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학술저널
저자정보
Han, Jian-Jun (Department of Cancer Intervention Treatment Center, Shandong Cancer Hospital and Institute) Xue, De-Wen (Department of Cancer Intervention Treatment Center, Shandong Cancer Hospital and Institute) Han, Qiu-Rong (Department of Obstetrics and Gynecology, Heze Municipal Hospital) Liang, Xiao-Hong (Department of Immunology Shandong University School of Medicine) Xie, Li (Department of Basic Research Center, Shandong Cancer Hospital and Institute) Li, Sheng (Department of Hepatobiliary Surgery, Shandong Cancer Hospital and Institute) Wu, Hui-Yong (Department of Cancer Intervention Treatment Center, Shandong Cancer Hospital and Institute) Song, Bao (Department of Basic Research Center, Shandong Cancer Hospital and Institute)
저널정보
아시아태평양암예방학회 Asian Pacific journal of cancer prevention : APJCP Asian Pacific journal of cancer prevention : APJCP 제15권 제23호
발행연도
2014.1
수록면
10,085 - 10,089 (5page)

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Background: The insulin-like growth factor (IGF) system comprises a group of proteins that play key roles in regulating cell growth, differentiation, and apoptosis in a variety of cellular systems. The aim of this study was to investigate the role of insulin-like growth factor binding protein 3 (IGFBP3) in hepatocellular carcinoma. Materials and Methods: Expression of IGF2, IGFBP3, and PTEN was analyzed by qRT-PCR. Lentivirus vectors were used to overexpress IGFBP3 in hepatocellular carcinoma cell (HCC) lines. The effect of IGFBP3 on proliferation was investigated by MTT and colony formation assays. Results: Expression of IGF2, IGFBP3, and PTEN in several HCC cell lines was lower than in normal cell lines. After 5-aza-2'-deoxycytidine/trichostatin A treatment, significant demethylation of the promoter region of IGFBP3 was observed in HCC cells. Overexpression of IGFBP3 induced apoptosis and reduced colony formation in HUH7 cells. Conclusions: Expression of IGF2, IGFBP3, and PTEN in several HCC cell lines was lower than in normal cell lines. After 5-aza-2'-deoxycytidine/trichostatin A treatment, significant demethylation of the promoter region of IGFBP3 was observed in HCC cells. Overexpression of IGFBP3 induced apoptosis and reduced colony formation in HUH7 cells.

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