Department of Radiation Oncology, The First Affiliated Hospital of 12480Xi'an Jiaotong University, Xi'an, Shaanxi, China.
Technol Cancer Res Treat. 2022 Jan-Dec;21:15330338221085373. doi: 10.1177/15330338221085373.
Evidence demonstrates that N6-methyladenosine (m6A) modification plays an increasingly important role in the development of tumors. The aim of this study is to explore the expression of m6A-related regulators in lung adenocarcinoma, identify the effect of altered key factors modified by m6A on the prognosis of patients with lung adenocarcinoma. A comprehensive analysis of m6A-related gene expressions in patients with lung adenocarcinoma based on The Cancer Genome Atlas database (TCGA) and the CBioPortal database. A prognostic risk score was established based on a linear combination of 4 key gene expression levels using the regression coefficients of the multivariate Cox regression models. Immunohistochemical staining analysis was performed to validate the relationship between the protein expression level of m6A regulators and the prognosis of patients retrospectively. The possible mechanism and prospective therapeutic targets of these key m6A molecules were explored by the M6A2Target database and the CMAP database. Mutation pattern analysis revealed that 32% of 656 patients had genetic alterations. Four genes (writer: methyltransferase like 3 [METTL3] and three readers: insulin like growth factor 2 mRNA binding protein 2 [IGF2BP2], heterogeneous nuclear ribonucleoprotein C [HNRNPC], and heterogeneous nuclear ribonucleoprotein A2/B1 [HNRNPA2B1]) were selected to construct a survival risk prediction model and the results of immunohistochemical staining showed that the expression of these four m6A genes was significantly different between lung adenocarcinoma tissues and normal lung tissues (< .01). The possible downstream genes and prospective therapeutic targets of these four m6A key molecules were discovered. These four m6A RNA methylation regulators may be effective prognostic and diagnostic factors which can provide auxiliary diagnosis and prognosis of lung adenocarcinoma.
证据表明,N6-甲基腺苷(m6A)修饰在肿瘤的发展中起着越来越重要的作用。本研究旨在探索肺腺癌中 m6A 相关调节剂的表达,确定 m6A 修饰的关键因素对肺腺癌患者预后的影响。
基于癌症基因组图谱数据库(TCGA)和 CBioPortal 数据库,对肺腺癌患者的 m6A 相关基因表达进行全面分析。根据多变量 Cox 回归模型的回归系数,基于 4 个关键基因表达水平的线性组合建立预后风险评分。通过回顾性免疫组织化学染色分析验证 m6A 调节剂的蛋白表达水平与患者预后之间的关系。通过 M6A2Target 数据库和 CMAP 数据库探索这些关键 m6A 分子的可能机制和潜在治疗靶点。
突变模式分析显示,656 名患者中有 32%存在遗传改变。选择四个基因(writer:甲基转移酶样 3 [METTL3]和三个 reader:胰岛素样生长因子 2 mRNA 结合蛋白 2 [IGF2BP2]、核不均一核糖核蛋白 C [HNRNPC]和核不均一核糖核蛋白 A2/B1 [HNRNPA2B1])构建生存风险预测模型,免疫组织化学染色结果显示,这四个 m6A 基因在肺腺癌组织和正常肺组织中的表达差异有统计学意义(<0.01)。发现了这四个 m6A 关键分子的下游基因和潜在的治疗靶点。
这四个 m6A RNA 甲基化调节剂可能是有效的预后和诊断因素,可为肺腺癌的辅助诊断和预后提供依据。