Predictive Potential of Glutathione S-Transferase Polymorphisms for Prognosis of Osteosarcoma Patients on Chemotherapy

被引:26
|
作者
Zhang, Shai-Lin [1 ]
Mao, Ning-Fang [2 ]
Sun, Jun-Ying [1 ]
Shi, Zhi-Cai [2 ]
Wang, Bing [1 ]
Sun, Yong-Jian [3 ]
机构
[1] Soochow Univ, Affiliated Hosp 1, Dept Orthopaed, Suzhou, Peoples R China
[2] Second Mil Med Univ, Changhai Hosp, Dept Orthopaed, Shanghai, Peoples R China
[3] So Med Univ, Nanfang Hosp, Dept Traumat Orthoped, Guangzhou, Guangdong, Peoples R China
关键词
GSTs; polymorphisms; osteosarcoma; predictive role; OVARIAN-CANCER; GENETIC POLYMORPHISMS; BREAST-CANCER; OSTEOGENIC-SARCOMA; ESCHERICHIA-COLI; DRUG-RESISTANCE; CLASS-MU; SUSCEPTIBILITY; ASSOCIATION; EXPRESSION;
D O I
10.7314/APJCP.2012.13.6.2705
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objective: To evaluate the predictive value of glutathione S-transferase (GST) gene polymorphisms for the prognosis of osteosarcoma patients receiving chemotherapy. Methods: A total of 159 patients were included in our study between January 2005 and December 2007., with follow-up until January 2012. Genotyping was based upon the duplex polymerase-chain-reaction with the PCR-CTPP method. Results: At the time of diagnosis, 15.4% of the patients presented with metastasis, while 22.3% developed metastasis during follow-up. At the time of final analysis on January 2012, the median follow-up was 45.5 months. Patients with null GSTM1 and GSTT1 had a higher event free survival rate than non-null genotype, but no significant association was found between the two genotypes and prognosis of osteosarcoma. Individuals with GSTP1 Val/Val genotype tended to live shorter than with the IIe/IIe genotype, and we found a significantly higher risk of death from osteosarcoma (adjusted HR=2.35, 95% CI=1.13-4.85). Conclusion: The GSTP1 gene polymorphism may have an important role in the prognosis of osteosarcoma patients with chemotherapy. Further analyses with larger samples and more genes encoding metabolizing and DNA repair enzymes are warranted.
引用
收藏
页码:2705 / 2709
页数:5
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