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索拉菲尼对人肝癌细胞株HepG2抑制作用的研究 被引量:2

DEPRESSANT EFFECTS OF SORAFENIB ON HUMAN LIVER CANCER CELL LINE HEPG2
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摘要 目的:探讨分子靶向药物索拉菲尼(Sorafenib)在体外对人肝癌细胞株HepG2的抑制作用。方法:采用MTT法检测Sorafenib对HepG2细胞的增殖抑制率,流式细胞仪分析细胞周期和凋亡率。结果:Sorafenib能明显抑制HepG2细胞增殖,呈时间-剂量依赖效应;6μmol/L的Sorafenib处理HepG2细胞72小时,HepG2细胞周期中的S期比例明显升高,G0-G1期、G2-M期比例明显下降,凋亡率明显上升(P<0.05,P<0.01)。结论:Sorafenib对体外人肝癌HepG2细胞具有明显的抑制作用,主要表现为抑制其增殖和促进其凋亡。 Objective:To investigate the depressant effects of Sorafenib on human liver cancer cell line HepG2 cells in vitro.Methods:MTT method was used to detect the antiproliferative ratio of Sorafenib on HepG2 cells, flow cytometry to analyze the cell cycle and apoptotic ratio.Results:Sorafenib could obviously inhibit proliferation of HepG2 cells and appeared time-dose-dependent effects.72 hours after the HepG2 cells were treated with Sorafenib in 6 μmol/L, the percentage of HepG2 ceils in S period increased, G0-G1 period and G2-M period HepG2 cells decreased, aopototic ratio of HepG2 cells increased significantly (P〈0.05, P〈0.01). Conclusions:Sorafenib can inhibit proliferation and promote apoptosis of human liver cancer cell line HepG2 cells in vitro.
出处 《承德医学院学报》 2009年第3期241-243,共3页 Journal of Chengde Medical University
关键词 索拉菲尼 人肝癌细胞株HEPG2 MTT法 流式细胞术 Sorafenib Human liver cancer cell line HepG2 MTT method Flow cytometry
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  • 1Wilhelm SM,Carter C,Tang L,et aI.BAY 43-9006 exhibits broad spectrum oral antitumor activity and targets the RAF/MEK/ERK pathway and receptor tyrosine kinases involved in tumor progression and angiogenesis [J].CancerRes,2004,64(19):7099-7109.
  • 2Tannapfel A,Sommerer EBenicke M,et al. Mutations of the BRAF gene in cholangiocarcinoma but not in hepa- tocellular carcinoma[J] .Gut,2003,52(5):706-712.
  • 3Hwang YH,Cho JY,KIM S,et al.Over-expression of c-raf- 1 proto-oncogene in liver cirrhosis and hepatocellular carcinoma[J].Hepatol Res,2004,29(2): 113-121.
  • 4Liu L,Cao Y,Chen C,et al.Sorafenib blocks the RAF/MEK/ ERK pathway,inhibits tumor angiogenesis, and induces tumor cell apoptosis in hepatocellular carcinoma model PLC/PRF/5 [J].Cancer Res,2036,66(24): 11851-11858.
  • 5伍婧,罗荣城,张华,崔彦芝.索拉菲尼联合三氧化二砷对肝癌细胞株的抑制作用[J].南方医科大学学报,2008,28(4):639-641. 被引量:18

二级参考文献12

  • 1陈建国,宋新明.中国肝癌发病水平的估算及分析[J].中国肿瘤,2005,14(1):28-31. 被引量:93
  • 2黄正京,周脉耕,王黎君.中国肝癌死亡率和乙肝病毒表面抗原携带率的地理分布研究[J].疾病监测,2007,22(4):242-245. 被引量:42
  • 3Scott MW, Christopher C, Li YT, et al. BAY43-9006 exhibits broad spectrum oral antitumor activity and targets the RAF/MEK/ERK pathway and receptor tyrosine kinases involved in tumor progression and angiogenesis [ J ]. Cancer Res, 2004, 64:7099-109.
  • 4Pelicano H, FengL, Zhou Y, et al. Inhibition of mitochondrial respiration: A novel strategy to enhance drug-induced apoptosis in human leukemia cells by a reactive oxygen species-mediated mechanism[J]. J Biol Chem, 2003, 278 (39): 37832 -9.
  • 5Beeram M, Patna IK, Row IE. Regulation of c-Raf-l: therapeutic implications [J]. Clin Adv Hematol Oncol, 2003, 1(8): 476-81.
  • 6Wiesenauer CA, Yip-Schneider MT, Wang Y, et al. Multiple anticancer effects of blocking MEK-ERK signaling in hepatocellular careinoma[J ]. J Am Coil Surg, 2004,198: 410-21.
  • 7Huynh H, Nguyen TT, Chow KH, et al. Over-expression of the mitogen-activated protein kinase (MAPK) kinasc(MEK)-MAPK in hepatocellular carcinoma: its role in tumor progression and apoptosis[J]. BMC Gastroenterol, 2003, 3: 19.
  • 8Tannapfel A, Sommerer F, Benicke M, et al. Mutations of the BRAF gene in cholangiocarcinoma but not in hepatocellular carcinoma [J]. Gut, 2003, 52: 706-12.
  • 9Hwang YH, choi JY, kim S, et al. Over-expression ofc-raf-1 protooncogene in liver cirrhosis and hepatocellular carcinoma [J]. Hepatol Res, 2004, 29:113-21.
  • 10Abou-Alfa GK, Schwartz L, Ricci S, et al. Phase Ⅱ study of sorafenib in patients with advanced hepatocellular carcinoma [J]. J Clin Oncol, 2006, 24(26): 4293-300.

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  • 1武卫红,温学森,赵宇.地黄寡糖及其药理活性研究进展[J].中药材,2006,29(5):507-510. 被引量:34
  • 2郭丽民,张汝学,贾正平,李茂星,王娟,尹强.地黄寡糖对HepG2胞细增殖及胰岛素抵抗的作用[J].中国中药杂志,2007,32(13):1328-1332. 被引量:28
  • 3Takai N, UedaT, Nishida M, et al. Histone deacetylase inhibitors induce growth inhibition, cell cycle arrest and apoptosis in human choriocarcinoma cells [J]. Int J Mol Med, 2008,21(1):109.
  • 4Cory S, Huang DC, Adams JM. The Bcl-2 family: roles in cell survival and oncogenesis [J]. Oncogene, 2003,22(53):85-90.
  • 5Bakri IM, Douglas CW. Inhibitory effect of garlic extract on oral bacteria [J]. Arch Oral Biol,2005,50(7):645-651.
  • 6Milner JA. Preclinieal perspectives on s Ⅱ lic and cancer [J]. Nutr, 2006,136(3) :827S-831S.
  • 7Tomada M, Kato S, Onuma M, et al. Water- soluble constitu- ents of Rehmanniae Radix. I. Cabohydrates and acids of Rehman- nia glutinosa f. hueichingensis[ J ]. Chem. Pharm. Bull, 1997, 19(7) : 1455 -1460.
  • 8M Lukan H and Swaan P W. Camptothecins: a review of their chemotherapentic potential [J]. Drugs, 2002, 6 ( 2 ) : 2039 - 2057.
  • 9郭楠,李稳宏,赵鹏,高蓉,朱骤海,何俊婷.不同炮制地黄中水苏糖含量研究[J].中成药,2008,30(12):1812-1814. 被引量:18
  • 10阮圣仁,张秀娟,安鹏,季宇彬.白藜芦醇对SGC-7901肿瘤细胞增殖的影响[J].中国药理学通报,2008,24(12):1656-1659. 被引量:10

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