Pharmacogenetic role of ERCC1 genetic variants in treatment response of platinum-based chemotherapy among advanced non-small cell lung cancer patients

被引:23
|
作者
Yu, Dianke [2 ,3 ]
Shi, Juan [4 ]
Sun, Tong [5 ,6 ]
Du, Xiaoli [7 ]
Liu, Li [4 ]
Zhang, Xiaojiao [4 ]
Lu, Chao [4 ]
Tang, Xiaohu [4 ]
Li, Meng [4 ]
Xiao, Lingchen [4 ]
Zhang, Zhouwei [4 ]
Yuan, Qipeng [1 ,4 ]
Yang, Ming [1 ,4 ]
机构
[1] Beijing Univ Chem Technol, Coll Life Sci & Technol, Beijing 100029, Peoples R China
[2] Chinese Acad Med Sci, State Key Lab Mol Oncol, Dept Etiol & Carcinogenesis, Canc Inst & Hosp, Beijing 100730, Peoples R China
[3] Peking Union Med Coll, Beijing 100021, Peoples R China
[4] Beijing Univ Chem Technol, Coll Life Sci & Technol, Beijing, Peoples R China
[5] Dana Farber Canc Inst, Dept Med Oncol, Boston, MA 02115 USA
[6] Harvard Univ, Sch Med, Boston, MA USA
[7] NCI, Cellular Oncol Lab, NIH, Bethesda, MD 20892 USA
基金
中国国家自然科学基金;
关键词
Chemotherapy; ERCC1; Meta-analysis; Pharmacogenetics; Platinum; NUCLEOTIDE EXCISION-REPAIR; DNA-REPAIR; POLYMORPHISMS; CISPLATIN; SURVIVAL; XPD; ENDONUCLEASE; METAANALYSIS; ASSOCIATION; EXPRESSION;
D O I
10.1007/s13277-011-0314-y
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The excision repair cross-complementation group 1 (ERCC1) plays an essential role in DNA repair and has been linked to resistance to platinum-based anticancer drugs among advanced non-small cell lung cancer (NSCLC) patients. We systematically evaluate whether ERCC1 Asn118Asn and C8092A genetic variants are associated with treatment response of platinum chemotherapy. We preformed a meta-analysis using ten eligible cohort studies (including 11 data-sets) with a total of 1,252 NSCLC patients to summarize the existing data on the association between the ERCC1 Asn118Asn and C8092A polymorphisms and response to platinum regiments. Odds ratio or hazard ratio with 95% confidence interval were calculated to estimate the correlation. We found that neither ERCC1 C8092A polymorphism nor Asn118Asn variant is associated with different response of platinum-based treatment among advanced NSCLC patients. Additionally, these two genetic variants are not related to treatment response in either Caucasian patients or Asian patients. Our meta-analysis indicates that the ERCC1 Asn118Asn and C8092A polymorphisms may not be good prognostic biomarkers for platinum-based chemotherapy in patients with stage III-IV NSCLC.
引用
收藏
页码:877 / 884
页数:8
相关论文
共 50 条
  • [1] Role of ERCC1 variants in response to chemotherapy and clinical outcome of advanced non-small cell lung cancer
    Huang, Shao-jun
    Wang, Yu-fei
    Jin, Zhi-yong
    Sun, Jia-yang
    Guo, Zhan-lin
    TUMOR BIOLOGY, 2014, 35 (05) : 4023 - 4029
  • [2] Genetic polymorphism of GSTP1 and ERCC1 correlated with response to platinum-based chemotherapy in non-small cell lung cancer
    Hongying Lv
    Ting Han
    Xiaoli Shi
    Yasai Yao
    Yongru Yao
    Wensheng Qiu
    Lu Yue
    Jun Liang
    Medical Oncology, 2014, 31
  • [3] Genetic polymorphism of GSTP1 and ERCC1 correlated with response to platinum-based chemotherapy in non-small cell lung cancer
    Lv, Hongying
    Han, Ting
    Shi, Xiaoli
    Yao, Yasai
    Yao, Yongru
    Qiu, Wensheng
    Yue, Lu
    Liang, Jun
    MEDICAL ONCOLOGY, 2014, 31 (08)
  • [4] Association Between Polymorphisms of ERCC1 and XPD and Clinical Response to Platinum-Based Chemotherapy in Advanced Non-Small Cell Lung Cancer
    Li, Fan
    Sun, Xinchen
    Sun, Ning
    Qin, Shukui
    Cheng, Hongyan
    Feng, Jifeng
    Chen, Baoan
    Cheng, Lu
    Lu, Zuhong
    Ji, Jiazhong
    Zhou, Yingfeng
    AMERICAN JOURNAL OF CLINICAL ONCOLOGY-CANCER CLINICAL TRIALS, 2010, 33 (05): : 489 - 494
  • [5] ERCC1 mRNA expression is not associated with response and survival after platinum-based chemotherapy regimens in advanced non-small cell lung cancer
    Booton, Richard
    Ward, Tim
    Ashcroft, Linda
    Morris, Julie
    Heighway, Jim
    Thatcher, Nick
    JOURNAL OF THORACIC ONCOLOGY, 2007, 2 (10) : 902 - 906
  • [6] Decreased ERCC1 Expression After Platinum-Based Neoadjuvant Chemotherapy in non-Small Cell Lung Cancer
    Podmaniczky, Eszter
    Fabian, Katalin
    Papay, Judit
    Puskas, Rita
    Gyulai, Marton
    Furak, Jozsef
    Tiszlavicz, Laszlo
    Losonczy, Gyoergy
    Timar, Jozsef
    Moldvay, Judit
    PATHOLOGY & ONCOLOGY RESEARCH, 2015, 21 (02) : 423 - 431
  • [7] Pharmacogenetics of platinum-based chemotherapy in non-small cell lung cancer: predictive validity of polymorphisms of ERCC1
    Hamilton, Gerhard
    Rath, Barbara
    EXPERT OPINION ON DRUG METABOLISM & TOXICOLOGY, 2018, 14 (01) : 17 - 24
  • [8] Genetic variants in ERCC1 and XPC predict survival outcome of non-small cell lung cancer patients treated with platinum-based therapy
    Zhang, Ruoxin
    Jia, Ming
    Xue, Huijing
    Xu, Yuan
    Wang, Mengyun
    Zhu, Meiling
    Sun, Menghong
    Chang, Jianhua
    Wei, Qingyi
    SCIENTIFIC REPORTS, 2017, 7
  • [9] Genetic variants in ERCC1 and XPC predict survival outcome of non-small cell lung cancer patients treated with platinum-based therapy
    Ruoxin Zhang
    Ming Jia
    Huijing Xue
    Yuan Xu
    Mengyun Wang
    Meiling Zhu
    Menghong Sun
    Jianhua Chang
    Qingyi Wei
    Scientific Reports, 7
  • [10] Association between ERCC1 polymorphisms and nephrotoxicity in non-small cell lung cancer patients undergoing platinum-based chemotherapy
    de Jong, Corine
    Deneer, Vera Henriette
    Kelder, Johannes
    Hunting, Cornelis Bernardus
    Herder, Gerarda
    JOURNAL OF CLINICAL ONCOLOGY, 2018, 36 (15)