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    Please use this identifier to cite or link to this item: https://ir.csmu.edu.tw:8080/ir/handle/310902500/17965


    Title: Lipocalin-2 induces apoptosis in human hepatocellular carcinoma cells through activation of mitochondria pathways
    Authors: Chien, Ming-Hsien
    Ying, Tsung-Ho
    Yang, Shun-Fa
    Yu, Ji-Kuen
    Hsu, Chih-Wei
    Hsieh, Shu-Ching
    Hsieh, Yi-Hsien
    Contributors: 中山醫大
    Keywords: Lipocalin 2;Hepatocellular carcinoma;Apoptosis;Mitochondrial membrane potential
    Date: 2012
    Issue Date: 2017-07-13T08:20:34Z (UTC)
    Publisher: Cell Biochemistry and Biophysics
    ISSN: 1085-9195
    Abstract: Abstract
    Lipocalin 2 (LCN2) is a secreted, iron-binding glycoprotein that is abnormally expressed in some malignant human cancers. However, the roles of LCN2 in hepatocellular carcinoma (HCC) cells are unknown. In this study, we suggested the LCN2 and LCN2R were weak detected in the HCC cell lines, LCN2 and LCN2R were found to be down-regulated in tumor tissues in 16 HCC patients. MTT, DAPI, TUNEL, and flow cytometry analyses revealed that LCN2 overexpression dramatically inhibited cell viability, induced apoptosis features of cell-cycle arrest in sub-G1 phase, in DNA fragmentation, and in condensation of chromatin in Huh-7 and SK-Hep-1 cells. Western blots were used to detect the activation of caspase, pro-apoptosis, and anti-apoptosis protein expression in overexpress-LCN2 HCC cells. LCN2-induced apoptosis was characterized by cleavage of caspase-9, -8, -3, and PARP protein, and a reduction in the mitochondrial membrane potential (MMP). Furthermore, LCN2 also enhanced the down-regulated Bcl-2 and up-regulated the expression of Bax. In addition, our experiments with caspase inhibitors LEHD-FMK and IETD-FMK prevent LCN2-induced apoptosis. We also demonstrated that treatment of overexpress-LCN2 HCC cells with the LCN2 neutralized antibody also significantly attenuated LCN2-induced cell apoptosis. These findings indicate that LCN2 overexpression can effectively induce apoptosis of HCC cells and may be used as a potent therapy against human HCC.
    URI: http://dx.doi.org/10.1007/s12013-012-9370-1
    https://ir.csmu.edu.tw:8080/ir/handle/310902500/17965
    Relation: Cell Biochemistry and Biophysics December 2012, Volume 64, Issue 3, pp 177–186
    Appears in Collections:[醫學系] 期刊論文

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