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Retrospective study of gene signatures and prognostic value of m6A regulatory factor in non-small cell lung cancer using TCGA database and the verification of FTO

机译:采用TCGA数据库的非小细胞肺癌M6A调控因子基因签名及预后价值的回顾性研究及FTO验证

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摘要

N6-methyladenosine (m6A) is the most common internal modification in eukaryotic mRNA. However, little is known about its role in non-small cell lung cancer (NSCLC). In this study, a total of 1017 NSCLC patients from the cancer genome atlas (TCGA) database with copy number variation (CNV) data were included. Log-rank tests and Cox regression model were used for survival analysis. The relationship between m6A regulators and clinicopathological features was evaluated using the chi-square test. The alteration of m6A regulators were related to T stage. Patients with any CNVs of regulators genes had worse overall survival (OS) than those with diploid genes. The deletion of m6A writer genes was an independent risk factor for poor OS, and the effect synergized with that of copy number gain of eraser genes. High expression of Fat mass-and obesity-associated gene (FTO) was associated with KRAS signaling up. Knockdown of FTO increased m6A content and inhibit proliferation of A549 lung cancer cell. Thus, we identified the genetic changes of m6A regulatory factors in NSCLC for the first time and found a significant relationship between these changes and poor clinical characteristics. FTO might play an important role in promoting NSCLC by decreasing m6A level and activating KRAS signaling.
机译:N6-甲基腺苷(M6A)是真核mRNA中最常见的内部修饰。然而,关于其在非小细胞肺癌(NSCLC)中的作用很少。在本研究中,包括来自癌症基因组Atlas(TCGA)数据库的1017名NSCLC患者,其中包括拷贝数变异(CNV)数据。日志秩测试和Cox回归模型用于生存分析。使用Chi-Square测试评估了M6A调节剂和临床病理学特征的关系。 M6a调节剂的改变与T阶段有关。患有任何CNV的调节因子基因的总体存活率比二倍体基因更差。缺失M6A作家基因是差的障碍的独立危险因素,并且效果与橡皮擦基因的拷贝数增益协同作用。脂肪质量和肥胖相关基因(FTO)的高表达与KRA信号相关联。 FTO敲低的M6A含量增加,抑制A549肺癌细胞的增殖。因此,我们首次鉴定了NSCLC中M6A调节因子的遗传变化,并发现这些变化与临床特征不良之间具有重要关系。 FTO在通过减少M6A水平和激活KRA信号来推广NSCLC在推广NSCLC中起着重要作用。

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