Evidence for an association of TP53 codon 72 polymorphism with breast cancer risk

被引:65
作者
Damin, Andrea P. S.
Frazzon, Ana P. G.
Damin, Daniel C.
Roehe, Adriana
Hermes, Vanessa
Zettler, Claudio
Alexandre, Claudio O. P.
机构
[1] Fdn Fac Fed Ciencias Med Porto Alegre, Mol Biol Lab, BR-90095170 Porto Alegre, RS, Brazil
[2] Fdn Fac Fed Ciencias Med Porto Alegre, Dept Pathol, BR-90095170 Porto Alegre, RS, Brazil
[3] Complexo Hosp Santa Casa, Porto Alegre, RS, Brazil
来源
CANCER DETECTION AND PREVENTION | 2006年 / 30卷 / 06期
关键词
TP53; polymorphism; codon; 72; breast cancer; risk factors; genotypes; arginine/proline; polymerase chain reaction-restriction fragment length polymorphism; PCR-RFLP; sequencing; Brazil; Hardy-Weinberg equilibrium;
D O I
10.1016/j.cdp.2006.09.007
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: A common Arg/Pro polymorphism at codon 72 of the TP53 gene has been investigated as a risk factor for cancer in different populations. So far, the results have been controversial. Our purpose was to investigate the association of this polymorphism with breast carcinoma in women from Southern Brazil, a high-risk area for breast cancer. Methods: Blood samples collected from 118 women with primary breast carcinoma and from 202 female blood donors were analyzed through polymerase chain reaction-restriction fragment length polymorphism and DNA sequencing. Results: The relative frequency of each allele was 0.75 for Arg and 0.25 for Pro in patients with cancer, and 0.62 for Arg and 0.38 for Pro in normal controls (P < 0.001). The Arg/Arg genotype was significantly associated with an increased risk for breast cancer (OR 2.9; 95% Cl 1.43-3.6; P < 0.002). No correlation between the genotype distribution and specific prognostic predictors for the disease outcome was observed. Discussion: TP53 codon 72 polymorphism might be implicated in breast carcinogenesis, with the Arg/Arg genotype being associated with an increased susceptibility for this malignancy. (c) 2006 International Society for Preventive Oncology. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:523 / 529
页数:7
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