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引用本文:孟娜娜,张瑞瑞,刘超,孙金月.新型化合物F-2对人肺癌NCI-H520细胞增殖、迁移及凋亡的影响[J].中国现代应用药学,2020,37(18):2223-2228.
MENG Nana,ZHANG Ruirui,LIU Chao,SUN Jinyue.Effects of a Novel Compound F-2 on Proliferation, Migration and Apoptosis of Human Lung Cancer NCI-H520 Cells[J].Chin J Mod Appl Pharm(中国现代应用药学),2020,37(18):2223-2228.
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新型化合物F-2对人肺癌NCI-H520细胞增殖、迁移及凋亡的影响
孟娜娜1,2, 张瑞瑞2, 刘超2, 孙金月1,2
1.山东师范大学生命科学学院, 济南 250014;2.山东省农业科学院农产品研究所, 济南 250100
摘要:
目的 探讨新型化合物F-2对人非小细胞肺癌NCI-H520细胞增殖、迁移及凋亡的影响。方法 CCK-8试验检测肺癌细胞增殖情况;采用划痕试验检测化合物对NCI-H520细胞迁移的情况;倒置显微镜观察化合物刺激对细胞形态的影响;流式细胞术检测化合物对细胞凋亡的影响;Western blotting检测化合物对细胞迁移及凋亡相关蛋白表达的影响。结果 化合物对NCI-H520细胞增殖有明显的抑制作用,且与浓度和时间呈依赖性关系。划痕试验结果表明化合物能够明显抑制肿瘤细胞迁移,并且Western blotting试验结果表明化合物处理NCI-H520细胞后可上调E-cadherin的表达,下调N-cadherin蛋白的表达。Annexin-V/PI双染法结果显示,化合物可诱导NCI-H520细胞发生凋亡,且随着药物浓度增加凋亡率上升,并且增加了BAX/Bcl-2蛋白表达比率。结论 化合物能够明显抑制肺癌细胞的增殖、迁移及诱导细胞凋亡,可能是通过阻断肿瘤细胞上皮间充质转化过程,调节细胞凋亡过程中相关基因表达从而发挥抗肿瘤作用。
关键词:  细胞迁移  细胞增殖  细胞凋亡  上皮间充质转化
DOI:10.13748/j.cnki.issn1007-7693.2020.18.009
分类号:R965.2
基金项目:山东省自然科学基金重大基础研究项目(ZR2018ZC0944)
Effects of a Novel Compound F-2 on Proliferation, Migration and Apoptosis of Human Lung Cancer NCI-H520 Cells
MENG Nana1,2, ZHANG Ruirui2, LIU Chao2, SUN Jinyue1,2
1.College of Life Sciences, Shandong Normal University, Jinan 250014, China;2.Institute of Agro-Food Science and Technology, Shandong Academy of Agricultural Sciences, Jinan 250100, China
Abstract:
OBJECTIVE To explore the effects of novel compound F-2 on proliferation, migration and apoptosis of human non-small cell lung cancer NCI-H520 cells. METHODS The proliferation of lung cancer cells was detected by CCK-8 test. The migration of NCI-H520 cells was detected by wound scratch test. The effect of compound stimulation on cell morphology was observed by inverted microscope. The effect of compounds on apoptosis was detected by flow cytometry. The effects of compounds on cell migration and apoptosis-related protein expression were detected by Western blotting. RESULTS The compounds significantly inhibited the proliferation of NCI-H520 cells and was dependent on concentration and time. The Wound scratch test showed that the compound could significantly inhibit the migration of tumor cells. Western blotting results showed that the compound could up-regulate the expression of E-cadherin and down-regulate the expression of N-cadherin in NCI-H520 cells. Annexin-V/PI double staining showed that the compound could induce apoptosis of NCI-H520 cells, and the apoptotic rate increased with the increase of drug concentration, and the expression ratio of BAX/Bcl-2 protein increased. CONCLUSION Compounds can significantly inhibit the proliferation, migration and induce apoptosis of lung cancer cells, which may be through blocking the epithelial-mesenchymal transition process of tumor cells and regulating the expression of related genes during apoptosis.
Key words:  cell migration  cell proliferation  cell apoptosis  epithelial-mesenchymal transition
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