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作 者:王中奇[1] 邓海滨[1] 张丽曼[1] 徐振晔[1]
机构地区:[1]上海中医药大学附属龙华医院肿瘤科,上海200032
出 处:《上海中医药大学学报》2011年第2期65-68,F0003,共5页Academic Journal of Shanghai University of Traditional Chinese Medicine
基 金:上海市教委科研创新项目(08YZ61);上海市浦东新区中医领军型人才项目(PWZl2009-04)
摘 要:目的:观察肺岩宁方及其拆方对C57小鼠Lewis肺癌肿瘤组织中血管内皮生长因子(vascularendothelial growth factor,VEGF)及其激酶功能区受体(kinase-domain insert containing receptor,KDR)mRNA与蛋白表达的影响。方法:建立C57小鼠Lewis肺癌模型,随机分为模型组、肺岩宁组、益气组、补肾组和抗癌组,每组10只。分别给予相应药物干预,均灌胃21 d,第22天处死。观察肺转移情况,取肿瘤组织,采用逆转录聚合酶链反应(RT-PCR)法和免疫组化SP法分别检测C57小鼠Lewis肺癌中VEGF和KDR mRNA及蛋白表达水平。结果:肺岩宁组与补肾组、抗癌组小鼠的肺转移率明显低于模型组与益气组(P<0.05)。C57小鼠Lewis肺癌组织中表达VEGF和KDR,但肺岩宁组与补肾组、抗癌组小鼠肿瘤组织中VEGF mRNA及蛋白的表达水平均明显低于模型组和益气组(P<0.05),肺岩宁方组和抗癌组小鼠肿瘤组织中KDR mR-NA及蛋白的表达水平均明显低于模型组和益气组(P<0.05)。结论:肺岩宁抑制C57小鼠Lewis肿瘤转移的机制可能与下调VEGF及其受体KDR mRNA和蛋白表达有关。Objective : To observe the effects of "Feiyanning Decoction" and its decomposed recipes on expressions of vascular endothelial growth factor (VEGF) and kinase-domain insert containing receptor (KDR) mRNA and proteins in Lewis tumors of C57 mice. Methods: The Lewis lung cancer model of C57BL/6 mice were established and divided into model group ( A), Feiyanning group ( B), nourishing-qi group ( C), tonifying-kidney group (D) and anti-cancer group (E) with 10 mice in each group. All the groups were treated by respective recipe for twenty-one days. The lung metastasis was observed and the expressions of VEGF and KDR mRNA and proteins were detected by reverse transcription-polymerase chain reaction (RT-PCR) method and immunohis- tochemical SP method respectively. Results: Compared with group A and C, the lung cancer metastasis rate decreased markedly in group B, D and E (P 〈0.05 ). The expressions of VEGF and KDR exist in Lewis lung tumor, while the expressions of VEGF mRNA and protein in group B, D and E were lower than that in group A and C ( P 〈 0.05 ) , and the expressions of KDR mRNA and protein in group B and E were lower than that in group A and C ( P 〈 0.05 ). Conclusion : " Feiyanning Decoction" can inhibit Lewis tumor metastasis in C57 mice and its mechanism may be related to down-regulating the expressions of VEGF and KDR mRNA and proteins.
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