5-Fu activates NKG2D ligands MICA/B promoter in transiently transfected A549 cell line
- VernacularTitle:5-Fu对A549细胞NKG2D配体MICA/B启动子活性的作用
- Author:
Dan, LUO
;
Jing-Xiang, ZHAO
;
Guang-Zhi, WEI
;
Yan, ZHANG
;
Zi-Ling, WANG
- Publication Type:Journal Article
- Keywords:
MICA/B;
promoter activity;
5-Fu
- From:Bulletin of The Academy of Military Medical Sciences
2009;33(6):535-538
- CountryChina
- Language:Chinese
-
Abstract:
Objective:To analyze the activities of human NKG2D ligand MICA/B promoter induced by 5-Fu.Methods:The 5'-end flanking regions of MICA /B promoter and their different truncated fragments were amplified from A549 genome by PCR. The resulting amplicons were cloned into pGL3-Basic vector to generate the MICA/B luciferase reporter plasmids. All the constructs were transiently transfected A549 cells. The promoter region activities were determined by dual-luciferase reporter assays. The effect of 5-Fu on the promoter activities of MICA/B was also tested.Results and Conclusion:The 5'-end flanking regions of MICA /B promoter and five of their different truncated fragments were successfully obtained. The normalized luciferase reporter gene activities driven by the above promoters and fragments were 3.61,2.26,1.63,0.313,0.711 and 0.663 for MICA and 17.49,10.11,7.398,0.822,0.997 and 0.49 for MICB,respectively. Promoter activities in transiently transfected A549 cells treated by 20,40,80,160 and 320 μg/m of 5-Fu increased 1.69,1.48,1.62,1.55 and 1.78 fold for MICA and 1.44,1.87,1.38,1.19 and 1.25 fold for MICB. Our results suggest that 5-FU can significantly up-regulate the promoter activity of both MICA and MICB.
