Wang Xiyong, Zhu Xiaoli, Zhang Hongming, Fan Xiaobo, Xue Xiulei, Chen Yan, Ding Chenbo, Zhao Jianwen, Wu Guoqiu
Medical school of Southeast University, Nanjing 210009, China.
Department of Respiratory Medicine, Zhongda Hospital, Southeast University, Nanjing, 210009, China.
J Cancer. 2017 Aug 23;8(14):2846-2853. doi: 10.7150/jca.19897. eCollection 2017.
To develop a qPCR method to examine the 202 isoform of excision repair cross-complementation group 1 (ERCC1_202) and to evaluate its clinical utility as a predictive biomarker for platinum-based chemotherapy in non-small cell lung cancer (NSCLC). The relative complementary DNA (cDNA) quantification for ERCC1_202 was conducted using a fluorescence-based, real-time detection method and β-actin was used as a reference gene. : A strong correlation was observed between ERCC1_202 mRNA and ERCC1 mRNA levels in NSCLC cells ( < 0.001). 28 patients completed this research. Our results implied that as ERCC1_202 levels increased, the risk of progression (HR = 4.296, = 0.011) and death (HR = 6.503, = 0.001) increased. At multivariate analysis, high expression of ERCC1_202 was shown to be an independent predictive factor for time to progression ( = 0.047), and progression-free survival ( = 0.014). However, the high expression of ERCC1_202 was not an independent predictive factor for response ( = 0.324). : This study suggests that the efficacy of platinum-based chemotherapy can be improved when customized according to the expression of ERCC1_202.
开发一种定量聚合酶链反应(qPCR)方法来检测切除修复交叉互补基因1(ERCC1)的202异构体(ERCC1_202),并评估其作为非小细胞肺癌(NSCLC)铂类化疗预测生物标志物的临床应用价值。使用基于荧光的实时检测方法对ERCC1_202进行相对互补脱氧核糖核酸(cDNA)定量,并将β-肌动蛋白用作参照基因。在NSCLC细胞中,观察到ERCC1_202信使核糖核酸(mRNA)与ERCC1 mRNA水平之间存在强相关性(<0.001)。28例患者完成了本研究。我们的结果表明,随着ERCC1_202水平升高,进展风险(风险比[HR]=4.296,P=0.011)和死亡风险(HR=6.503,P=0.001)增加。在多变量分析中,ERCC1_202高表达被证明是进展时间(P=0.047)和无进展生存期(P=0.014)的独立预测因素。然而,ERCC1_202高表达不是反应的独立预测因素(P=0.324)。本研究表明,根据ERCC1_202的表达定制铂类化疗方案可提高疗效。