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    Please use this identifier to cite or link to this item: https://ir.csmu.edu.tw:8080/ir/handle/310902500/11381


    Title: Genetic expression signatures of oral submucous fibrosis and oral cancer—A preliminary microarray report
    Authors: Liao, Pao-Hsin
    Yang, Hui-Wen
    Huang, Yu-Feng
    Contributors: 中山醫學大學
    Keywords: genetic signature;microarray;oral submucous fibrosis;SCC;XRCC5/Ku80
    Date: 2013
    Issue Date: 2015-07-16T09:53:29Z (UTC)
    ISSN: 1991-7902
    Abstract: Background/purpose

    Oral submucous fibrosis (OSF) is a potentially malignant disorder of oral squamous cell carcinoma (SCC). In this study, we obtained the genetic expression signatures of OSF and SCC by microarray analysis.

    Materials and methods

    Five patients with clinically evident OSF, five patients with SCC who also had existing OSF, and four normal volunteers who did not have a history of chewing betel quids were recruited. Biopsy specimens were obtained with an approved Institutional Review Board protocol. Total RNA from OSF or SCC was isolated and hybridized to a Human Oligo 1A (V2) Microarray (G4110B) chip against normal control RNA that was pooled from the four healthy volunteers.

    Results

    We found similar, but distinct genetic expression signatures for OSF and SCC. At the hierarchical clustering analysis, 24 known genes (23 upregulated and 1 downregulated) in OSF were differentially expressed consistently in all participants. Among the genes, XRCC5 was cloned and transfected into oral cancer GNM cells. The results demonstrated that the overexpression of XRCC5 increased the resistance of GNM cells to low-density X-ray irradiation and promoted the cell growth rate.

    Conclusion

    The distinct but similar genetic expression signatures seen in OSF and SCC suggested that this expression may be used as a supplemental diagnostic tool in pathology practice. This preliminary study showed that the XRCC5 gene promoted GNM cell growth and conferred resistance to low-density X-ray irradiation. Further studies on the effect of XRCC5 in oral cancer cells are in progress.
    URI: https://ir.csmu.edu.tw:8080/ir/handle/310902500/11381
    http://dx.doi.org/10.1016/j.jds.2013.02.017
    Relation: Journal of Dental Sciences Available online 28 April 2013 In Press, Corrected Proof — Note to users
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