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作 者:屠洋洋 俞耀军[1] 林海鸿[1] 林宪慧 孙维建[1] 卢明东[1] 周香[1] 余俊华[1] 郑志强[1]
机构地区:[1]温州医科大学附属第二医院,浙江温州325000
出 处:《中国中医急症》2014年第10期1801-1805,共5页Journal of Emergency in Traditional Chinese Medicine
基 金:浙江省卫生厅科研基金资助项目(2011KYA112)
摘 要:目的观察榄香烯对裸鼠胃癌移植瘤的作用并探讨其相关机制。方法雄性裸鼠建立人胃癌SCG-7901细胞裸鼠移植瘤模型,随机分为对照组、榄香烯组、PD98059组、榄香烯和PD98059联合组(榄香烯+PD98059组)。对比榄香烯和PD98059对裸鼠胃癌移植瘤的作用,测量对比裸鼠胃癌移植瘤的大小及药物对裸鼠生长的抑制作用。Western-blot方法检测各组ERK1/2蛋白、p-ERK1/2、p-P38蛋白的表达情况。结果 3个实验组在治疗后移植瘤大小与对照组比较明显减小,榄香烯组较对照组p-ERK1/2蛋白表达显著增多,3个治疗组相比对照组p-p38蛋白表达显著增加,两药联合比单一药物作用显著(均P<0.05或P<0.01)。结论榄香烯和PD98059都能促进肿瘤组织凋亡,其中榄香烯促进裸鼠胃癌移植瘤凋亡可能与p-ERK1/2蛋白和p-p38蛋白上调有关,而PD98059促进裸鼠胃癌移植瘤凋亡可能与p-P38蛋白上调有关。Objective: To observe the effect of elemene inducing nude mice transplanted tumor and to explore the relative mechanism. Method: male nude mice were chosen to establish SCG-7901 gastric transplanted tumor model and were divided into four groups:control group,elemene group (maximum tolerated dose of 200 mg/kg), PD98059 group(maximum tolerated dose 1 mg/kg) ,elemene and PD98059 joint group. The effect of elemene and PD98059 on nude mice gastric transplanted tumor were compared,and the size of transplanted tumor were mea- sured and the inhibitive effect on the growth of nude mice were determined. ERK1/2,P-ERK1/2 and P-P38 pro- tein expressions of each group were detected by Western blot method. Result: The size of nude mice transplanted tumors of three experimental groups significantly decreased after treatment compared with control group. And P- ERK1/2 protein expression of elemene group was more obvious than that of the control group. P-P38 protein ex- pression of three treatment groups increased much more significantly than that of the control group. Elemene and PD98059 combined treatment group had more obvious effect than single drug group. Conclusion: Both elemene and PD98059 can promote tumor tissue apoptosis. Elemene promoting nude mice gastric transplanted tumor apop- tosis may be related to increased P-ERK1/2 protein and P- P38 protein,while PD98059 promoting such apoptosis may be related to increased P- P38 protein.
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