期刊文献+

大豆苷元对人非小细胞肺癌A549、H1299细胞增殖、迁移能力的影响及机制 被引量:11

Effect of daidzein on proliferation and migration of lung cancer cells and its related mechanism
在线阅读 下载PDF
导出
摘要 目的探究大豆苷元(daidzein,Daid)对非小细胞性肺癌细胞株A549和H1299增殖、迁移能力的影响及可能机制。方法以A549和H1299为研究对象,CCK-8法检测Daid(0,5,10,25,50,100,200μmol·L^-1)抑制A549和H1299两种细胞的增殖情况。划痕和Transwell小室实验检测Daid对肺癌细胞迁移和侵袭能力的影响。Western blot检测Cleaved Caspase-3和LC3Ⅱ/Ⅰ等的蛋白表达。结果与对照组相比,Daid在体外可明显抑制肺癌细胞的增殖,且抑制作用呈浓度依赖关系。Daid(100μmol·L^-1)可明显降低人肺癌细胞A549和H1299的迁移侵袭能力。Western blot结果显示,Daid(100μmol·L^-1)预处理后,两种肺癌细胞的Cleaved Caspase-3及LC3Ⅱ/Ⅰ表达升高。结论Daid可抑制人非小细胞肺癌A549和H1299细胞的增殖,使上述细胞的迁移侵袭能力明显下降,其机制可能与Daid诱导细胞凋亡及自噬有关。 Aim To investigate the effect of Daidzein(Daid)on proliferation and migration of non-small cell lung cancer cell lines A549 and H1299 and its possible mechanism.Methods CCK-8 was adopted to detect cell proliferation of A549 and H1299 cells inhibited by Daid(0,5,10,25,50,100,200μmol·L^-1).The effect of Daid on proliferation and migration of lung cancer cells was detected by scratch healing and Transwell chamber assay.The protein expressions of cleaved Caspase-3 and LC3Ⅱ/Ⅰwere detected by Western blot.Results Daid had significantly inhibitory effects on the proliferation of lung cancer cells in vitro in a concentration-dependent manner when compared with control group.Daid(100μmol·L^-1)could inhibit the migration and invasion ability of human lung cancer cells A549 and H1299.Western blot results showed that the expressions of cleaved Caspase-3 and LC3Ⅱ/Ⅰwere elevated after Daid pretreatment.Conclusions Daid can inhibit the proliferation of human non-small cell lung cancer cells A549 and H1299,and reduce the migration and invasion of cells.The mechanism may be related to cell apoptosis and autophagy induced by Daid.
作者 成琼 李真 陈锦辉 向铮 张献伟 孔令非 CHENG Qiong;LI Zhen;CHEN Jin-hui;XIANG Zheng;ZHANG Xian-wei;KONG Ling-fei(Dept of Pathology,Henan Provincial People’s Hospital,People’s Hospital of Zhengzhou University,Zhengzhou 450003,China)
出处 《中国药理学通报》 CAS CSCD 北大核心 2020年第2期245-249,共5页 Chinese Pharmacological Bulletin
基金 河南省重大科技专项(No 161100311400) 河南省医学科技攻关计划联合共建项目(No 2018020400)。
关键词 大豆苷元 A549 H1299 肺癌 增殖 迁移 Daidzein A549 H1299 lung cancer proliferation migration
作者简介 成琼(1980-),女,博士,主治医师,研究方向:肿瘤的分子病理诊断及生物靶向治疗,E-mail:chengqiong2008@126.com;通讯作者:孔令非(1963-),男,主任医师,教授,硕士生导师,研究方向:肿瘤的分子病理诊断及生物靶向治疗,E-mail:lfkong9@163.com。
  • 相关文献

参考文献4

二级参考文献42

  • 1王秀美,周建峰.肺癌患者血清睾酮和雌二醇放射免疫测定的初步报告[J].实用癌症杂志,1994,9(1):29-29. 被引量:9
  • 2Ron D et al. Signal integration in the endoplasmic reticulum unfolded protein response. Nat Rev Mol Cell Biol, 2007, 8: 519-529.
  • 3Kim I et al. Cell death and endoplasmic reticulum stress: disease relevance and therapeutic opportunities. Nat Rev, 2008, 7: 1013-1030.
  • 4Malhotra JD et al. The endoplasmic reticulum and the unfolded protein response. Cell Dev Biol, 2007, 18:716-731.
  • 5Kouroku Yet al. ER stress (PERK/elF2α phosphorylation) mediates the polyglutamine-induced LC3 conversion, an essential step for autophagy formation. Cell Death Differ, 2007, 14:230-239.
  • 6Thuerauf DJ et al. Effects of the isoform-specific characteristics of ATF6a and ATF6b on endoplasmic reticulum stress response gene expression and cell viability. J Biol Chem, 2007, 282: 22865-22878.
  • 7Zhang YC et al. Inhibition of Ca2+ influx is required for mitochondrial reactive oxygen species-induced endoplasmic reticulum Ca2+ depletion and cell death in leukemia cells. Mol Pharm, 2006, 70(4): 1424-1434.
  • 8Ogata M et al, Autophagy is activated for cell survival after endoplasmic reticulum stress. Mol Cell Biol, 2006, 26: 9220- 9231.
  • 9Crighton D et al. DRAM, a p53-induced modulator of autophagy, is critical for apoptosis. Cell, 2006, 126:121-134.
  • 10Tasdemir E et al. Regulation of autophagy by cytoplasmic p53. Nat Cell Biol, 2008, 10(6):676-687.

共引文献23

同被引文献111

引证文献11

二级引证文献62

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