Wang Lingling, Zhang Chunze, Qin Litao, Xu Jingyue, Li Xiaobo, Wang Wenhong, Kong Lingqin, Zhou Taizhen, Li Xichuan
School of Basic Medical Sciences, Tianjin Medical University, Tianjin, China.
Tianjin Union Medical Center, Tianjin, China.
Oncotarget. 2017 Aug 3;9(1):1257-1265. doi: 10.18632/oncotarget.19838. eCollection 2018 Jan 2.
Nuclear factor E2-related factor 2 (NRF2), a transcription factor, is known as a potential therapeutic target of solid tumor for that it is a master regulator of the injury and inflammation response, including controlling antioxidant cell progress. Recent studies showed that NRF2 played significant roles in tumorigenesis and tumor progression, however no association and relationship between NRF2 expression and different clinical manifestation of solid tumor had been accurately evaluated. The present meta-analysis picked up 17 suitable articles from EMBASE, PubMed, and ISI Web of Science databases, including 2238 patients. Combined with results of hazard ratios (HRs) and 95% confidence intervals (CIs), we concluded that a higher expression of NRF2 would have worse impact on overall survival (HR = 2.29, 95% CI 1.80-2.91, < 0.05) and disease-free survival (HR = 2.34, 95% CI 1.36-4.00, < 0.05) by a random-effect model. Moreover, further results were positively correlated to the clinical diagnosis, curative effect observation and prognosis, including tumor differentiation, lymph node metastasis, distant metastasis and clinical stage. Consequently, our data shown that NRF2 is a potential poor prognostic factor in a variety of solid tumors.
核因子E2相关因子2(NRF2)是一种转录因子,因其是损伤和炎症反应的主要调节因子,包括控制抗氧化细胞进程,而被认为是实体瘤的潜在治疗靶点。最近的研究表明,NRF2在肿瘤发生和肿瘤进展中发挥着重要作用,然而,NRF2表达与实体瘤不同临床表现之间的关联和关系尚未得到准确评估。本荟萃分析从EMBASE、PubMed和ISI Web of Science数据库中筛选出17篇合适的文章,共纳入2238例患者。结合风险比(HRs)和95%置信区间(CIs)的结果,我们通过随机效应模型得出结论,NRF2的高表达对总生存期(HR = 2.29,95% CI 1.80 - 2.91,P < 0.05)和无病生存期(HR = 2.34,95% CI 1.36 - 4.00,P < 0.05)有更差的影响。此外,进一步的结果与临床诊断、疗效观察和预后呈正相关,包括肿瘤分化、淋巴结转移、远处转移和临床分期。因此,我们的数据表明,NRF2是多种实体瘤潜在的不良预后因素。