Validation of loci at 2q14.2 and 15q21.3 as risk factors for testicular cancer.


Loveday, C; Litchfield, K; Levy, M; Holroyd, A; Broderick, P; Kote-Jarai, Z; Dunning, AM; Muir, K; Peto, J; Eeles, R; Easton, DF; Dudakia, D; Orr, N; Pashayan, N; Reid, A; Huddart, RA; Houlston, RS; Turnbull, C; (2017) Validation of loci at 2q14.2 and 15q21.3 as risk factors for testicular cancer. Oncotarget, 9 (16). pp. 12630-12638. ISSN 1949-2553 DOI: https://doi.org/10.18632/oncotarget.23117

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Abstract

Testicular germ cell tumor (TGCT), the most common cancer in men aged 18 to 45 years, has a strong heritable basis. Genome-wide association studies (GWAS) have proposed single nucleotide polymorphisms (SNPs) at a number of loci influencing TGCT risk. To further evaluate the association of recently proposed risk SNPs with TGCT at 2q14.2, 3q26.2, 7q36.3, 10q26.13 and 15q21.3, we analyzed genotype data on 3,206 cases and 7,422 controls. Our analysis provides independent replication of the associations for risk SNPs at 2q14.2 (rs2713206 at <i>P</i> = 3.03 × 10<sup>-2</sup>; <i>P</i>-meta = 3.92 × 10-8; nearest gene, TFCP2L1) and rs12912292 at 15q21.3 (<i>P</i> = 7.96 × 10<sup>-11</sup>; <i>P</i>-meta = 1.55 × 10<sup>-19</sup>; nearest gene PRTG). Case-only analyses did not reveal specific associations with TGCT histology. TFCP2L1 joins the growing list of genes located within TGCT risk loci with biologically plausible roles in developmental transcriptional regulation, further highlighting the importance of this phenomenon in TGCT oncogenesis.

Item Type: Article
Faculty and Department: Faculty of Epidemiology and Population Health > Dept of Non-Communicable Disease Epidemiology
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PubMed ID: 29560096
URI: http://researchonline.lshtm.ac.uk/id/eprint/4647132

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