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    Please use this identifier to cite or link to this item: http://ir.cnu.edu.tw/handle/310902800/30918


    標題: IL-8 promotes HNSCC progression on CXCR1/2-meidated NOD1/RIP2 signaling pathway
    作者: Chan, Leong-Perng
    Wang, Ling-Feng
    Chiang, Feng-Yu
    Lee, Ka-Wo
    Kuo, Po-Lin
    Liang, Chia-Hua
    貢獻者: Kaohsiung Med Univ, Grad Inst Clin Med
    Kaohsiung Med Univ, Kaohsiung Med Univ Hosp, Dept Otolaryngol Head & Neck Surg
    Natl Sun Yat Sen Univ, Inst Med Sci & Technol
    Chia Nan Univ Pharm & Sci, Dept Cosmet Sci
    Chia Nan Univ Pharm & Sci, Inst Cosmet Sci
    關鍵字: HNSCC
    IL-8
    NOD1
    cancer progression
    inflammasomes
    日期: 2016-09
    上傳時間: 2018-01-18 11:37:55 (UTC+8)
    出版者: Impact Journals Llc
    摘要: NOD1 (nucleotide-binding oligomerization domain 1) is overexpressed in head and neck squamous cell carcinoma (HNSCC) cells, as is IL-8 in cancer cells. However, the mechanism of the IL-8-mediated overexpression of NOD in HNSCC not been identified. This study determines whether IL-8 promotes tumor progression via the NOD signaling pathway in HNSCC. Higher IL-8, NOD1 and receptor-interacting protein kinase (RIP2) expressions were observed in HNSCC tissue than in non-cancerous matched tissue (NCMT), whereas NOD2 was weakly expressed. Furthermore, IL-8 stimulated the proliferation of HNSCC cells (SCC4, SCC9 and SCC25) but not dysplastic oral mucosa DOK cells. Exposure to IL-8 increased the clonogenicity of HNSCC cells. IL-8 siRNA inhibited cell proliferation and cell colony formation, suggesting that IL-8 is involved in HNSCC cancer progression. The expressions of CXCR1 and CXCR2 were higher in HNSCC tissue than in NCMT. HNSCC cells that were exposed to IL-8 exhibited higher expression of CXCR1/2 than did controls. The blocking of IL-8 by siRNA reduced CXCR1/2 expression in HNSCC cells, suggesting that the cancer progression of HNSCC cells that is induced by IL-8 depends on CXCR1/2. Additionally, IL-8 is associated with increased NOD1 and RIP2 expression and reduced NOD2 expression in three types of HNSCC cells. The blocking of IL-8 by siRNA reduces IL-8, NOD1 and RIP2 expressions in HNSCC cells, but not the level of NOD2. These results suggest that IL-8 has an important role in HNSCC progression via a CXCR1/2-meidated NOD1/RIP2 signaling pathway.
    關聯: Oncotarget, v.7 n.38, pp.61820-61831
    Appears in Collections:[化妝品應用與管理系(所)] 期刊論文

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