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姜黄素对荷瘤裸鼠皮下移植瘤的影响
引用本文:江敏华,谢莹,胡凤霞,甘建和. 姜黄素对荷瘤裸鼠皮下移植瘤的影响[J]. 江苏临床医学杂志, 2010, 0(12): 7-11
作者姓名:江敏华  谢莹  胡凤霞  甘建和
作者单位:苏州大学附属第一医院感染病科,江苏苏州215006
摘    要:
目的观察姜黄素在体内对人肝癌细胞株SMMC-7721的抗肿瘤作用。方法用姜黄素在SMMC-7721肝癌细胞荷瘤裸鼠的瘤体内进行注射治疗,12 d后处死裸鼠,摘除瘤体,称瘤重,观察肿瘤生长变化,并通过免疫组化法检测Bcl-2、Bax、Caspase-3等与细胞凋亡相关因子的表达。结果姜黄素可抑制SMMC-7721细胞对裸鼠的致瘤能力,肿瘤体积较对照组显著减小(P〈0.01),质量也明显小于对照组(P〈0.01),肿瘤生长抑制率达47.7%,免疫组化结果显示阿的平能明显上调与细胞凋亡相关因子Bax和Caspase-3的表达和下调Bcl-2和Survivin的表达。结论姜黄素能抑制SMMC-7721细胞的体内致瘤能力。

关 键 词:姜黄素  凋亡  SMMC-7721细胞  体内成瘤

Effect of curcumin on subcutaneous transplantation tumor of human hepatoma in nude mice
JIANG Min-hua,XIE Ying,HU Feng-xia,GAN Jian-he. Effect of curcumin on subcutaneous transplantation tumor of human hepatoma in nude mice[J]. Journal of Jiangsu Clinical Medicine, 2010, 0(12): 7-11
Authors:JIANG Min-hua  XIE Ying  HU Feng-xia  GAN Jian-he
Affiliation:(Department of Infectious Diseases, First Affiliated Hospital of Suzhou University, Suzhou , Jiangsu , 215006)
Abstract:
Objective To study the anti-tumor effects of curcumin on human hepatocellular carcinoma SMMC-7721 Cells in vivo. Methods For in vivo study, we first established SMMC- 7721 tumor model by grafting SMMC-7721 cells in athymic nude mice, and then injected curcumin into the tumors. 12 days after injection, we sacrificed the mice, removed the tumors, weighed and calculated the ratios of tumor-suppression. We also detected the expressions of Bcl-2, Bax, Caspase -3 and Survivin with immumohistochemistry. Results The tumorigenicity of SMMC-7721 cells was significantly inhibited by curcumin. The size of the tumor in the curcumin treatment group was significantly smaller than that in the control group (P K 0.01), and the tumor weight was also markedly reduced in curcumin group than that in the control group [ (0. 485 ± 0. 178) g vs (0. 928 ± 0. 223) g, (P〈0.01) ]. The tumor growth inhibition rate was 47.7%. The in vivo data showed that curcumin suppressed the tumor growth conspicuously through down-regulating the expressions of bcl-2 and Survivin and up-regulating the expressions of bax and easpase-3. Conclusion Curcumin inhibits the in vivo tumorigenicity of SMMC-7721 cells.
Keywords:curcumin  apoptosis  SMMC-7721 cells  tumorigenicity
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