Wang June, Du Shenlin, Fan Wei, Wang Ping, Yang Weiqing, Yu Mingxia
Department of Clinical Laboratory & Center for Gene Diagnosis, Zhongnan Hospital of Wuhan University, Wuhan 430071, China.
Guangdong Provincial Key Laboratory of Medical Molecular Diagnostics, Guangdong Medical University, Dongguan 523808, China.
Oncotarget. 2017 Aug 24;8(43):75516-75527. doi: 10.18632/oncotarget.20466. eCollection 2017 Sep 26.
Recent studies have showed that the transforming acidic coiled coil 3 (TACC3), was aberrantly up-regulated in various solid tumors and was reported to be correlated with unfavorable prognosis in cancer patients. This study aimed to examine the relationship between TACC3 and relevant clinical outcomes. Pubmed, Web of Science, Embase and Cochrane Library were systematically searched to obtain all eligible articles. Pooled hazard ratios (HRs) and 95% confidence intervals (CIs) were calculated to evaluate the influence of TACC3 expression on overall survival (OS) and disease-free survival (DFS) in solid tumors patients. A total of 1943 patients from 11 articles were included. The result indicated that a significantly shorter OS was observed in patients with high expression level of TACC3 (HR=1.90, 95% CI=1.63-2.23). In the subgroup analysis, the association was also observed in patients with cancers of digestive system (HR=1.85, 95% CI=1.53-2.24). Statistical significance was also observed in subgroup meta-analysis stratified by the cancer type, analysis type and sample size. Furthermore, poorer DFS was observed in patients with high expression level of TACC3 (HR=2.67, 95% CI=2.10-3.40). Additionally, the pooled odds ratios (ORs) showed that increased TACC3 expression was also related to positive lymph node metastasis (OR=1.68, 95% CI=1.26-2.25), tumor differentiation (OR=1.90, 95% CI=1.25-2.88) and TNM stage (OR=1.66, 95% CI=1.25-2.20). In conclusion, the increased expression level of TACC3 was associated with unfavorable prognosis, suggesting that it was a valuable prognosis biomarker or a promising therapeutic target of solid tumors. Further studies should be conducted to confirm the clinical utility of TACC3 in human solid tumors.
近期研究表明,转化酸性卷曲螺旋蛋白3(TACC3)在多种实体瘤中异常上调,且据报道与癌症患者的不良预后相关。本研究旨在探讨TACC3与相关临床结局之间的关系。通过系统检索PubMed、科学网、Embase和Cochrane图书馆,获取所有符合条件的文章。计算合并风险比(HRs)和95%置信区间(CIs),以评估TACC3表达对实体瘤患者总生存期(OS)和无病生存期(DFS)的影响。共纳入来自11篇文章的1943例患者。结果表明,TACC3高表达患者的OS显著缩短(HR=1.90,95%CI=1.63-2.23)。在亚组分析中,消化系统癌症患者也观察到这种关联(HR=1.85,95%CI=1.53-2.24)。在按癌症类型、分析类型和样本量分层的亚组Meta分析中也观察到统计学意义。此外,TACC3高表达患者的DFS较差(HR=2.67,95%CI=2.10-3.40)。此外,合并优势比(ORs)表明,TACC3表达增加还与阳性淋巴结转移(OR=1.68,95%CI=1.26-2.25)、肿瘤分化(OR=1.90,95%CI=1.25-2.88)和TNM分期(OR=1.66,95%CI=1.25-2.20)相关。总之,TACC3表达水平升高与不良预后相关,表明它是实体瘤有价值的预后生物标志物或有前景的治疗靶点。应进一步开展研究以证实TACC3在人类实体瘤中的临床应用价值。