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Role of hepatocyte growth factor/c-Met signaling in regulating urokinase plasminogen activator on invasiveness in human hepatocellular carcinoma: a potential therapeutic target.

Role of hepatocyte growth factor/c-Met signaling in regulating urokinase plasminogen activator on invasiveness in human hepatocellular carcinoma: a potential therapeutic target. Research Abstract Details 

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  • Role of hepatocyte growth factor/c-Met signaling in regulating urokinase plasminogen activator on invasiveness in human hepatocellular carcinoma: a potential therapeutic target. Abstract Text:

    kyung hee leeKyung Hee Lee,eun young choiEun Young Choi,myung soo hyunMyung Soo Hyun,byung ik jangByung Ik Jang,tae nyeun kimTae Nyeun Kim,heon ju leeHeon Ju Lee,jong yuel eunJong Yuel Eun,hong gin kimHong Gin Kim,sung soo yoonSung Soo Yoon,dong sik leeDong Sik Lee,jung hye kimJung Hye Kim,jae-ryong kimJae-Ryong Kim,

    Hepatocyte growth factor (HGF), its transmembrane tyrosine kinase receptor (c-Met), and urokinase type plasminogen activator (uPA) is a key protein in the plasminogen activation system, which plays a proteolytically important role in the invasion and metastasis of various types of cancers. However, the mechanisms by which HGF/c-Met signaling mediates cancer progression and metastasis are unclear. This study was designed to investigate the roles of HGF/c-Met in tumor progression and metastasis in HepG2 and Hep3B hepatoma cell lines. Treatment with HGF increased c-Met phosphorylation in a dose-dependent manner. Activity of c-Met phosphorylation peaked 1-3 min after HGF treatment and then declined. HGF enhanced the protein level and the activity of uPA in HepG2 and Hep3B cells, and the uPAR protein level also increased in a HGF dose-dependent manner. HGF increased cell invasion through the Matrigel. A monoclonal antibody against human uPA receptor, mAb 3936, inhibited HGF-mediated tumor cell invasion in a dose-dependent manner. Down-regulation of uPA using uPA-shRNA induced a decrease in in vitro cell invasion. These results suggest that hepatoma cells express functional c-Met, which may provide a target for a therapeutic basis to interfere with metastases of cancer cells by inhibiting uPA system-mediated proteolysis.

    Role of hepatocyte growth factor/c-Met signaling in regulating urokinase plasminogen activator on invasiveness in human hepatocellular carcinoma: a potential therapeutic target. Publishing Authors By Initials

    kh leeKH Lee,ey choiEY Choi,ms hyunMS Hyun,bi jangBI Jang,tn kimTN Kim,hj leeHJ Lee,jy eunJY Eun,hg kimHG Kim,ss yoonSS Yoon,ds leeDS Lee,jh kimJH Kim,jr kimJR Kim,

    For similar abstracts research abstracts see: abstracts research

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    Role of hepatocyte growth factor/c-Met signaling in regulating urokinase plasminogen activator on invasiveness in human hepatocellular carcinoma: a potential therapeutic target. Journal Published:

    PUBLICATION TYPE: Journal Article

    Journal: Clinical & experimental metastasis

    VOLUME: 25

    Page Numbers: 89-96

    Journal Abbreviation: Clin. Exp. Metastasis

    ISSN: 0262-0898

    DAY: 9

    MONTH: 11

    YEAR: 2007

    Role of hepatocyte growth factor/c-Met signaling in regulating urokinase plasminogen activator on invasiveness in human hepatocellular carcinoma: a potential therapeutic target. Information

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    LANGUAGE: eng

    NlmUniqueID: 8409970

    Role of hepatocyte growth factor/c-Met signaling in regulating urokinase plasminogen activator on invasiveness in human hepatocellular carcinoma: a potential therapeutic target. Keywords Mesh Terms:

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    Grant and Affiliation Information for Role of hepatocyte growth factor/c-Met signaling in regulating urokinase plasminogen activator on invasiveness in human hepatocellular carcinoma: a potential therapeutic target.

    AFFILIATION: Department of Hemato-Oncology, College of Medicine, Yeungnam University, Daegu, Republic of Korea.

    Country: Netherlands

    Netherlands Research PublicationNetherlands Research Publication

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    MEDLINETA: Clin Exp Metastasis

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