Genome-wide association study for colorectal cancer identifies risk polymorphisms in German familial cases and implicates MAPK signalling pathways in disease susceptibility

• Published in: Carcinogenesis (New York) Vol. 31; no. 9; pp. 1612 - 1619
• Main Authors: Lascorz, Jesús, Försti, Asta, Chen, Bowang, Buch, Stephan, Steinke, Verena, Rahner, Nils, Holinski-Feder, Elke, Morak, Monika, Schackert, Hans K., Görgens, Heike, Schulmann, Karsten, Goecke, Timm, Kloor, Matthias, Engel, Cristoph, Büttner, Reinhard, Kunkel, Nelli, Weires, Marianne, Hoffmeister, Michael, Pardini, Barbara, Naccarati, Alessio, Vodickova, Ludmila, Novotny, Jan, Schreiber, Stefan, Krawczak, Michael, Bröring, Clemens D., Völzke, Henry, Schafmayer, Clemens, Vodicka, Pavel, Chang-Claude, Jenny, Brenner, Hermann, Burwinkel, Barbara, Propping, Peter, Hampe, Jochen, Hemminki, Kari
• Format: Journal Article
• Language: English
• Published: Oxford Oxford University Press 01.09.2010
• Subjects: Biological and medical sciences; Cancer and Oncology; Cancer och onkologi; Carcinogenesis; Carcinogenesis, carcinogens and anticarcinogens; Case-Control Studies; Clinical Medicine; Colorectal Neoplasms - epidemiology; Colorectal Neoplasms - genetics; European Continental Ancestry Group - genetics; Gastroenterology. Liver. Pancreas. Abdomen; Genetic Predisposition to Disease; Genome-Wide Association Study; Germany - epidemiology; Humans; Klinisk medicin; Medical and Health Sciences; Medical sciences; Medicin och hälsovetenskap; Mitogen-Activated Protein Kinases - genetics; Neoplasm Staging; Polymorphism, Single Nucleotide - genetics; Prognosis; Risk Factors; Signal Transduction - genetics; Stomach. Duodenum. Small intestine. Colon. Rectum. Anus; Tumors; Europe; Germany; Rectal disease; Genetic variability; Enzyme; Family study; Transferases; Colorectal cancer; Mitogen-activated protein kinase; Genotype; Malignant tumor; Colonic disease; Signal transduction; Association; Signaling pathway; Risk factor; Digestive diseases; Intestinal disease; Genome; Cancer; Polymorphism
• ISSN: 0143-3334; 1460-2180
• DOI: 10.1093/carcin/bgq146

Genetic susceptibility accounts for ∼35% of all colorectal cancer (CRC). Ten common low-risk variants contributing to CRC risk have been identified through genome-wide association studies (GWASs). In our GWAS, 610 664 genotyped single-nucleotide polymorphisms (SNPs) passed the quality control filtering in 371 German familial CRC patients and 1263 controls, and replication studies were conducted in four additional case–control sets (4915 cases and 5607 controls). Known risk loci at 8q24.21 and 11q23 were confirmed, and a previously unreported association, rs12701937, located between the genes GLI3 (GLI family zinc finger 3) and INHBA (inhibin, beta A) [P = 1.1 × 10−3, odds ratio (OR) 1.14, 95% confidence interval (CI) 1.05–1.23, dominant model in the combined cohort], was identified. The association was stronger in familial cases compared with unselected cases (P = 2.0 × 10−4, OR 1.36, 95% CI 1.16–1.60, dominant model). Two other unreported SNPs, rs6038071, 40 kb upstream of CSNK2A1 (casein kinase 2, alpha 1 polypeptide) and an intronic marker in MYO3A (myosin IIIA), rs11014993, associated with CRC only in the familial CRC cases (P = 2.5 × 10−3, recessive model, and P = 2.7 × 10−4, dominant model). Three software tools successfully pointed to the overrepresentation of genes related to the mitogen-activated protein kinase (MAPK) signalling pathways among the 1340 most strongly associated markers from the GWAS (allelic P value < 10−3). The risk of CRC increased significantly with an increasing number of risk alleles in seven genes involved in MAPK signalling events (Ptrend = 2.2 × 10−16, ORper allele = 1.34, 95% CI 1.11–1.61).