Kang Shan, Wang Dong-Jie, Li Wan-Sheng, Wang Na, Zhou Rong-Miao, Sun Dong-Lan, Duan Ya-Nan, Li Shi-Zhen, Li Xiao-Fei, Li Yan
Department of Obstetrics and Gynecology, Hebei Medical University, Fourth Hospital, Shijiazhuang, China.
Int J Gynecol Cancer. 2009 May;19(4):572-7. doi: 10.1111/IGC.0b013e3181a130ab.
This study was to investigate the association of p73 G4C14-to-A4T14 and Murine Double Minute2 (MDM2) 309T/G, Del1518+/- single nucleotide polymorphisms with the risk of epithelial ovarian cancer (EOC) in Chinese.
This hospital-based case-control study included 257 ovarian cancer patients and 257 healthy women who were matched for age. p73 and MDM2 genotypes were determined by polymerase chain reaction-restriction fragment length polymorphism.
There were no significant differences in allele frequencies and genotype distributions of the p73 G4C14-to-A4T14 polymorphism between cases and control women (P = 0.55 and 0.20, respectively). The frequencies of the G allele of the MDM2 309T/G polymorphism were significantly lower in ovarian cancer cases (46.7%) than those in healthy controls (54.7%), there was a statistical difference between the 2 groups (P = 0.01). Compared with the T/T genotype, the G allelotype (T/G+G/G genotype) significantly decreased the risk of developing EOC (odds ratio, 0.65; 95% confidence interval, 0.44-0.97). Although MDM2 Del1518+/- genotypes and allele frequencies did not differ between the case and the control groups (P = 0.68 and P = 0.45), Del1518 +/+ genotype tended to increase the risk of mucinous ovarian cancer or earlier ovarian cancer by stratification analysis according to histological subtypes or clinical stage. Besides, there was a significant interaction between p73 G4C14-to-A4T14 and MDM2 309T/G polymorphisms by the likelihood ratio test (P = 0.03; odds ratio, 0.89; 95% confidence interval, 0.80-0.99).
The MDM2 SNP309G allele significantly decreased the risk of EOC and might be a potentially protective factor for EOC development in Chinese women.
本研究旨在探讨在中国人群中,p73基因G4C14→A4T14单核苷酸多态性以及鼠双微体2(MDM2)基因309T/G、Del1518+/-单核苷酸多态性与上皮性卵巢癌(EOC)发病风险的相关性。
本基于医院的病例对照研究纳入了257例卵巢癌患者和257例年龄匹配的健康女性。采用聚合酶链反应-限制性片段长度多态性方法检测p73和MDM2基因的基因型。
病例组与对照组女性之间,p73基因G4C14→A4T14多态性的等位基因频率和基因型分布无显著差异(P值分别为0.55和0.20)。MDM2基因309T/G多态性中G等位基因在卵巢癌病例组中的频率(46.7%)显著低于健康对照组(54.7%),两组间存在统计学差异(P = 0.01)。与T/T基因型相比,G等位基因型(T/G + G/G基因型)显著降低了发生EOC的风险(比值比,0.65;95%置信区间,0.44 - 0.97)。尽管MDM2基因Del1518+/-的基因型和等位基因频率在病例组和对照组之间无差异(P值分别为0.68和0.45),但根据组织学亚型或临床分期进行分层分析时发现,Del1518 +/+基因型倾向于增加黏液性卵巢癌或早期卵巢癌的发病风险。此外,通过似然比检验发现p73基因G4C14→A4T14与MDM2基因309T/G多态性之间存在显著交互作用(P = 0.03;比值比,0.89;95%置信区间,0.80 - 0.99)。
MDM2基因SNP309G等位基因显著降低了EOC的发病风险,可能是中国女性EOC发生的潜在保护因素。