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首页> 外文期刊>Cell death & disease. >The novel 19q13 KRAB zinc-finger tumour suppressor ZNF382 is frequently methylated in oesophageal squamous cell carcinoma and antagonises Wnt/β-catenin signalling
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The novel 19q13 KRAB zinc-finger tumour suppressor ZNF382 is frequently methylated in oesophageal squamous cell carcinoma and antagonises Wnt/β-catenin signalling

机译:新型19q13 KRAB锌指肿瘤抑制物ZNF382在食道鳞状细胞癌中经常被甲基化,并拮抗Wnt /β-catenin信号传导

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摘要

Zinc finger proteins (ZFPs) are the largest transcription factor family in mammals. About one-third of ZFPs are Krüppel-associated box domain (KRAB)-ZFPs and involved in the regulation of cell differentiation/proliferation/apoptosis and neoplastic transformation. We recently identified ZNF382 as a novel KRAB-ZFP epigenetically inactivated in multiple cancers due to frequent promoter CpG methylation. However, its epigenetic alterations, biological functions/mechanism and clinical significance in oesophageal squamous cell carcinoma (ESCC) are still unknown. Here, we demonstrate that ZNF382 expression was suppressed in ESCC due to aberrant promoter methylation, but highly expressed in normal oesophagus tissues. ZNF382 promoter methylation is correlated with ESCC differentiation levels. Restoration of ZNF382 expression in silenced ESCC cells suppressed tumour cell proliferation and metastasis through inducing cell apoptosis. Importantly, ZNF382 suppressed Wnt/β-catenin signalling and downstream target gene expression, likely through binding directly to FZD1 and DVL2 promoters. In summary, our findings demonstrate that ZNF382 functions as a bona fide tumour suppressor inhibiting ESCC pathogenesis through inhibiting the Wnt/β-catenin signalling pathway.
机译:锌指蛋白(ZFP)是哺乳动物中最大的转录因子家族。大约三分之一的ZFP是Krüppel相关盒结构域(KRAB)-ZFP,并参与细胞分化/增殖/凋亡和肿瘤转化的调控。我们最近发现ZNF382是一种新型KRAB-ZFP,由于频繁的启动子CpG甲基化而在多种癌症中表观遗传失活。然而,其在食管鳞状细胞癌(ESCC)中的表观遗传学改变,生物学功能/机制和临床意义仍然未知。在这里,我们证明了ZNF382表达在ESCC中由于启动子异常甲基化而受到抑制,但在正常食道组织中高表达。 ZNF382启动子甲基化与ESCC分化水平相关。在沉默的ESCC细胞中ZNF382表达的恢复通过诱导细胞凋亡来抑制肿瘤细胞的增殖和转移。重要的是,ZNF382可能通过直接结合FZD1和DVL2启动子来抑制Wnt /β-catenin信号传导和下游靶基因表达。总而言之,我们的发现证明ZNF382通过抑制Wnt /β-catenin信号传导途径而发挥真正的肿瘤抑制作用,可抑制ESCC的发病机理。

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