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DC Field | Value | Language |
---|---|---|
dc.contributor.author | Lam-ubol A. | |
dc.contributor.author | Hopkin D. | |
dc.contributor.author | Letuchy E.M. | |
dc.contributor.author | Kurago Z.B. | |
dc.date.accessioned | 2021-04-05T03:36:29Z | - |
dc.date.available | 2021-04-05T03:36:29Z | - |
dc.date.issued | 2010 | |
dc.identifier.issn | 3603997 | |
dc.identifier.other | 2-s2.0-77956187379 | |
dc.identifier.uri | https://ir.swu.ac.th/jspui/handle/123456789/14689 | - |
dc.identifier.uri | https://www.scopus.com/inward/record.uri?eid=2-s2.0-77956187379&doi=10.1007%2fs10753-009-9175-6&partnerID=40&md5=0e0634803366ff6c893de8e0ba14d9db | |
dc.description.abstract | Bacteria and chronic inflammation are present in squamous cell carcinoma of the head and neck (HNSCC), but their roles in the pathogenesis of HNSCC are unclear. Our studies described here revealed that human monocytes co-cultured short term with HNSCC cells were more likely to express CD16, and CD16 + small mononuclear cells were common in HNSCC specimens. In addition, we identified monocytes as the primary source of LPS-induced IL-6 and TNF-alpha in the monocyte-HNSCC co-cultures. Remarkably, relative to LPS-stimulated monocytes cultured alone, HNSCC cells profoundly suppressed LPS-induced TNF-alpha in monocytes, without compromising IL-6 production. High levels of cytoprotective factors like IL-6 and low levels of TNF-alpha are important for the tumor microenvironment that enables tumor cell survival, affects monocyte differentiation and may contribute to tumor colonization by bacteria. This study provides novel observations that HNSCC cells affect monocyte phenotype and function, which are relevant to the regulation of the HNSCC microenvironment.© 2010 Springer Science+Business Media, LLC. | |
dc.subject | CD16 antigen | |
dc.subject | CD56 antigen | |
dc.subject | interleukin 6 | |
dc.subject | lipopolysaccharide | |
dc.subject | tumor necrosis factor alpha | |
dc.subject | Fc receptor | |
dc.subject | FCGR3B protein, human | |
dc.subject | glycosylphosphatidylinositol anchored protein | |
dc.subject | IL6 protein, human | |
dc.subject | interleukin 6 | |
dc.subject | lipopolysaccharide | |
dc.subject | lipopolysaccharide, E. coli 026-B6 | |
dc.subject | tumor necrosis factor alpha | |
dc.subject | antigen expression | |
dc.subject | article | |
dc.subject | cancer cell | |
dc.subject | cell differentiation | |
dc.subject | cell protection | |
dc.subject | cell survival | |
dc.subject | controlled study | |
dc.subject | cytokine production | |
dc.subject | cytokine release | |
dc.subject | head and neck carcinoma | |
dc.subject | human | |
dc.subject | human cell | |
dc.subject | keratinocyte | |
dc.subject | monocyte | |
dc.subject | mouth carcinoma | |
dc.subject | pathogenesis | |
dc.subject | phenotype | |
dc.subject | regulatory mechanism | |
dc.subject | squamous cell carcinoma | |
dc.subject | tumor microenvironment | |
dc.subject | upregulation | |
dc.subject | biosynthesis | |
dc.subject | cell culture | |
dc.subject | coculture | |
dc.subject | cytology | |
dc.subject | disease course | |
dc.subject | drug effects | |
dc.subject | head and neck tumor | |
dc.subject | immunology | |
dc.subject | inflammation | |
dc.subject | monocyte | |
dc.subject | mouth mucosa | |
dc.subject | pathology | |
dc.subject | phagocytosis | |
dc.subject | phenotype | |
dc.subject | secretion (process) | |
dc.subject | squamous cell carcinoma | |
dc.subject | stomatitis | |
dc.subject | tumor cell line | |
dc.subject | Carcinoma, Squamous Cell | |
dc.subject | Cell Line, Tumor | |
dc.subject | Cells, Cultured | |
dc.subject | Coculture Techniques | |
dc.subject | Disease Progression | |
dc.subject | Head and Neck Neoplasms | |
dc.subject | Humans | |
dc.subject | Inflammation | |
dc.subject | Interleukin-6 | |
dc.subject | Keratinocytes | |
dc.subject | Lipopolysaccharides | |
dc.subject | Monocytes | |
dc.subject | Mouth Mucosa | |
dc.subject | Phagocytosis | |
dc.subject | Phenotype | |
dc.subject | Receptors, IgG | |
dc.subject | Stomatitis | |
dc.subject | Tumor Necrosis Factor-alpha | |
dc.subject | Carcinoma, Squamous Cell | |
dc.subject | Cell Line, Tumor | |
dc.subject | Cells, Cultured | |
dc.subject | Coculture Techniques | |
dc.subject | Disease Progression | |
dc.subject | GPI-Linked Proteins | |
dc.subject | Head and Neck Neoplasms | |
dc.subject | Humans | |
dc.subject | Inflammation | |
dc.subject | Interleukin-6 | |
dc.subject | Keratinocytes | |
dc.subject | Lipopolysaccharides | |
dc.subject | Monocytes | |
dc.subject | Mouth Mucosa | |
dc.subject | Phagocytosis | |
dc.subject | Phenotype | |
dc.subject | Receptors, IgG | |
dc.subject | Stomatitis | |
dc.subject | Tumor Necrosis Factor-alpha | |
dc.title | Squamous carcinoma cells influence monocyte phenotype and suppress lipopolysaccharide-induced tnf-alpha in monocytes | |
dc.type | Article | |
dc.rights.holder | Scopus | |
dc.identifier.bibliograpycitation | Inflammation. Vol 33, No.4 (2010), p.207-223 | |
dc.identifier.doi | 10.1007/s10753-009-9175-6 | |
Appears in Collections: | Scopus 1983-2021 |
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