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黄芪甲苷配伍姜黄素对人卵巢癌HO-8910原位移植瘤转移的抑瘤作用
引用本文:杨苏钰,唐德才,曹子丰,张硕,时晓霞,尹刚.黄芪甲苷配伍姜黄素对人卵巢癌HO-8910原位移植瘤转移的抑瘤作用[J].中国实验方剂学杂志,2017,23(6):155-160.
作者姓名:杨苏钰  唐德才  曹子丰  张硕  时晓霞  尹刚
作者单位:江苏省中医药防治肿瘤协同创新中心, 南京中医药大学 基础医学院, 南京 210023,江苏省中医药防治肿瘤协同创新中心, 南京中医药大学 基础医学院, 南京 210023,江苏省中医药防治肿瘤协同创新中心, 南京中医药大学 基础医学院, 南京 210023,江苏省中医药防治肿瘤协同创新中心, 南京中医药大学 基础医学院, 南京 210023,江苏省中医药防治肿瘤协同创新中心, 南京中医药大学 基础医学院, 南京 210023,江苏省中医药防治肿瘤协同创新中心, 南京中医药大学 基础医学院, 南京 210023
基金项目:国家自然科学基金项目(81073012,81503267);江苏省自然科学基金项目(15KJB360003)
摘    要:目的:研究黄芪甲苷配伍姜黄素对人卵巢癌HO-8910原位移植瘤出现转移的抑瘤作用,探讨两者配伍对抗肿瘤是否有协同增效作用。方法:选取已建立荧光蛋白转染的HO-8910卵巢癌动物模型,设G1模型组,G2顺铂组,G3黄芪甲苷组,G4姜黄素组,G5黄芪甲苷+姜黄素配伍组,每组8只。称瘤重并计算抑瘤率;免疫组化法检测肿瘤组织基质金属蛋白酶2(matrix metallopeptidase 2,MMP2),B细胞淋巴瘤/白血病-2(apoptosis regulator,Bcl-2)的蛋白表达;实时荧光定量PCR(Realtime PCR)法检测MMP2,Bcl-2及miR21,miR15a,miR200a基因表达。结果:荷瘤鼠经治疗后,与模型组比较,瘤重均有所减小,配伍组瘤重明显低于其他组(P0.05)。免疫组化结果显示,与模型组比较,顺铂组、单体组MMP2,Bcl-2蛋白表达均降低,配伍组明显降低(P0.05);Real-time PCR结果显示,与模型组比较,中药组MMP2,Bcl-2,miR21基因表达均降低,配伍组明显下调(P0.05),miR15a,miR200a基因表达均增强,配伍组明显上调(P0.05)。结论:黄芪甲苷配伍姜黄素对人卵巢癌HO-8910原位移植瘤出现转移后有抑瘤作用,其作用机制可能与抑制MMP2,Bcl-2,miR21表达,上调miR15a,miR200a表达有关,黄芪甲苷配伍姜黄素确有协同增效作用。

关 键 词:黄芪甲苷  姜黄素  卵巢癌  B细胞淋巴瘤/白血病-2  基质金属蛋白酶2
收稿时间:2016/9/29 0:00:00

Anti-tumor Effect of Astragaloside Combined with Curcumin on Orthotopic Transplantation Tumor Tissue of HO-8910 Ovarian Carcinoma Metastasis
YANG Su-yu,TANG De-cai,CAO Zi-feng,ZHANG Shuo,SHI Xiao-xia and YIN Gang.Anti-tumor Effect of Astragaloside Combined with Curcumin on Orthotopic Transplantation Tumor Tissue of HO-8910 Ovarian Carcinoma Metastasis[J].China Journal of Experimental Traditional Medical Formulae,2017,23(6):155-160.
Authors:YANG Su-yu  TANG De-cai  CAO Zi-feng  ZHANG Shuo  SHI Xiao-xia and YIN Gang
Institution:Jiangsu Collaborative Innovation Center of Traditional Chinese Medicine Prevention and Treatment of Tumor, College of Basic Medicine, Nanjing University of Chinese Medicine, Nanjing 210023, China,Jiangsu Collaborative Innovation Center of Traditional Chinese Medicine Prevention and Treatment of Tumor, College of Basic Medicine, Nanjing University of Chinese Medicine, Nanjing 210023, China,Jiangsu Collaborative Innovation Center of Traditional Chinese Medicine Prevention and Treatment of Tumor, College of Basic Medicine, Nanjing University of Chinese Medicine, Nanjing 210023, China,Jiangsu Collaborative Innovation Center of Traditional Chinese Medicine Prevention and Treatment of Tumor, College of Basic Medicine, Nanjing University of Chinese Medicine, Nanjing 210023, China,Jiangsu Collaborative Innovation Center of Traditional Chinese Medicine Prevention and Treatment of Tumor, College of Basic Medicine, Nanjing University of Chinese Medicine, Nanjing 210023, China and Jiangsu Collaborative Innovation Center of Traditional Chinese Medicine Prevention and Treatment of Tumor, College of Basic Medicine, Nanjing University of Chinese Medicine, Nanjing 210023, China
Abstract:Objective: To study the anti-tumor effect of astragaloside combined with curcumin on human ovarian cancer HO-8910 orthotopic transplantation tumor metastasis and discuss whether the combination of astragalosideand curcumin has the synergies effect against tumor. Method: HO-8910 ovarian carcinoma animal models withfluorescent protein transfectionwere selected,including G1 model group, G2 Cisplatin group, G3 Astragaloside group, G4 curcumin group, G5 Astragaloside+curcumin group, n=8 in each group. The tumor was weighted and the inhibitory rate was calculated. The protein expression levelsof matrix metallopeptidase 2 (MMP2) and apoptosis regulator (Bcl-2) were detected by immunohistochemical method, and thegene expression levels of MMP2, Bcl-2, miR21, miR15a and miR200a were detected by Real-time PCR. Result: Tumor weights of the tumor-bearing nude mice after treatment were lower than those in model group; the tumor weight in Astragaloside+curcumin group was significantly lower than that in other groups(P<0.05).Immunohistochemical results showed that the levels of the protein expressions of MMP2,Bcl-2 in G2, G3 and G4 groups were lower than those in model group, and the levels in G5 group were significantly reduced (P<0.05). Real-time PCR results showed that the gene expression levels of MMP2, Bcl-2 and miR21 in Chinese medicine groups were lower than those in model group, and the levels in G5 groupweresignificantly reduced (P<0.05); the gene expression levels of miR15a, miR200a were higher than those in model group, and the levels in G5 group were significantly increased (P<0.05). Conclusion: The combination of astragaloside and curcumin has the suppression effect on human ovarian cancer HO-8910 orthotopic transplantation tumor metastasis, which may be associated with the down-regulation of MMP2, Bcl-2 and miR21 expressions and the up-regulation of miR15a and miR200a expressions. Therefore, the combination of astragaloside and curcumin has the synergies effect against tumor.
Keywords:astragaloside  curcumin  ovarian cancer  apoptosis regulator (Bcl-2)  matrix metallopeptidase 2 (MMP2)
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