Medical College, Hubei University of Arts and Science, Xiangyang, Hubei, China.
Department of Epidemiology and Biostatistics, Ministry of Education Key Laboratory of Environment and Health, School of Public Health, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei, China.
Cancer Med. 2022 Jan;11(1):281-294. doi: 10.1002/cam4.4431. Epub 2021 Dec 2.
Lung cancer is the leading cause of cancer morbidity and mortality worldwide, however, the individualized treatment is still unsatisfactory. DNA methylation can affect gene regulation and may be one of the most valuable biomarkers in predicting the prognosis of lung adenocarcinoma. This study was aimed to identify methylation CpG sites that may be used to predict lung adenocarcinoma prognosis.
The Cancer Genome Atlas (TCGA) database was used to detect methylation CpG sites associated with lung adenocarcinoma prognosis and construct a methylation signature model. Then, a Chinese cohort was carried out to estimate the association between methylation and lung adenocarcinoma prognosis. Biological function studies, including demethylation treatment, cell proliferative capacity, and gene expression changes in lung adenocarcinoma cell lines, were further performed.
In the TCGA set, three methylation CpG sites were selected that were associated with lung adenocarcinoma prognosis (cg14517217, cg15386964, and cg18878992). The risk of mortality was increased in lung adenocarcinoma patients with the gradual increase level of methylation signature based on three methylation sites levels (HR = 45.30, 95% CI = 26.69-66.83; p < 0.001). The C-statistic value increased to 0.77 when age, gender, and other clinical variables were added to the signature to prediction model. A similar situation was confirmed in Chinese lung adenocarcinoma cohort. In the biological function studies, the proliferative capacity of cell lines was inhibited when the cells were demethylated with 5-aza-2'-deoxycytidine (5-aza-2dC). The mRNA and protein expression levels of SEPT9 and HIST1H2BH (cg14517217 and cg15386964) were downregulated with different concentrations of 5-aza-2dC treatment, while cg18878992 showed the opposite result.
This study is the first to develop a three-CpG-based model for lung adenocarcinoma, which is a practical and useful tool for prognostic prediction that has been validated in a Chinese population.
肺癌是全球癌症发病率和死亡率的主要原因,但个体化治疗仍不尽人意。DNA 甲基化可影响基因调控,可能是预测肺腺癌预后最有价值的生物标志物之一。本研究旨在确定可能用于预测肺腺癌预后的甲基化 CpG 位点。
利用癌症基因组图谱(TCGA)数据库检测与肺腺癌预后相关的甲基化 CpG 位点,并构建甲基化特征模型。然后,进行了一项中国队列研究,以评估甲基化与肺腺癌预后之间的关联。进一步进行了肺腺癌细胞系的去甲基化治疗、细胞增殖能力和基因表达变化等生物学功能研究。
在 TCGA 队列中,选择了三个与肺腺癌预后相关的甲基化 CpG 位点(cg14517217、cg15386964 和 cg18878992)。基于三个甲基化位点水平,随着甲基化特征水平的逐渐升高,肺腺癌患者的死亡风险增加(HR=45.30,95%CI=26.69-66.83;p<0.001)。当将年龄、性别和其他临床变量添加到特征预测模型中时,C 统计值增加到 0.77。在中国肺腺癌队列中也得到了类似的证实。在生物学功能研究中,用 5-氮杂-2'-脱氧胞苷(5-aza-2dC)对细胞去甲基化后,细胞系的增殖能力受到抑制。用不同浓度的 5-aza-2dC 处理后,SEPT9 和 HIST1H2BH(cg14517217 和 cg15386964)的 mRNA 和蛋白表达水平下调,而 cg18878992 则表现出相反的结果。
本研究首次建立了一个基于三个 CpG 的肺腺癌模型,这是一个在中国人群中经过验证的实用且有用的预后预测工具。