IFN-γ和TNF-α诱导间充质干细胞促进结肠癌细胞的化疗抵抗
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第二军医大学东方肝胆外科医院肿瘤免疫与基因治疗实验室,第二军医大学第一附属医院长海医院,上海交通大学医学院附属仁济医院中心实验室,第二军医大学东方肝胆外科医院肿瘤免疫与基因治疗实验室,第二军医大学第一附属医院长海医院,第二军医大学东方肝胆外科医院肿瘤免疫与基因治疗实验室

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IFN-γ and TNF-α treated mesenchymal stem cells can enhance the chemotherapy resistance of colon cancer cells
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Tumor Immunology and Gene Therapy Center,Eastern Hepatobiliary Surgery Hospital,Second Military Medical University,Department of Phamacy,Changhai Hospital,the Second Military Medical University,Central Laboratory,Renji Hospital,Shanghai Jiao Tong University School of Medicine,Tumor Immunology and Gene Therapy Center,Eastern Hepatobiliary Surgery Hospital,Second Military Medical University,Department of Phamacy,Changhai Hospital,the Second Military Medical University,Tumor Immunology and Gene Therapy Center,Eastern Hepatobiliary Surgery Hospital,Second Military Medical University

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    摘要:

    目的 观察炎症因子干扰素γ(interferon-γ,IFN-γ)和肿瘤坏死因子α(tumor necrosis factor-α,TNF-α)诱导间充质干细胞(mesenchymal stem cells,MSCs)对结肠癌细胞化疗抵抗的影响及机制。 方法 应用炎症因子IFN-γ和TNF-α联合处理MSCs,收集条件培养上清,并将其作用于人结肠癌细胞系HCT116及HT29细胞,同时分别给予化疗药物顺铂和5-氟尿嘧啶处理。显微镜下观察各组细胞形态变化,MTT法和流式细胞术检测细胞增殖和凋亡情况,RT-PCR检测凋亡相关基因BaxBcl-2表达情况。 结果 经化疗药物处理,与未经条件培养上清培养的细胞比较,经条件培养上清培养的细胞形态学改变更轻微,细胞增殖率增高(P<0.05)、凋亡率降低(P<0.05),Bcl-2 mRNA表达水平上调、Bax mRNA表达水平下调。 结论 经炎症因子IFN-γ和TNF-α诱导的MSCs能够促进结肠癌细胞化疗抵抗能力。

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    Objective To observe the influence of interferon-γ(IFN-γ)and tumor necrosis factor-α(TNF-α)treated mesenchymal stem cells (MSCs) on the chemotherapy resistance of colon cancer cells(CRCs) and to discuss the related mechanism. Methods The supernatants of MSCs treated with IFN-γ and TNF-α were collected and used, together with chemotherapy drug cisplatin and 5-fluorouracil, to treat HCT116 and HT29 CRCs. Then the cellular morphology was observed under microscope, and the cell proliferation and apoptosis were examined by MTT and PI/Annexin Ⅴ-FITC assay. Furthermore, the mRNA levels of Bax and Bcl-2 were detected by RT-PCR. Results The CRCs treated with the supernatant of MSCs exposed to inflammatory factors, compared to CRCs treated with the supernatant of MSCs not exposed to inflammatory factors, had a slighter morphology changes, a significantly higher proliferation rate (P<0.05), and a significantly lower apoptosis rate following chemotherapy(P<0.05). Moreover, Bcl-2 mRNA level was higher and Bax mRNA level was lower in CRCs treated with the supernatant of MSCs exposed to inflammatory factors. Conclusion MSCs stimulated with inflammation factors IFN-γ and TNF-α can promote the chemotherapy resistance of human CRCs.

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  • 收稿日期:2015-04-22
  • 最后修改日期:2015-10-26
  • 录用日期:2015-12-15
  • 在线发布日期: 2016-01-22
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