Expression Status and Prognostic Value of m6A RNA Methylation Regulators in Lung Adenocarcinoma

被引:6
作者
Li, Xiuhong [1 ]
Feng, Zian [1 ]
Wang, Rui [2 ]
Hu, Jie [1 ]
He, Xiaodong [3 ]
Shen, Zuojun [1 ,2 ]
机构
[1] Univ Sci & Technol China, Affiliated Hosp 1, Dept Clin Lab, Div Life Sci & Med, Hefei 230001, Peoples R China
[2] Anhui Med Univ, Anhui Prov Hosp, Dept Clin Lab, Hefei 230001, Peoples R China
[3] Anhui Prov Ctr Clin Labs, Hefei 230001, Peoples R China
来源
LIFE-BASEL | 2021年 / 11卷 / 07期
关键词
m(6)A methylation; lung adenocarcinoma; prognostic signature; survival analysis; HEPATOCELLULAR-CARCINOMA; CANCER; GROWTH; CLASSIFICATION; TRANSLATION; SUPPRESSES; PROTEIN; GENES;
D O I
10.3390/life11070619
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
N-6-methyladenosine (m(6)A) RNA modification is the most abundant modification method in mRNA, and it plays an important role in the occurrence and development of many cancers. This paper mainly discusses the role of m(6)A RNA methylation regulators in lung adenocarcinoma (LUAD) to identify novel prognostic biomarkers. The gene expression data of 19 m(6)A methylation regulators in LUAD patients and its relevant clinical parameters were extracted from The Cancer Genome Atlas (TCGA) database. We selected three significantly differentially expressed m(6)A regulators in LUAD to construct the risk signature, and evaluated its prognostic prediction efficiency using the receiver operating characteristic (ROC) curve. Kaplan-Meier survival analysis and Cox regression analysis were used to identify the independent prognostic significance of the risk signature. The ROC curve indicated that the area under the curve (AUC) was 0.659, which means that the risk signature had a good prediction efficiency. The results of the Kaplan-Meier survival analysis and Cox regression analysis showed that the risk score can be used as an independent prognostic factor for LUAD. In addition, we explored the differential signaling pathways and cellular processes related to m(6)A methylation regulators in LUAD.
引用
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页数:13
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