A novel 4-gene signature for overall survival prediction in lung adenocarcinoma patients with lymph node metastasis

被引:38
|
作者
Wang, Yanfang [1 ]
Zhang, Quanli [2 ]
Gao, Zhaojia [3 ]
Xin, Shan [1 ,4 ]
Zhao, Yando [5 ]
Zhang, Kai [5 ]
Shi, Run [1 ]
Bao, Xuanwen [6 ,7 ]
机构
[1] Ludwig Maximilians Univ Munchen LMU, D-80539 Munich, Germany
[2] Jiangsu Key Lab Mol & Translat Canc Res, Nanjing 210009, Jiangsu, Peoples R China
[3] Nanjing Med Univ, Affiliated Changzhou Peoples Hosp 2, Dept Thorac Surg, Changzhou 213000, Peoples R China
[4] Helmholtz Ctr Munich, German Res Ctr Environm Hlth, Inst Mol Toxicol & Pharmacol, D-85764 Neuherberg, Germany
[5] Zhejiang Univ, Sir Run Run Shaw Hosp, Dept Cardiol, Sch Med, Hangzhou 310016, Zhejiang, Peoples R China
[6] Helmholtz Ctr Munich, Inst Radiat Biol, German Res Ctr Environm Hlth, D-85764 Neuherberg, Germany
[7] Tech Univ Munich, D-80333 Munich, Germany
关键词
Transcriptome; Lung adenocarcinoma (LUAD); Lymph node metastasis (LNM); mRNA signature; Weighted gene co-expression network analysis (WGCNA); Overall survival (OS); CANCER; EXPRESSION; VALIDATION; LDHA;
D O I
10.1186/s12935-019-0822-1
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Lung adenocarcinoma (LUAD) patients experiencing lymph node metastasis (LNM) always exhibit poor clinical outcomes. A biomarker or gene signature that could predict survival in these patients would have a substantial clinical impact, allowing for earlier detection of mortality risk and for individualized therapy. Methods: With the aim to identify a novel mRNA signature associated with overall survival, we analysed LUAD patients with LNM extracted from The Cancer Genome Atlas (TCGA). LASSO Cox regression was applied to build the prediction model. An external cohort was applied to validate the prediction model. Results: We identified a 4-gene signature that could effectively stratify a high-risk subset of these patients, and time-dependent receiver operating characteristic (tROC) analysis indicated that the signature had a powerful predictive ability. Gene Set Enrichment Analysis (GSEA) showed that the high-risk subset was mainly associated with important cancer-related hallmarks. Moreover, a predictive nomogram was established based on the signature integrated with clinicopathological features. Lastly, the signature was validated by an external cohort from Gene Expression Omnibus (GEO). Conclusion: In summary, we developed a robust mRNA signature as an independent factor to effectively classify LUAD patients with LNM into low- and high-risk groups, which might provide a basis for personalized treatments for these patients.
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页数:9
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