Lapidus R G, Nass S J, Butash K A, Parl F F, Weitzman S A, Graff J G, Herman J G, Davidson N E
Oncology Center, The Johns Hopkins University School of Medicine, Baltimore, Maryland 21231, USA.
Cancer Res. 1998 Jun 15;58(12):2515-9.
Southern analysis has shown that DNA from 25% of primary estrogen receptor (ER) alpha-negative breast tumors displays aberrant methylation at one site within the ER gene CpG island. To examine more sites and increase sensitivity, we developed a methylation-specific PCR assay to map methylation of the entire ER CpG island. The island was unmethylated in normal breast tissue and ER-positive breast cancer cell lines, but extensively methylated in all ER-negative cell lines and breast tumors examined. In addition, some of the ER-positive/progesterone receptor-negative and ER-positive/progesterone receptor-positive tumors (about 70% and 35%, respectively) displayed methylation of the ER CpG island, suggesting that this heterogeneity within tumor cell populations could potentially shed light on the etiology of ER-negative recurrent tumors arising from ER-positive tumors.
Southern印迹分析表明,25%的原发性雌激素受体(ER)α阴性乳腺癌肿瘤的DNA在ER基因CpG岛内的一个位点显示异常甲基化。为了检测更多位点并提高灵敏度,我们开发了一种甲基化特异性PCR检测方法来绘制整个ER CpG岛的甲基化图谱。该岛在正常乳腺组织和ER阳性乳腺癌细胞系中未甲基化,但在所有检测的ER阴性细胞系和乳腺肿瘤中广泛甲基化。此外,一些ER阳性/孕激素受体阴性和ER阳性/孕激素受体阳性肿瘤(分别约为70%和35%)显示ER CpG岛甲基化,这表明肿瘤细胞群体中的这种异质性可能有助于揭示ER阳性肿瘤产生的ER阴性复发性肿瘤的病因。