Xiao Yu, Zhu Xiang, Gu Yangchun, Chen Sen, Liang Li, Cao Baoshan
Department of Medical Oncology and Radiation Sickness,Peking University Third Hospital, Beijing 100191, China.
Department of Pathology, Peking University Third Hospital, Beijing 100191, China.
Zhongguo Fei Ai Za Zhi. 2018 Mar 20;21(3):241-250. doi: 10.3779/j.issn.1009-3419.2018.03.04.
There are significantly interindividual variations of the expression level of nuclear factor erythroid-2-related factor 2 (Nrf2) and/or Kelch-like ECH-associated protein 1 (Keap1) in our previous studies. It has been proven that Nrf2 or Keap1 is related to resistance of chemotherapeutic drugs and/or epidermal growth factor receptor tyrosine kinase inhibitors (EGFR-TKIs). However, the expression of Nrf2 and Keap1 in lung adenocarcinoma patients with different "driver gene" is not clear. The aim of this study is to investigate the protein expression level of Nrf2 and Keap1 in lung adenocarcinoma and to elucidate the correlation between Nrf2 or Keap1 expression and the status of EGFR gene mutation and to determine the effects of Nrf2 and Keap1 on the patients.
Immunohistochemical analysis of Nrf2 and Keap1 in tumor specimens was performed in a total of 104 lung adenocarcinoma patients with the status of EGFR gene mutations or EGFR wide-type.
The Nrf2 positive rate was 71.2% and Keap1 high expression rate was 34.6% in 104 patients. The Nrf2 positive rate significantly correlated with gender, stage and status of EGFR gene mutation (P<0.05), but not with age, smoking, differentiation and subtype of lung adenocarcinoma (P>0.05). The high expression of Keap1 was not significantly correlated with gender, age, smoking, differentiation, subtype of lung adenocarcinoma and status of EGFR gene mutation (P>0.05). The progression -free survival (PFS) and overall survival (OS) of the patients treated by EGFR-TKIs were significantly correlated with the expression level of Nrf2, but not with Keap1. The PFS and OS of the patients with Nrf2 high expression were significantly shorter than the patients with low/negative expression (P<0.05). Furthermore, Nrf2 high expression was the independent predictive factor for EGFR-TKIs induced PFS and OS (P<0.05).
The Nrf2 positive rate significantly correlated with the status of EGFR gene mutation in lung adenocarcinoma. The Nrf2 high expression significantly correlated with PFS and OS of EGFR-TKIs. Therefore, Nrf2 may be a biomarker for predicting response of EGFR-TKIs and a potential target for overcoming resistance of EGFR-TKIs.
在我们之前的研究中,核因子红细胞2相关因子2(Nrf2)和/或 Kelch样ECH相关蛋白1(Keap1)的表达水平存在显著的个体间差异。已证实Nrf2或Keap1与化疗药物和/或表皮生长因子受体酪氨酸激酶抑制剂(EGFR-TKIs)的耐药性有关。然而,不同“驱动基因”的肺腺癌患者中Nrf2和Keap1的表达情况尚不清楚。本研究旨在探讨肺腺癌中Nrf2和Keap1的蛋白表达水平,阐明Nrf2或Keap1表达与EGFR基因突变状态之间的相关性,并确定Nrf2和Keap1对患者的影响。
对104例具有EGFR基因突变状态或EGFR野生型的肺腺癌患者的肿瘤标本进行Nrf2和Keap1的免疫组织化学分析。
104例患者中,Nrf2阳性率为71.2%,Keap1高表达率为34.6%。Nrf2阳性率与性别、分期及EGFR基因突变状态显著相关(P<0.05),但与年龄、吸烟、肺腺癌的分化程度及亚型无关(P>0.05)。Keap1的高表达与性别、年龄、吸烟、肺腺癌的分化程度、亚型及EGFR基因突变状态均无显著相关性(P>0.05)。接受EGFR-TKIs治疗患者的无进展生存期(PFS)和总生存期(OS)与Nrf2的表达水平显著相关,而与Keap1无关。Nrf2高表达患者的PFS和OS显著短于低表达/阴性表达患者(P<0.05)。此外,Nrf2高表达是EGFR-TKIs诱导的PFS和OS的独立预测因素(P<0.05)。
肺腺癌中Nrf2阳性率与EGFR基因突变状态显著相关。Nrf2高表达与EGFR-TKIs的PFS和OS显著相关。因此,Nrf2可能是预测EGFR-TKIs疗效的生物标志物以及克服EGFR-TKIs耐药的潜在靶点。