Hahm K B, Cho K, Lee C, Im Y H, Chang J, Choi S G, Sorensen P H, Thiele C J, Kim S J
Laboratory of Cell Regulation, DBS, National Cancer Institute, Bethesda, Maryland 20892-5055, USA.
Nat Genet. 1999 Oct;23(2):222-7. doi: 10.1038/13854.
Chromosomal translocations resulting in the expression of chimaeric transcription factors are frequently observed in tumour cells, and have been suggested to be a common mechanism in human carcinogenesis. Ewing sarcoma and related peripheral primitive neuroectodermal tumours share recurrent translocations that fuse the gene EWSR1 (formerly EWS) from 22q-12 to FLI1 and genes encoding other ETS transcription factors (which bind DNA through the conserved ETS domain). It has been shown that transduction of the gene EWSR1-FLI1 (encoding EWS-FLI1 protein) can transform NIH3T3 cells, and that mutants containing a deletion in either the EWS domain or the DNA-binding domain in FLI1 lose this ability. This indicates that the EWS-FLI1 fusion protein may act as an aberrant transcription factor, but the exact mechanism of oncogenesis remains unknown. Because ETS transcription factors regulate expression of TGFBR2 (encoding the TGF-beta type II receptor, TGF-beta RII; Refs 9,14), a putative tumour suppressor gene, we hypothesized that TGFBR2 may be a target of the EWS-FLI1 fusion protein. We show here that Ewing sarcoma [corrected] (ES) cell lines with the EWSR1-FLI1 fusion have reduced TGF-beta sensitivity, and that fusion-positive ES cells and primary tumours both express low or undetectable levels of TGFBR2 mRNA and protein product. Co-transfection of FLI1 and the TGFBR2 promoter induces promoter activity, whereas EWSR1-FLI1 leads to suppression of TGFBR2 promoter activity and FLI1-induced promoter activity. Introduction of EWSR1-FLI1 into cells lacking the EWSR1-FLI1 fusion suppresses TGF-beta RII expression, whereas antisense to EWSR1-FLI1 in ES cell lines positive for this gene fusion restores TGF-beta RII expression. Furthermore, introduction of normal TGF-beta RII into ES cell lines restores TGF-beta sensitivity and blocks tumorigenicity. Our results implicate TGF-beta RII as a direct target of EWS-FLI1.
在肿瘤细胞中经常观察到导致嵌合转录因子表达的染色体易位,并且有人提出这是人类致癌作用的一种常见机制。尤因肉瘤和相关的外周原始神经外胚层肿瘤具有共同的反复出现的易位,这种易位将位于22q-12的EWSR1基因(以前称为EWS)与FLI1以及编码其他ETS转录因子(通过保守的ETS结构域结合DNA)的基因融合。已经表明,基因EWSR1-FLI1(编码EWS-FLI1蛋白)的转导可以转化NIH3T3细胞,并且在FLI1中EWS结构域或DNA结合结构域存在缺失的突变体失去这种能力。这表明EWS-FLI1融合蛋白可能作为一种异常转录因子起作用,但致癌的确切机制仍然未知。由于ETS转录因子调节TGFBR2(编码TGF-βII型受体,TGF-βRII;参考文献9,14)的表达,TGFBR2是一种假定的肿瘤抑制基因,我们推测TGFBR2可能是EWS-FLI1融合蛋白的一个靶点。我们在此表明,具有EWSR-FLI1融合的尤因肉瘤(ES)细胞系对TGF-β的敏感性降低,并且融合阳性的ES细胞和原发性肿瘤均表达低水平或无法检测到的TGFBR2 mRNA和蛋白产物。FLI1与TGFBR2启动子的共转染诱导启动子活性,而EWSR1-FLI1导致TGFBR2启动子活性和FLI1诱导的启动子活性受到抑制。将EWSR1-FLI1导入缺乏EWSR1-FLI1融合的细胞中会抑制TGF-βRII的表达,而在对该基因融合呈阳性的ES细胞系中针对EWSR1-FLI1的反义RNA可恢复TGF-βRII的表达。此外,将正常的TGF-βRII导入ES细胞系可恢复TGF-β敏感性并阻断致瘤性。我们的结果表明TGF-βRII是EWS-FLI1的直接靶点。