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启动子低甲基化导致肝细胞癌中 HAI-1 的表达上调。

Promoter Hypomethylation Is Responsible for Upregulated Expression of HAI-1 in Hepatocellular Carcinoma.

机构信息

Clinical Research Center, The Second Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou, Zhejiang 310009, China.

Department of Surgical Oncology, The First Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou, Zhejiang 310003, China.

出版信息

Dis Markers. 2019 Aug 28;2019:9175215. doi: 10.1155/2019/9175215. eCollection 2019.

Abstract

An upregulated expression of hepatocyte growth factor activator inhibitor type 1 (HAI-1) in hepatocellular carcinomas (HCC) associates with poor prognosis, but the underlying mechanism for expression regulation has not been elucidated. HAI-1 was expressed in HCC cell line Hep3B cells at a high level but absent or has a low level in other HCC cell lines HepG2 and SMMC7721 and immortal normal liver cell line L02 at transcriptional and translational levels, respectively. A dual-luciferase reporter assay showed that transcriptional activity of HAI-1 in the promoter region (-452 bp to -280 bp from the mRNA start site) was strongly enhanced in Hep3B and SMMC7721. Bisulfite genomic sequencing results of the HAI-1 promoter region showed an inverse correlation between levels of promoter methylation and expression in HCC cells. The expression level of HAI-1 in SMMC7721, HepG2, and L02 cells was elevated after 5-Aza-2'-deoxycytidine treatment. Hypomethylation of the HAI-1 promoter region contributed to the elevated HAI-1 expression in HCC tissues. In addition, the hypomethylation of the HAI-1 promoter region correlated with poor differentiation status of HCC tissues. Our findings indicate that promoter hypomethylation is an important mechanism for aberrant HAI-1 expression regulation in HCC.

摘要

肝细胞生长因子激活物抑制剂 1(HAI-1)在肝细胞癌(HCC)中的表达上调与预后不良相关,但表达调控的潜在机制尚未阐明。HAI-1 在 HCC 细胞系 Hep3B 细胞中高水平表达,但在其他 HCC 细胞系 HepG2 和 SMMC7721 以及永生化正常肝细胞系 L02 中分别在转录和翻译水平上缺失或低水平表达。双荧光素酶报告基因检测显示,HAI-1 在启动子区域(从 mRNA 起始位点上游-452bp 到-280bp)的转录活性在 Hep3B 和 SMMC7721 中得到了强烈增强。HAI-1 启动子区域的亚硫酸氢盐基因组测序结果表明,HCC 细胞中启动子甲基化水平与表达呈负相关。SMMC7721、HepG2 和 L02 细胞中 HAI-1 的表达水平在 5-Aza-2'-脱氧胞苷处理后升高。HAI-1 启动子区域的低甲基化导致 HCC 组织中 HAI-1 的表达升高。此外,HAI-1 启动子区域的低甲基化与 HCC 组织的低分化状态相关。我们的研究结果表明,启动子低甲基化是 HCC 中 HAI-1 表达异常调节的重要机制。

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