A robust six-gene prognostic signature for prediction of both disease-free and overall survival in non-small cell lung cancer

被引:51
作者
Zuo, Shuguang [1 ,2 ]
Wei, Min [1 ]
Zhang, Hailin [1 ]
Chen, Anxian [1 ]
Wu, Junhua [1 ]
Wei, Jiwu [1 ,3 ]
Dong, Jie [1 ]
机构
[1] Nanjing Univ, Med Sch, Jiangsu Key Lab Mol Med, Nanjing 210093, Jiangsu, Peoples R China
[2] Henan Univ, Huaihe Hosp, Ctr Translat Med, Kaifeng 475001, Henan, Peoples R China
[3] Nanjing Univ, Hightech Inst Suzhou, Suzhou 215123, Peoples R China
基金
中国国家自然科学基金;
关键词
Non-small cell lung cancer; Disease-free survival; Overall survival; Risk score; Prognostic signature; ELDERLY-PATIENTS; EGFR MUTATIONS; KRAS-MUTATION; EARLY-STAGE; EXPRESSION; CDCP1; OUTCOMES; MARKERS; GENES; ADENOCARCINOMA;
D O I
10.1186/s12967-019-1899-y
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
BackgroundThe high mortality of patients with non-small cell lung cancer (NSCLC) emphasizes the necessity of identifying a robust and reliable prognostic signature for NSCLC patients. This study aimed to identify and validate a prognostic signature for the prediction of both disease-free survival (DFS) and overall survival (OS) of NSCLC patients by integrating multiple datasets.MethodsWe firstly downloaded three independent datasets under the accessing number of GSE31210, GSE37745 and GSE50081, and then performed an univariate regression analysis to identify the candidate prognostic genes from each dataset, and identified the gene signature by overlapping the candidates. Then, we built a prognostic model to predict DFS and OS using a risk score method. Kaplan-Meier curve with log-rank test was used to determine the prognostic significance. Univariate and multivariate Cox proportional hazard regression models were implemented to evaluate the influences of various variables on DFS and OS. The robustness of the prognostic gene signature was evaluated by re-sampling tests based on the combined GEO dataset (GSE31210, GSE37745 and GSE50081). Furthermore, a The Cancer Genome Atlas (TCGA)-NSCLC cohort was utilized to validate the prediction power of the gene signature. Finally, the correlation of the risk score of the gene signature and the Gene set variation analysis (GSVA) score of cancer hallmark gene sets was investigated.ResultsWe identified and validated a six-gene prognostic signature in this study. This prognostic signature stratified NSCLC patients into the low-risk and high-risk groups. Multivariate regression and stratification analyses demonstrated that the six-gene signature was an independent predictive factor for both DFS and OS when adjusting for other clinical factors. Re-sampling analysis implicated that this six-gene signature for predicting prognosis of NSCLC patients is robust. Moreover, the risk score of the gene signature is correlated with the GSVA score of 7 cancer hallmark gene sets.ConclusionThis study provided a robust and reliable gene signature that had significant implications in the prediction of both DFS and OS of NSCLC patients, and may provide more effective treatment strategies and personalized therapies.
引用
收藏
页数:16
相关论文
共 53 条
[11]   Exploring TCGA Pan-Cancer Data at the UCSC Cancer Genomics Browser [J].
Cline, Melissa S. ;
Craft, Brian ;
Swatloski, Teresa ;
Goldman, Mary ;
Ma, Singer ;
Haussler, David ;
Zhu, Jingchun .
SCIENTIFIC REPORTS, 2013, 3
[12]   Plk1 overexpression induces chromosomal instability and suppresses tumor development [J].
de Carcer, Guillermo ;
Venkateswaran, Sharavan Vishaan ;
Salgueiro, Lorena ;
El Bakkali, Aicha ;
Somogyi, Kalman ;
Rowald, Konstantina ;
Montanes, Pablo ;
Sanclemente, Manuel ;
Escobar, Beatriz ;
de Martino, Alba ;
McGranahan, Nicholas ;
Malumbres, Marcos ;
Sotillo, Rocio .
NATURE COMMUNICATIONS, 2018, 9
[13]   Validation of a Histology-Independent Prognostic Gene Signature for Early-Stage, Non-Small-Cell Lung Cancer Including Stage IA Patients [J].
Der, Sandy D. ;
Sykes, Jenna ;
Pintilie, Melania ;
Zhu, Chang-Qi ;
Strumpf, Dan ;
Liu, Ni ;
Jurisica, Igor ;
Shepherd, Frances A. ;
Tsao, Ming-Sound .
JOURNAL OF THORACIC ONCOLOGY, 2014, 9 (01) :59-64
[14]   Prognostic value of EGFR and KRAS in circulating tumor DNA in patients with advanced non-small cell lung cancer: a systematic review and meta-analysis [J].
Fan, Gaowei ;
Zhang, Kuo ;
Ding, Jiansheng ;
Li, Jinming .
ONCOTARGET, 2017, 8 (20) :33922-33932
[15]   EGFR mutations as a prognostic and predictive marker in non-small-cell lung cancer [J].
Fang, Shu ;
Wang, Zhehai .
DRUG DESIGN DEVELOPMENT AND THERAPY, 2014, 8 :1595-1611
[16]   Expression, prognostic and predictive impact of VEGF and bFGF in non-small cell lung cancer [J].
Farhat, Fadi S. ;
Tfayli, Arafat ;
Fakhruddin, Najla ;
Mahfouz, Rami ;
Otrock, Zaher K. ;
Alameddine, Raafat S. ;
Awada, Ahmad H. ;
Shamseddine, Ali .
CRITICAL REVIEWS IN ONCOLOGY HEMATOLOGY, 2012, 84 (02) :149-160
[17]   Age alone is not a predictor for survival in glioblastoma [J].
Gately, Lucy ;
Collins, Anna ;
Murphy, Michael ;
Dowling, Anthony .
JOURNAL OF NEURO-ONCOLOGY, 2016, 129 (03) :479-485
[18]   The IASLC lung cancer staging project: Proposals for the revision of he TNM stage groupings in the forthcoming (seventh) edition of the TNM classification of malignant tumours [J].
Goldstraw, Peter ;
Crowley, John ;
Chansky, Kari ;
Giroux, Dorothy J. ;
Groome, Patti A. ;
Rami-Porta, Ramon ;
Postmus, Pieter E. ;
Rusch, Valerie ;
Sobin, Leslie .
JOURNAL OF THORACIC ONCOLOGY, 2007, 2 (08) :706-714
[19]   KRAS Mutation in Patients with Lung Cancer: A Predictor for Poor Prognosis but Not for EGFR-TKIs or Chemotherapy [J].
Guan, Ji-lin ;
Zhong, Wen-zhao ;
An, She-juan ;
Yang, Jin-ji ;
Su, Jian ;
Chen, Zhi-hong ;
Yan, Hong-hong ;
Chen, Zhi-yong ;
Huang, Zhi-min ;
Zhang, Xu-chao ;
Nie, Qiang ;
Wu, Yi-long .
ANNALS OF SURGICAL ONCOLOGY, 2013, 20 (04) :1381-1388
[20]   Mitotic Spindle Assembly and Genomic Stability in Breast Cancer Require PI3K-C2α Scaffolding Function [J].
Gulluni, Federico ;
Martini, Miriam ;
De Santis, Maria Chiara ;
Campa, Carlo Cosimo ;
Ghigo, Alessandra ;
Margaria, Jean Piero ;
Ciraolo, Elisa ;
Franco, Irene ;
Ala, Ugo ;
Annaratone, Laura ;
Disalvatore, Davide ;
Bertalot, Giovanni ;
Viale, Giuseppe ;
Noatynska, Anna ;
Compagno, Mara ;
Sigismund, Sara ;
Montemurro, Filippo ;
Thelen, Marcus ;
Fan, Fan ;
Meraldi, Patrick ;
Marchio, Caterina ;
Pece, Salvatore ;
Sapino, Anna ;
Chiarle, Roberto ;
Di Fiore, Pier Paolo ;
Hirsch, Emilio .
CANCER CELL, 2017, 32 (04) :444-+