Skip Navigation


Carcinogenesis Advance Access originally published online on April 15, 2009
Carcinogenesis 2009 30(6):991-996; doi:10.1093/carcin/bgp091
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Supplementary Data
Right arrow All Versions of this Article:
30/6/991    most recent
bgp091v1
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrowRequest Permissions
Google Scholar
Right arrow Articles by Wang, M.
Right arrow Articles by Zhang, Z.
PubMed
Right arrow PubMed Citation
Right arrow Articles by Wang, M.
Right arrow Articles by Zhang, Z.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

© The Author 2009. Published by Oxford University Press. All rights reserved. For Permissions, please email: journals.permissions@oxfordjournals.org

Common genetic variants on 8q24 contribute to susceptibility to bladder cancer in a Chinese population

Meilin Wang1,2,{dagger}, Miaomiao Wang1,{dagger}, Wei Zhang3, Lin Yuan1, Guangbo Fu4, Qingyi Wei5 and Zhengdong Zhang1,2,*

1 Department of Molecular and Genetic Toxicology
2 Department of Epidemiology and Biostatistics, School of Public Health, Cancer Center of Nanjing Medical University, 140 Hanzhong Road, Nanjing 210029, China
3 Department of Urology, The First Affiliated Hospital of Nanjing Medical University, Nanjing 210029, China
4 Department of Urology, The Huai-An First Affiliated Hospital of Nanjing Medical University, Huai-An 223300, China
5 Department of Epidemiology, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA

* To whom correspondence should be addressed. Tel: +86 25 86862937; Fax: +86 25 86527613; Email: zdzhang{at}njmu.edu.cn

A recent genome-wide association study identified two common variants that confer susceptibility to bladder cancer. We hypothesized that these variants are associated with risk of bladder cancer in Chinese populations. We genotyped rs9642880 G>T on 8q24 and rs710521 A>G on 3q28 in a two-stage case–control study of bladder cancer to evaluate the association and further examined the expression of MYC. We found that the rs9642880 G>T, but not the rs710521 A>G polymorphism, was associated with an increased risk of bladder cancer. Compared with the rs9642880 GG genotype, the GT/TT genotypes were associated with an odds ratio of 1.65 (95% confidence interval = 1.25–2.17), and this risk was more pronounced in young men and for low-risk tumors. Additional experiments revealed that the rs9642880 GT/TT genotypes were associated with enhanced levels of both MYC mRNA and protein in bladder tissues. Our findings suggested that the rs9642880 G>T polymorphism on 8q24 was independently associated with the risk of bladder cancer in Chinese populations.

Abbreviations: CI, confidence interval; GWA, genome-wide association; LD, linkage disequilibrium; OR, odds ratio; SNP, single nucleotide polymorphism


{dagger} These authors contributed equally to this work.

Received February 4, 2009; revised April 8, 2009; accepted April 10, 2009.


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
Cancer Epidemiol. Biomarkers Prev.Home page
M. C. Stern, D. Van Den Berg, J.-M. Yuan, D. V. Conti, M. Gago-Dominguez, M. C. Pike, Y.-B. Xiang, Y.-T. Gao, and V. K. Cortessis
Sequence Variant on 3q28 and Urinary Bladder Cancer Risk: Findings from the Los Angeles-Shanghai Bladder Case-Control Study
Cancer Epidemiol. Biomarkers Prev., November 1, 2009; 18(11): 3057 - 3061.
[Abstract] [Full Text] [PDF]



Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.