期刊文献+

肿瘤坏死因子α对Raji细胞Notch1蛋白表达的影响 被引量:2

Expression of TNF-α on Notch1 Expression in Raji Cells
下载PDF
导出
摘要 目的通过探讨肿瘤坏死因子α(TNF-α)作用淋巴瘤细胞系Raji细胞后Notch1蛋白表达的变化,进一步明确TNF-α对淋巴瘤细胞Notch信号途径的影响。方法采用半定量RT-PCR方法检测Raji细胞Notch1 mRNA的含量;用流式细胞术分析Raji细胞Notch1蛋白的表达及TNF-α作用后Notch1蛋白的变化。结果①半定量RT-PCR检测结果表明Raji细胞经TNF-α作用后Notch1mRNA的含量明显增高,且随TNF-α浓度的增加而增高,与对照组比较,差异有极显著性意义(P<0.01);②流式细胞术分析表明,Notch1蛋白在Raji细胞呈阳性表达,TNF-α作用组Notch1蛋白的平均荧光强度明显高于对照组,差异亦有极显著性意义(P<0.01)。结论TNF-α可上调Raji细胞内Notch1蛋白的表达;TNF-α可通过影响Notch信号途径在淋巴瘤细胞内发挥作用。 Objective To investigate the effect of TNF-α on the expression of Notch1 in Raji cell line. Methods The expression level of Notch1 mRNA and protein in Raji cells treated with TNF-α was detected by RT-PCR and flow cytometry respectively. Results The expression of Notch1 mRNA was up-regulated in a dose-dependent manner in Raji cells treated by TNF-α (P〈0.01). Raji cells treated with TNF-α had a higher fluorescence intensity of Notch1 protein as compared with untreated cells (P〈0.01). Conclusion Notch1 protein was expressed in Raji cells and the expression of Notch1 protein was increased after TNF-α treatment, suggesting that activated Notch1 signaling pathway plays an important role in pathogenesis of lymphoma and it might be a potential new target for treatment.
出处 《华中科技大学学报(医学版)》 CAS CSCD 北大核心 2008年第3期299-301,共3页 Acta Medicinae Universitatis Scientiae et Technologiae Huazhong
基金 国家自然科学基金资助项目(No30472267)
关键词 肿瘤坏死因子Α NOTCH1蛋白 RAJI细胞 TNF-α Notch1 Raji cell line
  • 相关文献

参考文献12

  • 1ARTAVANIS-TSAKONAS S, RAND M D, LAKE R J. Notch signaling: cell fate control and signal integration in development[J]. Science, 1999, 284(5415):770-776.
  • 2ZAGOURAS P, STIFANI S, BLAUMLLER C M, et al. Alterations in Notch signaling in neoplastic lesions of the human cervix[J]. Proc Natl Acad Sci USA, 1995, 92 (14):6414- 6418.
  • 3ASTER J C, PEAR W S. Notch signaling in leukemia[J]. Curr Opin Hematol, 2001, 8(4) :237-244.
  • 4PEAR W S, ASTER J C. T cell acute lymphoblastic leukemia/lymphoma: a human cancer commonly associated with aberrant Notchl signaling[J]. Curt Opin Hematol, 2004, 11 (6) :426-433.
  • 5JUNDT F, ANAGNOSTOPOULOS I, FORSTER R, et al. Activated Notchl signaling promotes tumor cell proliferation and survival in Hodgkin and anaplastic large cell lymphoma [J]. Blood,2002, 99(9):3398 3403.
  • 6SHELLY L L, FUCHS C, MIELE L. Notch-1 inhibits apoptosis in murine erythroleukemia cells and is necessary for differentiation induced by hybrid polar compounds[J]. J Cell Biochem,1999, 73(2) :164 175.
  • 7WENG A P, NAM Y, WOLFE M S, et al. Growth suppression of pre-T acute lymphoblastic leukemia cells by inhibition of notch signaling[J]. Mol Cell Biol, 2003, 23(2):655-664.
  • 8GO M J, EASTMAN D S, ARTAVANIS-TSAKONAS S. Cell proliferation control by Notch signaling in Drosophila development[J]. Development, 1998,125 (11) : 2031-2040.
  • 9赵洪云,陈运贤.肿瘤坏死因子基因多态性与血液系统恶性肿瘤[J].癌症,2003,22(2):216-220. 被引量:10
  • 10ANDO K, KANAZAWA S, TETSUKA T, et al. Induction of Notch signaling by tumor necrosis factor in rheumatoid synovial fibroblasts[J]. Oncogene, 2003, 22(49):7796-803.

二级参考文献35

  • 1[1]Gadducci A,Ferdeghini M,Castellani C,et al. Serum levels of tumor necrosis factor (TNF),soluble receptors for TNF (55-and-75kDa sTNFr),soluble CD14 (sCD14) in epithelial ovarian cancer [J]. Gymecol Oncol,1995,58:184- 188.
  • 2[2]Partanen R,Koskinen H,Hemminki K. Tumor necrosis factor-α (TNF-alpha) in patients who have asbestosis and develop cancer[J].Occup Environ Med,1995,52:316- 319.
  • 3[3]Okamoto T,Watanabe N,Yamauchi N,et al. Endogenous tumor necrosis factor exerts its protective function intracellularly against the cytotoxicity of exogenous tumor necrosis factor [J]. Cancer Res,1992,52:5278- 5281.
  • 4[4]Fujiki H,Suganuma M,Komori A,et al. A new tumor promotion pathway and its inhibitors[J].Cancer Detect Prev,1994,18(1):1- 7.
  • 5[5]Allen RD. Polymorphism of human TNF-α promoter-random variation or functional diversity?[J]. Mol Immunol,1999,36:1017- 1027.
  • 6[6]Wilson AG,Symons JA,Mcdowell TL,et al. Effects of polymorphism in the human tumor necrosis factor-α promoter on transcriptional activation [J]. Proc Natl Acad,1997,94:3195- 3199.
  • 7[7]Messer G,Spengler U,Jung MC,et al. Polymorphism structure of the tumor necrosis factor (TNF) locus: An NcoⅠ polymorphism in the first intron of the human TNF-beta gene correlates with a variant amino acid in position 26 and a reduced level of TNF-beta production [J]. J Exp Med,1991,173:209- 219.
  • 8[8]Kroeger KM,Abraham LJ. Identification of an AP-2 element in the -323 to -285 region of the TNF-alpha gene [J]. Biochem Mol Biol Int,1996,40:43- 51.
  • 9[9]Kroeger KM,Carcille KS,Abraham LJ. The -308 tumor necrosis factor-α promoter polymorphism effects transcription [J]. Mol Immunol,1997,34(5):391- 399.
  • 10[10]Kaijzel EL,Van KMV,Brinkman BMN,et al. Functional analysis of a human tumor necrosis factor-α (TNF-α ) promoter polymorphism related to joint damage in rheumatoid arithritis[J].Mol Med,1998,4:724- 733.

共引文献9

同被引文献18

  • 1Tay K,Dunleavy K,Wilson WH.Novel agents for B-cell non-Hodgkin's lymphoma:science and promise.Blood Rev,2010;24(2):69-82.
  • 2Fidza UM,Arias AM.Cell and molecular biology of Notch.JEndocrinol,2007;194(3):459-474.
  • 3Itoh M,Fu L,Tohda S.NF-kappa B activation induced by Notchligand stimulation in acute myeloid leukemia cells.Oncol Rep,2009;22(3):631-634.
  • 4Li M,Chen F,Clifton N,et al.Combined inhibition of Notchsignaling and Bcl-2/Bcl-Xl results in synergistic antimyelomaeffect.Mol Cancer Ther,2010;9(12):3200-3209.
  • 5Ellisen LW,Bird J,West DC,et al.TAN-1,the human homologof the Drosophila Notch gene,is broken by chromosomal translo-cations in T lymphoblastic neoplasms.Cell,1991;66(4):649-661.
  • 6Demarest RM,Dahmane N,Capobianco AJ.Notch is oncogenicdominant in T-cell acute lymphoblastic leukemia.Blood,2011;117(10):2749-2750.
  • 7Levis HD,Leveridge M,Strack PR,et al.Apoptosis in T cellacute lymphoblastic leukemia cells after cell cycle arrest induced byphamacological inhibition of notch signaling.Chem Biol,2007;14(2):209-219.
  • 8刘显文,祝颂松,胡静.Notch信号通路与关节软骨发育及骨关节炎[J].中国组织工程研究与临床康复,2010,14(11):2014-2017. 被引量:8
  • 9叶永斌,林骏,赵嘉佳,张兴梅,罗深秋.I型γ-分泌酶抑制剂对恶性胶质瘤细胞株增殖及凋亡的影响[J].中华神经医学杂志,2010,9(6):571-575. 被引量:2
  • 10李玉娟,郭冬梅,滕清良.Notch1和VEGF在多发性骨髓瘤发生、发展中的作用[J].山东医药,2011,51(11):108-109. 被引量:1

引证文献2

二级引证文献14

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