[No authors listed]
Cancers of the upper aerodigestive tract (UADT) include malignant tumors of the oral cavity, pharynx, larynx, and esophagus and account for 6.4% of all new cancers in Europe. In the context of a multicenter case-control study conducted in 14 centers within 10 European countries and comprising 1,511 cases and 1,457 controls (ARCAGE study), 115 single nucleotide polymorphisms (SNP) from 62 a priori-selected genes were studied in relation to UADT cancer. We found 11 SNPs that were statistically associated with UADT cancers overall (5.75 expected). Considering the possibility of false-positive results, we focused on SNPs in CYP2A6, MDM2, tumor necrosis factor (TNF), and gene amplified in squamous cell carcinoma 1 (GASC1), for which low P values for trend (P trend<0.01) were observed in the main effects analyses of UADT cancer overall or by subsite. The rare variant of CYP2A6 -47A>C (rs28399433), a phase I metabolism gene, was associated with reduced UADT cancer risk (P trend=0.01). Three SNPs in the MDM2 gene, involved in cell cycle control, were associated with UADT cancer. MDM2 IVS5+1285A>G (rs3730536) showed a strong codominant effect (P trend=0.007). The rare variants of two SNPs in the TNF gene were associated with a decreased risk; for TNF IVS1+123G>A (rs1800610), the P trend was 0.007. Variants in two SNPs of GASC1 were found to be strongly associated with increased UADT cancer risk (for both, P trend=0.008). This study is the largest genetic epidemiologic study on UADT cancers in Europe. Our analysis points to potentially relevant genes in various pathways.
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Kdm4c, CDH2, CDH11, NAT2, CDKN1A, CDKN2A, LZTS1, ADH1B, ADH1C, COMT, CTNNB1, CYP1A1, CYP1A2, CYP2A6, CYP2C8, CYP2C9, CYP3A4, NQO1, DRD2, EPHX1, ERBB2, ERCC1, ERCC4, ALDH2, FANCG, FHIT, KDM4C, ANKK1, GJB5, GSTA2, GSTM3, GSTP1, GSTT2, APEX1, IL1R1, ITGA3, LIG3, LTBP1, MDM2, MGMT, MPO, MTHFR, OGG1, DEC1, PCNA, POLB, WRAP53, SOD2, SULT1A1, TGFB1, TGFBR2, TNF, TNFAIP2, TP53, TYMS, XRCC1, XRCC2, XRCC3, DLEC1, CDH1
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