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    Please use this identifier to cite or link to this item: https://ir.csmu.edu.tw:8080/ir/handle/310902500/15918


    Title: Involvement of Viral and Chemical Factors with Oral Cancer in Taiwan
    Authors: Yang, Yu-Yen;Koh, Lim-Woh;Tsai, Ju-Hsin;Tsai, Chung-Hung;Wong, Eric Fook-Chuen;Lin, Shyh-Jye;Yang, Chi-Chiang
    Contributors: 中山醫學大學
    Keywords: Oral cancer;virus;arecoline
    Date: 2004
    Issue Date: 2016-09-05T08:50:05Z (UTC)
    Abstract: Background: The association between oral squamous cell carcinoma (OSCC) and viral and
    chemical factors is uncertain. Therefore the correlation of viral and chemical factors with oral
    cancer in Taiwan was investigated.
    Methods: Thirty-seven paraffin-embedded oral cancer biopsies and 36 normal oral tissue
    specimens were examined by the polymerase chain reaction method for six viruses: HPV,
    CMV, EBV, HSV-1, HSV-2 and HHV-8. To elucidate the role of arecoline in the oncogenesis of
    oral cancer, human buccal fibroblasts, oral submucosal fibroblasts and three cancer cell lines
    KB, GNM and TSCCa were used for MTT cytotoxity assay and flow cytometry DNA content
    analysis.
    Results: Two (5.4%) HSV-1-positive and four (10.8%) HPV-positive cases were recognized in
    oral cancer biopsies. Among the four HPV-positive tissues, two were further typed as HPV-16,
    one was identified as HPV-18- and HSV-1-positive; and one contained both HPV-16 and HPV-
    18. One sample presented HSV-1 only. Arecoline, at a concentration lower than 0.8 µg/ml,
    increased cell growth (all cell types); at higher concentrations (25–400 µg/ml) it was cytotoxic.
    The cell cycle was demonstrated to be altered either by low or high concentrations of arecoline
    treatment, depending on the cells treated.
    Conclusions: The data demonstrated that HPV, HSV-1 and betel quid chewing were significantly
    associated with OSCC, but HSV-2, CMV, EBV and HHV-8 were not. We suggest that the
    most determinative factor for oral cancer may be chemical in nature rather than viral infection.
    URI: https://ir.csmu.edu.tw:8080/ir/handle/310902500/15918
    Relation: Jpn J Clin Oncol 2004;34(4)176–183
    Appears in Collections:[醫學檢驗暨生物技術學系暨碩士班] 期刊論文

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