Suppression of Epstein-Barr nuclear antigen 1 (EBNA1) by RNA interference inhibits proliferation of EBV-positive Burkitt’s lymphoma cells

被引:0
|
作者
Mei Hong
Yoshihiro Murai
Tomohiko Kutsuna
Hiroyuki Takahashi
Kazuhiro Nomoto
Chun-Mei Cheng
Shin Ishizawa
Qing-Li Zhao
Ryohei Ogawa
Brian V. Harmon
Koichi Tsuneyama
Yasuo Takano
机构
[1] Toyama Medical and Pharmaceutical University,Department of Pathology, School of Medicine
[2] Toyama Medical and Pharmaceutical University,Department of Radiological Sciences, School of Medicine
[3] Queensland University of Technology,School of Life Sciences
来源
Journal of Cancer Research and Clinical Oncology | 2006年 / 132卷
关键词
EBV; EBNA1; RNA interference; Burkitt’s lymphoma; Cell growth;
D O I
暂无
中图分类号
学科分类号
摘要
Purpose: Epstein-Barr virus (EBV) is associated with the development of several lymphoid and epithelial malignancies, including Burkitt’s lymphoma. The EBV latent protein, EBV Nuclear Antigen 1 (EBNA1), is detectable in almost all types of EBV-associated tumors and is essential for replication and maintenance of the latent episome of EBV. We here examined whether the RNA interference (RNAi) technique could be employed to suppress expression of EBNA1 in EBV-positive Burkitt’s lymphoma cells. Methods: A Raji cell line expressing small hairpin RNAs (shRNAs) against EBNA1 was established and EBNA1 mRNA level was determined by real-time RT-PCR analysis. We investigated the effects of EBNA1 silence on lymphoma cell growth and cell cycle progression. Results: Transfection of an EBNA1 RNAi plasmid resulted in substantial loss of EBNA1 mRNA and significantly inhibited proliferation of Raji cells relative to the control plasmid case. Suppression of EBNA1 was also associated with downregulation of EBV oncogene EBNA2, a decreased PCNA labeling index and increased G0/G1 fraction in cell cycle analysis. Conclusions: These findings point to potential therapeutic applications for vector-mediated siRNA delivery to control EBV-associated malignant disorders.
引用
收藏
页码:1 / 8
页数:7
相关论文
共 48 条
  • [41] Epigenetic Alteration of the Cancer-Related Gene TGFBI in B Cells Infected with Epstein-Barr Virus and Exposed to Aflatoxin B1: Potential Role in Burkitt Lymphoma Development
    Manara, Francesca
    Jay, Antonin
    Odongo, Grace Akinyi
    Mure, Fabrice
    Maroui, Mohamed Ali
    Diederichs, Audrey
    Sirand, Cecilia
    Cuenin, Cyrille
    Granai, Massimo
    Mundo, Lucia
    Hernandez-Vargas, Hector
    Lazzi, Stefano
    Khoueiry, Rita
    Gruffat, Henri
    Herceg, Zdenko
    Accardi, Rosita
    CANCERS, 2022, 14 (05)
  • [42] Differential effect of IL-4 and IL-13 on CD44 expression in the Burkitt's lymphoma B cell line BL30/B95-8 and in Epstein-Barr virus(EBV) transformed human B cells: Loss of IL-13 receptors on Burkitt's lymphoma B cells
    Gee, K
    Kozlowski, M
    Kryworuchko, M
    Diaz-Mitoma, F
    Kumar, A
    CELLULAR IMMUNOLOGY, 2001, 211 (02) : 131 - 142
  • [43] Functional role of phosphatidylinositol 3-kinase/Akt pathway on cell growth and lytic cycle of epstein-barr virus in the Burkitt's lymphoma cell line, P3HR-1
    Mori, Takako
    Sairenji, Takeshi
    VIRUS GENES, 2006, 32 (03) : 327 - 334
  • [44] Tofacitinib induces G1 cell-cycle arrest and inhibits tumor growth in Epstein-Barr virus-associated T and natural killer cell lymphoma cells
    Ando, Shotaro
    Kawada, Jun-ichi
    Watanabe, Takahiro
    Suzuki, Michio
    Sato, Yoshitaka
    Torii, Yuka
    Asai, Masato
    Goshima, Fumi
    Murata, Takayuki
    Shimizu, Norio
    Ito, Yoshinori
    Kimura, Hiroshi
    ONCOTARGET, 2016, 7 (47) : 76793 - 76805
  • [45] Epstein-Barr Virus Nuclear Antigen 3C Inhibits Expression of COBLL1 and the ADAM28-ADAMDEC1 Locus via Interaction with the Histone Lysine Demethylase KDM2B
    Gillman, Adam C. T.
    Parker, Gillian
    Allday, Martin J.
    Bazot, Quentin
    JOURNAL OF VIROLOGY, 2018, 92 (21)
  • [46] In ACPA-positive RA patients, antibodies to EBNA35-58Cit, a citrullinated peptide from the Epstein-Barr nuclear antigen-1, strongly cross-react with the peptide β60-74Cit which bears the immunodominant epitope of citrullinated fibrin
    Cornillet, M.
    Verrouil, E.
    Cantagrel, A.
    Serre, G.
    Nogueira, L.
    IMMUNOLOGIC RESEARCH, 2015, 61 (1-2) : 117 - 125
  • [47] Transcription of Epstein-Barr virus-encoded nuclear antigen 1 promoter Qp is repressed by transforming growth factor-β via Smad4 binding element in human BL cells
    Liang, CL
    Tsai, CN
    Chung, PJ
    Chen, JL
    Sun, CM
    Chen, RH
    Hong, JH
    Chang, YS
    VIROLOGY, 2000, 277 (01) : 184 - 192
  • [48] In ACPA-positive RA patients, antibodies to EBNA35-58Cit, a citrullinated peptide from the Epstein–Barr nuclear antigen-1, strongly cross-react with the peptide β60-74Cit which bears the immunodominant epitope of citrullinated fibrin
    M. Cornillet
    E. Verrouil
    A. Cantagrel
    G. Serre
    L. Nogueira
    Immunologic Research, 2015, 61 : 117 - 125