Polymorphism of IL-1α, IL-1β and IL-10 in patients with advanced ovarian cancer:: Results of a prospective study with 147 patients

被引:30
|
作者
Braicu, Elena Ioana
Mustea, Alexander
Toliat, Mohammad R.
Pirvulescu, Cristina
Konsgen, Dominique
Sun, Pengming
Nuernberg, Peter
Lichtenegger, Werner
Sehouli, Jalid
机构
[1] Univ Med Berlin, Dept Gynecol & Obstet, Charite, D-13353 Berlin, Germany
[2] Iuliu Hatieganu Med Univ, Dept Obstet & Gynecol, Cluj Napoca, Romania
[3] Univ Cologne, Cologne Ctr Genom, Cologne, Germany
[4] Peking Univ, Peoples Hosp, Beijing 100871, Peoples R China
关键词
ovarian cancer; cytokines; polymorphism; IL-1; alpha; beta; IL-10;
D O I
10.1016/j.ygyno.2006.10.014
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objective. Interleukin I (IL-1) and IL-10 are critically involved in tumorigenesis. We investigated polymorphisms of IL-1 and IL-10 genes in patients with ovarian cancer (OC). Methods. In a prospective, case-control study 147 patients with OC and 129 patients without history of any malignancy (CG) were genotyped for IL-1 gene (IL-1 alpha-889 T/C and IL-1 beta -511 C/T) and IL-10 gene (IL-10 - 1082 G/A, -819 C/T and -592 C/A) using pyrosequencing. Results. IL-10 polymorphisms in -819 and -592 positions correlated with the postoperative residual tumor mass (P = 0.036 and p = 0.035, respectively). The chance of achieving optimal tumor debulking was 1.49 times greater for patients with the C/C genotype at - 819 and - 512 positions than for patients with other genotypes. There were no significant associations between allelic frequencies for IL-1 alpha and IL-1 beta in OC. IL-10 -819 CC and -592 CC genotypes were associated in univariate analysis with a better disease-free and overall survival. Conclusions. IL-10 promoter polymorphism may be related with the ability to achieve optimal tumor debulking. Polymorphism in IL-10 gene seems to influence the overall and disease-free survival rate. Subsequent multi-institutional studies with high number of patients are warranted to confirm these results. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:680 / 685
页数:6
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