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陈慧聪, 刘运江, 赵继东, 曹淼, 李欣慧, 任曙光, 张香梅, 单保恩. IFN-γ通过下调CXCL8抑制食管鳞状细胞癌的增殖和迁移[J]. 肿瘤防治研究, 2022, 49(3): 187-191. DOI: 10.3971/j.issn.1000-8578.2022.21.0901
引用本文: 陈慧聪, 刘运江, 赵继东, 曹淼, 李欣慧, 任曙光, 张香梅, 单保恩. IFN-γ通过下调CXCL8抑制食管鳞状细胞癌的增殖和迁移[J]. 肿瘤防治研究, 2022, 49(3): 187-191. DOI: 10.3971/j.issn.1000-8578.2022.21.0901
CHEN Huicong, LIU Yunjiang, ZHAO Jidong, CAO Miao, LI Xinhui, REN Shuguang, ZHANG Xiangmei, SHAN Baoen. IFN-γ Inhibits Proliferation and Migration of Esophageal Squamous Cell Carcinoma by Downregulating CXCL8 Expression[J]. Cancer Research on Prevention and Treatment, 2022, 49(3): 187-191. DOI: 10.3971/j.issn.1000-8578.2022.21.0901
Citation: CHEN Huicong, LIU Yunjiang, ZHAO Jidong, CAO Miao, LI Xinhui, REN Shuguang, ZHANG Xiangmei, SHAN Baoen. IFN-γ Inhibits Proliferation and Migration of Esophageal Squamous Cell Carcinoma by Downregulating CXCL8 Expression[J]. Cancer Research on Prevention and Treatment, 2022, 49(3): 187-191. DOI: 10.3971/j.issn.1000-8578.2022.21.0901

IFN-γ通过下调CXCL8抑制食管鳞状细胞癌的增殖和迁移

IFN-γ Inhibits Proliferation and Migration of Esophageal Squamous Cell Carcinoma by Downregulating CXCL8 Expression

  • 摘要:
    目的 研究干扰素-γ(IFN-γ)对食管鳞状细胞癌细胞株Eca9706增殖及迁移能力的影响,并初步探讨其作用机制。
    方法 体外进行细胞培养,用干扰素-γ作用细胞,镜下观察细胞形态变化,CCK-8实验检测细胞增殖能力,划痕实验和Transwell实验检测细胞迁移能力。采用Quantitative Real-time PCR法检测趋化因子CXCL8(白介素8)的表达效率,ELISA实验检测细胞CXCL8分泌量的变化。
    结果 与空白对照组比较,接受不同浓度干扰素-γ作用后的Eca9706细胞,细胞形态未发生明显改变。CCK-8实验证实,IFN-γ作用后的Eca9706细胞增殖能力显著降低(P < 0.01)。划痕实验发现IFN-γ使Eca9706细胞迁移能力显著下降(P < 0.01)。Transwell实验显示IFN-γ作用后,Eca9706细胞的迁移能力受到明显抑制(P < 0.01)。同时,接受干扰素-γ作用后,Eca9706细胞的CXCL8基因表达水平显著下调(P < 0.01),CXCL8分泌量显著降低(P < 0.05)。
    结论 干扰素-γ可抑制食管癌细胞株Eca9706的增殖和迁移能力,其可能与抑制Eca9706细胞的CXCL8的表达和分泌相关。

     

    Abstract:
    Objective To investigate the effect of IFN-γ on the proliferation and migration of esophageal squamous cell carcinoma cell line Eca9706 and related mechanism.
    Methods Cells were cultured in vitro and treated with interferon-γ. Cell morphology changes were observed under microscope, cell proliferation ability was detected by CCK-8 experiment, and cell migration ability was detected by cell scratch experiment and Transwell experiment. Real-time PCR method was used to detect the expression efficiency of chemokine CXCL8 (interleukin 8), and the ELISA experiment was used to detect the change of CXCL8 secretion.
    Results Compared with the blank control group, Eca9706 cells treated with different concentrations of interferon-γ did not change significantly in cell morphology. CCK8 experiment confirmed that the proliferation ability of Eca9706 cells after IFN-γ treatment was significantly reduced (P < 0.01). Cell scratch experiment found that IFN-γ significantly decreased the migration ability of Eca9706 cells (P < 0.01). Transwell experiment showed that after IFN-γ treatment, the migration ability of Eca9706 cells was significantly inhibited (P < 0.01). CXCL8 gene expression level in Eca9706 cells treated with interferon-γ was significantly down-regulated (P < 0.01), and the amount of CXCL8 secretion significantly reduced (P < 0.05).
    Conclusion Interferon-γ can inhibit the proliferation and migration of esophageal cancer cell line Eca9706, which may be related to its inhibition of the expression and secretion of CXCL8.

     

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