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
  • [31] Epstein-Barr virus-encoded EBNA1 enhances RNA polymerase III-dependent EBER expression through induction of EBER-associated cellular transcription factors
    Owen, Thomas J.
    O'Neil, John D.
    Dawson, Christopher W.
    Hu, Chunfang
    Chen, Xiaoyi
    Yao, Yunhong
    Wood, Victoria H. J.
    Mitchell, Louise E.
    White, Robert J.
    Young, Lawrence S.
    Arrand, John R.
    MOLECULAR CANCER, 2010, 9
  • [32] Activation of the lytic program of the Epstein-Barr virus in Burkitt's lymphoma cells leads to a two steps downregulation of expression of the proapoptotic protein BimEL, one of which is EBV-late-gene expression dependent
    Oussaief, Lassad
    Hippocrate, Aurelie
    Clybouw, Cyril
    Rampanou, Aurore
    Ramirez, Vanessa
    Desgranges, Claude
    Vazquez, Aime
    Khelifa, Ridha
    Joab, Irene
    VIROLOGY, 2009, 387 (01) : 41 - 49
  • [33] (-)-Epigallocatechin-3-gallate inhibition of Epstein-Barr virus spontaneous lytic infection involves ERK1/2 and PI3-K/Akt signaling in EBV-positive cells
    Liu, Sufang
    Li, Hongde
    Chen, Lin
    Yang, Lifang
    Li, Lili
    Tao, Yongguan
    Li, Wei
    Li, Zijian
    Liu, Haidan
    Tang, Min
    Bode, Ann M.
    Dong, Zigang
    Cao, Ya
    CARCINOGENESIS, 2013, 34 (03) : 627 - 637
  • [34] Epstein-Barr virus LMP1 protein promotes proliferation and inhibits differentiation of epithelial cells via activation of YAP and TAZ
    Singh, Deo R.
    Nelson, Scott E.
    Pawelski, Abigail S.
    Kansra, Alisha S.
    Fogarty, Stuart A.
    Bristol, Jillian A.
    Ohashi, Makoto
    Johannsen, Eric C.
    Kenney, Shannon C.
    PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2023, 120 (20)
  • [35] Triptolide inhibits proliferation of Epstein-Barr virus-positive B lymphocytes by down-regulating expression of a viral protein LMP1
    Zhou, Heng
    Guo, Wei
    Long, Cong
    Wang, Huan
    Wang, Jingchao
    Sun, Xiaoping
    BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2015, 456 (03) : 815 - 820
  • [36] The Epstein-Barr virus latent membrane protein 1 induces interleukin-10 in Burkitt's lymphoma cells but not in Hodgkin's cells involving the p38/SAPK2 pathway
    Vockerodt, M
    Haier, B
    Buttgereit, P
    Tesch, H
    Kube, D
    VIROLOGY, 2001, 280 (02) : 183 - 198
  • [37] Unusually high frequency of a 69-bp deletion within the carboxy terminus of the LMP-1 oncogene of Epstein-Barr virus detected in Burkitt's lymphoma of Turkish children
    Tacyildiz, N
    Cavdar, AO
    Ertem, U
    Oksal, A
    Kutluay, L
    Uluoglu, O
    Lin, JC
    LEUKEMIA, 1998, 12 (11) : 1796 - 1805
  • [38] Alzheimer's disease risk associated with changes in Epstein-Barr virus nuclear antigen 1-specific epitope targeting antibody levels
    Sim, Kyu-Young
    An, Jaekyeung
    Bae, So-Eun
    Yang, Taewoo
    Ko, Gwang-Hoon
    Hwang, Jeong-Ryul
    Choi, Kyu Yeong
    Park, Jung Eun
    Lee, Jung Sup
    Kim, Byeong C.
    Lee, Kun Ho
    Park, Sung-Gyoo
    JOURNAL OF INFECTION AND PUBLIC HEALTH, 2024, 17 (07)
  • [39] Morphologic differences between latent membrane protein-1 (LMP-1)-positive and negative tumour cells in Epstein-Barr virus (EBV)-related childhood Hodgkin's disease - A morphometric study
    Panayiotides, J
    Kanavaros, P
    Protopapa, E
    Vlachonikolis, J
    Tzardi, M
    Kalmanti, M
    Delides, G
    PATHOLOGY RESEARCH AND PRACTICE, 1996, 192 (03) : 210 - 214
  • [40] Identification of MEF2B, EBF1, and IL6R as Direct Gene Targets of Epstein-Barr Virus (EBV) Nuclear Antigen 1 Critical for EBV-Infected B-Lymphocyte Survival
    Tempera, Italo
    De Leo, Alessandra
    Kossenkov, Andrew V.
    Cesaroni, Matteo
    Song, Hui
    Dawany, Noor
    Showe, Louise
    Lu, Fang
    Wikramasinghe, Priyankara
    Lieberman, Paul M.
    JOURNAL OF VIROLOGY, 2016, 90 (01) : 345 - 355