ABCB1/4 gallbladder cancer risk variants identified in India also show strong effects in Chileans
Autor
Boekstegers, Felix
Marcelain, Katherine
Barahona-Ponce, Carol
Baez Benavides, Pablo F.
Müller, Bettina
De Toro, Gonzalo
Retamales, Javier
Barajas, Olga
Ahumada, Monica
Morales, Erik
Sanhueza, Verónica
Loader, Denisse
Rivera, María T.
Gutiérrez, Lorena
Bernal, Giuliano
Ortega, Alejandro
Montalvo, Domingo
Portiño, Sergio
Bertrán, María E.
Gabler, F.
Spencer, Loreto
Olloquequi, Jordi
González-Silos, Rosa
Fischer, Christine
Scherer, Dominique
Jenab, Mazda
Aleksandrova, Krasimira
Katzke, Verena
Weiderpass, Elisabete
Moradi, Tahereh
Fischer, Krista
Bossers, Willem
Brenner, Hermann
Hveem, Kristian
Eklund, Niina
Völker, Uwe
Waldenberger, Melanie
Fuentes-Guajardo, Macarena
González-José, Rolando
Bedoya, Gabriel
Bortolini, María C.
Canizales, Samuel
Gallo, Carla
Ruiz-Linares, Andres
Rothhammer, Francisco
Lorenzo-Bermejo, Justo
Fecha
2020Resumen
Background: The first large-scale genome-wide association study of gallbladder cancer (GBC) recently identified and validated three susceptibility variants in the ABCB1 and ABCB4 genes for individuals of Indian descent. We investigated whether these variants were also associated with GBC risk in Chileans, who show the highest incidence of GBC worldwide, and in Europeans with a low GBC incidence. Methods: This population-based study analysed genotype data from retrospective Chilean case-control (255 cases, 2042 controls) and prospective European cohort (108 cases, 181 controls) samples consistently with the original publication. Results: Our results confirmed the reported associations for Chileans with similar risk effects. Particularly strong associations (per-allele odds ratios close to 2) were observed for Chileans with high Native American (=Mapuche) ancestry. No associations were noticed for Europeans, but the statistical power was low. Conclusion: Taking full advantage of genetic and ethnic differences in GBC risk may improve the efficiency of current prevention programs.
Fuente
Cancer epidemiology, 65, 101643Link de Acceso
Click aquí para ver el documentoIdentificador DOI
doi.org/10.1016/j.canep.2019.101643Colecciones
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