Ikeda J-i, Morii E, Kimura H, Tomita Y, Takakuwa T, Hasegawa J-i, Kim Y-K, Miyoshi Y, Noguchi S, Nishida T, Aozasa K
Department of Pathology, Osaka University Graduate School of Medicine, Yamada-oka 2-2, Suita 565-0871, Japan.
J Pathol. 2006 Sep;210(1):75-84. doi: 10.1002/path.2026.
CDCP1 is a novel stem cell marker that is expressed in several types of cancer. The mechanisms by which CDCP1 expression is regulated, and the clinical implications of this marker, have not been clarified. In this report, we examine the epigenetic regulation of CDCP1 expression in cell lines and clinical samples from patients with breast cancer. Many CpG sequences were localized around the transcription initiation site of CDCP1. These CpG motifs were found to be poorly methylated in cell lines with high levels of CDCP1 expression and heavily methylated in cell lines with low levels of CDCP1 expression. The in vitro methylation of CpG sites decreased CDCP1 promoter activity, and the addition of a demethylating reagent restored activity. In 25 breast cancer samples, an inverse correlation was noted between the CDCP1 expression level and the proportion of methylated to non-methylated CpG sites. Tumours with high-level CDCP1 expression showed higher levels of proliferation, as revealed by immunohistochemical detection of the MIB-1 antigen, than tumours with low-level CDCP1 expression. These findings indicate that the expression of CDCP1 is regulated by methylation of its promoter region in tumours. CDCP1 expression may prove to be useful in the further characterization of cancers.
CDCP1是一种新型干细胞标志物,在多种癌症类型中均有表达。CDCP1表达的调控机制及其作为标志物的临床意义尚未阐明。在本报告中,我们研究了乳腺癌患者细胞系和临床样本中CDCP1表达的表观遗传调控。许多CpG序列位于CDCP1转录起始位点周围。这些CpG基序在CDCP1高表达的细胞系中甲基化程度较低,而在CDCP1低表达的细胞系中甲基化程度较高。CpG位点的体外甲基化降低了CDCP1启动子活性,添加去甲基化试剂可恢复活性。在25例乳腺癌样本中,CDCP1表达水平与甲基化和未甲基化CpG位点的比例呈负相关。通过免疫组化检测MIB-1抗原发现,CDCP1高表达的肿瘤比CDCP1低表达的肿瘤增殖水平更高。这些发现表明,肿瘤中CDCP1的表达受其启动子区域甲基化的调控。CDCP1表达可能有助于进一步表征癌症。