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吲哚-3-甲醇对人喉癌Hep-2细胞增殖的抑制作用研究 被引量:1

Study on the mechanism of Hep-2 cells proliferation inhibition induced by indoel-3-carbinol
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摘要 目的研究吲哚-3-甲醇对人喉癌上皮细胞(Hep-2)增殖及凋亡的影响。方法实验分为5组,4个浓度实验组(吲哚-3-甲醇,0,50,100,150μmol·L-1)与对照组(二甲基亚砜)。用水溶性四氮唑法检测吲哚-3-甲醇对Hep-2细胞增殖的影响,用Hochest33258染色及流式细胞仪检测吲哚-3-甲醇诱导的Hep-2细胞的凋亡,用蛋白免疫印迹方法检测凋亡相关信号分子livin蛋白表达情况。结果经4个浓度实验组及对照组处理48 h后,Hep-2细胞的凋亡率分别为(3.95±0.68)%,(8.54±1.35)%,(21.28±2.32)%,(38.65±4.85)%和(4.26±0.58)%。表明吲哚-3-甲醇以浓度依赖方式抑制Hep-2增殖,诱导细胞凋亡和Livin蛋白表达。结论吲哚-3-甲醇可抑制Hep-2细胞增殖,其诱导细胞凋亡可能与Livin蛋白表达的抑制相关。 Objective To study the effect of indoel -3 -carbinol on Hep-2 cells in vitro.Methods There was divided into 5 groups, the 4 test groups (the concerntration of indoel-3-carbinol, 0, 50, 100, 150μmol· L-1) and the control group(dimethyl sulfoxide).The inhibition of cell proliferation was assayed by method of WST-1.And the apopto-sis was shown with Hochest33258 staining and flow cytometry.The mechanism of apoptosis, and the expressions of the livin protein were detected by Western blotting assay.Results After being disposed by the test groups with 4 different concerntration of indoel-3-carbinol and the control group, the apoptosis rate of Hep-2 cells were(3.95 ±0.68)%, ( 8.54 ±1.35 )%, ( 21.28 ±2.32 )%, ( 38.65 ±4.85 )%, and (4.26 ±0.58)%, respectively.The indoel -3 -carbinol could inhibit the proliferation of Hep-2 cells with the dose-dependent manner and the apoptosis could be induced too.Furthermore, the expressions of Livin appeared to be decreased significantly as compared with the control group.Conclusion The indoel-3-carbinol could induce apoptosis of Hep-2 cells in the manner of dose-dependent, and Livin might play a role during above processes.
出处 《中国临床药理学杂志》 CAS CSCD 北大核心 2015年第11期932-934,959,共4页 The Chinese Journal of Clinical Pharmacology
基金 浙江省自然科学基金资助项目(Y15H130014) 温州市科技局科学基金资助项目(Y20140375)
关键词 吲哚-3-甲醇 人喉癌上皮细胞 细胞增殖 细胞凋亡 indole -3 -carbinol Hep -2 cell cell proliferation cell apoptosis
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参考文献8

  • 1Safe S. Cancer chemotherapy with indole -3 - carbinol, bis( 3 - indolyl) methane and synthetic analogs [ J ] . Cancer Left, 2010, 269 : 326 - 338.
  • 2Aggarwal BB, Ichikawa H. Molecular targets and anticance potential of indole - 3 -carbinol and its derivatives [J] . Cell Cycle, 2008, 4 : 1201 - 1215.
  • 3Brew CT, Mcgrath DR, Spigelman AD. Indole -3 -carbinol acti- vates the ATM signaling pathway independent of DNA damage to sta- bilize p53 and induce G1 arrest of human mammary epithelial cells [ J]. lnt J Cancer, 2006,118:857 - 868.
  • 4Rahman KM, Sarkar ARH. Indole - 3 - carbinol ( 13C ) induces apoptosis in tumorigenic but not in nontumorigenic breast epithelial ceils[ J ]. Nutr Cancer,2003,45 : 101 - 112.
  • 5朱伟,李文学,魏青,杨光宇,刘华章,杨杏芬.吲哚-3-甲醇通过抑制Survivin表达诱导人鼻咽癌细胞的凋亡[J].毒理学杂志,2009,23(5):356-359. 被引量:2
  • 6戈畅,樊赛军.吲哚-3-甲醇(I3C)抗肿瘤作用的研究进展[J].中国肺癌杂志,2009,12(9):1044-1046. 被引量:2
  • 7刘学军,陈波蓓,凡启军,倪丽艳,高金建,黄赛瑜,黄加云.凋亡抑制基因Livin在喉癌组织中的表达及其与p53、Bcl-2表达的相关性研究[J].中国耳鼻咽喉头颈外科,2014,21(10):511-514. 被引量:6
  • 8Rahman KM, Aranha O, Sarkar RH. Indole- 3 -carbinol (13C) induces apoptosis in tumorigenic but not in nontumorigenic breast epi- thelial cells[ J]. Nutr Cancer,2003, 45 : 101 - 112.

二级参考文献26

  • 1魏玺(综述),黄焰(审校).乳腺癌分子靶向药物治疗[J].中外健康文摘:医药月刊,2006,3(11):82-84. 被引量:2
  • 2Safe S. Cancer chemotherapy with indole-3-carbinol, bis(3'- indolyl)methane and synthetic analogs[J]. Cancer Lett,2008, 269:326-338.
  • 3Kim YS, Milner JA. Targets for indole232carbinol in cancer prevention[J]. J Nutr Biochem, 2005, 16:652-731.
  • 4Aggarwal BB, Ichikawa H. Molecular Targets and Anticancer Potential of Indole-3-Carbinol and Its Derivatives [ J ]. Cell Cycle,2005,4 : 1201-1215.
  • 5Xu M, Bailey AC, Hernaez JF, et al. Protection by green tea, black tea, and indole-3-carbinol against 2-amino-3- methylimidazo[4, 5-f ] quinoline-induced DNA adducts and colonic aberrant crypts in the FM4 rat [ J ]. Carcinogenesis, 1996,17 : 1429-1434.
  • 6Hanh HG, Gloria AB, David HHN, et al. Indole-3-Carbinol (I3C) Inhibits Cyelin-dependent Kinase-2 Function in Human Breast Cancer Cells by Regulating the Size Distribution, Associated Cyelin E Forms, and Subcellular Localization of the CDK2 Protein Complex [ J ]. Biolo Chem, 2005, 280 : 8756- 8764.
  • 7Takahashi N, Dashwood RH, Bjeldaness LF, et al. Mechanisms of indole-3-carbinal ( I3C ) anticarcinogenesis: Inhibition of aflatoxin B1 DNA adduction and mutagenesis by I3C acid condensation products[ J]. Food Chem Toxic, 1995, 33 : 851-857.
  • 8Arif JM, Gairola CG, Kelloff GJ, et al. Inhibition of cigarette smoke related DNA adduets in rat tissues by indole-3-carbinol [J]. Murat Res,2000,452:11-18.
  • 9Jones AM. Programmed cell death in development and defense [J]. Plant Physiol, 2001,125:94-97.
  • 10Tamm I, Wang Y, SausviUe E, et al. IAP2family protein survivin inhibits caspase activity and apoptosis induced by Fas, Bax, Caspase and anticancer drugs [ J ] . Cancer Res, 1998, 58: 5315.

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