中华实验外科杂志
中華實驗外科雜誌
중화실험외과잡지
CHINESE JOURNAL OF EXPERIMENTAL SURGERY
2011年
1期
136-138
,共3页
于顺江%陈力%陈怡东%王京
于順江%陳力%陳怡東%王京
우순강%진력%진이동%왕경
转录因子%基因表达%横纹肌肉瘤
轉錄因子%基因錶達%橫紋肌肉瘤
전록인자%기인표체%횡문기육류
Transcription factor%Gene expression%Rhabdomyosarcomas
目的 探讨转录因子Sp1调节儿童横纹肌肉瘤成纤维细胞生长因子受体4(FGFR4)基因表达的作用及其调节的分子机制.方法 应用细胞及分子生物学技术如细胞转染、RNA和蛋白质印迹等方法检测2种不同横纹肌肉瘤细胞株中的FGFR4 mRNA和蛋白的表达,观察Sp1对FG-FR4表达的调节作用,探讨Sp1凋节FGFR4基因表达的机制.结果 Sp1在儿童横纹肌肉瘤中可高度表达,Sp1与FGFR4启动区结合并上调了FGFR4的表达.Sp1的这一调节作用不受FGFR4启动区甲基化作用的影响.结论 Sp1促进FGFR4在儿童横纹肌肉瘤细胞中的表达,该作用可能是通过Sp1与FGFR4启动区的顺式元件直接结合而实现的.
目的 探討轉錄因子Sp1調節兒童橫紋肌肉瘤成纖維細胞生長因子受體4(FGFR4)基因錶達的作用及其調節的分子機製.方法 應用細胞及分子生物學技術如細胞轉染、RNA和蛋白質印跡等方法檢測2種不同橫紋肌肉瘤細胞株中的FGFR4 mRNA和蛋白的錶達,觀察Sp1對FG-FR4錶達的調節作用,探討Sp1凋節FGFR4基因錶達的機製.結果 Sp1在兒童橫紋肌肉瘤中可高度錶達,Sp1與FGFR4啟動區結閤併上調瞭FGFR4的錶達.Sp1的這一調節作用不受FGFR4啟動區甲基化作用的影響.結論 Sp1促進FGFR4在兒童橫紋肌肉瘤細胞中的錶達,該作用可能是通過Sp1與FGFR4啟動區的順式元件直接結閤而實現的.
목적 탐토전록인자Sp1조절인동횡문기육류성섬유세포생장인자수체4(FGFR4)기인표체적작용급기조절적분자궤제.방법 응용세포급분자생물학기술여세포전염、RNA화단백질인적등방법검측2충불동횡문기육류세포주중적FGFR4 mRNA화단백적표체,관찰Sp1대FG-FR4표체적조절작용,탐토Sp1조절FGFR4기인표체적궤제.결과 Sp1재인동횡문기육류중가고도표체,Sp1여FGFR4계동구결합병상조료FGFR4적표체.Sp1적저일조절작용불수FGFR4계동구갑기화작용적영향.결론 Sp1촉진FGFR4재인동횡문기육류세포중적표체,해작용가능시통과Sp1여FGFR4계동구적순식원건직접결합이실현적.
Objective To investigate the role of transcription factor Sp1 in the fibroblast growth factor receptor 4 (FGFR4) expression regulation and to obtain insight into the regulatory mechanisms goveming FGFR4 gene regulation and overexpression in human infant rhabdomyosarcomas. Methods By using a series of cellular and molecular biology methods like transfection, Northern blotting, Western blotting etc., the mRNA and protein expression of FGFR4 was detected. The regulatory effects of Sp1 on the FGFR4 expression in the human rhabdomyosarcoma-derived cells were analyzed. Results Sp1 could be express highly in the human rhabdomyosarcoma-derived cells, and its binding to FGFR4 promoter could upregulate the FGFR4 expression, which was influenced by the methylation of FGFR4 promoter. Conclusion Sp1 induces the expression of FGFR4 in human infant rhabdomyosarcomas by directly binding of Sp1 with DNA cis elements in FGFR4 gene promoter region.