Down-regulation of survivin suppresses uro-plasminogen activator through transcription factor JunB.
10.3858/emm.2011.43.9.057
- Author:
Kyung Hee LEE
1
;
Eun Young CHOI
;
Sung Ae KOH
;
Min Kyoung KIM
;
Kyeong Ok KIM
;
Si Hyung LEE
;
Byung Ik JANG
;
Se Won KIM
;
Sang Woon KIM
;
Sun Kyo SONG
;
Joon Hyuk CHOI
;
Jae Ryong KIM
Author Information
1. Department of Hematology-Oncology, College of Medicine, Yeungnam University, Daegu 705-717, Korea.
- Publication Type:Original Article ; Research Support, Non-U.S. Gov't
- Keywords:
BIRC5 protein, human;
hepatocyte growth factor;
neoplasm metastasis;
transcription factor AP-1;
urokinase-type plasminogen activator
- MeSH:
Apoptosis;
Cell Hypoxia;
Cell Line, Tumor;
*Cytoprotection;
Glutathione Peroxidase/metabolism;
Herbicides/*toxicity;
Humans;
L-Lactate Dehydrogenase/metabolism;
Lung/*cytology/*drug effects/metabolism;
Malondialdehyde/metabolism;
Oxidative Stress;
Paraquat/*toxicity;
Reactive Oxygen Species/*metabolism;
Superoxide Dismutase/metabolism
- From:Experimental & Molecular Medicine
2011;43(9):501-509
- CountryRepublic of Korea
- Language:English
-
Abstract:
Survivin, a member of the inhibitors of apoptosis protein family, is expressed during development and in various human cancers. However, the clinical relevance of survivin in cancer is still a matter of debate. Genes induced by hepatocyte growth factor (HGF) were screened using cDNA microarray technology in the stomach cancer cell lines, NUGC3 and MKN28. The levels of JunB, survivin, and uro-plasminogen activator (uPA) were up-regulated in cells treated with HGF in a dose-dependent manner. HGF-induced up regulation of JunB, survivin, and uPA was inhibited by pre-treatment with a MEK inhibitor (PD 98059). HGF-induced up-regulation of uPA was repressed by survivin knockdown. HGF enhanced the binding activity of JunB to the survivin promoter in control cells, but not in the JunB-shRNA cells. Transfection with survivin-shRNA resulted in a decrement of cell proliferation, as determined with MTT assays. In an in vitro invasion assay, significantly fewer cells transfected with survivin shRNA than control cells were able to invade across a Matrigel membrane barrier. In conclusion, survivin appeared to play an important role in the up-regulation of uPA induced by HGF via JunB and might contribute to HGF-mediated tumor invasion and metastasis, which may serve as a promising target for gastric cancer therapy.
