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毒黄素对非小细胞肺癌A549细胞株作用的实验研究

明 浩,宗 赟,谢荃沁,陈陆俊,徐 斌,李 翀,蒋敬庭

  

  1. 213003 江苏常州 苏州大学附属第三医院呼吸内科
  • 收稿日期:2015-10-13 修回日期:2015-11-24 出版日期:2016-02-29 发布日期:2016-02-29
  • 通讯作者: 李 翀

Experimental study of toxoflavin on human non-small cell lung cancer cells A549

MING Hao, ZONG Yun, XIE Quanqin, CHEN Lujun, XU Bin, LI Chong, JIANG Jingting.

  

  1. Department of Respiration,the Third Affiliated Hospital of Soochow University, Changzhou 213003, China
  • Received:2015-10-13 Revised:2015-11-24 Online:2016-02-29 Published:2016-02-29
  • Contact: LI Chong

摘要: 目的 研究毒黄素不同浓度和不同作用时间对非小细胞肺癌A549细胞增殖、凋亡和迁移的影响。方法 分别取0.5、0.375、0.25和0.125 μmol/L毒黄素作用于A549细胞(实验组),以不加毒黄素为对照组,分别培养24 h和48 h。采用CCK-8试剂盒、Annexin V-FITC/PI凋亡试剂盒检测A549细胞增殖抑制率和凋亡率。划痕实验对比0.125 μmol/L毒黄素组和对照组(0 μmol/L毒黄素)在12、24和48 h细胞迁移率。结果 0.5、0.375、0.25和0.125 μmol/L毒黄素组24 h细胞增殖抑制率分别为(93.51±3.69)%、(40.38±3.08)%、(23.54±2.58)%和(13.07±2.37)%,48 h为(90.53±3.58)%、(53.72±3.02)%、(34.44±3.10)%和(24.78±2.43)%。0.5、0.375、0.25和0.125 μmol/L毒黄素组24 h细胞凋亡率分别为(78.68±2.22)%、(43.66±2.53)%、(20.81±2.59)%和(6.25±0.96)%,高于对照组的(1.57±0.52)%;0.5、0.375、0.25和0.125 μmol/L毒黄素组48 h细胞凋亡率分别为(88.66±3.16)%、(59.86±2.81)%、(27.89±3.48)%和(9.91±1.33)%,高于对照组的(1.59±0.55)%。0.125 μmol/L毒黄素组12、24和48 h细胞迁移率分别为7%、11%和16%,低于对照组相应的14%、26%和39%。结论 毒黄素对A549细胞有明显增殖抑制和促凋亡作用,并呈时间和剂量依赖性,且可抑制A549细胞迁移活性。

Abstract:

Objective To investigate the inhibitory effects of toxoflavin on proliferation, apoptosis and migration of non-small cell lung cancer A549 cells. Methods The cultured A549 cells were treated with toxoflavin(0.5, 0.375, 0.25, 0.125 μmol/L) for 24 h and 48 h, the control group was treated with cell culture media only. CCK-8 assay was used to test the growth inhibitory rate and Annexin V/propidium iodide(PI)staining assay was applied to detect the apoptosis rate. The cell migration rate of 12 h, 24 h, 48 h were measured by the wound healing assay. Results The cell growth inhibition rates of A549 cells in experimental groups were (93.51±3.69)%,(40.38±3.08)%,(23.54±2.58)%,(13.07±2.37)% in 24 h and(90.53±3.58)%,(53.72±3.02)%,(34.44±3.10)%,(24.78±2.43)% in 48 h. The cell apoptosis rates of A549 cells in expremental groups were (78.68±2.22)%,(43.66±2.53)%,(20.81±2.59)%,(6.25±0.96)% in 24 h and(88.66±3.16)%, (59.86±2.81)%,(27.89±3.48)%,(9.91±1.33)% in 48 h, and those of control group were(1.57±0.52)% in 24 h and(1.59±0.55)% in 48 h respectively. The A549 cell migration rate of 12 h,24 h,48 h in experimental group(0.125 μmol/L) was 7%,11% and 16%,but it was 14%,26% and 39% in control group. Conclusion Toxoflavin could significantly inhibit proliferation and promote apoptosis of A549 cells in a dose and time dependent manner, and it could also weaken the migration capacity of A549 cells.

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