期刊文献+

Rho激酶抑制剂Y27632对非小细胞肺癌增殖、凋亡及侵袭转移的影响

Effects of Rho kinase inhibitor Y27632 on proliferation,apoptosis and invasion of non-small cell lung cancer
下载PDF
导出
摘要 目的探讨Rho激酶抑制剂Y27632对非小细胞肺癌细胞增殖、凋亡及侵袭转移的影响。方法采用5、10、20、40、80μmol/L Y27632处理非小细胞肺癌细胞A549后,设不加药物的为对照组。分别在24、48、72 h 3个不同刺激时间点应用四甲基偶氮唑盐比色法(MTT法)检测A549细胞的吸光度并计算增殖抑制率和半数抑制浓度(IC_(50)),膜联蛋白-增强型绿色荧光蛋白(Annexin-EGFP)/碘化丙啶(PI)双染流式细胞术检测Y27632处理24、48 h后的细胞凋亡情况,PI单染流式细胞术检测Y27632处理48 h后细胞周期各时相(G_0/G_1、S和G_2/M期)分布情况,Transwell试验检测Y27632处理48 h后的穿膜细胞数。结果 Y27632可抑制A549的增殖(与对照组比较,P<0.05),呈剂量和时间依赖性,且IC50值随作用时间的延长而降低;与对照组比较,Y27632处理后的凋亡率、G_0/G_1期细胞比例均升高,而S、G_2/M期细胞比例均降低,各浓度间的差异均有统计学意义(P<0.05);Transwell实验发现Y27632可抑制A549细胞的侵袭,如0、5、10、20、40、80μmol/L Y27632处理后的穿膜细胞数依次为(78.1±6.0)、(62.3±5.7)、(51.7±5.2)、(42.3±6.9)、(36.4±5.3)和(22.8±4.6)个,差异均有统计学意义(P<0.05)。结论 Y27632可抑制A549细胞的增殖并诱导凋亡及G_0/G_1期阻滞,同时可抑制细胞侵袭,在肺癌治疗上有一定价值。 Objective To investigate the effect of Rho kinase inhibitor Y27632 on cell proliferation, apoptosis and invasion and metastasis of non-small cell lung cancer. Methods The non-small cell lung cancer cells A549 were treated with different concen-trations of Y27632 ( 5, 10, 20, 40, 80μmol/L) and the cells without treatment were set as the control group. The absorbance of A549 cells was detected by MTT method at 24, 48, 72 h after stimulation, and the inhibitory rates of proliferation and half inhibitory concen-trations ( IC50 ) were calculated accordingly. The cell apoptotic rates were measured at 24 and 48 h by Annexin-enhanced green fluores-cent protein (Annexin-EGFP)/iodinated propidium (PI) double staining via flow cytometry. The distribution of cell cycle, including G0/G1 , S and G2/M, were detected by PI single staining with flow cytometry. The number of cells penetrating the membrane was de-tected by Transwell test. Results Y27632 can inhibit the proliferation of A549 ( compared with the control group P〈0?05) in a dose-and time-dependence manner, and the IC50 value decreased with the prolongation of the time. Compared with the control group, the ap-optotic rates and G0/G1 phase cell proportions were increased, and the proportions of S and G2/M cells were decreased, and the differ-ences among different concentrations were statistically significant ( P〈0?05) . Transwell experiments showed that Y27632 could inhibit the invasion of A549 cells. For instance, the number of cells penetrating the membrane were (78?1±6), (62?3±5?7), (51?7±5?2), (42?3±6?9), (36?4±5?3) and (22?8±4?6) for treatment with 0, 5, 10, 20, 40, 80 mol/L Y27632, respectively. Conclusion In addition to the inhibition effect on cell invasion, Y27632 can inhibit the proliferation of A549 cells and induce apoptosis and G0/G1 ar-rest, having a certain value in the treatment of lung cancer.
作者 朱颖 刘渤娜
出处 《临床肿瘤学杂志》 CAS 2016年第3期199-203,共5页 Chinese Clinical Oncology
关键词 RHO激酶 Y27632 非小细胞肺癌 增殖 凋亡 细胞周期 Rho kinase Y27632 Non-small cell lung cancer Proliferation Apoptosis Cell cycle
  • 相关文献

参考文献7

二级参考文献98

  • 1马健,杨罗艳,吴洪涛,谭孝其.膀胱癌组织中Rock-2和MMP-2的表达及相互关系的研究[J].中外健康文摘:医药月刊,2007,4(5):51-53. 被引量:2
  • 2Matsui T,Amano M,Yamamoto T,et al.Rho-associated kinase,a novel serine / threonine kinase,as a putative target for small GTP binding protein Rho[J].EMBO J,1996,15(9):J2208-2216. 被引量:1
  • 3Mueller BK,Mack H,Teusch N.Rho kinase,a promising drug target for neurological disorders[J].Nat Rev Drug Discov,2005,4(5):387-398. 被引量:1
  • 4Zheng R,Iwase A,Shen R,et al.Neuropeptide-stimulated cell migration in prostate cancer cells is mediated by RhoA kinase signaling and inhibited by neutral endopeptidase[J].Oncogene,2006,25(44):5942-5952. 被引量:1
  • 5Kawanishi H,Matsui Y,Ito M,et al.Secreted CXCL1 is a potential mediator and marker of the tumor invasion of bladder cancer[J].Clin Cancer Res,2008,14(9):2579-2587. 被引量:1
  • 6Villalonga P,Ridley AJ.Rho GTPases and cell cycle control[J].Growth Factors,2006,24(3):159-164. 被引量:1
  • 7Loirand G,Guerin P,Pacaud P.Rho kinases in cardiovascu-lar physiology and pathophysiology[J].Circ Res,2006,98 (3):322-334. 被引量:1
  • 8Nakajima M,Hayashi K,Eqi Y,et al.Effect of Wf-536,a novel ROCK inhibitor,against metastasis of B16 melanoma[J].Cancer Chemoth Pharm,2003,52(4):319-324. 被引量:1
  • 9Jemal A,Brcy F,Center MM,et al.Global cancer statistics[J].CA-Cancer J Clin,2011,61(2):69-90. 被引量:1
  • 10Gomez del Pulqar T,Benitah SA,Valeron PF,et al.Rho GTPase expression in tumourigenesis:evidence for a sig-nificant link[J].Bio essays,2005,27(6):602-613. 被引量:1

共引文献12

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