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Experimental & Molecular Medicine ; : 380-386, 2004.
Article in English | WPRIM | ID: wpr-119638

ABSTRACT

The early growth response gene-1 (Egr-1) is a tumor suppressor which plays an important role in cell growth, differentiation and apoptosis. Egr-1 has been shown to be down-regulated in many types of tumor tissues. Trifluoperazine (TFP), a phenothiazine class of antipsychotics, restored serum-induced Egr-1 expression in several cancer cell lines. We investigated the effect of Egr-1 expression on the TFP-induced inhibition of cell growth. Ectopic expression of Egr-1 enhanced the TFP-induced antiproliferative activity and downregulated cyclin D1 level in U87MG glioma cells. Our results suggest that antipsychotics TFP exhibits antiproliferative activity through up-regulation of Egr-1.


Subject(s)
Humans , Cell Cycle , Cell Proliferation/drug effects , Cyclin D1/metabolism , DNA-Binding Proteins/genetics , Gene Expression , Glioma/metabolism , Immediate-Early Proteins/genetics , Promoter Regions, Genetic/drug effects , Transcription Factors/genetics , Trifluoperazine/pharmacology , Tumor Cells, Cultured
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