基础医学与临床 ›› 2022, Vol. 42 ›› Issue (3): 436-440.doi: 10.16352/j.issn.1001-6325.2022.03.026

• 研究论文 • 上一篇    下一篇

华蟾素抑制人鼻咽癌细胞系CNE2和HONE1增殖

赵霞, 蔡庆春*, 丁瑞敏, 张倩   

  1. 河南中医药大学第三附属医院, 河南 郑州 450004
  • 收稿日期:2021-03-23 修回日期:2021-07-12 出版日期:2022-03-05 发布日期:2022-03-04
  • 通讯作者: * 13803864943@163.com
  • 基金资助:
    河南省中医管理局基金(2018ZY1013)

Cinobufagin inhibits proliferation of human nasopharyngeal carcinoma cell lines CNE2 and HONE1

ZHAO Xia, CAI Qing-chun*, DING Rui-min, ZHANG Qian   

  1. The Third Affiliated Hospital of Henan University of Traditional Chinese Medicine, Zhengzhou 450004, China
  • Received:2021-03-23 Revised:2021-07-12 Online:2022-03-05 Published:2022-03-04
  • Contact: * 13803864943@163.com

摘要: 目的 评估华蟾素(Cin)对人鼻咽癌(NPC)细胞系(CNE2和HONE1)的生物学作用以及发挥功效的机制。方法 用不同浓度梯度(0、5、15和45 mg/L)Cin分别处理CNE2和HONE1细胞24、48和72 h后,用CCK-8法检测细胞活性。48 h后,用相差显微镜观察细胞形态;TUNEL荧光染色法检测细胞凋亡;DCF荧光法评估细胞内的活性氧簇(ROS)水平;蛋白质免疫印迹法检测凋亡相关蛋白表达。结果 Cin呈浓度依赖性抑制NPC细胞活性(P<0.05,P<0.01和P<0.001),并且导致细胞出现拉丝和稀疏现象。Cin促进NPC细胞凋亡并增加细胞内ROS水平(P<0.05,P<0.01或P<0.001)。Cin抑制Bax和线粒体细胞色素c(Cytc)的表达(P<0.05,P<0.01或P<0.001),但促进Bcl-2、cleaved caspase-3和胞质Cytc的表达(P<0.01或P<0.001)。结论 Cin可抑制NPC细胞的增殖并促进细胞凋亡。

关键词: 华蟾素, 鼻咽癌, 凋亡, 增殖

Abstract: Objective To evaluate the biological effect of cinobufagin(Cin) on nasopharyngeal carcinoma (NPC) cells lines(CNE2 and HONE1) and the mechanism of its efficacy. Methods CNE2 and HONE1 cells were treated with different concentrations (0, 5, 15 and 45 mg/L) of Cin for 24, 48 and 72 h respectively and cell viability was detected by CCK-8 assay. After 48 hrs, cell morphology was observed by phase contrast microscopy; cell apoptosis was detected by TUNEL fluorescence staining; the level of reactive oxygen species (ROS) in cells were assessed by DCF fluorescence assay; the expression levels of apoptosis-related proteins were detected by Western blot. Results Cin inhibited the cell activity of NPC cells in a concentration-dependent manner (P<0.05, P<0.01 or P<0.001) and the cells showed filament and sparse morphology. Cin promoted apoptosis and increased intracellular ROS level in NPC cells (P<0.05, P<0.01 or P<0.001). Cin inhibited the expression of Bax and mitochondrial cytochrome c (Cytc) (P<0.05, P<0.01 or P<0.001) but promoted the expression of Bcl-2, cleaved caspase-3 and cytoplasmic Cytc (P<0.01 or P<0.001). Conclusions Cin can inhibit cell proliferation and promote apoptosis of NPC cells.

Key words: cinobufagin, nasopharyngeal carcinoma, apoptosis, proliferation

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