Association between ERCC1 and ERCC2 gene polymorphisms and chemotherapy response and overall survival in osteosarcoma

被引:17
|
作者
Cao, Z. H. [1 ,2 ]
Yin, H. P. [2 ]
Jiang, N. [2 ]
Yu, B. [1 ]
机构
[1] Southern Med Univ, Nanfang Hosp, Dept Traumat Orthoped, Guangzhou, Guangdong, Peoples R China
[2] Inner Mongolia Med Univ, Affiliated Hosp 2, Dept Minimally Invas Spine Surg, Hohhot, Peoples R China
关键词
ERCC1; ERCC2; Polymorphism; Clinical outcome; Osteosarcoma; CELL LUNG-CANCER; PLATINUM-BASED CHEMOTHERAPY; DNA-REPAIR GENES; CISPLATIN CHEMOTHERAPY; GASTRIC-CANCER; BONE-TUMOR; PROGNOSIS; MARKER;
D O I
10.4238/2015.August.21.21
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 aimed to evaluate the influence of four SNPs in ERCC1 and ERCC2 on the response to cisplatin-based treatment and on clinical outcome in patients with osteosarcoma. We identified 186 patients with osteosarcoma diagnosed between April 2009 and April 2011 who were eligible for inclusion in our study. Genotyping of ERCC1 rs11615, rs3212986, and rs2298881; and ERCC2 rs1799793 and rs13181 was conducted by a polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) assay. By conditional logistic regression analysis, patients carrying the CC genotypes of ERCC1 rs11615 and rs2298881 were shown to be more likely to have good response to chemotherapy when compared with patients carrying wildtype genotypes; the ORs (95% CIs) were 2.56 (1.02-7.35) and 3.01 (1.07-9.71), respectively. By Cox regression analysis, individuals carrying the CC genotype of ERCC1 rs11615 were associated with longer overall survival time and decreased risk of death from osteosarcoma; the hazards ratio (95% CI) was 0.32 (0.07-0.98). In summary, our results suggested that the ERCC1 rs11615 and rs2298881 polymorphisms play important roles in the response to chemotherapy mediated by the DNA repair pathway and in the clinical outcome of osteosarcoma.
引用
收藏
页码:10145 / 10151
页数:7
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