Glutathione S-transferase P1 and DNA Polymorphisms with the Response to Chemotherapy and the Prognosis of Bone Tumor

被引:45
|
作者
Yang, Li-Min [1 ]
Li, Xiu-Hua [1 ]
Bao, Cui-Fen [2 ]
机构
[1] Liaoning Med Coll, Affiliated Hosp 1, Dept Orthopaed, Jinzhou, Peoples R China
[2] Liaoning Med Univ, Cent Lab, Jinzhou, Peoples R China
关键词
GSTP1; DNA repaird gene; chemotherapy; polymorphisms; response; OSTEOSARCOMA PATIENTS; COLORECTAL-CANCER; ASSOCIATION; SURVIVAL; ERCC2;
D O I
10.7314/APJCP.2012.13.11.5883
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Osteosarcoma is the most common primary bone malignancy in children and adolescents, and its clinical outcome is poor. We evaluated the response of GSTP1, ERCC1 and ERCC2 to chemotherapy among osteosarcoma patients, and the role of these genes on the prognosis of osteosarcoma. 187 patients with osteosarcoma were administered with methotrexate, cisplatin/adriamycin, actinomycin D, cyclophosphamide, or vincristine treatment. GSTP1, ERCC1 and ERCC2 polymorphism was genotyped by PCR-RFLP assay. The results showed the average survival time of 187 patients were 38.4 months. 97 patients showed response to neoadjuvant chemotherapy. The GSTP1 Val and ERCC2 A/A genotypes had significantly higher rates of response to chemotherapy, with adjusted OR (95% CI) of 2.19 (1.15-6.21) and 2.88 (1.14-13.25). Individuals with ERCC2 A/A genotype were likely to have a lower risk of death from oseosarcoma, and the adjusted HR was 0.32 (0.13-0.95). Our study indicated test of GSTP1 and ERCC2 Lys751Gln polymorphisms might be a candidate pharmacogenomic factors to be explored in the future to identify the osteosarcoma patients who might benefit from chemotherapy.
引用
收藏
页码:5883 / 5886
页数:4
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