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γ-生育三烯酚抑制人胃腺癌SGC-7901细胞侵袭和迁移及其机制探讨 被引量:3

Inhibitory effects of γ-tocotrienol on invasion and migration of human gastric cancer SGC-7901 cells and its mechanism
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摘要 目的:探讨γ-生育三烯酚(γ-tocotrienol,γ-T3)对人胃腺癌SGC-7901细胞侵袭和迁移的抑制作用及其可能的分子机制。方法:用不同浓度(0、15、30、45、60和100μmol/L)的γ-T3作用SGC-7901细胞后,采用CCK-8法、细胞划痕愈合实验和Transwell侵袭实验分别检测细胞增殖、迁移和侵袭能力的变化,然后采用蛋白质印迹法检测细胞中环氧合酶2(cyclooxygenase-2,COX-2)和核因子κB(nuclear factor-kappa B,NF-κB)信号通路蛋白的表达。结果:15~100μmol/Lγ-T3作用SGC-7901细胞24、48和72 h后,细胞增殖能力受到明显抑制,且呈时间和剂量依赖性(P值均<0.01)。15~60μmol/Lγ-T3单独作用或与10 ng/mL肿瘤坏死因子α(tumor necrosis factor-alpha,TNF-α)联合作用SGC-7901细胞24 h后,细胞迁移和侵袭能力均被明显抑制(P值均<0.01)。15~60μmol/Lγ-T3作用SGC-7901细胞24 h后,NF-κB、NF-κB p65和COX-2蛋白的表达水平均随着作用浓度的增加呈明显降低趋势(P值均<0.01)。结论:γ-T3可抑制人胃腺癌SGC-7901细胞的侵袭和转移,其作用机制可能与阻滞NF-κB信号通路和下调COX-2蛋白表达有关。 Objective: To investigate the effects of ~,-tocotrienol (~,-T3) on the invasion and migration of human gastric cancer SGC-7901 cells as well as its possible molecular mechanism.Methods: The different concentrations (0, 15, 30, 45, 60, and 100μmol/L) of γ-T3 were used to treat SGC-7901 cells. Then the proliferation, migration and invasion of SGC-7901 cells were detected by CCK-8 assay, cell scratch wound healing assay and Transwell invasion assay, respectively. Furthermore, the expressions of cyclooxygenase-2 (COX-2) and nuclear factor-kappa B (NF-κB) signal pathway proteins were detected by Western blotting. Results: After treatment with different concentrations (1 5-100μmol/L ) of γ-T3 for 24, 48 and 72 h, the proliferation of SGC-7901cells was evidently inhibited in a time- and dose-dependent manner (all P 〈 0.01). After treatment with γ-T3 (1 5-60 μmol/L) alone or combined with tumor necrosis factor-alpha (TNF-α) (10 ng/mL) for 24 h, the migration and invasion abilities of SGC-7901 cells were significantly inhibited (all P 〈 0.01). The expressions of NF-κB, NF-κB p65 and COX-2 proteins were significantly down-regulated in SGC-7901 cells after γ-T3 (1 5-60μmol/L) treatment for 24 h (all P 〈 0.01). Conclusion: γ-T3 can inhibit the invasion and migration of human gastric cancer SGC-7901 cells. Its mechanism may be associated with blocking NF-κB signal pathway and reducing the expression of COX-2 protein.
出处 《肿瘤》 CAS CSCD 北大核心 2017年第5期441-447,共7页 Tumor
基金 国家自然科学基金面上项目(编号:81273061)~~
关键词 胃肿瘤 生育三烯酚类 肿瘤浸润 细胞迁移分析 NF-ΚB Stomach neoplasms Tocotrienols Neoplasm invasiveness Cell migrationassays NF-kappa B
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  • 1黄伟,张瑶珍,李登举,周剑锋.HL-60及其耐药细胞之间线粒体膜及线粒体中Bid差异研究[J].肿瘤,2005,25(2):122-124. 被引量:2
  • 2孙文广,陈炳卿,王琪,徐伟丽,刘慧坤.γ-生育三烯酚抑制人胃癌SGC-7901细胞增殖及促凋亡作用[J].毒理学杂志,2007,21(1):1-4. 被引量:2
  • 3WARGOVICH M J, WOODS C, HOLLIS D M,et al. Herbals,cancer prevention and health[ J]. J Nutr,2001 , 131 ( 11 ) : 3034- 3036.
  • 4IKEDA S, TOHYAMA T, YOSHIMURA H, et al. Dietary alphatocopherol decreases alpha-tocotrienol but not gamma-tocotrienol concentration in rats[J]. J Nutr, 2003, 133(2) : 428-434.
  • 5MCINTYRE B S, BRISKI K P, GAPOR A, et al. Antiproliferarive and apoptotic effects of tocopherols and tocotrienols on preneo- plastic and neoplastic mouse mammary epithelial cells [ J ]. Proc Soc Exp Biol Med, 2000, 224(4) : 292-301.
  • 6XIE S Q, WANG J H, MA H X, et al. Polyamine transporter recognization and antitumor effects of anthracenymethyl homospermidine [ J ]. Toxicology, 2009, 263 (2/3) : 127-133.
  • 7O' BRIEN P J, IRWIN W, DIAZ D, et al. High concordance of drug-induced human hepatotoxicity with in vitro cytotoxicity measured in a novel cell-based model using high content screening [J]. Arch Toxicol, 2006, 80(9) : 580-604.
  • 8HOLST C M, STAAF J, JONSSON G, et al. Molecular mecha- nisms underlying N1, N11-diethylnorspermine-induced apoptosis in a human breast cancer cell line [ J ]. Anticancer Drugs, 2008, 19(9) : 871-883.
  • 9HIDALGO A, BRANDOLINI A, RATTI S. Influence of genetic and environmental factors on selected nutritional traits of Triticum monococcum[J]. J Agric Food Chem, 2009, 57 (14) : 6342- 6348.
  • 10DEWSON G, KLUCK R M. Mechanisms by which Bak and Bax permeabilise mitochondria during apoptosis[ J]. J Cell Sci, 2009, 122(16) : 2801-2808.

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