TLR-3 polymorphism is an independent prognostic marker for stage II colorectal cancer

被引:66
作者
Castro, F. A. [1 ,2 ]
Forsti, A. [1 ,3 ]
Buch, S. [4 ,5 ]
Kalthoff, H. [6 ,7 ]
Krauss, C. [6 ]
Bauer, M. [6 ]
Egberts, J. [6 ]
Schniewind, B. [6 ]
Broering, D. C. [6 ]
Schreiber, S. [5 ]
Schmitt, M. [2 ]
Hampe, J. [5 ]
Hemminki, K. [1 ,3 ]
Schafmayer, C. [4 ,6 ]
机构
[1] German Canc Res Ctr, Div Mol Genet Epidemiol, D-69120 Heidelberg, Germany
[2] German Canc Res Ctr, Div Genome Modificat & Carcinogenesis, D-69120 Heidelberg, Germany
[3] Lund Univ, Ctr Primary Hlth Care Res, Clin Res Ctr, Malmo, Sweden
[4] Univ Kiel, POPGEN Biobank Project, Kiel, Germany
[5] Univ Kiel, Dept Gen Internal Med, Kiel, Germany
[6] Univ Kiel, Dept Gen & Thorac Surg, Kiel, Germany
[7] Univ Kiel, Inst Expt Canc Res, Comprehens Canc Ctr N, Kiel, Germany
关键词
Alimentary tract; Variants; Prognosis and survival; TOLL-LIKE RECEPTOR-3; NF-KAPPA-B; COLON-CANCER; SURVIVAL; CHEMOTHERAPY; INFLAMMATION; ASSOCIATION; INDUCTION; APOPTOSIS; PROMOTER;
D O I
10.1016/j.ejca.2010.12.011
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Clinicopathologic stage is still the main parameter to evaluate the prognosis of newly diagnosed colorectal cancer (CRC) patients. Although molecular markers have been suggested for follow up of treated CRC patients, their complete clinical application is still under evaluation. Materials and methods: To evaluate the association of immune-related genes with CRC prognosis and survival, a total of 19 single nucleotide polymorphisms (SNPs) were genotyped in 614 German patients within the Kiel cohort (POPGEN). Results: A promoter variant (rs1800872) in the Interleukin-10 (IL-10) gene was associated with an increased lymph node metastasis involvement [odds ratio (OR) = 2.1, 95% confidence interval (CI) = 1.03-4.2, for carriers of the TT genotype]. More importantly, among 582 followed up patients the SNP rs3775291 in the toll-like receptor 3 (TLR-3) gene was associated with CRC specific survival (150 events). Patients carrying the TT genotype had a 93% increased risk of death compared with the CC carriers [hazard ratio (HR) = 1.93, 95% CI 1.14-3.281. The observed effect of the TLR-3 variant was restricted to stage II patients (HR = 4.14, 95% CI 1.24-13.84) and to patients who did not receive adjuvant therapy (HR = 3.2, 95% CI 1.4-7.7). Conclusions: Our results may provide additional candidates for risk assessment in stage II CRC patients for treatment decision. Further validation of the presented findings is warranted. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1203 / 1210
页数:8
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