Biological and predictive role of ERCC1 polymorphisms in cancer

被引:16
作者
Formica, V. [1 ]
Doldo, E. [2 ]
Antonetti, F. R. [1 ]
Nardecchia, A. [1 ]
Ferroni, P. [3 ]
Riondino, S. [1 ,3 ]
Morelli, C. [1 ]
Arkenau, H. T. [4 ]
Guadagni, F. [3 ]
Orlandi, A. [2 ]
Roselli, M. [1 ]
机构
[1] Tor Vergata Clin Ctr Univ Hosp, Dept Syst Med, Med Oncol Unit, Viale Oxford 81, I-00133 Rome, Italy
[2] Tor Vergata Univ Hosp, Inst Pathol Anat, Dept Biomed & Prevent, Rome, Italy
[3] San Raffaele Roma Open Univ, Dept Human Sci & Qual Life Promot, Rome, Italy
[4] Sarah Cannon Res Inst, Drug Dev Unit, London, England
关键词
ERCC1; Oxaliplatin; Single nucleotide polymorphisms; Colorectal cancer; NUCLEOTIDE EXCISION-REPAIR; ADVANCED COLORECTAL-CANCER; RELATIVE DOSE INTENSITY; MESSENGER-RNA LEVELS; GENE-SPECIFIC REPAIR; DNA-REPAIR; ADJUVANT CHEMOTHERAPY; XERODERMA-PIGMENTOSUM; OXALIPLATIN; CISPLATIN;
D O I
10.1016/j.critrevonc.2017.01.016
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Excision repair cross-complementation group 1 (ERCCI) is a key component in DNA repair mechanisms and may influence the tumor DNA-targeting effect of the chemotherapeutic agent oxaliplatin. Germline ERCCI polymorphisms may alter the protein expression and published data on their predictive and prognostic value have so far been contradictory. In the present article we review available evidence on the clinical role and utility of ERCC1 polymorphisms and, in the absence of a 'perfect' trial, what we call the 'sliding doors' trial, we present the data of ERCC1 genotyping in our local patient population. We found a useful predictive value for oxaliplatin-induced risk of anemia. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:133 / 143
页数:11
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