Song Dong-Jian, Yue Li-Fang, Zhang Da, Yang He-Ying, Fan Yu-Xia, Yue Ming, Pei Hang, Wang Jia-Xiang
Department of Pediatric Surgery, First Affiliated Hospital of Zhengzhou University, Zhengzhou 450052, China.
Zhongguo Dang Dai Er Ke Za Zhi. 2013 Aug;15(8):638-43.
To investigate the mRNA expression and promoter methylation status of p73 gene in the peripheral blood of children with Wilms' tumor (WT), and their relationship.
Forty-five children with WT were selected as the case group, and 15 sex- and age- matched children (without malignancies) who visited the hospital for physical examination or other reasons were selected as the control group. Peripheral blood was collected from both groups. Real-time quantitative PCR and methylation-specific PCR were used to determine the mRNA expression level and promoter methylation status of p73 gene. Their relationship with clinicopathological features and the effect of promoter methylation on mRNA expression of p73 gene were analyzed in the case group.
The relative quantity (RQ) of p73 mRNA in the case group was significantly higher than in the control group (3.2 ± 0.9 vs 1.6 ± 1.1; P<0.01). The positive rate of p73 gene promoter methylation in the case group was significantly lower than in the control group (20% vs 73%; P<0.01). In the case group, the RQ of p73 mRNA was significantly higher in children with methylated p73 gene promoter than in those with unmethylated p73 gene promoter (P<0.01). In children with methylated p73 gene promoter, the RQ of p73 mRNA was significantly higher in the case group than in the control group (P<0.01). In children with unmethylated p73 gene promoter, there was no significant difference in RQ of p73 mRNA between the case and control groups (P=0.810).
Aberrant promoter methylation of p73 gene in peripheral blood is one of the gene expression regulations in children with WT, and it is related to the onset and development of WT. The p73 gene may play a role as oncogene in WT patients with p73 gene promoter methylation and mRNA overexpression is associated with promoter methylation status of p73 gene.
探讨肾母细胞瘤(WT)患儿外周血中p73基因的mRNA表达及启动子甲基化状态及其关系。
选取45例WT患儿作为病例组,选取15例因体格检查或其他原因来院就诊的性别和年龄匹配的无恶性肿瘤患儿作为对照组。采集两组患儿的外周血。采用实时定量PCR和甲基化特异性PCR检测p73基因的mRNA表达水平和启动子甲基化状态。分析病例组中其与临床病理特征的关系以及启动子甲基化对p73基因mRNA表达的影响。
病例组p73 mRNA的相对定量(RQ)显著高于对照组(3.2±0.9 vs 1.6±1.1;P<0.01)。病例组p73基因启动子甲基化阳性率显著低于对照组(20% vs 73%;P<0.01)。病例组中,p73基因启动子甲基化的患儿p73 mRNA的RQ显著高于未甲基化患儿(P<0.01)。p73基因启动子甲基化的患儿中,病例组p73 mRNA的RQ显著高于对照组(P<0.01)。p73基因启动子未甲基化的患儿中,病例组和对照组p73 mRNA的RQ无显著差异(P=0.810)。
外周血中p73基因启动子异常甲基化是WT患儿基因表达调控方式之一,与WT的发生发展有关。p73基因在p73基因启动子甲基化的WT患者中可能作为癌基因发挥作用,且mRNA过表达与p73基因启动子甲基化状态有关。