The expression profile and clinic significance of the SIX family in non-small cell lung cancer

被引:62
作者
Liu, Qian [1 ]
Li, Anping [2 ]
Tian, Yijun [1 ]
Liu, Yu [3 ]
Li, Tengfei [2 ]
Zhang, Cuntai [3 ]
Wu, Jennifer D. [4 ]
Han, Xinwei [2 ]
Wu, Kongming [1 ]
机构
[1] Huazhong Univ Sci & Technol, Tongji Med Coll, Tongji Hosp, Dept Oncol, Wuhan 430030, Peoples R China
[2] Zhengzhou Univ, Affiliated Hosp 1, Dept Intervent Radiol, Zhengzhou 450052, Peoples R China
[3] Huazhong Univ Sci & Technol, Tongji Med Coll, Tongji Hosp, Dept Geriatr, Wuhan 430030, Peoples R China
[4] Med Univ South Carolina, Hollings Canc Ctr, Dept Microbiol & Immunol, Charleston, SC USA
来源
JOURNAL OF HEMATOLOGY & ONCOLOGY | 2016年 / 9卷
基金
国家高技术研究发展计划(863计划); 中国国家自然科学基金;
关键词
SIX family genes; Lung cancer; Tumor marker; Prognosis; Meta-analysis; GENE-EXPRESSION; ADJUVANT CHEMOTHERAPY; HOMEOBOX GENES; BREAST-CANCER; TUMOR-GROWTH; SINE-OCULIS; SIX1; ADENOCARCINOMA; SURVIVAL; METAANALYSIS;
D O I
10.1186/s13045-016-0339-1
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: The SIX family homeobox genes have been demonstrated to be involved in the tumor initiation and progression, but their clinicopathological features and prognostic values in non-small cell lung cancer (NSCLC) have not been well defined. We analyzed relevant datasets and performed a systemic review and a meta-analysis to assess the profile of SIX family members in NSCLC and evaluate their importance as biomarkers for diagnosis and prediction of NSCLC. Methods: This meta-analysis included 17 studies with 2358 patients. Hazard ratio (HR) and 95 % confidence interval (CI) were calculated to represent the prognosis of NSCLC with expression of the SIX family genes. Heterogeneity of the ORs and HRs was assessed and quantified using the Cochrane Q and I-2 test. Begg's rank correlation method and Egger's weighted regression method were used to screen for potential publication bias. Bar graphs of representative datasets were plotted to show the correlation between the SIX expression and clinicopathological features of NSCLC. Kaplan-Meier survival curves were used to validate our prognostic analysis by pooled HR. Results: The systematic meta-analysis unveiled that the higher expressions of SIX1-5 were associated with the greater possibility of the tumorigenesis. SIX4 and SIX6 were linked to the lymph node metastasis (LNM). SIX2, SIX3, and SIX4 were correlated with higher TNM stages. Furthermore, the elevated expressions of SIX2, SIX4, and SIX6 predicted poor overall survival (OS) in NSCLC (SIX2: HR = 1.14, 95 % CI, 1.00-1.31; SIX4: HR = 1.39, 95 % CI, 1.16-1.66; SIX6: HR = 1.18, 95 % CI, 1.00-1.38) and poor relapse-free survival (RFS) in lung adenocarcinoma (ADC) (SIX2: HR = 1. 42, 95 % CI, 1.14-1.77; SIX4: HR = 1.52, 95 % CI, 1.09-2.11; SIX6: HR = 1.25, 95 % CI, 1.01-1.56). Conclusions: Our report demonstrated that the SIX family members play distinct roles in the tumorigenesis of NSCLC and can be potential biomarkers in predicting prognosis of NSCLC patients.
引用
收藏
页码:1 / 13
页数:13
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