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人食管鳞状细胞癌中热休克蛋白 B2 的启动子甲基化。

Promoter methylation of heat shock protein B2 in human esophageal squamous cell carcinoma.

机构信息

Department of Otolaryngology, Head and Neck Cancer Research Division, The Johns Hopkins University, School of Medicine, 1550 Orleans Street, CRB II-5M, Baltimore, MD 21231, USA.

出版信息

Int J Oncol. 2011 Apr;38(4):1129-35. doi: 10.3892/ijo.2011.918. Epub 2011 Jan 21.

Abstract

Hypermethylation of gene promoters and the corresponding loss of gene expression are recognized as a hallmark of human cancer, and DNA methylation has emerged as a promising biomarker for the detection of human esophageal squamous cell carcinoma (ESCC). To identify novel genes methylated in ESCC, we screened 35 candidate genes identified from an oligonucleotide microarray. Among them, the heat shock protein B2 (HSPB2) was methylated in 95.7% (67/70) of primary ESCCs, whereas no methylation was found in normal esophageal tissues from ESCC patients (0%, 0/20). RT-PCR analysis revealed that HSPB2 expression was silenced or weakly expressed in most ESCC cell lines, and re-activated by the demethylating agent 5-aza-2'-deoxy-cytidine. These results indicate that promoter methylation of HSPB2 is one of the causal factors for loss or down-regulation of HSPB2 expression. mRNA expression of HSPB2 in ESCC tissues was significantly down-regulated compared to normal tissues. Our data suggest that promoter methylation of HSPB2 deserves further attention as a novel molecular biomarker in human ESCC.

摘要

基因启动子的高甲基化和相应的基因表达缺失被认为是人类癌症的一个标志,DNA 甲基化已成为检测人类食管鳞状细胞癌(ESCC)的有前途的生物标志物。为了鉴定 ESCC 中甲基化的新基因,我们从寡核苷酸微阵列中筛选了 35 个候选基因。其中,热休克蛋白 B2(HSPB2)在 95.7%(67/70)的原发性 ESCC 中发生甲基化,而在 ESCC 患者的正常食管组织中未发现甲基化(0%,0/20)。RT-PCR 分析显示,HSPB2 在大多数 ESCC 细胞系中表达沉默或弱表达,并被去甲基化剂 5-氮杂-2'-脱氧胞苷重新激活。这些结果表明 HSPB2 启动子甲基化是 HSPB2 表达缺失或下调的一个原因。与正常组织相比,ESCC 组织中 HSPB2 的 mRNA 表达明显下调。我们的数据表明,HSPB2 启动子甲基化值得进一步关注,作为人类 ESCC 的一种新的分子生物标志物。

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