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作 者:倪克锋[1] 丁志山[2] 黄挺[1] 蒋福升[2] 林胜友[3] 吴良村[3] 黄伶[1]
机构地区:[1]浙江中医药大学附属广兴医院(杭州市中医院),杭州310006 [2]浙江中医药大学生命科学学院 [3]浙江中医药大学附属第一医院
出 处:《浙江中医药大学学报》2008年第6期732-734,共3页Journal of Zhejiang Chinese Medical University
基 金:浙江省中医管理局立项资助项目(NO:2006C104)~~
摘 要:[目的]观察三叶青总黄酮对H-22荷瘤小鼠瘤体的抑制作用,探讨其作用机理。[方法]小鼠肝癌H-22细胞右前肢腋窝皮下接种造膜,观察低、中、高剂量三叶青黄酮对荷瘤小鼠抑瘤率、脾脏指数、胸腺指数的影响,并通过定量RT-PCR检测小鼠皮下移植瘤Fasp-3、CytC的表达情况。[结果]低、中、高剂量三叶青黄酮对H-22荷瘤小鼠的瘤重抑制率分别为34.28%、32.56%和29.24%;皮下移植瘤Fasp-3、CytC mRNA的表达低剂量组明显高于空白组(P<0.05)。[结论]三叶青黄酮可显著抑制肿瘤细胞,这一作用与其能促进肿瘤细胞的促凋亡基因Fasp-3、CytC的表达相关。[Objective]Observe H-22 solid tumor growth inhibition by Tetrastigma hemsleyanum Diels et Gilg flavone(TDGF) and analyse its mechanism. [Methods]Solid tumor-bearing Kunming mice were obtained using mice hepatoma H-22 cell line, tumor growth inhibition ratio of TDGF was assessed and compared, thymus index and spleen index were also recorded to evaluate the function of TDGF; Moreover,the gene expression level of Fasp-3,CytC were detected through quantitate RT-PCR. [Results]Low, moderate and high dose treatment groups showed inhibition H-22 solid tumor activity with inhibition ratio 34.28%, 32.56% and 29.24% respectively. Gene analysis showed that low dose group can up-regulate Fasp-3,CytC mRNA expression with significant deviation compared with control group(P〈0.05). [Conclusion]TDGF can inhibit H-22 solid tumor growth in vivo, which maybe educed by up-regulating the expression of apoptosis related genes Fast〉3 and CytC.
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