CXCL12 G801A polymorphism is a risk factor forSporadic prostate cancer susceptiblifity

被引:75
作者
Hirata, Hiroshi
Hinoda, Yuji
Kikuno, Nobuyuki
Kawamoto, Ken
Dahiya, Angela V.
Suehiro, Yutaka
Tanaka, Yuichiro
Dahiya, Rajvir
机构
[1] Vet Affairs Med Ctr, Urol Res Ctr 112F, Dept Urol, San Francisco, CA 94121 USA
[2] Univ Calif San Francisco, San Francisco, CA 94121 USA
[3] Yamaguchi Univ, Grad Sch Med, Dept Lab Med, Yamaguchi, Japan
关键词
FACTOR-I; CELL-MIGRATION; SDF-1; GENE; EXPRESSION; P53; SUSCEPTIBILITY; CXCR4; METASTASIS; VARIANTS; CODON-72;
D O I
10.1158/1078-0432.CCR-07-0859
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: The chemokine CXCL12 and its receptor CXCR4 have been found to be associated with cancer metastasis. A single nucleoticle polymorphism of CXCL12 G801A has been described and is regarded as a target for cis-acting factor that has the ability to up-regulate CXCL12 expression. Currently, there are no reports investigating the role of CXCL 12 G801A polymorphism in prostate cancer (PC). Experimental Design: We genotyped CXCL12 G801A and p53Arg72Pro in 167 PC patients and 167 age-matched healthy subjects. Genotyping was done with PCR-RFLP and confirmed by direct DNA sequencing. To investigate the effect of the CXCL12 G801A polymorphism on CXCL12 and CXCR4 expression, immunohistochemistry was done in genotyped PC tissues. Results: A significant increase in the GA + AA genotype of the CXCL12 G801A polymorphism was observed in PC patients compared with healthy controls. The frequency of CXCL12 AA genotype was significantly higher in a group of patients with lymph node metastasis (23%) compared with those without metastasis (7%). The frequency of CXCL12 expression in AA + GA genotype carriers was significantly higher than that in GG genotype carriers. Among the carriers with CXCL12 GA + AA genotypes, CXCR4 expression was also significantly higher compared with those with the GG genotype. Moreover, among the groups with both CXCL12-and CXCR4-positive staining, the frequency of the CXCL12 GA + AA genotype was high. Although we did not find a significant relationship between the frequency of the Arg/Pro + Pro/Pro genotype of p53 Arg72Pro and susceptibility in PC, there was a combined effect of CXCL12 GA + AA genotype and the p53 72ArglPro + Pro/Pro genotype on the frequency of PC. These results indicate that the p53 codon 72 polymorphism may interact with CXCL12 G801A. Conclusions: This is the first report showing that CXCL12 G801A polymorphism may be a risk factor for PC. Moreover, this study suggests that this polymorphism can be an important marker for detecting microinvasion and PC metastasis.
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页码:5056 / 5062
页数:7
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