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    Please use this identifier to cite or link to this item: http://ir.nhri.org.tw/handle/3990099045/6087


    Title: Proteomic analysis of gemcitabine-induced drug resistance in pancreatic cancer cells
    Authors: Chen, YW;Liu, JY;Lin, ST;Li, JM;Huang, SH;Chen, JY;Wu, JY;Kuo, CC;Wu, CL;Lu, YC;Chen, YH;Fan, CY;Huang, PC;Law, CH;Lyu, PC;Chou, HC;Chan, HL
    Contributors: National Institute of Cancer Research;Institute of Cellular and Systems Medicine
    Abstract: Currently, the most effective agent against pancreatic cancer is gemcitabine (GEM), which inhibits tumor growth by interfering with DNA replication and blocking DNA synthesis. However, GEM-induced drug resistance in pancreatic cancer compromises the therapeutic efficacy of GEM. To investigate the molecular mechanisms associated with GEM-induced resistance, 2D-DIGE and MALDI-TOF mass spectrometry were performed to compare the proteomic alterations of a panel of differential GEM-resistant PANC-1 cells with GEM-sensitive pancreatic cells. The proteomic results demonstrated that 33 proteins were differentially expressed between GEM-sensitive and GEM-resistant pancreatic cells. Of these, 22 proteins were shown to be resistance-specific and dose-dependent in the regulation of GEM. Proteomic analysis also revealed that proteins involved in biosynthesis and detoxification are significantly over-expressed in GEM-resistant PANC-1 cells. In contrast, proteins involved in vascular transport, bimolecular decomposition, and calcium-dependent signal regulation are significantly over-expressed in GEM-sensitive PANC-1 cells. Notably, both protein-protein interaction of the identified proteins with bioinformatic analysis and immunoblotting results showed that the GEM-induced pancreatic cell resistance might interplay with tumor suppressor protein p53. Our approach has been shown here to be useful for confidently detecting pancreatic proteins with differential resistance to GEM. Such proteins may be functionally involved in the mechanism of chemotherapy-induced resistance.
    Date: 2011-11-01
    Relation: Molecular BioSystems. 2011 Nov 1;7(11):3065-3074.
    Link to: http://dx.doi.org/10.1039/c1mb05125c
    Cited Times(WOS): https://www.webofscience.com/wos/woscc/full-record/WOS:000295844100015
    Cited Times(Scopus): http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=80054042816
    Appears in Collections:[劉界元(2003-2010)] 期刊論文
    [郭呈欽] 期刊論文

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