast, among DNMT1 low expression patients, the Wnt signaling pathway was not correlated with NHERF1 expression. In conclusion, Wnt signaling increases DNMT1 expression. DNMT1 contributes to promoter hypermethylation and epigenetic NHERF1 silencing in colon cancer. In addition, we provide novel insight into the mechanisms underlying the regulation of NHERF1 expression and occurrence/progression of colon cancer.
NHERF1 下调并被鉴定为结直肠癌的新标志物。然而,结肠癌中 NHERF1 下调的分子机制尚不清楚。在本研究中,我们证明了 NHERF1 mRNA 水平下调并与结肠癌患者的结局相关。NHERF1 表达与 EMT 表型相关。观察到结肠癌中 NHERF1 启动子高甲基化水平。通过去甲基化处理可恢复 NHERF1 表达。此外,在 TCGA 数据集观察到 NHERF1 甲基化和 mRNA 表达之间存在负相关。此外,DNMT1 在体内抑制 NHERF1 表达。发现 DNMT1 表达与 NHERF1 呈负相关,DNMT1 抑制剂也可恢复 NHERF1 表达。DNMT1 和 NHERF1 受 Wnt 信号通路调节。此外,在 DNMT1 高表达患者中,Wnt 信号通路与 NHERF1 表达呈负相关。相比之下,在 DNMT1 低表达患者中,Wnt 信号通路与 NHERF1 表达无相关性。总之,Wnt 信号增加 DNMT1 表达。DNMT1 有助于结肠癌中启动子超甲基化和表观遗传 NHERF1 沉默。此外,我们为 NHERF1 表达调控以及结肠癌发生/进展的机制提供了新的见解。