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沙利度胺对人结肠癌细胞增殖及迁移的影响 被引量:3

Effects and mechanisms of thalidomide on human colorectal cancer cell
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摘要 目的:观察沙利度胺对人结肠癌细胞HCT116增殖和迁移的影响,并初步探讨其影响机制。方法:分别用不同浓度沙利度胺处理人结肠癌细胞HCT116,采用MTT法检测沙利度胺对人结肠癌细胞增殖的影响,平板克隆试验法检测沙利度胺对单个细胞克隆增殖的作用,流式细胞术检测细胞周期分布,Transwell细胞培养小室检测沙利度胺对细胞迁移的影响,蛋白免疫印迹检测沙利度胺对细胞P53、CXCR4蛋白的作用。结果:MTT检测显示不同浓度沙利度胺对HCT116细胞增殖无影响,平板克隆试验表明其对细胞克隆生长具有抑制作用,流式细胞检测显示100 mg/L沙利度胺处理组G2/M期细胞比例明显高于对照组(P<0.05),沙利度胺组HCT116细胞迁移数明显少于对照组,P53蛋白、CXCR4蛋白表达与对照组比较无明显变化。结论:沙利度胺抑制结肠癌细胞克隆增殖的作用,可能与其影响细胞周期有关;抑制结肠癌细胞迁移的作用,与CXCR4蛋白表达无关。 Objective:To investigate the effects and mechanisms of thalidomide on human colorectal cancer cell HCT116.Methods:HCT116 cells were treated with different concentration of thalidomide.The influence on proliferation was measured by MTT assay.The effect on single colorectal cell colon was detected with plate colony formation assay.Flow cytometry(FCM) was conducted to determine the effect on cell cycle of HCT116 cells.The changes of migration capability were evaluated using transwell assay.The levels of P53 and CXCR4 proteins were detected by western blotting.Results:The result of MTT assay showed thalidomide had no effect on colon cancer cells.Thalidomide inhibited the plate colony formation of HCT116 cells.FCM showed that cells treated with thalidomide were arrested in G2/M phase.The migration capability was decreased significantly,which was independent of CXCR4 protein expression. Conclusion:The inhibition effect of thalidomide on the colony formation of colorectal cancer cell line is likely to be associated with cell cycle arrest.The migration inhibition effect of thalidomide is independent of CXCR4 protein expression.
出处 《新医学》 2011年第6期374-376,385,F0003,共5页 Journal of New Medicine
关键词 沙利度胺 结肠癌 克隆形成 细胞周期 迁移 Thalidomide Colorectal cancer Colony formation Cell cycle migration
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  • 1LIU W M, HENRY JY, MEYER B, et al. Inhibition of metastatic potential in colorectal carcinoma in vivo and in vitro using immunomodulatory drugs (IMiDs) [ J ]. Br J Cancer, 2009,101 (5): 803-812. 被引量:1

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  • 1李臣,陈明清,董坚.表观遗传学与结直肠癌的关系研究进展[J].实用癌症杂志,2010,25(5):546-548. 被引量:4
  • 2王烜 ,欧阳钦 .沙利度胺对炎症性肠病疗效的实验研究[J].四川大学学报(医学版),2005,36(4):548-551. 被引量:6
  • 3杨义明,杜钢军,林海红.沙利度胺治疗肝癌的实验研究(英文)[J].第一军医大学学报,2005,25(8):925-928. 被引量:2
  • 4Sehmidt M,Kim Y,Gast SM.Inereased in vivo efficacy of lenalidomide and thalidomide by addition of ethaerynieaeid[J].In vivo,2011,25 (3):325-333. 被引量:1
  • 5Katoh M, Katoh M. Human FOX gene family(Review). Int J Oncol, 2004, 25 : 1495-1500. 被引量:1
  • 6Katoh M, Igarashi M, Fukuda H, et al. Cancer genetics and genomics of human FOX family genes. Cancer Lett, 2013, 328: 198-206. 被引量:1
  • 7Lo PK, Lee JS, Chen H, et al. Cytoplasmic misloeal- ization of overexpressed FOXF1 is associated with the malignancy and metastasis of colorectal adenocarcino- mas. Exp Mol Pathol, 2013, 94: 262-269. 被引量:1
  • 8Watson JE, Doggett NA, Albertson DG, et al. Integra- tion of high-resolution array comparative genomic hybrid- ization analysis of chromosome 16q with expression array data refines common regions of loss at 16q23-qter and i- dentifies underlying candidate tumor suppressor genes in prostate cancer. Oncogene, 2004, 23: 3487-3494. 被引量:1
  • 9Lo PK, Lee JS, Liang X, et al. Epigenetic inactivation of the potential tumor suppressor gene FOXF1 in breast cancer. Cancer Res. 2010. 70: 6047-6058. 被引量:1
  • 10Waters MF, Laing AB, Ambikapathy A, et al. Treatment of ulcerative colitis with thalidomide [J]. Br Med J, 1979, 1(6166) :792. 被引量:1

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