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细胞因子IFN-γ和IL-1β对人喉鳞癌细胞粘附和浸润能力的影响 被引量:3

Effects of IFN-γ and IL-1β the adhesive and invasive behaviors of human laryngeal carcinoma cell lines
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摘要 目的研究细胞因子干扰素γ(IFNγ)和白介素1β(IL1β)对人喉鳞癌细胞株Hep2及AMCHN8细胞粘附及浸润的生物学性状的影响。探讨细胞因子IFNγ和IL1β改变喉鳞癌细胞粘附和浸润性状的机制。方法应用细胞粘附抑制实验和快速体外浸润实验检测经细胞因子IFNγ和IL1β作用后的Hep2及AMCHN8细胞体外粘附和浸润情况。采用流式细胞仪检测经细胞因子IFNγ和IL1β作用后的喉鳞癌细胞Hep2及AMCHN8整合素α6、β4的表达。结果IFNγ和IL1β对两种喉鳞癌细胞株的生物学性状的影响各异。IFNγ可体外抑制Hep2及AMCHN8细胞的粘附和浸润。IL1β可增强AMCHN8细胞的粘附和浸润,但对Hep2细胞的粘附和浸润无影响。IFNγ和IL1β对两种喉鳞癌细胞整合素α6、β4蛋白表达有不同的调控作用。结论IFNγ和IL1β可能是通过调控不同的粘附分子进而影响喉癌细胞株的生物学性状。 Objective To study the effects of IFN-γ and IL-1β on the adhesive and invasive behaviors of human laryngeal carcinoma cell lines. Methods Adherence inhibition assay and in vitro invasive assay were used following IFN-γ and IL-1β incubated with Hep-2 and AMC-HN8 cells for 48 hours. How cytometry was used to exam the expression of the integrine α6, β4 in Hep-2 and AMC- HN8 cells. Results The effects of IFN-γ and IL-1β on Hep-2 and AMC-HN8 cell lines were different. IFN-γ could inhibit the adhesive and invasive behaviors of Hep-2 and AMC-HN8 cells. IL-1β could enhance the adhesive and invasive behaviors of AMC-HN8 cells, which had no effect on Hep-2 cells. The regulation of IFN-γ and IL-1β on Hep-2 and AMC-HN8 cell lines was differet. Conclusion It is suggested that IFN-γ and IL-1β have different effects on the adhesive and invasive behaviors of human laryngeal carcinoma cell lines through diverse adhesive molecules.
出处 《中国耳鼻咽喉颅底外科杂志》 CAS 2005年第4期217-220,224,共5页 Chinese Journal of Otorhinolaryngology-skull Base Surgery
基金 上海市科委资助项目(No.004119017)
关键词 喉肿瘤/病理学 细胞因子 整合素 粘附 浸润 Laryngeal neoplasms/nathol Cytokine Integrin Adhesive Invasive
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  • 1Kim SY, Chu KC, Lee H R, et al. Establishment and characterization of nine new head and neck cancer cell lines[J]. Acta otolaryngol (stockh), 1997, 117(5): 775-784.
  • 2Pia Santala, Jyrki Heino. Regulation of Integrin-type Cell Adhesion Receptors by Cytokines[J]. The Journal of Biological Chemistry, 1991, 26(34): 23505-23509.
  • 3Valen FV, Hanenberg H, Jurgens H. Expression of functional very late antigen-α1, -α2, -α3, and -α6 Integrins on Ewing's Sarcoma and primitive peripheral neuroectodermal tumour cells and modulation by interferon-γ and tumour necrosis factor-α[J]. European Journal of Cancer, 1994, 30(14): 2119-2125.
  • 4Albini A, Iwamoto Y, Kleinman HK, et al. A rapid in vitro assay for quantitating the invasive potential of tumor cell[J]. Cancer Research, 1987, 15; 47(12): 3239-3245.
  • 5Martin-Henao GA, Quiroga R, Sureda A, et al. L-selectin expression is low on CD34+ cells from patients with chronic myeloid leukemia and interferon-a up-regulates this expression[J]. Haematologia, 2000, 85(2): 139-146.
  • 6Bendall LJ, Kortlepel K, Gottlieb DJ. Bone marrow fibroblast exposure to the inflammatory cytokines tumor necrosis factor-alpha and interferon-gamma increases adhesion of acute myeloid leukemia cells and alters the adhesive mechanism[J]. Exp Hematol, 1997, 25(2): 132-139.
  • 7Hayashi H, Shimizu R, Fujii K, et al. Resistance to IL-1 anti-proliferative effect, accompanied by characteristics of advanced melanoma, permits invasion of human melanoma cells in vitro, but not metastasis in the nude mouse[J]. Int J Cancer, 1997, 71(3): 416-421.
  • 8Anasagasti MJ, Alvarez A, Martin JJ, et al. Sinusoidal endothelium release of hydrogen peroxide enhances very late antigen-4-mediated melanoma cell adherence and tumor cytotoxicity during interleukin-1 promotion of hepatic melanoma metastasis in mice[J]. Heptatology, 1997, 25(4): 840-846.
  • 9Hsieh MC, Wu CW, Wu LH, et al. Heat shock and cytokines modulate the expression of adhesion molecules on different human gastric-cancer cell lines[J]. Int J Cancer, 1996, 4; 67(5): 690-694.
  • 10Saito H, Kurose I, Ebinuma H, et al. Kupffer cell-mediated cytotoxicity against hepatoma cells occurs through production of nitric oxide and adhesion via ICAM-1/CD18[J]. Int Immunel, 1996, 8(7): 1165-1172.

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