Li K K C, Goodall J, Goding C R, Liao S-K, Wang C-H, Lin Y-C, Hiraga H, Nojima T, Nagashima K, Schaefer K-L, Lee K A W
Department of Biology, HK University of Science & Technology, Kowloon, HK, China.
Br J Cancer. 2003 Sep 15;89(6):1072-8. doi: 10.1038/sj.bjc.6601212.
Clear cell sarcoma (CCS) is associated with the EWS/ATF1 oncogene that is created by chromosomal fusion of the Ewings Sarcoma oncogene (EWS) and the cellular transcription factor ATF1. The melanocytic character of CCS suggests that the microphthalmia-associated transcription factor (Mitf), a major inducer of melanocytic differentiation, may be miss-expressed in CCS. Accordingly, we show that the mRNA and protein of the melanocyte-specific isoform of Mitf (Mitf-M) are present in several cultured CCS cell lines (Su-ccs-1, DTC1, Kao, MST-1, MST-2 and MST-3). The above cell lines thus provide a valuable experimental resource for examining the role of Mitf-M in both CCS and melanocyte differentiation. Melanocyte-specific expression of Mitf-M is achieved via an ATF-dependent melanocyte-specific cAMP-response element in the Mitf-M promoter, and expression of Mitf-M in CCS cells suggests that EWS/ATF1 (a potent and promiscuous activator of cAMP-inducible promoters) may activate the Mitf-M promoter. Surprisingly, however, the Mitf-M promoter is not activated by EWS/ATF1 in transient assays employing CCS cells, melanocytes or nonmelanocytic cells. Thus, our results indicate that Mitf-M promoter activation may require an appropriate chromosomal context in CCS cells or alternatively that the Mitf-M promoter is not directly activated by EWS/ATF1.
透明细胞肉瘤(CCS)与EWS/ATF1致癌基因相关,该基因由尤因肉瘤致癌基因(EWS)与细胞转录因子ATF1的染色体融合产生。CCS的黑素细胞特征表明,小眼畸形相关转录因子(Mitf)作为黑素细胞分化的主要诱导因子,可能在CCS中表达异常。因此,我们发现Mitf黑素细胞特异性异构体(Mitf-M)的mRNA和蛋白存在于几种培养的CCS细胞系(Su-ccs-1、DTC1、Kao、MST-1、MST-2和MST-3)中。上述细胞系为研究Mitf-M在CCS和黑素细胞分化中的作用提供了宝贵的实验资源。Mitf-M的黑素细胞特异性表达是通过Mitf-M启动子中一个依赖ATF的黑素细胞特异性cAMP反应元件实现的,并且Mitf-M在CCS细胞中的表达表明EWS/ATF1(一种cAMP诱导型启动子的强效且多效性激活剂)可能激活Mitf-M启动子。然而,令人惊讶的是,在使用CCS细胞、黑素细胞或非黑素细胞的瞬时试验中,Mitf-M启动子并未被EWS/ATF1激活。因此,我们的结果表明,Mitf-M启动子的激活可能需要CCS细胞中合适的染色体环境,或者Mitf-M启动子不是由EWS/ATF1直接激活的。