Department of Head and Neck Surgery, The University of Texas MD Anderson Cancer Center, Houston, Texas, United States of America.
PLoS One. 2012;7(11):e49361. doi: 10.1371/journal.pone.0049361. Epub 2012 Nov 7.
The p14(ARF)/MDM2/p53 pathway plays an important role in modulation of DNA damage and oxidative stress responses. The aim of this study was to determine whether genetic variants in MDM2 and p14(ARF) are associated with risk of salivary gland carcinoma (SGC).
Four single nucleotide polymorphisms (SNPs) in MDM2 and p14(ARF) (MDM2-rs2279744, MDM2-rs937283, p14(ARF)-rs3731217, and p14(ARF)-rs3088440) were genotyped in 156 patients with SGC and 511 cancer-free controls. Multivariate logistic regression analysis was performed to calculate odds ratios (ORs) and 95% confidence intervals (CIs).
MDM2-rs2279744 was significantly associated with a moderately increased risk of SGC (OR, 1.5, 95% CI, 1.1-2.2). There was a trend toward significantly increased SGC risk with increasing number of risk genotypes of the four polymorphisms (P(trend) = 0.004). Individuals carrying 3-4 risk genotypes in MDM2 and p14(ARF) were at increased SGC risk (OR, 2.0, 95% CI, 1.1-2.7) compared with individuals carrying 0-2 risk genotypes. Moreover, the combined effect of risk genotypes of MDM2 and p14(ARF) was more pronounced among young subjects (≤ 45 years), female subjects, subjects with race/ethnicity other than non-Hispanic white, ever-smokers, and ever-drinkers.
Our results support the involvement of SNPs of MDM2 and p14(ARF), either alone or more likely in combination, in susceptibility to SGC. Larger studies are needed to validate our findings.
p14(ARF)/MDM2/p53 通路在调节 DNA 损伤和氧化应激反应中起着重要作用。本研究旨在确定 MDM2 和 p14(ARF)中的遗传变异是否与唾液腺癌 (SGC)的风险相关。
在 156 名 SGC 患者和 511 名无癌症对照中,对 MDM2 和 p14(ARF)中的四个单核苷酸多态性 (SNP) (MDM2-rs2279744、MDM2-rs937283、p14(ARF)-rs3731217 和 p14(ARF)-rs3088440)进行了基因分型。采用多变量逻辑回归分析计算比值比 (OR) 和 95%置信区间 (CI)。
MDM2-rs2279744 与 SGC 的中度风险增加显著相关 (OR,1.5,95%CI,1.1-2.2)。随着四个多态性的风险基因型数量的增加,SGC 的风险呈显著增加趋势 (P(trend) = 0.004)。与携带 0-2 个风险基因型的个体相比,携带 MDM2 和 p14(ARF)中 3-4 个风险基因型的个体患 SGC 的风险增加 (OR,2.0,95%CI,1.1-2.7)。此外,在年轻 (≤ 45 岁)、女性、非非裔白人、吸烟者和饮酒者中,MDM2 和 p14(ARF)的风险基因型联合作用更为明显。
我们的结果支持 MDM2 和 p14(ARF)中的 SNP 单独或更可能联合参与 SGC 的易感性。需要更大的研究来验证我们的发现。