期刊文献+

青蒿烯对人宫颈癌Hela细胞凋亡的影响及作用机制 被引量:7

Effect of artemisitene on apoptosis of cervcal cancer cell line Hela
下载PDF
导出
摘要 目的:研究青蒿烯对宫颈癌Hela细胞凋亡的影响,并初步探讨青蒿烯诱导Hela细胞凋亡的作用机制。方法:通过MTT法分析不同浓度青蒿烯对Hela细胞增殖活力的影响;运用Hoechst33258荧光染色法和流式细胞术检测青蒿烯对Hela细胞诱导凋亡的影响;应用caspase-3/7活性检测试剂盒检测青蒿烯处理后Hela细胞caspase-3/7活性的变化情况;Western blot法检测caspase-3/7,Fas-L和Fas蛋白水平的变化。结果:与对照组相比,青蒿烯抑制Hela细胞的增殖(P<0.05,P<0.01),且显著地诱导Hela细胞凋亡(P<0.01);青蒿烯促进aspase3/7的活化,增加caspase-3/7的切割以及Fas-L的表达。结论:青蒿烯具有诱导宫颈癌Hela细胞凋亡的作用,这一作用可能与青蒿烯上调Fas-L的表达,激活死亡受体信号通路有关。 Objective To investigate the pro-apoptotic activity of artemisitene on cervical cancer cell line Hela and its mechanisms. Methods The inhibitory effect of artemisitene on the proliferation of Hela cells was measured by MTT assay. Hoechst33258 fluorescence staining and flow cytometry were employed to determine the pro-apoptotic effect of artemisitene on Hela cells. The activity of caspase-3 / 7 was analyzed by caspase-3 / 7activity assay kit. Westren blot was used to detect the protein levels of cleaved caspase-3 / 7, Fas-L and Fas.Results MTT assay showed that artemisitene inhibited Hela cells proliferation(P〈0.05,P〈0.01). Moreover,Hela cells were significantly induced to apoptosis by artemisitene. Accordingly, the enhanced activity and increased cleaved form of caspase-3 / 7 were observed in artemisitene-treated group. In addition, artemisitne promoted the expression of Fas-L. Conclusion Artemisitene significantly induced apoptosis of Hela cells. The effect may be related to the up-regulation of Fas-L, and subsequent activated death receptor apoptotic signaling pathway.
作者 李磊 姚亚超
出处 《实用医学杂志》 CAS 北大核心 2016年第9期1384-1387,共4页 The Journal of Practical Medicine
基金 国家自然科学基金(编号:81400639 81502507) 广州医科大学博士启动基金(编号:2014C39)
关键词 宫颈肿瘤 青蒿烯 凋亡 FAS-L Cervical neoplasms Artemisitene Apoptosis
  • 相关文献

参考文献9

  • 1SHI C, LI H, YANG Y, et al. Anti-inflammatory and immunoregulatoiy timctions of atlemisinin and its derivatives [J]. Mediators hfflamm, 2015, 2015: 435713.
  • 2HO WE, PEH HY, CHAN TK, et al. Artemisinins: pharmacologica actions beyond anti-malarial [J]. Pharmacnl Ther, 2014, 142(1): 126-139.
  • 3付彦辉,钟俊,罗素琴,侯庆伟,王国成,战明哲.青蒿素的化学合成研究进展[J].中国药学杂志,2014,49(10):795-805. 被引量:19
  • 4张天,孙权权,陈嘉荣,庞诗语,袁亚维.MicroRNA-451通过靶向RAB14抑制鼻咽癌细胞的生长、侵袭和迁移能力[J].实用医学杂志,2015,31(3):355-360. 被引量:6
  • 5VILLA-MORALES M, FERNANDEZ-PIQUERAS J. Targeting the Fas/FasL signaling pathway in cancer therapy [J]. Expert Opin Ther Targets, 2012, 16( 1 ) : 85-101.
  • 6ZHAO C, QIN G, GAO W, et al. Potent proapoptotic actions of dihydroartemisinin in gemcitabine-resistant A549 cells [J]. Cell Signal, 2014, 26(10): 2223-2233.
  • 7QIN G, WU L, LIU H, et al. Artesunate induces apoptosis via a ROS-independent and Bax-mediated intrinsic pathway in HepG2 cells[J]. Exp Cell Res, 2015, 336(2) : 308-317.
  • 8LI L, YA0 YC, FANG SH, et al. Pigment epithelial-derived factor (PEDF)-triggered lung cancer cell apoptosis relies on p53 protein-driven Fas ligand (Fas-L) up-regulation and Fas protein cell surface translocation [J]. J Biol Chem, 2014, 289 (44) : 30785-30799.
  • 9BONOFIGLIO D, GABRIELE S, AQUILA S, et al. Peroxisome proliferator-aetivated receptor gamma activates fas ligand gene promoter inducing apoptosis in human breast cancer cells [ J ]. Breast Cancer Res Treat, 2009, 113 (3) : 423-434.

二级参考文献22

  • 1梅林,石开云.青蒿素生物合成研究进展[J].中国药业,2006,15(19):27-28. 被引量:7
  • 2石开云,梅林,蔡中文,张秋.青蒿素前体研究进展[J].中国药业,2007,16(10):25-26. 被引量:3
  • 3Zongaro S, Kukema H , I)/Anlnni S, et al. The 3' UTR nfFMR1 niRNA is a target of miR-101 , miR-129-5p and miR-221 : implications for the molecular pathology of FXTAS at thesynapse [J]‘ Hum Mol Genet, 2013,22( 10) : 1971-1982.
  • 4/hang JX, Qian I), Wang KW , et al. Mi(ToKNA-29c enhanresllie sensitivities of human nasophai*yngeal carcinoma lo cisplatin-hased chemotherapy and radiotherapy [J j. Cancer Lell,2013 ,329(1):91-98.
  • 5IJ (;,Liu Y, Su Z, et al. MicroRNA-324-3p regulales nasopha-ryngeal carcinoma radioresistanr-e by Hirertly tiirgeting WNT2B[J]. Kur J Cancer, 2013.49( 11) ;2596-2607.
  • 6Qu C, Liang Z, Huang J, et al. MiR-205 Heter mines the ra-dioresistance of human nasopharyngeal carcinoma l>y directlytargeting PTKN [J]. Cell Cycle, 2012,11(4):785-7%.
  • 7Tian Y , Nan Y , Han L, et al. MicroKNA miR-451 downrt*fil-iates the PI3K/AKT pathway ihnnigh CAB39 in human glioma[J]. Ini J Onrol, 2012,40(4) : 1105-1112.
  • 8Liu N,Jiang N, Guo R, et al. MiR-451 inhibits cell growth andinvasion by targeting MIF and is associated with survival in na-sopharyngeal carcinoma [J]. Mol Cancer,2013,12( 1) : 123.
  • 9Zhang Z,Luo X,Ding S, et al. MicroRNA-451 regulates p38MAPK signaling by targeting of Ywhaz and suppresses themesangial hypertrophy in early diabetic nephropathy [J]. FEBSLett, 2012,586(1):20-26.
  • 10Wang R, Wang ZX, Yang JS, et al. MicroRNA-451 functionsas a tumor suppressor in human non-small cell lung cancer bytargeting ras-related protein 14 (RAB14) [J]. Oncogene,2011,30(23):2644-2658.

共引文献23

同被引文献74

引证文献7

二级引证文献68

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部