Identification of a melanoma susceptibility locus and somatic mutation in TET2.


Journal Article

Although genetic studies have reported a number of loci associated with melanoma risk, the complex genetic architecture of the disease is not yet fully understood. We sought to identify common genetic variants associated with melanoma risk in a genome-wide association study (GWAS) of 2298 cases and 6654 controls. Thirteen of 15 known loci were replicated with nominal significance. A total of 69 single-nucleotide polymorphisms (SNPs) were selected for in silico replication in two independent melanoma GWAS datasets (a total of 5149 cases and 12 795 controls). Seven novel loci were nominally significantly associated with melanoma risk. These seven SNPs were further genotyped in 234 melanoma cases and 238 controls. The SNP rs4698934 was nominally significantly associated with melanoma risk. The combined odds ratio per T allele = 1.18; 95% confidence interval (1.10-1.25); combined P = 7.70 × 10(-) (7). This SNP is located in the intron of the TET2 gene on chromosome 4q24. In addition, a novel somatic mutation of TET2 was identified by next-generation sequencing in 1 of 22 sporadic melanoma cases. TET2 encodes a member of TET family enzymes that oxidizes 5-methylcytosine to 5-hydroxymethylcytosine (5hmC). It is a putative epigenetic biomarker of melanoma as we previously reported, with observation of reduced TET2 transcriptional expression. This study is the first to implicate TET2 genetic variation and mutation in melanoma.

Full Text

Duke Authors

Cited Authors

  • Song, F; Amos, CI; Lee, JE; Lian, CG; Fang, S; Liu, H; MacGregor, S; Iles, MM; Law, MH; Lindeman, NI; Montgomery, GW; Duffy, DL; Cust, AE; Jenkins, MA; Whiteman, DC; Kefford, RF; Giles, GG; Armstrong, BK; Aitken, JF; Hopper, JL; Brown, KM; Martin, NG; Mann, GJ; Bishop, DT; Bishop, JAN; GenoMEL consortium, ; Kraft, P; Qureshi, AA; Kanetsky, PA; Hayward, NK; Hunter, DJ; Wei, Q; Han, J

Published Date

  • September 2014

Published In

Volume / Issue

  • 35 / 9

Start / End Page

  • 2097 - 2101

PubMed ID

  • 24980573

Pubmed Central ID

  • 24980573

Electronic International Standard Serial Number (EISSN)

  • 1460-2180

Digital Object Identifier (DOI)

  • 10.1093/carcin/bgu140


  • eng

Conference Location

  • England