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

Silvia Selinski, Meinolf Blaszkewicz, Katja Ickstadt, Holger Gerullis, Thomas Otto, Emanuel Roth, Frank Volkert, Daniel Ovsiannikov, Oliver Moormann, Gergely Banfi, Peter Nyirady, Sita H. Vermeulen, Montserrat Garcia-Closas, Jonine D. Figueroa, Alison Johnson, Margaret R. Karagas, Manolis Kogevinas, Nuria Malats, Molly Schwenn, Debra T. SilvermanStella Koutros, Nathaniel Rothman, Lambertus A. Kiemeney, Jan G. Hengstler, Klaus Golka

Research output: Article

7 Citations (Scopus)


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.

Original languageEnglish
Pages (from-to)1167-1179
Number of pages13
Issue number12
Publication statusPublished - dec. 1 2017


ASJC Scopus subject areas

  • Cancer Research

Cite this

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., ... Golka, K. (2017). Identification and replication of the interplay of four genetic high-risk variants for urinary bladder cancer. Carcinogenesis, 38(12), 1167-1179.