首页> 外文期刊>西安医科大学学报(英文版) >ANTITUMOR MECHANISM OF GEM10 BY THE NATURAL KILLER ACTIVITY AND INTERLEUKIN-2 PRODUCTION
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ANTITUMOR MECHANISM OF GEM10 BY THE NATURAL KILLER ACTIVITY AND INTERLEUKIN-2 PRODUCTION

机译:自然杀手活性和白介素2产生的GEM10的反演机理。

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Objective To investigate the anti-tumor effects of GeM10 by the natural killer(NK) cells activities and the production of Interleukin-2 (IL-2) in peripheral blood mononuclear cells (PBMNCs). Methods Assay of human NK cells activities by dye rejection assay in vitro and production of IL-2 in PBMNC by IL-2 bioassay with IL-2 dependent cell line CTLL2 and MTT colorometric method. Results GeM10 could significantly stimulate NK activities (60μg*mL -1 GeM10: 17.077±7.665, 120μg*mL-1 GeM10: 24.9±13.04; control: 7.72±4.64, P<0.05). GeM10 could up-regulate the production of IL-2 of PBMNCs in tumor patients(60μg*mL-1 GeM10: 2.965±1.183; 120μg*mL-1 GeM10: 2.28±0.847; control: 1.792±0.823, P<0.05).Conclusion The GeM10 not only can stimulate the NK activities but also increase the IL-2 production by PBMNCs in tumor patients. These findings indicate that the GeM10 may have promise as an anti-tumor drug and a biological response modifier in clinic.
机译:目的探讨天然杀伤(NK)细胞活性对GeM10的抗肿瘤作用以及外周血单核细胞(PBMNCs)IL-2(IL-2)的产生。方法采用体外染色排斥法测定人NK细胞活性,IL-2依赖性细胞株CTLL2和MTT比色法通过IL-2生物测定法检测PBMCC中IL-2的产生。结果GeM10可显着刺激NK活性(60μg* mL -1 GeM10:17.077±7.665,120μg* mL-1 GeM10:24.9±13.04;对照组:7.72±4.64,P <0.05)。 GeM10可上调肿瘤患者PBMCCs的IL-2产生(60μg* mL-1 GeM10:2.965±1.183;120μg* mL-1 GeM10:2.28±0.847;对照:1.792±0.823,P <0.05)。结论GeM10不仅可以刺激肿瘤患者的NK活性,而且可以增加PBMNCs的IL-2产生。这些发现表明,GeM10有望在临床上作为抗肿瘤药物和生物反应修饰剂。

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