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丁酸钠对结肠癌细胞SW480凋亡及Survivin基因和VEGF表达水平的影响

Effects of Sodium Butyrate on the Expression of Survivin and VEGF,and on the Apoptosis of SW480 Colon Carcinoma Cells
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摘要 目的:观察丁酸钠对结肠癌细胞株SW480的生长抑制、凋亡情况以及对生成素(Survivin)表达水平的影响,探讨其预防结肠癌的作用机制。方法:人传代结肠癌细胞株SW480经不同浓度丁酸钠处理后,在不同时段收集细胞,分别用四唑蓝法检测肿瘤细胞生长增殖率,流式细胞仪检测细胞周期和凋亡变化,免疫细胞化学技术观察对Survivin基因和血管内皮生长因子(VEGF)表达水平。结果:随着培养液中丁酸浓度的不断升高和培养时间的延长,SW480细胞的生长逐渐受到抑制。G1期细胞明显增多,S期细胞明显减少,细胞凋亡率逐渐增高。Sur-vivin基因和VEGF随着丁酸浓度的不断升高而表达下降。结论:丁酸钠能抑制SW480细胞株增生,诱导凋亡,并抑制Survivin基因和VEGF表达。 Objective: To study the effect of sodium butyrate on the growth and apoptosis of SW480 colon carcinoma cells and the expression of survivin gene, and to explore their mechanisms in colon cancer prevention. Methods: The subculture of human colon cancer cell line SW480 was treated with different concentration of butyrate. The cells were collected after different time of cultivation. The cell proliferation rate and apoptosis were measured by MTT and flow cytometer, meanwhile, immunochemistry were used to observe the expression of survivin gene and VEGF (vascular endothelial growth factor) in SW480 cell line after treated by sodium butyrate. Results: By increasing the butyrate concentration and culturing time, the proliferation of SW480 cell was inhibited gradually. The percent of G1 stage cell was increased gradually whereas the percent of S stage cell was decreased. The apoptosis rate of SW480 was increased gradually at the same time. By increasing the butyrate concentration, the expression of survivin and VEGF decreased gradually. Conclusion: Sodium hutyrate can inhibit the expression of survivin and VEGF, and induce the apoptosis of SW480 cell line.
出处 《武汉大学学报(医学版)》 CAS 北大核心 2009年第2期169-172,176,I0004,共6页 Medical Journal of Wuhan University
关键词 丁酸钠 结肠癌细胞 细胞凋亡 SURVIVIN VEGF Sodium Butyrate Colon Cancer Cell Cell Apoptosis Survivin VEGF
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参考文献9

  • 1Bonjer H J, Hop WCJ, Nelson H, et al. Laparoscopically assisted vs open colectomy for colon cancer-A meta-analysis[J]. Arch Surg, 2007,142(3) :298-303.
  • 2Collins R, Cranny G, Bureh J, et al. A systematic review of duplex ultrasound, magnetic resonance angiography and computed tomography angiography for the diagnosis and assessment of symptomatic, lower limb peripheral arterial disease[J].Health Technol Assess, 2007,11(20):iii-iv, xi-xiii, 1-184.
  • 3Kostyniuk CL,Dehm SM,Batten D, et al. Tile ubiquitous and tissue specific promoters of the human SRC- gene are repressed by inhibitors of histon deacetylases[J].Oncogene, 2002, 21(41):6 340-6 347.
  • 4Zaffaroni N,Pennati M,Daidone MG. Survivin as a target for new anticancer interventions [J]. J Cell Mol Med,2005,9(2) :360-372.
  • 5Yang D, Schneider S, Azuma M, et al. Gene expression levels of epidermal growth factor receptor, survivin, and vascular endothelial growth factor as molec ular markers of lymph node involvement in patients with locally advanced rectal cancer clinical colorectal cancer[J]. 2006, 6 (4): 305-312.
  • 6崔路佳,高善玲,裴凤华.丁酸钠抗肿瘤作用的新进展[J].世界华人消化杂志,2005,13(14):1744-1746. 被引量:3
  • 7邵荣江,艾中立,张力,王璐,刘汉燕,王波涌.丁酸钠诱导人肝癌SMMC-7721细胞凋亡作用的评价[J].数理医药学杂志,2004,17(3):213-216. 被引量:5
  • 8Greenberg VL, Williams JM, Boghaert E,et al. Buryrate alters the expression and activity of cell cycle components in and plastic thyroid carcinoma cells[J]. Thyroid, 2001,11(1) :21-29.
  • 9王黎,李琨琨,刘益清,唐芙爱,李振峰,杨荟玉.Survivin,VEGF,b-FGF在大肠肿瘤中的表达及其与肿瘤血管形成的关系[J].临床医学,2004,24(2):5-7. 被引量:1

二级参考文献40

  • 1赵洁,苏琦.组蛋白乙酰化/去乙酰化与白血病的研究进展[J].肿瘤学杂志,2004,10(6):436-439. 被引量:19
  • 2Huang L, Sowa Y, Sakai T, et al. Activation of the p21wAF1/CIPI promoter independent of p53 by the histone deacetylase inhibitor suberoylanilide hydroxamic acid (SAHA) through the Sp-lsites Oncogene,2000,19:5712~5719.
  • 3Kerr JER, winterford CM, Biol ADA, et al. Apoptosis: its significance in cancer and cancer therapy. Cancer, 1994,15:2013.
  • 4Yamamoto H, Fujimoto J. Okamoto E, et al. Suppression of growth of hepatocellular carcinoma sodium butyrate in vitro and invivo. Int J Cancer, 1998,76:897-902.
  • 5Kool M, Van der Linden M, De Haas M, et al. MRP3, an organic anion transporter able to transport anticancer drugs. Proc Natl Acad Sci USA, 1999,96(12):6914-6919.
  • 6Yoshida M, Furumai R, Nishiyama M, et al. Histone deacetylase as a new target for cancer chemotherapy. Cancer Chemother Pharmacol, 2001,48 :S20-S26.
  • 7Livtak DA, et al. Induction of apoptosis in human gastric cancer by sodium butyrate. Anticancer Res, 2000,20(2A):779-784.
  • 8Archer SY, Meng S, Wu J, et al. Butyrate inhibits colon carcinoma cell growth through two distinct path ways. Surgery, 1998,124:248-253.
  • 9Yu X, Guo ZS, Marcu MG, et al. Modulation of p53, ErbBl,ErbB2, and Raf-1 expression in lung cancer cells by depsipeptide FR901228. Journal of the National Cancer Institute, 2002,94: 504-513.
  • 10Hinnebusch BF, Meng S, Wu JT, Archer SY, Hodin RA. The effects of short-chain fatty acids on human colon cancer cell phenotype are associated with histone hyperacetylation. J Nutr2002;132:1012-1017.

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