Exp Mol Med.  2009 Mar;41(3):180-188. 10.3858/emm.2009.41.3.021.

Reactive oxygen species regulate the generation of urokinase plasminogen activator in human hepatoma cells via MAPK pathways after treatment with hepatocyte growth factor

Affiliations
  • 1Department of Hemato-Oncology, College of Medicine, Yeungnam University, Daegu 705-717, Korea.
  • 2Department of Biochemistry and Molecular Biology, College of Medicine, Yeungnam University, Daegu 705-717, Korea. kimjr@med.yu.ac.kr
  • 3Aging-associated Vascular Disease Research Center, College of Medicine, Yeungnam University, Daegu 705-717, Korea.

Abstract

Tumor cells are known to produce larger amounts of reactive oxygen species (ROS) than normal cells. Although numerous reports have indicated the importance of ROS in urokinase plasminogen activator (uPA) production, the precise mechanisms remain controversial. In our study, we investigated the effect of ROS on uPA generation in human hepatoma cells, HepG2 and Hep 3B. We determined the effects of hepatocyte growth factor (HGF) on the regulation of ROS, which resulted in suppression of ROS production, as measured with the fluorescent probe, 2'-7'-dichlorofluorescein diacetate. The role of HGF in modulating ROS production, particularly that regulated by Rac-1, was determined. HGF suppressed the increment in Rac-1-regulated ROS in both cell lines. Treatment with 200 microM of H2O2 showed a 1.6-2.1 fold increment in HGF, but a little increment occurred at 500 microM of H2O2. It looks no dose dependent manner. Combined treatment with H2O2 and HGF, resulted in a slightly increased production of HGF compared to no treatment (control). Also, H2O2 upregulated uPA expression in both hepatoma cell lines. To identify the downstream pathways regulated by ROS, we treated cells with PD 98059, an MEK inhibitor, and SB 203580, a p38 inhibitor, after treatment with H2O2, and showed negative control between ERK and p38 kinase activities for uPA regulation. We found that HGF modulate Rac-1-regulated ROS production through activation of Akt and ROS regulates uPA production via MAP kinase, which provides a novel clue to clarify the mechanism underlying hepatoma progression.

Keyword

hepatocyte growth factor; metastasis; mitogen-activated protein kinases; neoplasm metastasis; reactive oxygen species; urokinase-type plasminogen activator

MeSH Terms

Cell Line, Tumor
Fluorescent Dyes/chemistry
Hepatocyte Growth Factor/pharmacology/*physiology
Humans
Hydrogen Peroxide/pharmacology
Imidazoles/pharmacology
Liver Neoplasms/drug therapy
Mitogen-Activated Protein Kinases/antagonists & inhibitors/*metabolism
Pyridines/pharmacology
Reactive Oxygen Species/*metabolism
Recombinant Proteins/pharmacology
Urokinase-Type Plasminogen Activator/*biosynthesis
rac1 GTP-Binding Protein/metabolism
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