首页> 外文会议>2011 International Conference on Human Health and Biomedical Engineering >The experimental investigation of SBHL on reversing acquired multi-drug resistance on S180 mouse tumor bearing model
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The experimental investigation of SBHL on reversing acquired multi-drug resistance on S180 mouse tumor bearing model

机译:SBHL逆转S180荷瘤小鼠模型获得性多药耐药性的实验研究。

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Observe the influence of solasodine hydrochloride (SBHL) on mouse S180's tumor model's acquired multi-drug resistance by measuring the tumor chemo sensitivity, tumor cell apoptosis and gene expression level of P-glycoprotein(P-gp), Lung Cancer Resistance Protein(LRP) and Topoisomerase II. Methods Establish the Multi-drug Resistance (MDR) mouse S180 tumor model by low dose chemotherapy. Treat the mouse S180 tumor model with standard chemotherapy drug CTX and 5-FU with or without SBHL for 4 weeks respectively. At the end of study, the size of tumor was measured and the growth of inhibition was calculated. Tumor cells were isolated from each group then stained with PI followed by flow cytometry. The percentage of apoptosis was calculated based on the PI positive cells vs total cells. The expression of P-gp, LRP and TOPOII in each group was compared by flow cytomery as well. Results The combination treatment of chemotherapy and SBHL significantly increased the inhibition of tumor growth. The SBHL combination treatment also significantly induced tumor cell apoptosis compared to control group. Further study demonstrated that the SBHL combination treatment reduced the expression of P-gp, LRP and TOPOII. Conclusion SBHL can reverse the S180 mouse tumor model's acquired multi-drug resistance by increase tumor chemo sensitivity. The mechanism of this reversal maybe related to the reduction of P-gp, LRP and TOPOII expression.
机译:通过测量肿瘤化疗,肿瘤细胞凋亡和基因表达水平,肺癌抗性蛋白(LRP),观察盐酸溶层盐酸溶溶溶的盐酸溶溶胶(SBHL)对小鼠S180肿瘤模型获得多药物抗性的影响(P-GP)和拓扑异构酶II。方法通过低剂量化疗建立多药物抗性(MDR)小鼠S180肿瘤模型。用标准化疗药物CTX和5-FU对小鼠S180肿瘤模型分别与或不含SBHL 4周。在研究结束时,测量肿瘤的尺寸并计算抑制的生长。从每组中分离肿瘤细胞,然后用PI染色,然后流式细胞术染色。基于PI阳性细胞对凋亡的百分比对总细胞进行计算。通过流动的细胞组织比较每组P-GP,LRP和TOPOII的表达。结果化疗和SBHL的组合治疗显着提高了肿瘤生长的抑制。与对照组相比,SBHL组合治疗也显着诱导肿瘤细胞凋亡。进一步的研究表明,SBHL组合治疗降低了P-GP,LRP和TOPOII的表达。结论SBHL可以通过提高肿瘤化疗敏感性来逆转S180小鼠肿瘤模型获得的多药抵抗力。这种逆转的机制可能与降低p-GP,LRP和TopoII表达有关。

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