期刊文献+

全反式维甲酸对人喉癌细胞株Hep-2体外增殖及Survivin表达的影响 被引量:1

Effects of all-trans retinoic acid on growth of Hep-2 laryngeal carcinoma cells and expression of Survivin
下载PDF
导出
摘要 目的进一步探讨全反式维甲酸(ATRA)对人喉癌的治疗机制。方法取对数生长期人喉癌细胞株Hep-2,以1×105/ml细胞密度接种于96孔培养板,置于CO2培养箱中24h后随机分为观察组和对照组,观察组分别加入终浓度为10-7、10-6、10-5mol/L的ATRA,对照组为空白对照。观察两组细胞增殖抑制率(IR)、细胞凋亡率、Survivin表达水平。结果观察组Hep-2细胞IR及细胞凋亡率均显著高于对照组,Survivin表达显著低于对照组,且呈时间和剂量依赖性。结论ATRA对人喉癌细胞株Hep-2生长有抑制作用,同时可诱导其凋亡,机制可能与Survivin基因表达下调有关。 Objective To investigate the treatment mechanism of all-trans retinoic acid(ATRA) on laryngeal carcinoma. Methods Hep-2 laryngeal carcinoma ceils in logarithmic phase were inoculated into 96 weil-Gibco,and divided into the observed group and the control group, the former was treated by ATRA with the concentration of 10^-7. 10^-6, 10^-5 mmol/L. The inhibition rates (IR) of proliferation were detechted by MTT assay. The apoptosis was analyzed by Hoechst 33258 fluorescence staining. The expression of Survivin was detected through immunoeytochemistry method. Results The IR and apoptosis rates of Hep-2 ceils in observed group were higher than those in the control group , while the expression of Survivin was lower ,all in a close and time dependent manner. Conclusion ATRA can inhibit the growth of Hep-2 laryngeal carcinoma ceils and induce its apoptosis, down-regulation of Survivin gene probably contributes to it.
出处 《山东医药》 CAS 北大核心 2009年第11期30-32,共3页 Shandong Medical Journal
关键词 全反式维甲酸 喉癌细胞 细胞凋亡 生长素 all-trans retinoic acid laryngeal carcinoma cell apoptosis Survivin
  • 相关文献

参考文献7

  • 1Barna G,Sebestyen A,Weischede S,et al. Different ways to induce apoptosis by fenretinide and all-trans retinoic acid in human B lmpluanacells[J]. Anticancer Res,2005,25 (6B) :4179-4185.
  • 2阴梅云,郑力芬,阎蕴力.阿克拉霉素与顺铂联合应用对卵巢癌细胞的抑制作用[J].中华妇产科杂志,2003,38(4):247-248. 被引量:3
  • 3E1 -Metwally TH, Hussein MR, Pour PM ,et al. High concentrations of refinoids induce differentiation and late apoptosis in pancreatic cancer cells it, vitro[J]. Cancer Biol Ther,2005,4(5) :602-611.
  • 4Huss WJ, Lai L, Barrios RJ, et al. Retnoic acid slows progression and promotes apoptosis of spontaneous proslate cancer[J].Prostate, 2004,61 (2) :142-152.
  • 5邱元正,肖健云,田勇泉,赵素萍,曹利,李桂源.维甲酸诱导后CK13基因在鼻咽癌中的表达研究[J].中国耳鼻咽喉颅底外科杂志,2003,9(5):290-292. 被引量:4
  • 6Jinfeng M, Kimura W, Sakurai F, et al. Histopathological study of in-traducal papillary mucinous tumor of the pancreas : special reference to the roles of Survivin and p53 in tumorienesis of IPMT[J]. Int J Gastrointest Cancer,2002,32 (2-3) :73-81.
  • 7Fuessel S, Kueppers B, Ning S, et al. Systematic in vitro evaluation of Survivin directed antisense oligodeoxynucleotides in bladder cancer cells[J]. J Urol,2004,171 (6 Pt 1 ) :2471-2476.

二级参考文献9

  • 1金正均.合并用药中的相加[J].中国药理学报,1980,1:70-73.
  • 2Lain PK, To EW, Chan ES, et al. In vitro inhibition of head and neck c2mcer-cell growth by human recombinant interferon-alpha and 13-cis retinoic acid[J]. Br J Biomed Sci, 2001, 58(4) : 226-9.
  • 3Rugg E, Magee G, Wilson N, et al. Identification of two novel mutations in karation 13 as the cause of white sponge naevtts[J].Oral Dis, 1999, 5(4) : 321 - 324.
  • 4Mofifuji M, Taniguehi S, Sakai H, et al. Differetial expression of cytokeratin after orthotopic implantation of newly established human tongue cancer cell lines of definded metastatic ability[J]. Am J Pathol, 2000, 156(4) : 1317- 1326.
  • 5Theodore TP, Alphonse K. Role of eytoskeleton in genome regulation and cancer[J]. Inter Rev Cytol, 1992, 132(1) : 75 - 107.
  • 6Romano V, Raimondi E, Bosco P, et al. Chromosomal mapping of human cytokatin 13 gene[J]. Genomics, 1992, 14(2): 495-497.
  • 7Wasoma A, Alam Y, Dogma B, et al. Isolation sequence and expression of the gene encoding human karatin 13[J]. Gene, 1998,215(2) : 269 -279.
  • 8Kim SY, Berger D, Yim SO, et al. Coordinate control of growth and cytokeratin 13 expression by retinoic acid[J]. Mol-Carcinog,1996, 16(1): 6-11.
  • 9邱元正,田勇泉,肖健云,陶正德,赵素萍,李桂源.细胞角蛋白基因13在鼻咽癌中的表达研究[J].中华肿瘤杂志,2000,22(2):129-131. 被引量:16

共引文献5

同被引文献8

  • 1周亭芳,庄英帜,曹建国.罗格列酮增强顺铂抑制人肺腺癌细胞增殖作用[J].中国药理学通报,2005,21(1):88-91. 被引量:13
  • 2Roman J.Peroxisome proliferator-activated receptor gamma and lung cancer biology:implications for therapy.Investig Med,2008,56(2):528-533.
  • 3Laurora S,Pizzimenti S,Briatore F,Fraioli A,et al.Peroxisome proliferator-activated receptor ligands affect growth-related gene expression in human leukemic cells.Pharmacol Exp Ther,2003,305 (2):932-942.
  • 4Krishnan A,Nair SA,Pillai MR.Biology of PPAR gamma in cancer:a critical review on existing lacunae.Curr Mol Med,2007,7(6):532-540.
  • 5Sato M,Yajima Y,Kawashima S,et al.Synergistic potentiation of thiazolidinedione-induced ST 13 preadipocyte differentiation by RAR synergists.Biochem Biophys Res Commun,2001,280(3):646-651.
  • 6Kawamata H,Tachibana M,Fujimori T,et al.Differentiation-inducing therapy for solid tumors.Curr Pharm Des,2006,12(3):379-385.
  • 7Tsubouchi Y,Sano H,Kawahito Y,et al.Inhibition of human lung cancer cell growth by the peroxisome proliferator-activated receptor-gamma agonists through induction of apoptosis.Biochem Biophys Res Commun,2000,270(2):400-405.
  • 8黄海雯,吴德沛,陈广华,常惠荣,Chow HCH,Leung AYH,Liang R.罗格列酮与全反式维甲酸联合对骨髓瘤细胞增殖抑制作用及其机制探讨[J].中华血液学杂志,2009,30(4):242-246. 被引量:5

引证文献1

二级引证文献1

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部