Interleukin-6 signalling regulates vascular endothelial growth factor-C synthesis and lymphangiogenesis in human oral squamous cell carcinoma |
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Authors: | Shinriki Satoru Jono Hirofumi Ueda Mitsuharu Ota Kazutoshi Ota Tomoko Sueyoshi Takanao Oike Yuichi Ibusuki Mutsuko Hiraki Akimitsu Nakayama Hideki Shinohara Masanori Ando Yukio |
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Affiliation: | Department of Diagnostic Medicine, Graduate School of Medical Sciences, Kumamoto University, Japan. satorus@fc.kuh.kumamoto-u.ac.jp |
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Abstract: | Lymph node metastasis is associated with resistance to conventional therapy and poor survival of patients with oral squamous cell carcinoma (OSCC). Although lymphangiogenesis is well known to be associated with the occurrence of lymph node metastasis in various cancers, the precise mechanisms of lymphangiogenesis in OSCC are largely unknown. IL-6, a potent pro-inflammatory cytokine, has been shown to play active roles in various cancers, including OSCC. This study aimed to investigate the involvement of IL-6 signalling in lymphatic metastasis and to evaluate the efficacy of tocilizumab, a humanized anti-human IL-6 receptor antibody, as an anti-lymphangiogenic agent for OSCC. This investigation confirmed that levels of expression of IL-6 protein and VEGF-C mRNA in OSCC tissues were significantly correlated with lymph node metastasis in patients with OSCC, as assessed by immunohistochemical analysis and real-time quantitative RT-PCR. In vitro studies showed that IL-6 regulated VEGF-C mRNA expression in a human OSCC cell line, SAS cells, through the phosphoinositide 3-kinase-Akt pathway. In addition, treatment with tocilizumab led to markedly reduced VEGF-C mRNA expression and OSCC-related lymphangiogenesis in SAS xenografts. Together, these data suggest that tocilizumab acted as expected: it inhibited lymph node metastasis in OSCC by reducing tumour lymphangiogenesis. |
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Keywords: | interleukin‐6 interleukin‐6 receptor tocilizumab oral squamous cell carcinoma vascular endothelial growth factor‐C lymphangiogenesis lymph node metastasis |
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