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Abstract


Introduction and Objectives:
@EN Retinoic acid (RA) is known as a potent chemopreventive agent in bladder tumor. Recently, RA has gained attention for upregulation of transduced gene expression via long terminal repeat (LTR) transcriptional promotion. In this study, we
investigated
the possible dual effect of RA, growth inhibition of transduced gene expression which contains LTR promotor in human bladder carcinoma cell lines.
@ES Materials and Methods:
@EN Human bladder carcinoma cell lines (T-24, J-82, HT-1197, ATCC) were transduced with Moloney murine leukemia virus containing cDNA of TNF-¥á. The growth of transduced and parent cell line was measured by tetrazolium based colorimetric assay
(MTT).
Transduced TNF-¥á gene expression was determined by ELISA method.
@ES Results:
@EN TNF-¥á production was increased approximately twofold after treatment with RA(10¥ìM) in all three cell lines. This increase was dependent on RA concentration. RA treatment of transduced and parent cell line resulted in dose dependent
inhibition
of
cell proliferation (up to 80% inhibition with 10¥ìM RA) in all parental and transduced cell lines.
@ES Conclusions:
@EN These results indicate that RA shows dual effect in cytokine gene transduced bladder carcinoma cells with retroviral vector containing LTR promotor and could be a supplement to the gene therapy of bladder cancer.

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