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活化的p-AKT分子在各种血液系统恶性肿瘤和实体瘤中的预后作用:一项荟萃分析

Prognostic Role of the Activated p-AKT Molecule in Various Hematologic Malignancies and Solid Tumors: A Meta-Analysis.

作者信息

Yao Zhen, Gao Guangyu, Yang Jiawen, Long Yuming, Wang Zhenzhen, Hu Wentao, Liu Yulong

机构信息

Department of Nuclear Accident Medical Emergency, The Second Affiliated Hospital of Soochow University, Suzhou, China.

Department of Ultrasound, Xingtang Hospital, Suzhou, China.

出版信息

Front Oncol. 2020 Dec 10;10:588200. doi: 10.3389/fonc.2020.588200. eCollection 2020.

Abstract

Cancer is one of the main causes of human death worldwide. Recently, many studies have firmly established the causal relationship between oxidative stress and cancer initiation and progression. As a key protein in PI3K/Akt signaling pathway, p-AKT (phosphorylated Akt) participates in the process of oxidative stress and plays a prognostic role in various hematologic tumors and solid tumors. We conducted a comprehensive search of the PubMed, Embase and Cochrane libraries to identify studies published in the past decade involving cancer patients expressing p-AKT that reported overall survival (OS) during follow-up. In this study, 6,128 patients in total were evaluated from 29 enrolled articles, and we concluded that overexpression of p-AKT was closely related to worse OS in cancer patients with a hazard ratio (HR) of 2.33 (95% CI: 1.67-4.00). Furthermore, we conducted a subgroup analysis, and the results indicated that overexpression of p-AKT was associated with worse OS in hematological tumor (HR: 1.64, 95% CI: 1.41-1.92), and solid tumor (HR: 2.44, 95% CI: 1.61-5.26). High expression of p-AKT is related to poor prognosis of various hematologic tumors and solid tumors.

摘要

癌症是全球人类死亡的主要原因之一。最近,许多研究已确凿地证实了氧化应激与癌症发生和发展之间的因果关系。作为PI3K/Akt信号通路中的一种关键蛋白,p-AKT(磷酸化Akt)参与氧化应激过程,并在各种血液肿瘤和实体瘤中发挥预后作用。我们全面检索了PubMed、Embase和Cochrane数据库,以识别过去十年发表的涉及表达p-AKT的癌症患者的研究,这些研究报告了随访期间的总生存期(OS)。在本研究中,共从29篇纳入文章中评估了6128例患者,我们得出结论,p-AKT过表达与癌症患者较差的总生存期密切相关,风险比(HR)为2.33(95%CI:1.67-4.00)。此外,我们进行了亚组分析,结果表明,p-AKT过表达与血液肿瘤(HR:1.64,95%CI:1.41-1.92)和实体瘤(HR:2.44,95%CI:1.61-5.26)较差的总生存期相关。p-AKT的高表达与各种血液肿瘤和实体瘤的不良预后相关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/203a/7758503/b9cfdae5418c/fonc-10-588200-g001.jpg

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