Expression of ERCC1 and BRCA1 predict the clinical outcome of non-small cell lung cancer in patients receiving platinum-based chemotherapy

被引:10
作者
Wang, T. B. [1 ]
Zhang, N. L. [1 ]
Wang, S. H. [1 ]
Li, H. Y. [1 ]
Chen, S. W. [1 ]
Zheng, Y. G. [1 ]
机构
[1] Zhengzhou Univ, Luoyang Ctr Hosp, Dept Resp Med, Luoyang, Peoples R China
关键词
Non-small cell lung cancer; BRCA1; RRM1; RRM2; Overall survival; EXCISION-REPAIR; SUSCEPTIBILITY; POLYMORPHISMS; CISPLATIN;
D O I
10.4238/2014.May.9.15
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We examined mRNA expression levels of ERCC1, BRCA1, RRM1, and human beta-tubulin-III (TUBB3) in non-small-cell lung carcinoma (NSCLC) patients and investigated the association between expression of these genes and the clinical outcome of NSCLC treatment. A total of 366 patients who underwent surgery for NSCLC were included in this study. All patients received third-generation platinum-based chemotherapy as first-line treatment. The relative cDNA quantification for ERCC1, RRM1, BRCA1, and TUBB3 was determined using a fluorescence-based, real-time detection method. We found that low expression of ERCC1 and BRCA1 was associated with a good response to platinum-based chemotherapy, with an odds ratio [95% confidence interval (CI)] of 2.09 (1.33-3.27) and 2.92 (1.85-4.62), respectively. Multivariate Cox regression analysis indicated that patients with low expression of ERCC1 and BRCA1 attained a longer overall survival time than those with high expression, with a hazard ratio (95% CI) of 0.42 (0.23-0.77) and 0.39 (0.21-0.71), respectively. However, RMM1 and TUBB2 expressions were not correlated with clinical outcome of NSCLC. In conclusion, we found that low expression of ERCC1 and BRCA1 can be useful for selecting NSCLC patients who would benefit from chemotherapy and warrants further investigation in prospective studies.
引用
收藏
页码:3704 / 3710
页数:7
相关论文
共 19 条
[1]  
[Anonymous], PRINCIPLES PRACTICE
[2]   Gene expression and polymorphisms of DNA repair enzymes:: Cancer susceptibility and response to chemotherapy [J].
Camps, Carlos ;
Sirera, Rafael ;
Iranzo, Vega ;
Taron, Miquel ;
Rosell, Rafael .
CLINICAL LUNG CANCER, 2007, 8 (06) :369-375
[3]  
Crino L., 2010, Ann Oncol, V21, pv103
[4]   ERCC1 predicts outcome in patients with gastric cancer treated with adjuvant cisplatin-based chemotherapy [J].
De Dosso, Sara ;
Zanellato, Elena ;
Nucifora, Martina ;
Boldorini, Renzo ;
Sonzogni, Angelica ;
Biffi, Roberto ;
Fazio, Nicola ;
Bucci, Eraldo ;
Beretta, Ottavio ;
Crippa, Stefano ;
Saletti, Piercarlo ;
Frattini, Milo .
CANCER CHEMOTHERAPY AND PHARMACOLOGY, 2013, 72 (01) :159-165
[5]   mRNA Expression and Clinical Significance of ERCC1, BRCA1, RRM1, TYMS and TUBB3 in Postoperative Patients with Non-Small Cell Lung Cancer [J].
Han, Yi ;
Wang, Xiao-Bin ;
Xiao, Ning ;
Liu, Zhi-Dong .
ASIAN PACIFIC JOURNAL OF CANCER PREVENTION, 2013, 14 (05) :2987-2990
[6]  
International Agency for Research on Cancer (IARC), 2008, LUNG CANC INC MORT P
[7]   Genetic variation in the DNA repair genes is predictive of outcome in lung cancer [J].
Matakidou, Athena ;
el Galta, Rachid ;
Webb, Emily L. ;
Rudd, Matthew F. ;
Bridle, Helen ;
Consortium, The Gelcaps ;
Eisen, Tim ;
Houlston, Richard S. .
HUMAN MOLECULAR GENETICS, 2007, 16 (19) :2333-2340
[8]  
MILLER AB, 1981, CANCER, V47, P207, DOI 10.1002/1097-0142(19810101)47:1<207::AID-CNCR2820470134>3.0.CO
[9]  
2-6
[10]   ERCC1 Can Be a Prognostic Factor in Hilar Cholangiocarcinoma and Extrahepatic Bile Duct Cancer, But Not in Intrahepatic Cholangiocarcinoma [J].
Park, Kyun Woo ;
Jung, Eun-Seon ;
Kim, Dong-Gu ;
Yoo, Young-Kyung ;
Hong, Tae-Ho ;
Lee, In Seok ;
Koh, Yoon Ho ;
Kim, Ji-Hoon ;
Lee, Myung Ah .
CANCER RESEARCH AND TREATMENT, 2013, 45 (01) :63-69