姜黄素对膀胱癌细胞增殖及凋亡的影响

杨家荣; 陈磊; 杨慧; 潘铁军

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姜黄素对膀胱癌细胞增殖及凋亡的影响

论著 | 更新时间：2026-01-09

- 姜黄素对膀胱癌细胞增殖及凋亡的影响
- Curcumin inhibits proliferation of cell strain of bladder carcinoma and induces its apoptosis
- 陆军军医大学学报 2007年29卷第24期页码：2350-2353
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  中图分类号： R285.5;R329.28;R737.14
- 纸质出版：2007
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杨家荣,陈磊,杨慧,潘铁军.姜黄素对膀胱癌细胞增殖及凋亡的影响[J].陆军军医大学学报(原第三军医大学学报),2007,29(24):2350-2353.

　YANG Jia-rong,CHEN Lei,YANG Hui,PAN Tie-jun.Curcumin inhibits proliferation of cell strain of bladder carcinoma and induces its apoptosis[J].J Amry Med Univ (J Third Mil Med Univ),2007,29(24):2350-2353.
杨家荣,陈磊,杨慧,潘铁军.姜黄素对膀胱癌细胞增殖及凋亡的影响[J].陆军军医大学学报(原第三军医大学学报),2007,29(24):2350-2353. DOI：

　YANG Jia-rong,CHEN Lei,YANG Hui,PAN Tie-jun.Curcumin inhibits proliferation of cell strain of bladder carcinoma and induces its apoptosis[J].J Amry Med Univ (J Third Mil Med Univ),2007,29(24):2350-2353. DOI：

摘要

目的探讨中药姜黄素对膀胱癌细胞(T24)增殖及凋亡的影响及可能机制。方法以培养的T24细胞为研究对象，姜黄素组加入终浓度为1、10、100 μmol/L的姜黄素，对照组不加姜黄素，12、24、48 h后观察 T24 细胞的形态变化，分别用MTT法、TUNEL染色、RT-PCR、免疫印迹及图像分析技术检测各组细胞生长、凋亡发生、AKT1蛋白及转录水平、caspase 3蛋白含量的变化。结果姜黄素组T24细胞生长抑制率显著上升，细胞凋亡发生显著升高，AKT1蛋白活性水平降低，转录水平无显著变化，caspase 3蛋白含量显著升高。结论姜黄素能抑制T24细胞的生长并促进其凋亡，其发生与其抑制T24细胞PKB/AKT信号通路有关。

Abstract

Objective To investigate the effect and possible mechanism of curcumin on the proliferation and apoptosis of cell strain of bladder carcinoma. Methods In curcumin group

T24 cells were treated with curcumin of 1

100 μmol/L respectively

while no curcumin treatment in control group. The growth

apoptosis

AKT1 protein activity and mRNA level

caspase 3 content of T24 cells were observed by MTT

TUNEL

RT-PCR

immunoblot and image analysis technology 12

24 and 48 h after the commencement of curcumin treatment. Results In the curcumin group

the inhibition rate

apoptosis and the content of caspase 3 of T24 cells increased significantly. The activity of AKT1 protein decreased

but the mRNA level of AKT1 showed no changes. Conclusion Curcumin can inhibit the growth of T24 cells and induce the cell apoptosis

which mechanism is related to the inhibition of AKT1 signal pathway of T24 cells.

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