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Identification and replication of the interplay of four genetic high-risk variants for urinary bladder cancer

Authors :
Gergely Bánfi
Klaus Golka
Péter Nyirády
Silvia Selinski
Emanuel Roth
Núria Malats
Nathaniel Rothman
Daniel Ovsiannikov
Frank Volkert
Montserrat Garcia-Closas
Lambertus A. Kiemeney
Manolis Kogevinas
Thomas Otto
Oliver Moormann
Jan G. Hengstler
M. Blaszkewicz
Debra T. Silverman
Molly Schwenn
Alison Johnson
Holger Gerullis
Margaret R. Karagas
Stella Koutros
Katja Ickstadt
Jonine D. Figueroa
Sita H. Vermeulen
Source :
Recercat. Dipósit de la Recerca de Catalunya, instname, Carcinogenesis, 38, 1167-1179, Carcinogenesis, Carcinogenesis, 38, 12, pp. 1167-1179, Selinski, S, Blaszkewicz, M, Ickstadt, K, Gerullis, H, Otto, T, Roth, E, Volkert, F, Ovsiannikov, D, Moormann, O, Banfi, G, Nyirady, P, Vermeulen, S H, Garcia-closas, M, Figueroa, J D, Johnson, A, Karagas, M R, Kogevinas, M, Malats, N, Schwenn, M, Silverman, D T, Koutros, S, Rothman, N, Kiemeney, L A, Hengstler, J G & Golka, K 2017, ' Identification and replication of the interplay of four genetic high risk variants for urinary bladder cancer ', Carcinogenesis: Integrative Cancer Research . https://doi.org/10.1093/carcin/bgx102, Dipòsit Digital de la UB, Universidad de Barcelona
Publisher :
Oxford University Press

Abstract

We identified and replicated specific combinations of three and four genetic variants that enhance bladder cancer risk in 5049 cases and 5452 controls. Different combinations were relevant in never, former and current smokers. The highest OR was obtained in never smokers (OR = 2.59).<br />Little is known whether genetic variants identified in genome-wide association studies interact to increase bladder cancer risk. Recently, we identified two- and three-variant combinations associated with a particular increase of bladder cancer risk in a urinary bladder cancer case–control series (Leibniz Research Centre for Working Environment and Human Factors at TU Dortmund (IfADo), 1501 cases, 1565 controls). In an independent case–control series (Nijmegen Bladder Cancer Study, NBCS, 1468 cases, 1720 controls) we confirmed these two- and three-variant combinations. Pooled analysis of the two studies as discovery group (IfADo-NBCS) resulted in sufficient statistical power to test up to four-variant combinations by a logistic regression approach. The New England and Spanish Bladder Cancer Studies (2080 cases and 2167 controls) were used as a replication series. Twelve previously identified risk variants were considered. The strongest four-variant combination was obtained in never smokers. The combination of rs1014971[AA] near apolipoprotein B mRNA editing enzyme, catalytic polypeptide-like 3A (APOBEC3A) and chromobox homolog 6 (CBX6), solute carrier family 1s4 (urea transporter), member 1 (Kidd blood group) (SLC14A1) exon single nucleotide polymorphism (SNP) rs1058396[AG, GG], UDP glucuronosyltransferase 1 family, polypeptide A complex locus (UGT1A) intron SNP rs11892031[AA] and rs8102137[CC, CT] near cyclin E1 (CCNE1) resulted in an unadjusted odds ratio (OR) of 2.59 (95% CI = 1.93–3.47; P = 1.87 × 10−10), while the individual variant ORs ranged only between 1.11 and 1.30. The combination replicated in the New England and Spanish Bladder Cancer Studies (ORunadjusted = 1.60, 95% CI = 1.10–2.33; P = 0.013). The four-variant combination is relatively frequent, with 25% in never smoking cases and 11% in never smoking controls (total study group: 19% cases, 14% controls). In conclusion, we show that four high-risk variants can statistically interact to confer increased bladder cancer risk particularly in never smokers.

Details

ISSN :
01433334
Database :
OpenAIRE
Journal :
Recercat. Dipósit de la Recerca de Catalunya, instname, Carcinogenesis, 38, 1167-1179, Carcinogenesis, Carcinogenesis, 38, 12, pp. 1167-1179, Selinski, S, Blaszkewicz, M, Ickstadt, K, Gerullis, H, Otto, T, Roth, E, Volkert, F, Ovsiannikov, D, Moormann, O, Banfi, G, Nyirady, P, Vermeulen, S H, Garcia-closas, M, Figueroa, J D, Johnson, A, Karagas, M R, Kogevinas, M, Malats, N, Schwenn, M, Silverman, D T, Koutros, S, Rothman, N, Kiemeney, L A, Hengstler, J G & Golka, K 2017, ' Identification and replication of the interplay of four genetic high risk variants for urinary bladder cancer ', Carcinogenesis: Integrative Cancer Research . https://doi.org/10.1093/carcin/bgx102, Dipòsit Digital de la UB, Universidad de Barcelona
Accession number :
edsair.doi.dedup.....30ed2f3e3e1c994a886ae18312c71ff1
Full Text :
https://doi.org/10.1093/carcin/bgx102