The CYP1A1 Ile462Val Polymorphism and Platinum Resistance of Epithelial Ovarian Neoplasms

被引:18
作者
Heubner, Martin [1 ,2 ]
Wimberger, Pauline [2 ]
Riemann, Kathrin [1 ]
Kasimir-Bauer, Sabine [2 ]
Otterbach, Friedrich [3 ]
Kimmig, Rainer [2 ]
Siffert, Winfried [1 ]
机构
[1] Univ Duisburg Essen, Inst Pharmacogenet, Fac Med, D-45147 Essen, Germany
[2] Univ Duisburg Essen, Clin Obstet & Gynaecol, Fac Med, D-45147 Essen, Germany
[3] Univ Duisburg Essen, Inst Pathol, Fac Med, D-45147 Essen, Germany
关键词
Ovarian cancer; Polymorphism; CYP1A1; platinum resistance; HORMONE-THERAPY; PHASE-II; CANCER; EXPRESSION; CELLS; RISK; METABOLISM; LETROZOLE; GENOTYPES; RECEPTOR;
D O I
10.3727/096504010X12626118079903
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The role of estrogens in ovarian carcinogenesis and progression of ovarian cancer is unclear. Cytochrome P450 is involved in estrogen metabolism, and polymorphisms have been associated with functional changes and risk for ovarian cancer. In this study, we investigated (he impact of the CYP1A1 Ile462Val polymorphism upon tumor risk and disease progression in ovarian cancer patients. One hundred and eleven ovarian cancer patients who had been treated tit the University Hospital of Essen between 1999 and 2007 and 1 19 age-matched healthy female controls were enrolled in this study. Genotyping was performed using PCR-RFLP. The distribution of genotypes was statistically significant different between ovarian cancer patients and healthy controls. We observed a significant association of the Ile allele with ovarian cancer (OR 2.6, 95% Cl 1.5-4.7, p = 0.001). Clinical parameters Such as overall Survival, FIGO stage, grading, and age tit diagnosis did not differ significantly. We observed a statistically significant association between the 462Val allele and platinum resistance, which was defined as a time interval <6 months to disease progression after administration of a platinum-based primary chemotherapy (OR 5.9, 95% Cl 1.5-23.2. p = 0.005). We observed a significant association between the presence of the 462Ile allele with ovarian cancer. While there is uncertainty about the potential involvement of CYP1A1 in the metabolism of platinum-containing agents, Our findings suggest an association between the 462Val allele and the development of platinum resistance in ovarian tumors. If confirmed in a larger, independent collective, Our findings would have important relevance with respect to the clinical consequences for the primary chemotherapy of ovarian cancer patients.
引用
收藏
页码:343 / 347
页数:5
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