Correlation between miR-200 Family Overexpression and Cancer Prognosis

被引:13
作者
Liu, Wen [1 ]
Zhang, Kaiping [2 ,3 ]
Wei, Pengfei [4 ,5 ]
Hu, Yue [1 ]
Peng, Yaqin [1 ]
Fang, Xiang [2 ,3 ]
He, Guoping [1 ]
Wu, Limin [1 ]
Chao, Min [2 ,3 ]
Wang, Jing [1 ]
机构
[1] Univ Sci & Technol China, Anhui Prov Hosp, Affiliated Hosp 1, Prenatal Diagnost Ctr,Dept Obstet & Gynecol, Hefei, Anhui, Peoples R China
[2] Anhui Med Univ, Anhui Prov Childrens Hosp, Dept Urol, Hefei, Anhui, Peoples R China
[3] Anhui Med Univ, Childrens Hosp, Hefei, Anhui, Peoples R China
[4] Univ Sci & Technol China, Hefei Natl Lab Phys Sci Microscale, CAS Key Lab Innate Immun & Chron Dis, Innovat Ctr Cell Signaling Network,Sch Life Sci, Hefei, Anhui, Peoples R China
[5] Univ Sci & Technol China, Med Ctr, Hefei, Anhui, Peoples R China
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
DOWN-REGULATION; MESENCHYMAL TRANSITION; CLINICAL-SIGNIFICANCE; PREDICTIVE BIOMARKER; OVARIAN-CANCER; MICRORNA-200C; METASTASIS; MIR-429; METAANALYSIS; EXPRESSION;
D O I
10.1155/2018/6071826
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The correlation between miR-200 family overexpression and cancer prognosis remains controversial. Therefore, we conducted a systematic review and meta-analysis by searching PubMed, Embase, Cochrane Library, China Biology Medicine disc (CBM), and China National Knowledge Infrastructure (CNKI) to identify eligible studies. Hazard ratios (HRs) with 95% confidence intervals (CIs) were calculated to evaluate the strength of the correlations. Additionally, different subgroup analyses and publication bias test were performed. Eventually, we analyzed 23 articles that included five tumor types and 3038 patients. Consequently, high expression of miR-200 family in various tumors was associated with unfavorable overall survival (OS) in both univariate (HR = 1.32, 95% CI: 1.14-1.54, P < 0.001) and multivariate (HR = 1.32, 95% CI: 1.16-1.49, P < 0.001) analyses. Likewise, a similar result was found in different subgroups of the patient source, cancer type, test method, sample source, miR-200 component, and sample size. However, no association of miR-200 family was detected with recurrence- or relapse-free survival (RFS) (univariate: HR 1.02, 95% CI: 0.96-1.09, P = 0.47; multivariate: HR = 1.07, 95% CI: 1.00-1.14, P = 0.07), progression-free survival (PFS) (univariate: HR = 0.96, 95% CI: 0.54-1.70, P = 0.88; multivariate: HR = 1.17, 95% CI: 0.86-1.61, P = 0.32), and disease-free survival (DFS) (univariate: HR = 0.90, 95% CI: 0.74-1.09, P = 0.29; multivariate: HR = 0.98, 95% CI: 0.68-1.41, P = 0.90). Our findings have provided convincing evidence that miR-200 family overexpression suggested poor prognosis of various cancer types, which efforts may raise the potential use of miR-200 family for cancer prognosis in clinical practice.
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页数:16
相关论文
共 52 条
[1]   The functions of animal microRNAs [J].
Ambros, V .
NATURE, 2004, 431 (7006) :350-355
[2]   Circulating miR-200c and miR-141 and outcomes in patients with breast cancer [J].
Antolin, Silvia ;
Calvo, Lourdes ;
Blanco-Calvo, Moises ;
Paz Santiago, Maria ;
Jose Lorenzo-Patino, Maria ;
Haz-Conde, Mar ;
Santamarina, Isabel ;
Figueroa, Angelica ;
Miguel Anton-Aparicio, Luis ;
Valladares-Ayerbes, Manuel .
BMC CANCER, 2015, 15
[3]   PUBLICATION BIAS AND DISSEMINATION OF CLINICAL RESEARCH [J].
BEGG, CB ;
BERLIN, JA .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1989, 81 (02) :107-115
[4]   Human microRNA genes are frequently located at fragile sites and genomic regions involved in cancers [J].
Calin, GA ;
Sevignani, C ;
Dan Dumitru, C ;
Hyslop, T ;
Noch, E ;
Yendamuri, S ;
Shimizu, M ;
Rattan, S ;
Bullrich, F ;
Negrini, M ;
Croce, CM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (09) :2999-3004
[5]  
Cao Q, 2014, INT J CLIN EXP PATHO, V7, P2392
[6]   Regulation of ovarian cancer progression by microRNA-187 through targeting Disabled homolog-2 [J].
Chao, A. ;
Lin, C-Y ;
Lee, Y-S ;
Tsai, C-L ;
Wei, P-C ;
Hsueh, S. ;
Wu, T-I ;
Tsai, C-N ;
Wang, C-J ;
Chao, A-S ;
Wang, T-H ;
Lai, C-H .
ONCOGENE, 2012, 31 (06) :764-775
[7]   MiR-373 drives the epithelial-to-mesenchymal transition and metastasis via the miR-373-TXNIP-HIF1α-TWIST signaling axis in breast cancer [J].
Chen, De ;
Dang, Bian-Li ;
Huang, Jin-zhou ;
Chen, Min ;
Wu, Di ;
Xu, Man-Li ;
Li, Rong ;
Yan, Guang-Rong .
ONCOTARGET, 2015, 6 (32) :32701-32712
[8]   Circulating Plasma MiR-141 Is a Novel Biomarker for Metastatic Colon Cancer and Predicts Poor Prognosis [J].
Cheng, Hanyin ;
Zhang, Lina ;
Cogdell, David E. ;
Zheng, Hong ;
Schetter, Aaron J. ;
Nykter, Matti ;
Harris, Curtis C. ;
Chen, Kexin ;
Hamilton, Stanley R. ;
Zhang, Wei .
PLOS ONE, 2011, 6 (03)
[9]   The Functions of MicroRNA-200 Family in Ovarian Cancer: Beyond Epithelial-Mesenchymal Transition [J].
Choi, Pui-Wah ;
Ng, Shu-Wing .
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2017, 18 (06)
[10]   Dynamic epigenetic regulation of the microRNA-200 family mediates epithelial and mesenchymal transitions in human tumorigenesis [J].
Davalos, V. ;
Moutinho, C. ;
Villanueva, A. ;
Boque, R. ;
Silva, P. ;
Carneiro, F. ;
Esteller, M. .
ONCOGENE, 2012, 31 (16) :2062-2074