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  • Bone invasive properties of oral squamous cell carcinoma and its interactions with alveolar bone cells: an in vitro study.

    Author(s)
    Qallandar, Omel Baneen
    Ebrahimi, Faeza
    Islam, Farhadul
    Wahab, Riajul
    Qiao, Bin
    Reher, Peter
    Gopalan, Vinod
    Lam, Alfred King-yin
    Griffith University Author(s)
    Gopalan, Vinod
    Reher, Peter
    Lam, Alfred K.
    Islam, Farhad
    Year published
    2019
    Metadata
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    Abstract
    BACKGROUND: Co-culture of cancer cells with alveolar bone cells could modulate bone invasion and destructions. However, the mechanisms of interaction between oral squamous cell carcinoma (OSCC) and bone cells remain unclear. OBJECTIVE: The aim of this study is to analyse the direct and indirect effects of OSCC cells in the stimulation of osteolytic activity and bone invasion. METHOD: Direct co-culture was achieved by culturing OSCC (TCA8113) with a primary alveolar bone cell line. In the indirect co-culture, the supernatant of TCA8113 cells was collected to culture the alveolar bone cells. To assess the bone invasion properties, ...
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    BACKGROUND: Co-culture of cancer cells with alveolar bone cells could modulate bone invasion and destructions. However, the mechanisms of interaction between oral squamous cell carcinoma (OSCC) and bone cells remain unclear. OBJECTIVE: The aim of this study is to analyse the direct and indirect effects of OSCC cells in the stimulation of osteolytic activity and bone invasion. METHOD: Direct co-culture was achieved by culturing OSCC (TCA8113) with a primary alveolar bone cell line. In the indirect co-culture, the supernatant of TCA8113 cells was collected to culture the alveolar bone cells. To assess the bone invasion properties, in vitro assays were performed. RESULTS: The proliferation of co-cultured cancer cells was significantly (p<0.05) higher in comparison to the monolayer control cells. However, the proliferation rates were not significantly different between direct and indirect co-cultured cells with indirect co-cultured cells proliferated slightly more than the direct co-cultured cells. Invasion and migration capacities of co-cultured OSCC and alveolar bone cells enhanced significantly (p<0.05) when compared to that of control monolayer counterparts. Most importantly, we noted that OSCC cells directly co-cultured with alveolar bone cells stimulated pronounced bone collagen destruction. In addition, stem cells and epithelial-mesenchymal transition markers have shown significant changes in their expression in co-cultured cells. CONCLUSIONS: In conclusion, the findings of this study highlight the importance of the interaction of alveolar bone cells and OSCC cells in co-culture setting in the pathogenesis of bone invasion. This may help in the development of potential future biotherapies for bone invasion in OSCC.
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    Journal Title
    Curr Cancer Drug Targets
    DOI
    https://doi.org/10.2174/1568009618666181102144317
    Note
    This publication has been entered into Griffith Research Online as an Advanced Online Version.
    Subject
    Medicinal and biomolecular chemistry
    Oncology and carcinogenesis
    Pharmacology and pharmaceutical sciences
    Publication URI
    http://hdl.handle.net/10072/385007
    Collection
    • Journal articles

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