Zhu Wei, Li Guixian, Guo Haina, Chen Honglang, Xu Xiujuan, Long Jiali, Zeng Chao, Wang Xiaojun
Department of Pathology, School of Basic Medicine, Guangdong Medical University, Dongguan, Guangdong Province, China. Email:
Asian Pac J Cancer Prev. 2017 Nov 26;18(11):2903-2909. doi: 10.22034/APJCP.2017.18.11.2903.
Background: Metastasis associated gene 1(MTA1) is one of the most deregulated molecules in human cancer and leads to cancer progression and metastasis. We performed a meta-analysis to determine the correlations between MTA1 expression and the clinicopathological characteristics of non-small cell lung cancer (NSCLC). Methods: We searched PubMed, Springer, Science Direct, Google Scholar and China National Knowledge Infrastructure (CNKI) for relevant articles. For statistical analyses, we used R3.1.1 software. The fixed or random effects model was employed based on the results of the statistical test for homogeneity. Results: Seven studies involving 660 NSCLC patients were included. The proportion of MTA1 overexpression with 95% confidence interval (95% CI) was 0.53(95%CI: 0.43-0.62) in NSCLC patients; 0.47(95%CI: 0.40-0.55) in age <60 years and 0.52(95%CI: 0.34-0.70) in age ≥60 years; 0.5(95%CI: 0.41- 0.62) in males and 0.51(95%CI: 0.39-0.62) in females; 0.59(95%CI: 0.48-0.69) in squamous cell carcinoma (SC) and 0.57(95%CI: 0.46-0.67) in adenocarcinoma (AC); 0.39(95%CI: 0.23-0.56) in well-differentiated tumors, 0.44(95%CI: 0.37-0.51) in moderately differentiated tumors and 0.55(95%CI: 0.37-0.51) in poorly differentiated tumors; 0.48(95%CI: 0.36-0.60) in clinical grade (III-IV) NSCLC and 0.75 (95%CI: 0.69-0.81) in clinical grade (I-II) NSCLC; 0.58(95%CI: 0.45-0.71) in T Stage (T1/T2) NSCLC; 0.68(95%CI: 0.49-0.82) in NSCLC patients with lymph node positivity and 0.51(95%CI: 0.43-0.58) in NSCLC patients with lymph node negativity. Conclusions: These results indicated that MTA1 might be a valuable biomarker in the diagnosis of NSCLC. MTA1 overexpression was significantly associated with age ≥60 years, gender, histopathological type, clinical grade (I-II), T stage (T1/T2) and lymph node positivity in NSCLC patients.
转移相关基因1(MTA1)是人类癌症中失调最严重的分子之一,可导致癌症进展和转移。我们进行了一项荟萃分析,以确定MTA1表达与非小细胞肺癌(NSCLC)临床病理特征之间的相关性。方法:我们在PubMed、Springer、Science Direct、谷歌学术和中国知网(CNKI)上搜索相关文章。进行统计分析时,我们使用了R3.1.1软件。根据同质性统计检验结果采用固定效应或随机效应模型。结果:纳入了7项涉及660例NSCLC患者的研究。NSCLC患者中MTA1过表达的比例及95%置信区间(95%CI)为0.53(95%CI:0.43 - 0.62);年龄<60岁患者中为0.47(95%CI:0.40 - 0.55),年龄≥60岁患者中为0.52(95%CI:0.34 - 0.70);男性中为0.5(95%CI:0.41 - 0.62),女性中为0.51(95%CI:0.39 - 0.62);鳞状细胞癌(SC)中为0.59(95%CI:0.48 - 0.69),腺癌(AC)中为0.57(95%CI:0.46 - 0.67);高分化肿瘤中为0.39(95%CI:0.23 - 0.56),中分化肿瘤中为0.44(95%CI:0.37 - 0.51),低分化肿瘤中为0.55(95%CI:0.37 - 0.51);临床分级(III - IV)的NSCLC患者中为0.48(95%CI:0.36 - 0.60),临床分级(I - II)的NSCLC患者中为0.75(95%CI:0.69 - 0.81);T分期(T1/T2)的NSCLC患者中为0.58(95%CI:0.45 - 0.71);有淋巴结转移的NSCLC患者中为0.68(95%CI:0.49 - 0.82),无淋巴结转移的NSCLC患者中为0.51(95%CI:0.43 - 0.58)。结论:这些结果表明,MTA1可能是NSCLC诊断中有价值的生物标志物。MTA1过表达与NSCLC患者年龄≥60岁、性别、组织病理学类型、临床分级(I - II)、T分期(T1/T2)及淋巴结转移显著相关。