A robust 6-mRNA signature for prognosis prediction of pancreatic ductal adenocarcinoma

被引:16
作者
Zhou, Chenhao [1 ,2 ]
Zhao, Yue [3 ,4 ]
Yin, Yirui [1 ,2 ]
Hu, Zhiqiu [5 ]
Atyah, Manar [1 ,2 ]
Chen, Wanyong [1 ,2 ,5 ]
Meng, Zhefeng [5 ]
Mao, Huarong [5 ]
Zhou, Qiang [1 ,2 ]
Tang, Weiguo [5 ]
Wang, Pengcheng [5 ]
Li, Zhanming [5 ]
Weng, Jialei [5 ]
Bruns, Christiane [3 ]
Popp, Marie [3 ]
Popp, Felix [3 ]
Dong, Qiongzhu [5 ,6 ]
Ren, Ning [1 ,2 ,5 ]
机构
[1] Fudan Univ, Zhongshan Hosp, Liver Canc Inst, Dept Liver Surg, 180 Fenglin Rd, Shanghai 200032, Peoples R China
[2] Minist Educ, Key Lab Carcinogenesis & Canc Invas, 180 Fenglin Rd, Shanghai 200032, Peoples R China
[3] Univ Hosp Cologne, Dept Gen Visceral & Canc Surg, Cologne, Germany
[4] Otto von Guericke Univ, Dept Surg, Magdeburg, Germany
[5] Fudan Univ, Minhang Hosp, Inst Fudan Minhang Acad Hlth Syst, Shanghai, Peoples R China
[6] Fudan Univ, Inst Biomed Sci, 131 Dongan Rd, Shanghai 200032, Peoples R China
来源
INTERNATIONAL JOURNAL OF BIOLOGICAL SCIENCES | 2019年 / 15卷 / 11期
基金
中国国家自然科学基金;
关键词
Pancreatic ductal adenocarcinoma; molecular signature; survival; MALIGNANT CHARACTER; SIGNALING PATHWAY; CANCER; SURVIVAL; CARCINOMA; INPP4B; ASSOCIATION; BURDEN; GRADE;
D O I
10.7150/ijbs.32899
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Pancreatic ductal adenocarcinoma (PDAC) is one of the most fatal malignancies worldwide. PDAC prognostic and diagnostic biomarkers are still being explored. The aim of this study is to establish a robust molecular signature that can improve the ability to predict PDAC prognosis. 155 overlapping differentially expressed genes between tumor and non-tumor tissues from three Gene Expression Omnibus (GEO) datasets were explored. A least absolute shrinkage and selection operator method (LASSO) Cox regression model was employed for selecting prognostic genes. We developed a 6-mRNA signature that can distinguish high PDAC risk patients from low risk patients with significant differences in overall survival (OS). We further validated this signature prognostic value in three independent cohorts (GEO batch, P < 0.0001; ICGC, P = 0.0036; Fudan, P = 0.029). Furthermore, we found that our signature remained significant in patients with different histologic grade, TNM stage, locations of tumor entity, age and gender. Multivariate cox regression analysis showed that 6-mRNA signature can be an independent prognostic marker in each of the cohorts. Receiver operating characteristic curve (ROC) analysis also showed that our signature possessed a better predictive role of PDAC prognosis. Moreover, the gene set enrichment analysis (GSEA) analysis showed that several tumorigenesis and metastasis related pathways were indeed associated with higher scores of risk. In conclusion, identifying the 6-mRNA signature could provide a valuable classification method to evaluate clinical prognosis and facilitate personalized treatment for PDAC patients. New therapeutic targets may be developed upon the functional analysis of the classifier genes and their related pathways.
引用
收藏
页码:2282 / 2295
页数:14
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