Wang Guimin, Firoz Elnaz F, Rose Amy, Blochin Elen, Christos Paul, Pollens Danuta, Mazumdar Madhu, Gerald William, Oddoux Carole, Lee Peng, Osman Iman
The Ronald O. Perelman Department of Dermatology, NYU Cancer Institute, New York University School of Medicine, New York, New York, USA.
Int J Clin Exp Pathol. 2009;2(4):353-60. Epub 2008 Dec 4.
MDM2 is a key negative regulator of tumor suppressor p53. A single nucleotide polymorphism in the MDM2 promoter, SNP309, enhances transcriptional activation of MDM2 and has been associated with early onset of several types of cancer. In this study, we attempted to determine if the MDM2 SNP309 polymorphism plays a role in the aggressive phenotype seen in African American (AA) prostate cancer by examining the association between MDM2 SNP309 and MDM2 protein levels in prostate cancer (PCa) patients of different racial backgrounds. Prospectively enrolled PCa patients (AA=51, CA=50) were evaluated for MDM2 SNP309 and MDM2 protein expression. MDM2 overexpression, defined as >10% of tumor cells in three tissue cores, was assessed using immunohistochemistry on tissue microarray. MDM2 protein expression was significantly greater in CA than AA patients (78% versus 45% respectively, p=0.0007). Germline DNA was analyzed by PCR-RFLP then confirmed by DNA sequencing. MDM2 SNP309 genotype frequencies did not differ significantly between AA and CA PCa patients (AA: TT 68.6%, TG 25.5%, GG 5.9%; CA: TT 62.0%, TG 20.0%, GG 18.0%; p=0.16), suggesting that the MDM2 SNP309 allele does not play a significant role in the observed overexpression.
MDM2是肿瘤抑制因子p53的关键负调控因子。MDM2启动子中的单核苷酸多态性SNP309可增强MDM2的转录激活作用,并与多种癌症的早发相关。在本研究中,我们试图通过检测不同种族背景的前列腺癌(PCa)患者中MDM2 SNP309与MDM2蛋白水平之间的关联,来确定MDM2 SNP309多态性是否在非裔美国人(AA)前列腺癌的侵袭性表型中发挥作用。对前瞻性纳入的PCa患者(AA = 51例,CA = 50例)进行MDM2 SNP309和MDM2蛋白表达评估。使用组织微阵列免疫组化法评估MDM2过表达情况,定义为三个组织芯中肿瘤细胞>10%。CA患者的MDM2蛋白表达显著高于AA患者(分别为78%和45%,p = 0.0007)。通过PCR-RFLP分析种系DNA,然后通过DNA测序进行确认。AA和CA PCa患者之间的MDM2 SNP309基因型频率无显著差异(AA:TT 68.6%,TG 25.5%,GG 5.9%;CA:TT 62.0%,TG 20.0%,GG 18.0%;p = 0.16),这表明MDM2 SNP309等位基因在观察到的过表达中不发挥重要作用。