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MDM4 SNP34091 (rs4245739) and its effect on breast‐ colon‐ lung‐ and prostate cancer risk

机译:MDM4 SNP34091(rs4245739)及其对乳腺癌结肠癌肺癌和前列腺癌的风险

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摘要

The MDM4 protein plays an important part in the negative regulation of the tumor suppressor p53 through its interaction with MDM2. In line with this, MDM4 amplification has been observed in several tumor forms. A polymorphism (rs4245739 A>C; ) in the MDM4 3′ untranslated region has been reported to create a target site for hsa‐miR‐191, resulting in decreased MDM4 mRNA levels. In this population‐based case–control study, we examined the potential association between MDM4 , alone and in combination with the MDM2 SNP309T>G (rs2279744), and the risk of breast‐, colon‐, lung‐, and prostate cancer in Norway. was genotyped in 7,079 cancer patients as well as in 3,747 gender‐ and age‐matched healthy controls. MDM4 SNP34091C was not associated with risk for any of the tumor forms examined, except for a marginally significant association with reduced risk for breast cancer in a recessive model (OR = 0.77: 95% CI = 0.59–0.99). Stratifying according to MDM2 SNP309 status, we observed a reduced risk for breast cancer related to MDM4 SNP34091CC among individuals harboring the MDM2 SNP309GG genotype (OR = 0.41; 95% CI = 0.21–0.82). We conclude, MDM4 status to be associated with reduced risk of breast cancer, in particular in individuals carrying the MDM2 SNP309GG genotype, but not to be associated with either lung‐, colon‐ or prostate cancer.
机译:通过与MDM2相互作用,MDM4蛋白在肿瘤抑制因子p53的负调控中起重要作用。与此相一致,已经观察到几种肿瘤形式的MDM4扩增。据报道,在MDM4 3'非翻译区中存在一个多态性(rs4245739 A> C;),可为hsa-miR-191创建目标位点,从而导致MDM4 mRNA水平降低。在这项基于人群的病例对照研究中,我们研究了挪威单独使用MDM4和与MDM2 SNP309T> G(rs2279744)联合使用与乳腺癌,结肠癌,肺癌和前列腺癌风险之间的潜在关联。 。在7,079名癌症患者以及3,747名性别和年龄匹配的健康对照中进行了基因分型。 MDM4 SNP34091C与任何一种检查的肿瘤形式均不相关,除了在隐性模型中与乳腺癌风险降低之间有显着相关性外(OR = 0.77:95%CI = 0.59-0.99)。根据MDM2 SNP309状态进行分层,我们观察到具有MDM2 SNP309GG基因型的个体中与MDM4 SNP34091CC相关的乳腺癌风险降低(OR = 0.41; 95%CI = 0.21-0.82)。我们得出的结论是,MDM4状态与乳腺癌风险降低相关,特别是在携带MDM2 SNP309GG基因型的个体中,与肺癌,结肠癌或前列腺癌无关。

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