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      Sox-4 is a positive regulator of Hep3B and HepG2 cells' apoptosis induced by prostaglandin (PG)A(2) and delta(12)-PGJ(2).

      Experimental & Molecular Medicine
      Apoptosis, drug effects, Blotting, Western, Calcimycin, pharmacology, Caspase 1, metabolism, Caspase Inhibitors, Etoposide, Gene Expression Regulation, Neoplastic, High Mobility Group Proteins, genetics, Humans, Liver Neoplasms, enzymology, pathology, Oligopeptides, Prostaglandin D2, analogs & derivatives, Prostaglandins A, SOXC Transcription Factors, Trans-Activators, Transfection, Tumor Cells, Cultured

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          Abstract

          We reported earlier that expression of Sox-4 was found to be elevated during prostaglandin (PG) A(2) and delta(12)-PGJ(2) induced apoptosis in human hepatocarcinoma Hep3B cells. In this study, the role of Sox-4 was examined using human Hep3B and HepG2 cell lines. Sox-4 induction by several apoptotic inducer such as A23187 (Ca(2+) ionophore) and etoposide (topoisomerase II inhibitor) and Sox-4 transfection into the cells were able to induce apoptosis as observed by the cellular DNA fragmentation. Antisense oligonucleotide of Sox-4 inhibited the induction of Sox-4 expression and blocked the formation of DNA fragmentation by PGA(2) and delta(12)-PGJ(2) in Hep3B and HepG2 cells. Sox-4-induced apoptosis was accompanied with caspase-1 activation indicating that caspase cascade was involved in this apoptotic pathway. These results indicate that Sox-4 is involved in Hep3B and HepG2 cells apoptosis as an important apoptotic mediator.

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