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Induction of plasminogen activator inhibitor-2 is associated with suppression of invasive activity in TPA-mediated differentiation of human prostate cancer cells.
Shimizu, Takahisa; Sato, Kimiyoshi; Suzuki, Toshihiro; Tachibana, Ken; Takeda, Ken.
Afiliación
  • Shimizu T; Department of Hygiene-Chemistry, Faculty of Pharmaceutical Sciences, Tokyo University of Science, 2641 Yamazaki, Noda-shi, Chiba 278-8510, Japan.
Biochem Biophys Res Commun ; 309(2): 267-71, 2003 Sep 19.
Article en En | MEDLINE | ID: mdl-12951044
ABSTRACT
We previously reported that 12-O-tetra-decanoylphorbol-13-acetate (TPA) induces microglia-like differentiation and decreases malignancy in human prostate cancer TSU-Pr1 cells. To investigate the mechanism underlying differentiation and decrease of malignancy in TSU-Pr1 cells treated with TPA, we attempted to identify genes expressed differentially during the differentiation using differential display. We successfully detected plasminogen activator inhibitor type-2 (PAI-2) as one gene up-regulated by TPA treatment. The change in expression of PAI-2 by TPA was blocked by treatment with protein kinase C or mitogen-activated protein kinase inhibitors. We also found that secretion of PAI-2 protein was increased by TPA treatment. Moreover, we demonstrated that suppression of invasive activity of TSU-Pr1 cells by TPA treatment was blocked by co-treatment with anti-PAI-2 antibody. These results suggest that induction of PAI-2 is associated with suppression of invasive activity in TSU-Pr1 cells treated with TPA.
Asunto(s)
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Base de datos: MEDLINE Asunto principal: Neoplasias de la Próstata / Acetato de Tetradecanoilforbol / Regulación Neoplásica de la Expresión Génica / Inhibidor 2 de Activador Plasminogénico Tipo de estudio: Risk_factors_studies Idioma: En Revista: Biochem Biophys Res Commun Año: 2003 Tipo del documento: Article
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Base de datos: MEDLINE Asunto principal: Neoplasias de la Próstata / Acetato de Tetradecanoilforbol / Regulación Neoplásica de la Expresión Génica / Inhibidor 2 de Activador Plasminogénico Tipo de estudio: Risk_factors_studies Idioma: En Revista: Biochem Biophys Res Commun Año: 2003 Tipo del documento: Article