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p-4EBP1在人类恶性肿瘤中预后价值的Meta分析。

Meta-analysis of the prognostic value of p-4EBP1 in human malignancies.

作者信息

Zhang Tao, Guo Jianrong, Li Huili, Wang Jiliang

机构信息

Department of Gastrointestinal Surgery, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430022, Hubei, China.

出版信息

Oncotarget. 2017 Dec 7;9(2):2761-2769. doi: 10.18632/oncotarget.23031. eCollection 2018 Jan 5.

Abstract

Phosphorylated 4E-binding protein 1 (p-4EBP1) is the inactivated form of 4EBP1, which is a downstream mediator in the mTOR signaling pathway and a vital factor in the synthesis of some oncogenic proteins. This meta-analysis was conducted to assess the predicative value of p-4EBP1 expression in human malignancies. The PubMed and Embase databases were carefully searched. Articles comparing the prognostic worthiness of different p-4EBP1 levels in human malignancies were collected for pooled analyses and methodologically appraised using the Newcastle-Ottawa Scale (NOS). A total of 39 retrospective cohorts with an overall sample size of 3,980 were selected. Patients with lower p-4EBP1 expression had better 3-year ( < 0.00001), 5-year ( < 0.00001), and 10-year ( = 0.03) overall survival and better 3-year ( < 0.0001) and 5-year ( = 0.0005) disease-free survival. Subgroup analyses confirmed the unfavorable prognosis associated with p-4EBP1 overexpression. These findings were further validated by sensitivity analyses. Harbord and Peters tests revealed no publication bias within the included studies. It thus appears higher expression of p-4EBP1 indicates a poor prognosis in human malignancies.

摘要

磷酸化4E结合蛋白1(p-4EBP1)是4EBP1的失活形式,它是mTOR信号通路中的下游介质,也是某些致癌蛋白合成中的关键因子。本荟萃分析旨在评估p-4EBP1表达在人类恶性肿瘤中的预测价值。我们仔细检索了PubMed和Embase数据库。收集比较人类恶性肿瘤中不同p-4EBP1水平预后价值的文章进行汇总分析,并使用纽卡斯尔-渥太华量表(NOS)进行方法学评估。共选择了39个回顾性队列,总样本量为3980。p-4EBP1表达较低的患者3年(<0.00001)、5年(<0.00001)和10年(=0.03)总生存率更高,3年(<0.0001)和5年(=0.0005)无病生存率更高。亚组分析证实了p-4EBP1过表达与不良预后相关。这些发现通过敏感性分析得到进一步验证。Harbord和Peters检验显示纳入研究中不存在发表偏倚。因此,p-4EBP1表达较高似乎表明人类恶性肿瘤预后较差。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/883d/5788677/819d51e9afa9/oncotarget-09-2761-g001.jpg

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