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肺癌中表面活性蛋白A2基因的DNA甲基化谱及表达

DNA methylation profile and expression of surfactant protein A2 gene in lung cancer.

作者信息

Grageda Melissa, Silveyra Patricia, Thomas Neal J, DiAngelo Susan L, Floros Joanna

机构信息

1Pediatric Critical Care Division, Department of Pediatrics, Pennsylvania State Children's Hospital, The Pennsylvania State University College of Medicine , Hershey, PA , United States.

出版信息

Exp Lung Res. 2015 Mar;41(2):93-102. doi: 10.3109/01902148.2014.976298. Epub 2014 Dec 16.

Abstract

Knowledge of the methylation profile of genes allow for the identification of biomarkers that may guide diagnosis and effective treatment of disease. Human surfactant protein A (SP-A) plays an important role in lung homeostasis and immunity, and is encoded by two genes (SFTPA1 and SFTPA2). The goal of this study was to identify differentially methylated CpG sites in the promoter region of the SFTPA2 gene in lung cancer tissue, and to determine the correlation between the promoter's methylation profile and gene expression. For this, we collected 28 pairs of cancerous human lung tissue and adjacent noncancerous (NC) lung tissue: 17 adenocarcinoma (AC), 9 squamous cell carcinoma (SCC), and 2 AC with SCC features, and we evaluated DNA methylation of the SFTPA2 promoter region by bisulfite conversion. Our results identified a higher methylation ratio in one CpG site of the SFTPA2 gene in cancerous tissue versus NC tissue (0.36 versus 0.11, p = 0.001). When assessing AC samples, we also found cancerous tissues associated with a higher methylation ratio (0.43 versus 0.10, p = 0.02). In the SCC group, although cancerous tissue showed a higher methylation ratio (0.22 versus 0.11), this difference was not statistically significant (p = 0.35). Expression of SFTPA2 mRNA and total SP-A protein was significantly lower in cancer tissue when compared to adjacent NC tissue (p < 0.001), and correlated with the hypermethylated status of an SFTPA2 CpG site in AC samples. The findings of this pilot study may hold promise for future use of SFTPA2 as a biomarker for the diagnosis of lung cancer.

摘要

了解基因的甲基化谱有助于识别可指导疾病诊断和有效治疗的生物标志物。人表面活性蛋白A(SP-A)在肺稳态和免疫中起重要作用,由两个基因(SFTPA1和SFTPA2)编码。本研究的目的是鉴定肺癌组织中SFTPA2基因启动子区域差异甲基化的CpG位点,并确定启动子甲基化谱与基因表达之间的相关性。为此,我们收集了28对人肺癌组织和相邻的非癌(NC)肺组织:17例腺癌(AC)、9例鳞状细胞癌(SCC)和2例具有SCC特征的AC,并通过亚硫酸氢盐转化评估SFTPA2启动子区域的DNA甲基化。我们的结果显示,癌组织中SFTPA2基因一个CpG位点的甲基化率高于NC组织(0.36对0.11,p = 0.001)。在评估AC样本时,我们还发现癌组织的甲基化率更高(0.43对0.10,p = 0.02)。在SCC组中,尽管癌组织的甲基化率较高(0.22对0.11),但差异无统计学意义(p = 0.35)。与相邻的NC组织相比,癌组织中SFTPA2 mRNA和总SP-A蛋白的表达显著降低(p < 0.001),并且与AC样本中SFTPA2 CpG位点的高甲基化状态相关。这项初步研究的结果可能为未来将SFTPA2用作肺癌诊断生物标志物带来希望。

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