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华蟾素对肺癌NCI-A549移植瘤裸鼠的抑制作用及机制研究

熊飞 施嫣嫣 沈久成 程洪兰 杭永付

中国临床药理学与治疗学2018,Vol.23Issue(10):1103-1108,6.
中国临床药理学与治疗学2018,Vol.23Issue(10):1103-1108,6.DOI:10.12092/j.issn.1009-2501.2018.10.004

华蟾素对肺癌NCI-A549移植瘤裸鼠的抑制作用及机制研究

Inhibitory effect and mechanism of cinobufotalin on lung cancer NCI-A549 xenograft in nude mice

熊飞 1施嫣嫣 2沈久成 1程洪兰 1杭永付3

作者信息

  • 1. 苏州大学附属第二医院,苏州215000,江苏
  • 2. 苏州市中医医院,苏州215000,江苏
  • 3. 苏州大学附属第一医院,苏州215000,江苏
  • 折叠

摘要

Abstract

AIM: To investigate the anti-tumor effect and mechanism of cinobufotalin on lung cancer cells NCI-A549. METHODS: Forty BALB/c nude mice were randomly divided into the normal group, the mock group, the cinobufotalin group and the DDP ( cisplatin) group. Body weight change, tumor inhibition rate, blood function, liver and kidney function of the mice in each group were detected. Western blot was used to investigate the expression of apoptosis-associated proteins. RESULTS:Cinobu-fotalin significantly inhibited the growth of A549 xenograft, but had no significant effect on the blood, liver and kidney function of the mice. The tumor-in-hibition rate of the cinobufotalin group and the DDP group was 58. 0% and 82. 3% , respectively. West- ern blot results showed that cinobufotalin significant-ly up-regulated the expression of Bax/Bcl-2, promo-ted the expression of cleaved-caspase-3, cleaved-PARP, and inhibited the expression of p-AKT (ser473). CONCLUSION: Cinobufotalin can sig-nificantly inhibit the growth of lung cancer A549 xenograft. Its molecular mechanism might be related to the inhibition of PI3K/AKT pathway activation. Based on this mechanism, cinobufotalin can acceler-ate cell apoptosis.

关键词

华蟾素/肺癌/移植瘤/凋亡/PI3K/AKT通路

Key words

cinobufotalin/lung cancer/xeno-graft/apoptosis/PI3K/AKT pathway

分类

医药卫生

引用本文复制引用

熊飞,施嫣嫣,沈久成,程洪兰,杭永付..华蟾素对肺癌NCI-A549移植瘤裸鼠的抑制作用及机制研究[J].中国临床药理学与治疗学,2018,23(10):1103-1108,6.

基金项目

国家自然科学基金青年项目(81402830) (81402830)

中国临床药理学与治疗学

OACSCDCSTPCD

1009-2501

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