de Nigris F, Mega T, Berger N, Barone M V, Santoro M, Viglietto G, Verde P, Fusco A
Centro di Endocrinologia ed Oncologia Sperimentale del Consiglio Nazionale delle Ricerche c/o Dipartimento di Biologia e Patologia Cellulare e Molecolare, Facoltà di Medicina e Chirurgia, Università degli Studi di Napoli, Naples, Italy.
Cancer Res. 2001 Mar 1;61(5):2267-75.
The proteins of the Ets family are transcription factors involved in signal transduction, cell cycle progression, and differentiation. In this study, we report that thyroid cell neoplastic transformation is associated with a dramatic increase in ETS transcriptional activity, which is dependent on the accumulation of Ets-1, Ets-2, and other Ets-related proteins. Inhibition of ETS transactivation activity by the Ets-dominant negative construct (Ets-Z) induced programmed cell death in human thyroid carcinoma cell lines but not in normal thyroid cells. Apoptotic cell death induced by Ets-Z was dependent on the reduction of c-MYC protein levels, because it was prevented by overexpression of c-myc. Taken together, these data indicate that the induction of Ets-1 and Ets-2 transcription factors plays a pivotal role in thyroid cell neoplastic transformation.
Ets家族蛋白是参与信号转导、细胞周期进程和分化的转录因子。在本研究中,我们报告甲状腺细胞的肿瘤转化与ETS转录活性的显著增加相关,这依赖于Ets-1、Ets-2和其他Ets相关蛋白的积累。Ets显性负性构建体(Ets-Z)对ETS反式激活活性的抑制在人甲状腺癌细胞系中诱导程序性细胞死亡,但在正常甲状腺细胞中则不然。Ets-Z诱导的凋亡性细胞死亡依赖于c-MYC蛋白水平的降低,因为c-myc的过表达可阻止这种情况。综上所述,这些数据表明Ets-1和Ets-2转录因子的诱导在甲状腺细胞的肿瘤转化中起关键作用。