Integrative analysis of miRNA and mRNA expression profiles reveals a novel mRNA/miRNA signature to improve risk classification for patients with gastric cancer

被引:3
作者
Yin, Xiang [1 ]
Zhang, Fumin [1 ]
Guo, Zhongwu [1 ]
Kong, Weiyuan [1 ]
Wang, Yuanyuan [2 ]
机构
[1] Daqing Oilfield Gen Hosp, Dept Minimally Invas Tumor Surg, Daqing, Peoples R China
[2] Daqing Long Nan Hosp, Dept Gastroenterol, 35 Patriotism Rd, Daqing 163453, Heilongjiang, Peoples R China
关键词
gastric cancer; mRNA expression profiles; microRNA expression profiles; signature; prognosis; MICRORNA DYSREGULATION; SURVIVAL; PROGNOSIS; RECURRENCE; BIOMARKERS; DISCOVERY;
D O I
10.3892/ol.2019.10536
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Gastric cancer (GC) is one of the most common types of malignant cancer and is associated with poor prognosis. Although the prognosis of patients with GC is associated with grade, stage and lymph node metastases, these traditional clinical features are inadequate to predict the outcome of GC. Therefore, there has been an increased focus on identifying novel molecular biomarkers for early diagnosis and prognosis, in order to improve outcomes in GC. In the present study, an integrative analysis of microRNA (miRNA) expression profiles, mRNA expression profiles and clinical characteristics was performed in a large cohort of patients with GC in order to identify an integrative prognostic model for improving postoperative risk classification. An integrative mRNA/miRNA signature (IMMIS), comprised of three miRNAs and one mRNA, was identified from a large number of differentially expressed miRNAs and mRNAs using univariate and multivariate Cox regression analysis. The prognostic value of the IMMIS was validated in the discovery cohort, testing cohort and The Cancer Genome Atlas (TCGA) cohort. The present results suggested that the identified signature had a reliable predictive performance and could classify the patients into high- and low-risk groups with significantly different overall survival times. In the discovery cohort, the hazard ratio (HR) was 2.805 with a 95% CI=1.722-4.567 (P<0.001). The median overall survival time as 1.49 vs. 3.85 years. In the testing cohort, the HR was 1.625 with a 95% CI=1.004-2.638 (P=0.039) and the median overall survival time was 2.17 vs. 4.62 years. In the TCGA cohort, the HR was 2.139 with a 95% CI=1.519-3.012 (P<0.001) and the median overall survival time was 1.53 vs. 4.62 years. The IMMIS constituted a reliable independent prognostic factor compared with clinical covariates, including age, sex, grade and stage, as indicated by multivariate and stratified analyses. Furthermore, comparative analysis revealed that the predictive value of the IMMIS was superior to the mRNA-based signature alone. The present results suggested the potential value of the IMMIS as a promising novel biomarker for improving the clinical management of patients with GC.
引用
收藏
页码:2330 / 2339
页数:10
相关论文
共 38 条
[1]   An Integrative Model of miRNA and mRNA Expression Signature for Patients of Breast Invasive Carcinoma with Radiotherapy Prognosis [J].
Bing, Zhitong ;
Tian, Jinhui ;
Zhang, Jingyun ;
Li, Xiuxia ;
Wang, Xiaohu ;
Yang, Kehu .
CANCER BIOTHERAPY AND RADIOPHARMACEUTICALS, 2016, 31 (07) :253-260
[2]   Gene expression profile predicts patient survival of gastric cancer after surgical resection [J].
Chen, CN ;
Lin, JJ ;
Chen, JJW ;
Lee, PH ;
Yang, CY ;
Kuo, ML ;
Chang, KJ ;
Hsieh, FJ .
JOURNAL OF CLINICAL ONCOLOGY, 2005, 23 (29) :7286-7295
[3]   Cancer Statistics in China, 2015 [J].
Chen, Wanqing ;
Zheng, Rongshou ;
Baade, Peter D. ;
Zhang, Siwei ;
Zeng, Hongmei ;
Bray, Freddie ;
Jemal, Ahmedin ;
Yu, Xue Qin ;
He, Jie .
CA-A CANCER JOURNAL FOR CLINICIANS, 2016, 66 (02) :115-132
[4]   MicroRNA-184 inhibits cell proliferation and invasion, and specifically targets TNFAIP2 in Glioma [J].
Cheng, Zhe ;
Wang, Hang Zhou ;
Li, Xuetao ;
Wu, Zhiwu ;
Han, Yong ;
Li, Yanyan ;
Chen, Guilin ;
Xie, Xueshun ;
Huang, Yulun ;
Du, Ziwei ;
Zhou, Youxin .
JOURNAL OF EXPERIMENTAL & CLINICAL CANCER RESEARCH, 2015, 34
[5]   Molecular classification of gastric cancer [J].
Chia, N. -Y. ;
Tan, P. .
ANNALS OF ONCOLOGY, 2016, 27 (05) :763-769
[6]   Gene Expression Signature-Based Prognostic Risk Score in Gastric Cancer [J].
Cho, Jae Yong ;
Lim, Jae Yun ;
Cheong, Jae Ho ;
Park, Yun-Yong ;
Yoon, Se-Lyun ;
Kim, Soo Mi ;
Kim, Sang-Bae ;
Kim, Hoguen ;
Hong, Soon Won ;
Park, Young Nyun ;
Noh, Sung Hoon ;
Park, Eun Sung ;
Chu, In-Sun ;
Hong, Waun Ki ;
Ajani, Jaffer A. ;
Lee, Ju-Seog .
CLINICAL CANCER RESEARCH, 2011, 17 (07) :1850-1857
[7]   A novel microRNA signature predicts survival in stomach adenocarcinoma [J].
Ding, Bowen ;
Gao, Xujie ;
Li, Hui ;
Liu, Liren ;
Hao, Xishan .
ONCOTARGET, 2017, 8 (17) :28144-28153
[8]  
Guo LY, 2017, ONCOTARGET, V8, P68483, DOI 10.18632/oncotarget.19590
[9]   Gastric cancer: Classification, histology and application of molecular pathology [J].
Hu, Bing ;
El Hajj, Nassim ;
Sittler, Scott ;
Lammert, Nancy ;
Barnes, Robert ;
Meloni-Ehrig, Aurelia .
JOURNAL OF GASTROINTESTINAL ONCOLOGY, 2012, 3 (03) :251-261
[10]   Current perspectives toward the identification of key players in gastric cancer microRNA dysregulation [J].
Ishimoto, Takatsugu ;
Baba, Hideo ;
Izumi, Daisuke ;
Sugihara, Hidetaka ;
Kurashige, Junji ;
Iwatsuki, Masaaki ;
Tan, Patrick .
INTERNATIONAL JOURNAL OF CANCER, 2016, 138 (06) :1337-1349