ERCC1_202 Is A Prognostic Biomarker in Advanced Stage Non-Small Cell Lung Cancer Patients Treated with Platinum-Based Chemotherapy

被引:8
作者
Wang, Xiyong [1 ,2 ]
Zhu, Xiaoli [1 ,2 ]
Zhang, Hongming [1 ,2 ]
Fan, Xiaobo [1 ]
Xue, Xiulei [1 ]
Chen, Yan [1 ]
Ding, Chenbo [1 ]
Zhao, Jianwen [1 ]
Wu, Guoqiu [1 ,3 ]
机构
[1] Southeast Univ, Sch Med, Nanjing 210009, Peoples R China
[2] Southeast Univ, Zhongda Hosp, Dept Resp Med, Nanjing 210009, Peoples R China
[3] Southeast Univ, Zhongda Hosp, Ctr Clin Lab Med, Nanjing 210009, Peoples R China
基金
美国国家科学基金会;
关键词
non-small cell lung cancer; ERCC-1; 202; isoform; Cisplatin; resistance; MESSENGER-RNA EXPRESSION; DNA-REPAIR; CISPLATIN; BRCA1; SURVIVAL; EXCISION; ISOFORM; RRM1;
D O I
10.7150/jca.19897
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: 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). Methods: The relative complementary DNA (cDNA) quantification for ERCC1_ 202 was conducted using a fluorescence-based, real-time detection method and beta-actin was used as a reference gene. Results: A strong correlation was observed between ERCC1_ 202 mRNA and ERCC1 mRNA levels in NSCLC cells (P < 0.001). 28 patients completed this research. Our results implied that as ERCC1_ 202 levels increased, the risk of progression (HR = 4.296, P = 0.011) and death (HR = 6.503, P = 0.001) increased. At multivariate analysis, high expression of ERCC1_ 202 was shown to be an independent predictive factor for time to progression (P = 0.047), and progression-free survival (P = 0.014). However, the high expression of ERCC1_ 202 was not an independent predictive factor for response (P = 0.324). Conclusions: This study suggests that the efficacy of platinum-based chemotherapy can be improved when customized according to the expression of ERCC1_ 202.
引用
收藏
页码:2846 / 2853
页数:8
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