%0 Journal Article %T 黄芪多糖对气阴两虚Lewis肺癌荷瘤小鼠肿瘤生长、转移及细胞周期的影响 %A 明海霞 %A 李杨 %A 杨玲玲 %A 白彦丽 %J 肿瘤防治研究 %D 2018 %R 10.3971/j.issn.1000-8578.2018.17.0220 %X 摘要 目的 观察黄芪多糖抑制气阴两虚Lewis肺癌荷瘤小鼠的生长、转移及对肺癌细胞周期的影响。方法 体外培养Lewis肺癌细胞,随机分为对照组和中药组,流式细胞术检测细胞周期;C57BL/6J小鼠90只,设空白组10只,余80只刨花烟熏并灌胃温热性的中药,移植Lewis肺癌实体肿瘤建立气阴两虚荷瘤小鼠模型并随机分为8组,比较各组小鼠抑瘤率及q值,计数外周血细胞及骨髓细胞,ELISA测定血清IL-2、IFN-γ、TNF-α、IL-10、HIF-1α、VEGF、MMP-2的含量。结果 黄芪多糖将Lewis 肺癌细胞阻滞于S期,随着药物浓度的增加,细胞凋亡逐渐增加;联合用药各组的抑瘤率高于黄芪多糖各组和顺铂组,q值均在0.85~1.15之间;与顺铂组比较,联合用药中、高剂量组小鼠外周血细胞及骨髓细胞的数量,IL-2、INF-γ、TNF-α均显著升高,IL-10、 HIF-1α、VEGF、MMP-2均显著降低(P<0.05, P<0.01)。结论 黄芪多糖在体外对Lewis肺癌细胞有抑制作用,体内与顺铂联合能抑制气阴两虚Lewis荷瘤小鼠肺癌细胞的生长、转移,提高外周血细胞和骨髓细胞的细胞数量,提高IL-2、INF-γ、TNF-α的含量,减少IL-10、HIF-1α、VEGF、MMP-2的含量 %K 黄芪多糖 %K 气阴两虚 %K Lewis肺癌 %K 细胞周期 %K 抗瘤增效 %K G6PD对大肠癌细胞生长侵袭的影响及其与HKⅡ的相关性 %K Mechanism of D-bifunctional Protein Promoting Formation of Hepatocellular Carcinoma in Rat via STAT3 %K Effect of STAT1 on Cell Cycle of Human Glioma U251 Cells and Related Mechanism %K Role of Gadd45 Protein Family in Tumorigenesis and Development %K Effect of Cyclin G1 on Radiosensitivity of Hepatocellular Carcinoma HepG2 Cells and Its Mechanism %K Effect of IL-4/IL-4R on Biological Behavior of Hepatocellular Carcinoma and Its Underlying Mechanism %K Progress of Relationships of Calprotectin with Tumours %K GM-CSF Enhances Effect of TMZ on High-grade Glioma Cells %K Effects of Gefitinib Combined with Bruceolic Oil Emulsion on Human Lung Adenocarcinoma Cell Lines and Its Mechanism %K Effects of SHP-1 Overexpression on Biological Characteristics of K562 Cells %K Effect of Silencing Toll-like Receptor 4 Expression on Cell Cycle and Apoptosis of Human Lung Adenocarcinoma Cells A549 %K Tumor Suppressor Roles of miR-100 in Esophageal Squamous Cell Carcinoma Cell Line Ec-109 %K Cisplatin-induced Senescence and Senescence-related Gene Expression Profiles in#br# Human Nasopharyngeal Carcinoma Cells CNE2 %K Role of IL-1RAP in Gliomas Cells and Its Relationship with STAT3 %K Effects of MNNG on Proliferation %K Cycle and Apoptosis of Kazakh Normal Esophageal Epithelial Cells %U http://www.zlfzyj.com/CN/abstract/abstract9118.shtml