Lee Amie Y, He Biao, You Liang, Dadfarmay Sina, Xu Zhidong, Mazieres Julien, Mikami Iwao, McCormick Frank, Jablons David M
Thoracic Oncology Laboratory, Department of Surgery, Comprehensive Cancer Center, University of California, San Francisco, CA 94115, USA.
Oncogene. 2004 Aug 26;23(39):6672-6. doi: 10.1038/sj.onc.1207881.
Secreted frizzled-related proteins (sFRPs) comprise a family of five secreted glycoproteins that antagonize Wnt signaling. Aberrant activation and upregulation of the Wnt pathway is a key feature of many cancers. Thus, role of sFRP as a negative regulator of Wnt signaling may have important implications in tumorigenesis, and its downregulation has been correlated with human cancers. Recently, we reported Wnt signaling and dishevelled (Dvl) overexpression in malignant pleural mesothelioma (MM). Here, we report significant transcriptional downregulation of the SFRP gene family in MM primary tissues and cell lines as well as several other cancer cell lines (breast, lung, glioma, and cervical) compared to normal cells. One or more SFRPs were downregulated in approximately 85% (18 of 21) of primary MM tumor specimens compared to normal pleural tissue. Eight of the nine cancer cell lines we examined showed silencing of the SFRP family. Methylation-specific PCR (MSP) analysis showed that SFRP1, SFRP4, and SFRP5 gene promoters are frequently methylated in MM primary tissue (>80%). Furthermore, transfection of the SFRP gene construct into MM cell lines lacking SFRP expression resulted in apoptosis and growth suppression. Our results suggest that methylation silencing of SFRPs may be one of the important mechanisms of aberrant Wnt signaling activation in MM.
分泌型卷曲相关蛋白(sFRPs)由五种分泌型糖蛋白组成,它们可拮抗Wnt信号通路。Wnt通路的异常激活和上调是许多癌症的关键特征。因此,sFRP作为Wnt信号负调节因子的作用可能在肿瘤发生中具有重要意义,其下调与人类癌症相关。最近,我们报道了恶性胸膜间皮瘤(MM)中Wnt信号通路和散乱蛋白(Dvl)的过表达。在此,我们报道与正常细胞相比,MM原发性组织和细胞系以及其他几种癌细胞系(乳腺癌、肺癌、神经胶质瘤和宫颈癌)中SFRP基因家族存在显著的转录下调。与正常胸膜组织相比,约85%(21个中的18个)的原发性MM肿瘤标本中一种或多种SFRP下调。我们检测的9个癌细胞系中有8个显示SFRP家族沉默。甲基化特异性PCR(MSP)分析表明,SFRP1、SFRP4和SFRP5基因启动子在MM原发性组织中经常发生甲基化(>80%)。此外,将SFRP基因构建体转染到缺乏SFRP表达的MM细胞系中会导致细胞凋亡和生长抑制。我们的结果表明,SFRPs的甲基化沉默可能是MM中Wnt信号异常激活的重要机制之一。