Prognostic role of the long non-coding RNA, SPRY4 Intronic Transcript 1, in patients with cancer: a meta-analysis

被引:12
作者
Wang, Miaojuan [1 ]
Dong, Xuejun [1 ]
Feng, Yi [1 ]
Sun, Honggang [1 ]
Shan, Ningping [1 ]
Lu, Tao [1 ]
机构
[1] Zhejiang Univ, Shaoxing Hosp, Shaoxing Peoples Hosp, Clin Lab Ctr, Shaoxing, Peoples R China
关键词
lncRNA; SPRY4-IT1; prognosis; overall survival; meta-analysis; PREDICTS POOR-PROGNOSIS; LYMPH-NODE METASTASIS; PROMOTES TUMORIGENESIS; CELL-PROLIFERATION; UP-REGULATION; SPRY4-IT1; EXPRESSION; APOPTOSIS; BIOMARKER; SURVIVAL;
D O I
10.18632/oncotarget.16735
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Recent studies have emphasized the important role of long non-coding RNAs (lncRNAs) in cancer development. The present study performed a meta-analysis to investigate whether lncRNA, SPRY4 Intronic Transcript 1(SPRY4-IT1) can be served as a potential biomarker for prognosis in human cancers. The eligible studies were collected by searching multiple online databases (Pubmed, EMBASE, CNKI, Web of Science and Google Scholar) and meta-analysis was performed to explore the association between the expression levels of SPRY4-IT1 and overall survival (OS), disease-free survival (DFS) and clinicopathological parameters. A total of 1329 patients from 13 studies were included for meta-analysis. The meta-analysis results showed that high expression level of SPRY4-IT1 was significantly associated with shorter OS in cancer patients (HR = 3.20, 95% CI: 2.59-3.90, P<0.001) except in the patients with non-small cell lung cancer (NSCLC). Increased SPRY4-IT1 expression level was correlated with shorter DFS in patients with gastric cancer and ovarian cancer. SPRY4-IT1 expression level was not correlated with the clinicopathological parameters including age (P = 0.37), gender (P = 0.87), tumor size (P = 0.47) and invasion depth (P = 0.52), and increased SPRY4-IT1 expression level was significantly associated with distant metastasis (odds ratio (OR) = 1.96, 95% CI: 1.24-3.08, P = 0.004), lymph node metastasis (OR = 3.96, 95% CI: 1.48-5.54, P<0.001), advanced tumor/node/metastasis stage (OR = 3.72, 95% CI = 2.91-4.76, P<0.001) and poor tumor differentiation (OR = 1.86, 95% CI = 1.35-2.58, P<0.001) in cancer patients except in patients with NSCLC. In summary, the meta-analysis results suggested that increased expression level of SPRY4-IT1 was positively associated with unfavorable prognosis and advanced features of cancers in cancer patients but not in patients with NSCLC.
引用
收藏
页码:33713 / 33724
页数:12
相关论文
共 37 条
[1]  
[Anonymous], MOL BIOSYSTEMS
[2]  
[Anonymous], J CANC RES CLIN ONCO
[3]   Long noncoding RNA SPRY4-IT1 promotes malignant development of colorectal cancer by targeting epithelial-mesenchymal transition [J].
Cao, Dong ;
Ding, Qiong ;
Yu, Wubin ;
Gao, Ming ;
Wang, Yilian .
ONCOTARGETS AND THERAPY, 2016, 9 :5417-5425
[4]   Upregulation of long noncoding RNA SPRY4-IT1 correlates with tumor progression and poor prognosis in cervical cancer [J].
Cao, Yang ;
Liu, Yinglei ;
Lu, Xiaoyan ;
Wang, Ying ;
Qiao, Haifeng ;
Liu, Manhua .
FEBS OPEN BIO, 2016, 6 (09) :954-960
[5]  
Chen T, 2016, MINERVA MED, V107, P251
[6]   Long noncoding RNA SPRY4-IT1 promotes esophageal squamous cell carcinoma cell proliferation, invasion, and epithelial-mesenchymal transition [J].
Cui, Fei ;
Wu, Duoguang ;
He, Xiaotian ;
Wang, Wenjian ;
Xi, Jingle ;
Wang, Minghui .
TUMOR BIOLOGY, 2016, 37 (08) :10871-10876
[7]   Prognostic Value of Long Non-Coding RNA HOTAIR in Various Cancers [J].
Deng, Qiwen ;
Sun, Huiling ;
He, Bangshun ;
Pan, Yuqin ;
Gao, Tianyi ;
Chen, Jie ;
Ying, Houqun ;
Liu, Xian ;
Wang, Feng ;
Xu, Yong ;
Wang, Shukui .
PLOS ONE, 2014, 9 (10)
[8]  
Elkholi R, 2014, CANCER METAB, V2, DOI 10.1186/2049-3002-2-16
[9]   Role of long noncoding RNA UCA1 as a common molecular marker for lymph node metastasis and prognosis in various cancers: a meta-analysis [J].
He, Anbang ;
Hu, Rong ;
Chen, Zhicong ;
Liao, Xinhui ;
Li, Jianfa ;
Wang, Dailian ;
Lv, Zhaojie ;
Liu, Yuchen ;
Wang, Feng ;
Mei, Hongbing .
ONCOTARGET, 2017, 8 (01) :1937-1943
[10]  
Jemal A, 2009, CA-CANCER J CLIN, V59, P225, DOI [10.3322/caac.20006, 10.3322/caac.21254, 10.3322/caac.21332, 10.3322/caac.21551, 10.3322/caac.20073, 10.3322/caac.21387, 10.3322/caac.21654, 10.3322/caac.21601]