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中华乳腺病杂志(电子版) ›› 2010, Vol. 04 ›› Issue (05) : 581 -587. doi: 10.3877/cma.j.issn.1674-0807.2010.05.010

实验研究

乳腺癌Runx3基因启动子甲基化状态及其与病理特征的关系
田声望1, 贾绍昌2,(), 陈坚2   
  1. 1.213200金坛,江苏省金坛市人民医院肿瘤内科
    2.210012南京,解放军八一医院全军肿瘤中心
  • 收稿日期:2009-10-28 出版日期:2010-10-01
  • 通信作者: 贾绍昌

Analysis of the status of Runx3 gene promoter methylation in breast cancer and its relationship with pathological features

Sheng-wang TIAN1, Shao-chang JIA,1(), Jian CHEN1   

  1. 1.Jintan People's Hospital,Jintan 213200,China
  • Received:2009-10-28 Published:2010-10-01
  • Corresponding author: Shao-chang JIA
引用本文:

田声望, 贾绍昌, 陈坚. 乳腺癌Runx3基因启动子甲基化状态及其与病理特征的关系[J/OL]. 中华乳腺病杂志(电子版), 2010, 04(05): 581-587.

Sheng-wang TIAN, Shao-chang JIA, Jian CHEN. Analysis of the status of Runx3 gene promoter methylation in breast cancer and its relationship with pathological features[J/OL]. Chinese Journal of Breast Disease(Electronic Edition), 2010, 04(05): 581-587.

目的

探讨乳腺癌组织中Runx3基因启动子甲基化状态及其与乳腺癌临床病理特征之间的关系。

方法

2007年2 月至2009年4月收集经病理确诊的56例乳腺癌患者癌组织及相应的癌旁组织。采用甲基化特异聚合酶链反应检测Runx3基因启动子区Cp G 岛的甲基化状态,并检测其对Runx3基因表达的影响和分析其与乳腺癌临床病理特征之间的关系。统计学分析采用χ2 检验和Pearson 相关分析法。

结果

乳腺癌组织中Runx3基因启动子区Cp G 岛甲基化率(55.4%)显著高于癌旁组织中的甲基化率(10.7%),二者之间差异有统计学意义(χ2=25.225,P=0.000)。Runx3基因的异常甲基化和乳腺癌患者的临床分期及淋巴结转移有关(P=0.018,P=0.010),但与患者的年龄、肿瘤直径大小及组织学类型无关(P>0.050)。Runx3 mRNA 表达与Runx3启动子甲基化呈弱相关(r=0.343,P=0.010)。

结论

Runx3基因启动子甲基化状态导致Runx3基因mRNA 表达降低或缺失。Runx3基因启动子区甲基化可能是导致Runx3基因在乳腺癌中失活的分子机制之一。

Objective

To analyze the status of Runx3 gene promoter methylation and explore its association with the expression of Runx3 gene and clinicopathological factors of breast cancer.

Methods

From February 2007 to April 2009,a total of 56 breast cancer tissue samples and corresponding pericancer tissues were collected and used for this study.All samples were confirmed pathologically.Methylation-specific PCR (polymerase chain reaction)was performed to detect the promoter hypermethylation of Runx3 gene,and analyze its influence on the expression of Runx3 gene and the relationship between Runx3 promoter methylation and clinicopathological factors in breast cancer.Chi-square test and Pearson test were used for statistical analysis.

Results

The rate of promoter hypermethylation of Runx3 gene in the breast cancer tissues(55.4%)was significantly higher than that in the pericancer tissues(10.7%),with statistical difference between the two(χ2=25.225,P=0.000).Runx3 gene hypermethylation was related with clinical staging and lymph node metastasis(P=0.018,P=0.010),but not related with the age,tumour size and histological types(P>0.050).There was a light association between the expression of Runx3 m RNA and Runx3 promoter methylation (r=0.343,P=0.010).

Conclusions

Runx3 promoter methylation can lead to a decrease or absence in the runx3 mRNA expression in breast cancer.The promoter methylation of Runx3 gene can induce the inhibition of Runx3 m RNA expression,which might be one of the mechanisms of Runx3 gene inactivation in human breast cancer.

图1 乳腺癌组织和对应癌旁组织基因组DNA 中Runx3基因启动子甲基化检测 N:癌旁组织;T:肿瘤组织;U:未甲基化引物扩增;M:甲基化引物扩增;Positive:淋巴细胞DNA;Negative:水
表1 乳腺癌Runx3表达与Runx3启动子甲基化之间的相关性(例)
图2 RT-PCR 检测Runx3基因m RNA 的表达 N:癌旁组织;T:肿瘤组织;GAPDH:内参照
表2 乳腺癌Runx3甲基化与临床病理特征的关系
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