Association of Telomerase Reverse Transcriptase Promoter Mutations with the Prognosis of Glioma Patients: a Meta-Analysis
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  • 作者:Xiaogang Wang ; Xiaoming Li ; Feng Xu ; Youqian Zhang ; Hongwei Liu…
  • 关键词:TERT promoter mutation ; Gliomas ; Survival
  • 刊名:Molecular Neurobiology
  • 出版年:2016
  • 出版时间:May 2016
  • 年:2016
  • 卷:53
  • 期:4
  • 页码:2726-2732
  • 全文大小:513 KB
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  • 作者单位:Xiaogang Wang (1)
    Xiaoming Li (1)
    Feng Xu (1)
    Youqian Zhang (1)
    Hongwei Liu (2)
    Yingqun Tao (1)

    1. Department of Neurosurgery, General Hospital of Shenyang Military Area Command, Shenyang, 110840, China
    2. Department of Neuroscience, Xiangya Hospital, Central South University, Changsha, 410008, China
  • 刊物主题:Neurosciences; Neurobiology; Cell Biology; Neurology;
  • 出版者:Springer US
  • ISSN:1559-1182
文摘
Previous studies have found that telomerase reverse transcriptase (TERT) has vital roles in the development of malignant diseases including glioma. The occurrence of TERT promoter mutations in gliomas is frequent. So far, several studies on the association between TERT promoter mutations and prognosis of gliomas had been published, but the conclusion was still not uncertain. The aim of the present meta-analysis was to assess the association between TERT promoter mutations and survival of glioma patients by pooling data from published studies. PubMed, Embase, and Web of Science were searched for articles on the association between TERT promoter mutations and survival of glioma patients until June 30, 2015. Hazard ratios (HR) and the 95 % confidence intervals (CIs) were utilized to analyze the prognosis of glioma patients with TERT promoter mutations. Heterogeneity of included studies was assessed using Cochrane’s Q test and I 2 method. Eleven studies with a total of 3,444 glioma patients were finally included into the meta-analysis. Nine studies reported the HRs adjusting for other confounding factors. Meta-analysis of total 11 studies suggested that TERT promoter mutations were significantly associated with worse prognosis of patients with gliomas (HR = 2.07, 95 % CI = 1.58–2.71, P < 0.00001). Meta-analysis of nine studies with adjusted outcomes suggested that TERT promoter mutations were independently associated with worse prognosis of patients with gliomas (HR = 2.28, 95 % CI = 1.72–3.01, P < 0.00001). In conclusion, TERT promoter mutation is a promising biomarker for predicting worse prognosis for patients with gliomas. More prospective well-designed cohort studies are needed to further validate its prognostic role in gliomas.

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