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人参皂甙激活恶性胸水中的TILs及其与吉西他滨协同抗癌作用的实验研究 被引量:9

The Synergetic Effect of Ginsenoside and Gemcitabine on Human Lung Cancer Cells Derived from Pleural Effusion
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摘要 目的 研究人参皂甙 (GS)对癌性胸水中肿瘤浸润淋巴细胞 (TILs)增殖及抗肿瘤活性的影响 ,探讨活化后的TILs与吉西他滨 (GCM)的协同抗癌作用。方法 采用3 H -TdR释放法检测TILs的增殖及抗肿瘤活性 ,MTT比色法测定TILs与GCM的协同抗癌作用。结果  ( 1 )以GS处理TILs 72h ,其增殖速度明显高于PBS对照组 (P <0 .0 5 ) ,且GS浓度为 2~ 64μg mL时能增强IL - 2对TILs增殖的促进作用。 ( 2 )联合使用GS与白介素 - 2 (IL - 2 )能进一步提高TILs的抗肿瘤活性 ,对肺癌细胞的抑制率明显高于对照组 (P <0 .0 5 ) ,并且可减少IL - 2的剂量 ,其最适浓度为 2 3.7μg mL。 ( 3)GS和IL - 2合用后活化的TILs能提高GCM的细胞毒性 ,与单独使用GCM相比 ,P <0 .0 1。结论 GS是一种有应用前景的TILs诱导活化剂 ,在肿瘤免疫化疗中可能具有较重要的地位。 Objective:Our research aimed at studying whether GS can promote tumor infiltrating lymphocytes (TILs) derived from malignant pleural effusion proliferating and enhance their anti-tumor potency,elucidating the synergetic effect of TILs and gemcitabine (GCM).Methods:The proliferation and tumor cytotoxicity of TILs were determined by 3 H-TdR releasing assay.The synergetic effect of TILs and GCM was detected by MTT colorimetric assay.Results:(1)TILs treated with GS for 72 hours grew quicker than control groups(P<0.05),and GS can enhance the effect of IL-2 in accelerating TILs proliferation when its concentration is 2~64 μg/mL.(2)When used in combination with interleukin-2(IL-2),GS was capable of enhancing the tumor cytotoxicity of TILs in further,the inhibition rate to lung cancer cells was markedly higher than controls(P<0.05).On the other hand,GS can decrease the concerntration of IL-2 needed to show equivalent effect.The best concerntration of GS was 23.7 μg/mL.(3)TILs achivation by GS and IL-2 was capable of augmenting the tumor cytotoxicity of GCM (P<0.05).Conclusions: GS was a kind of antitumor agent which may be useed in clinical practice in future by inducing and activating TILs,thus it may play an important role in immunochemotherapy of malignant pleural effusion.
出处 《南华大学学报(医学版)》 2002年第1期7-10,共4页 Journal of Nanhua University(Medical Edition)
基金 湖南省科技厅立项课题 (99SSY30 0 8)
关键词 人参皂甙 肿瘤浸润淋巴细胞 吉西他滨 协同抗癌作用 中药 药理 ginsenoside tumor infiltrating lymphocytes gemcitabine synergetic tumor cytotoxicity
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