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    Please use this identifier to cite or link to this item: https://ir.csmu.edu.tw:8080/ir/handle/310902500/19232


    Title: Chemotherapeutic effects of luteolin on radio-sensitivity enhancement and interleukin-6/signal transducer and activator of transcription 3 signaling repression of oral cancer stem cells
    Authors: DG, Tu
    WT, Lin
    CC, Yu
    SS, Lee
    CY, Peng
    Lin, T
    CH, Yu
    Contributors: 中山醫學大學
    Keywords: cancer stem cells;luteolin;oral carcinomas;radio-sensitivity
    Date: 2016-12
    Issue Date: 2018-06-20T09:15:33Z (UTC)
    Publisher: J Formos Med Assoc
    ISSN: 0929-6646
    Abstract: BACKGROUND/PURPOSE:
    Previously, we successfully identified oral cancer stem cells (OCSC) displaying enhanced stemness and tumorigenic potentials. In the study, we investigated the chemotherapeutic effect of the flavonoid luteolin, commonly found in fruits and vegetables, on targeting OCSC.

    METHODS:
    Oralspheres was applied to isolate OCSC. aldehyde dehydrogenase 1 activity and CD44 positivity of OCSC with luteolin treatment were assessed by flow cytometry analysis. Radio-sensitivity of OCSC treated with luteolin was examined. Invasion and colony-forming assays were performed to assess oncogenicity in OCSC. The expression of interleukin-6 (IL-6)/signal transducer and activator of transcription 3 (STAT3) was examined by enzyme-linked immunosorbent assay and western blot analysis.

    RESULTS:
    We showed that luteolin effectively inhibited the proliferation rate, self-renewal, aldehyde dehydrogenase 1 activity, and CD44 positivity of OCSC but did not cause significant cytotoxicity of normal epithelial cells. Moreover, luteolin restored radio-sensitivity in OCSC. Combined treatment with luteolin and radiation displayed synergistic effect on invasiveness and clonogenicity of OCSC. Mechanistically, treatment of luteolin resulted in inactivation of IL-6/STAT3 signaling.

    CONCLUSION:
    These results suggest that combined treatment of luteolin and radiation therapy can attenuate tumorigenicity of OCSC through IL-6/STAT3 signaling inactivation.
    URI: http://dx.doi.org/10.1016/j.jfma.2016.08.009
    https://ir.csmu.edu.tw:8080/ir/handle/310902500/19232
    Relation: J Formos Med Assoc. 2016 Dec;115(12):1032-1038.
    Appears in Collections:[牙醫學系暨碩士班] 期刊論文

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