4.4 Article

Increased expression of Toll-like receptor-9 has close relation with tumour cell proliferation in oral squamous cell carcinoma

Journal

ARCHIVES OF ORAL BIOLOGY
Volume 56, Issue 9, Pages 877-884

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.archoralbio.2011.01.010

Keywords

Toll-like receptor-9(TLR-9); Oral squamous cell carcinoma (OSCC); Ki-67; Cell proliferation; Inflammatory chemokines

Funding

  1. National Natural Science Foundation of China [30772430, 30801301]
  2. Shanghai Municipal Education Commission
  3. Science and Technology Commission of Shanghai Municipality [10dz1951300]

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Objective: Toll-like receptor-9 (TLR-9), a new member of the interleukin-1 receptor superfamily, was recently found to have a high level of expression in many carcinoma specimens. The objective of this study was to examine the TLR-9 expression and its role in tumour cell proliferation in oral squamous cell carcinoma. Materials and methods: Western blot and immunohistochemistry were used to detect TLR-9 protein in oral squamous cell carcinoma (OSCC) Tca-8113 cell lines and clinical specimens (n = 60). The relationship between TLR-9 expression and clinicopathologic features was analysed. Cell proliferation and inflammatory chemokines secretion were tested by MTT and ELISA methods respectively. Results: Results showed that TLR-9 expression level was higher in OSCC tissues than in paired adjacent normal tissues (P < 0.01), and the expression level of TLR-9 was significantly associated with tumour size (P = 0.001), tumour clinical stage (P = 0.003) and Ki-67 expression (P < 0.01). In vitro results also suggested that stimulation of Tca-8113 cells with TLR-9 agonist CpG-ODN could significantly increase tumour cell proliferation as well as subsequent IL-1 alpha and IL-6 secretions (P < 0.01), which could be partially inhibited by usage of anti-TLR-9 protein. Conclusions: It was therefore hypothesized that increased expression of TLR-9 may be of great value in assessing the development of OSCC, and could be used as a new target for OSCC prevention and therapy in future. (C) 2011 Elsevier Ltd. All rights reserved.

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