An Analysis of Growth, Differentiation and Apoptosis Genes with Risk of Renal Cancer

被引：28

作者：

Dong, Linda M. ^{[1
]}

Brennan, Paul ^{[2
]}

Karami, Sara ^{[1
]}

Hung, Rayjean J. ^{[3
]}

Menashe, Idan ^{[1
]}

Berndt, Sonja I. ^{[1
]}

Yeager, Meredith ^{[4
]}

Chanock, Stephen ^{[4
]}

Zaridze, David ^{[5
]}

Matveev, Vsevolod ^{[5
]}

Janout, Vladimir ^{[6
]}

Kollarova, Hellena ^{[6
]}

Bencko, Vladimir ^{[7
]}

Schwartz, Kendra ^{[8
,9
]}

Davis, Faith ^{[10
]}

Navratilova, Marie ^{[11
]}

Szeszenia-Dabrowska, Neonila ^{[12
]}

Mates, Dana ^{[13
]}

Colt, Joanne S. ^{[1
]}

Holcatova, Ivana ^{[7
]}

Boffetta, Paolo ^{[3
]}

Rothman, Nathaniel ^{[1
]}

Chow, Wong-Ho ^{[1
]}

Rosenberg, Philip S. ^{[1
]}

Moore, Lee E. ^{[1
]}

机构：

[1] NCI, Div Canc Epidemiol & Genet, Bethesda, MD 20892 USA

[2] Intl Agcy Res Canc, Lyon, France

[3] Mt Sinai Hosp, Samuel Lunenfeld Res Inst, Toronto, ON, Canada

[4] NCI, Core Genotyping Facil, Gaithersburg, MD USA

[5] Inst Carcinogenesis, Moscow, Russia

[6] Palacky Univ, Olomouc, Czech Republic

[7] Inst Hyg & Epidemiol, Prague, Czech Republic

[8] Wayne State Univ, Dept Family Med & Publ Hlth Sci, Detroit, MI USA

[9] Wayne State Univ, Karmanos Canc Inst, Detroit, MI USA

[10] Univ Illinois, Dept Biostat & Epidemiol, Chicago, IL 60680 USA

[11] Masaryk Memorial Canc Inst, Brno, Czech Republic

[12] Inst Occupat Med, Lodz, Poland

[13] Inst Publ Hlth, Bucharest, Romania

来源：

PLOS ONE | 2009年 / 4卷 / 03期

基金：

美国国家卫生研究院;

关键词：

D O I：

10.1371/journal.pone.0004895

中图分类号：

O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];

学科分类号：

07 ; 0710 ; 09 ;

摘要：

We conducted a case-control study of renal cancer (987 cases and 1298 controls) in Central and Eastern Europe and analyzed genomic DNA for 319 tagging single-nucleotide polymorphisms (SNPs) in 21 genes involved in cellular growth, differentiation and apoptosis using an Illumina Oligo Pool All (OPA). A haplotype-based method (sliding window analysis of consecutive SNPs) was used to identify chromosome regions of interest that remained significant at a false discovery rate of 10%. Subsequently, risk estimates were generated for regions with a high level of signal and individual SNPs by unconditional logistic regression adjusting for age, gender and study center. Three regions containing genes associated with renal cancer were identified: caspase 1/5/ 4/12(CASP 1/5/ 4/12), epidermal growth factor receptor (EGFR), and insulin-like growth factor binding protein-3 (IGFBP3). We observed that individuals with CASP1/5/4/12 haplotype (spanning area upstream of CASP1 through exon 2 of CASP5) GGGCTCAGT were at higher risk of renal cancer compared to individuals with the most common haplotype (OR: 1.40, 95% CI: 1.10-1.78, p-value = 0.007). Analysis of EGFR revealed three strong signals within intron 1, particularly a region centered around rs759158 with a global p = 0.006 (GGG: OR: 1.26, 95% CI: 1.04-1.53 and ATG: OR: 1.55, 95% CI: 1.14-2.11). A region in IGFBP3 was also associated with increased risk (global p = 0.04). In addition, the number of statistically significant (p-value, 0.05) SNP associations observed within these three genes was higher than would be expected by chance on a gene level. To our knowledge, this is the first study to evaluate these genes in relation to renal cancer and there is need to replicate and extend our findings. The specific regions associated with risk may have particular relevance for gene function and/or carcinogenesis. In conclusion, our evaluation has identified common genetic variants in CASP1, CASP5, EGFR, and IGFBP3 that could be associated with renal cancer risk.

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