Genome-wide interaction study of smoking and bladder cancer risk.

نویسندگان

  • Jonine D Figueroa
  • Summer S Han
  • Montserrat Garcia-Closas
  • Dalsu Baris
  • Eric J Jacobs
  • Manolis Kogevinas
  • Molly Schwenn
  • Nuria Malats
  • Alison Johnson
  • Mark P Purdue
  • Neil Caporaso
  • Maria Teresa Landi
  • Ludmila Prokunina-Olsson
  • Zhaoming Wang
  • Amy Hutchinson
  • Laurie Burdette
  • William Wheeler
  • Paolo Vineis
  • Afshan Siddiq
  • Victoria K Cortessis
  • Charles Kooperberg
  • Olivier Cussenot
  • Simone Benhamou
  • Jennifer Prescott
  • Stefano Porru
  • H Bas Bueno-de-Mesquita
  • Dimitrios Trichopoulos
  • Börje Ljungberg
  • Françoise Clavel-Chapelon
  • Elisabete Weiderpass
  • Vittorio Krogh
  • Miren Dorronsoro
  • Ruth Travis
  • Anne Tjønneland
  • Paul Brenan
  • Jenny Chang-Claude
  • Elio Riboli
  • David Conti
  • Manuela Gago-Dominguez
  • Mariana C Stern
  • Malcolm C Pike
  • David Van Den Berg
  • Jian-Min Yuan
  • Chancellor Hohensee
  • Rebecca Rodabough
  • Geraldine Cancel-Tassin
  • Morgan Roupret
  • Eva Comperat
  • Constance Chen
  • Immaculata De Vivo
  • Edward Giovannucci
  • David J Hunter
  • Peter Kraft
  • Sara Lindstrom
  • Angela Carta
  • Sofia Pavanello
  • Cecilia Arici
  • Giuseppe Mastrangelo
  • Margaret R Karagas
  • Alan Schned
  • Karla R Armenti
  • G M Monawar Hosain
  • Chris A Haiman
  • Joseph F Fraumeni
  • Stephen J Chanock
  • Nilanjan Chatterjee
  • Nathaniel Rothman
  • Debra T Silverman
چکیده

Bladder cancer is a complex disease with known environmental and genetic risk factors. We performed a genome-wide interaction study (GWAS) of smoking and bladder cancer risk based on primary scan data from 3002 cases and 4411 controls from the National Cancer Institute Bladder Cancer GWAS. Alternative methods were used to evaluate both additive and multiplicative interactions between individual single nucleotide polymorphisms (SNPs) and smoking exposure. SNPs with interaction P values < 5 × 10(-) (5) were evaluated further in an independent dataset of 2422 bladder cancer cases and 5751 controls. We identified 10 SNPs that showed association in a consistent manner with the initial dataset and in the combined dataset, providing evidence of interaction with tobacco use. Further, two of these novel SNPs showed strong evidence of association with bladder cancer in tobacco use subgroups that approached genome-wide significance. Specifically, rs1711973 (FOXF2) on 6p25.3 was a susceptibility SNP for never smokers [combined odds ratio (OR) = 1.34, 95% confidence interval (CI) = 1.20-1.50, P value = 5.18 × 10(-) (7)]; and rs12216499 (RSPH3-TAGAP-EZR) on 6q25.3 was a susceptibility SNP for ever smokers (combined OR = 0.75, 95% CI = 0.67-0.84, P value = 6.35 × 10(-) (7)). In our analysis of smoking and bladder cancer, the tests for multiplicative interaction seemed to more commonly identify susceptibility loci with associations in never smokers, whereas the additive interaction analysis identified more loci with associations among smokers-including the known smoking and NAT2 acetylation interaction. Our findings provide additional evidence of gene-environment interactions for tobacco and bladder cancer.

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

The Effect of Smoking and Opium on Bladder Cancer in Yazd Province: A Case - Control Study

Introduction: Bladder cancer is regarded as the most common urinary malignancy in the world. As other cancers, its incidence has increased in recent years. Hence, the present study was conducted to investigate the relationship between smoking and opium and bladder cancer in residents of Yazd province. Materials and Methods: This case-control study was performed on 200 patients with ...

متن کامل

Bladder cancer epidemiology and genetic susceptibility

Bladder cancer is the most common malignancy of the urinary system. The incidence of bladder cancer of men is higher than that of women (approximately 4:1). Here, we summarize the bladder cancer-related risk factors, including environmental and genetic factors. In recent years, although the mortality rate induced by bladder cancer has been stable or decreased gradually, the public health effect...

متن کامل

Rs401681 polymorphism in TERT-CLPTM1L was associated with bladder cancer risk: A meta-analysis

Objective(s):Genome-wide association studies have identified a number of genetic variants of telomerase reverse transcriptase (TERT), cleft lip and palate transmembrane1-like (CLPTM1L) associated with the risk of bladder cancer. Rs401681 polymorphism in TERT-CLPTM1L was of special interest for bladder cancer risk, whereas the results were inconclusive. Materials and Methods:Publications illustr...

متن کامل

The post GWAS era: strategies to identify gene-gene and gene-environment interactions in urinary bladder cancer

Bladder cancer is a smoking-and occupational exposure-related disease with a sub-Both family studies and large genome-wide association analyses support a polygenetic basis for uri-nary bladder carcinomas, mainly because there is no evidence for a major gene (Aben et al. Several of these moderate-risk variants, especially those categorized as phase II metabolism genes, have been shown to modulat...

متن کامل

Evaluation of Long Stress-Induced Non-coding Transcripts 5 Polymorphism in Iranian Patients with Bladder Cancer

Background: Bladder cancer (BC) is the most commonly diagnosed genitourinary cancer in Iran, presented in both men and women. BC is a multifactorial trait resulting from the complex interaction between several genes and environmental factors. Long stress-induced non-coding transcript 5 (LSINCT5), a member of the long non-coding RNAs, is abundantly expressed in high proliferative cells, as well ...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:
  • Carcinogenesis

دوره 35 8  شماره 

صفحات  -

تاریخ انتشار 2014