Identification of BTG1 Status in Solid Cancer for Future Researches Using a System Review and Meta-analysis

被引:2
作者
Chen, Xiu-qiong [1 ]
Meng, Fan-qiao [2 ]
Xiong, Hua [1 ]
Wang, Ya-li [1 ]
Tang, Wen-hua [1 ]
Zhou, Yang-mei [1 ]
Zou, Yan-mei [1 ]
机构
[1] Huazhong Univ Sci & Technol, Tongji Med Coll, Tongji Hosp, Ctr Canc, Wuhan 430030, Peoples R China
[2] Tianjin Med Univ, Tianjin, Peoples R China
关键词
solid tumor; B-cell translocation gene 1 protein; prognosis; CELL TRANSLOCATION GENE-1; GASTRIC-CANCER; EXPRESSION; CARCINOMA; APOPTOSIS; PATHOGENESIS; MACROPHAGES; PROGRESSION; INDUCTION; INDICATOR;
D O I
10.1007/s11596-020-2150-z
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
Abundant studies have been conducted to identify how B-cell translocation gene 1 protein (BTG1) gene affects the differentiation, proliferation, metastasis of cancer cells, and how it further regulates the generation or development of diseases to influence the prognosis of patients. However, the data from single research were not powerful enough. The correlations between BTG1 expression and mechanisms of tumorigenesis or prognosis of patients are still in controversial. Our system review and meta-analysis provided a complete explanation about the association between BTG1 expression and clinicopathological features or prognosis of patients, which further laid a foundation for future research on BTG1. Fifteen eligible studies consisting of 1992 participants were included. We uncovered that BTG1 expression in solid tumors was associated with lymph node status (RR=0.66, 95% CI: 0.58-0.75, P=0.142), TMN stage status (RR=2.13, 95% CI: 1.71-2.65, P=0.001), T category (RR=1.90, 95% CI: 1.20-3.00, P=0.000), histological differentiation (RR=1.91, 95% CI: 1.55-2.37, P=0.012), vascular invasion (RR=0.90, 95% CI: 0.57-1.41, P=0.001). BTG1 low expression was significantly associated with overall survival (OS) (HR=0.47, 95% CI: 0.38-0.67, P=0.000). It concluded that BTG1 possessed the potential value for future research and could be recommended as a significant biomarker in solid tumor.
引用
收藏
页码:85 / 94
页数:10
相关论文
共 46 条
[1]  
[Anonymous], 2017, HELICOBACTER
[2]   Interaction of PRMT1 with BTG/TOB proteins in cell signalling:: molecular analysis and functional aspects [J].
Berthet, C ;
Guéhenneux, F ;
Revol, V ;
Samarut, C ;
Lukaszewicz, A ;
Dehay, C ;
Dumontet, C ;
Magaud, JP ;
Rouault, JP .
GENES TO CELLS, 2002, 7 (01) :29-39
[3]   Gastric Cancer: Clinical Aspects, Epidemiology and Molecular Background [J].
Bornschein, Jan ;
Rokkas, Theodore ;
Selgrad, Michael ;
Malfertheiner, Peter .
HELICOBACTER, 2011, 16 :45-52
[4]   Quantifying, displaying and accounting for heterogeneity in the meta-analysis of RCTs using standard and generalised Q statistics [J].
Bowden, Jack ;
Tierney, Jayne F. ;
Copas, Andrew J. ;
Burdett, Sarah .
BMC MEDICAL RESEARCH METHODOLOGY, 2011, 11
[5]  
Bray F, 2018, CA-CANCER J CLIN, V68, P394, DOI [10.3322/caac.21492, 10.3322/caac.21609]
[6]   Repression by oxidative stress of NOS and cytokine gene induction in macrophages results from AP-1 and NF-κB inhibition mediated by B cell translocation gene-1 activation [J].
Cho, IJ ;
Lee, AK ;
Lee, SJ ;
Lee, MG ;
Kim, SG .
FREE RADICAL BIOLOGY AND MEDICINE, 2005, 39 (11) :1523-1536
[7]   Identification of B-cell translocation gene 1 as a biomaker for monitoring the remission of acute myeloid leukemia [J].
Cho, JW ;
Kim, JJ ;
Park, SG ;
Lee, DH ;
Lee, SC ;
Kim, HJ ;
Park, BC ;
Cho, SY .
PROTEOMICS, 2004, 4 (11) :3456-3463
[8]   THE COMPARISON OF PERCENTAGES IN MATCHED SAMPLES [J].
COCHRAN, WG .
BIOMETRIKA, 1950, 37 (3-4) :256-266
[9]  
Cortes U, 2000, MOL CARCINOGEN, V27, P57, DOI 10.1002/(SICI)1098-2744(200002)27:2<57::AID-MC1>3.0.CO
[10]  
2-I