Baicalein inhibits growth of Epstein-Barr virus-positive nasopharyngeal carcinoma by repressing the activity of EBNA1 Q-promoter

被引:26
作者
Zhang, Yaqian [1 ]
Wang, Huan [1 ]
Liu, Yu [1 ]
Wang, Chao [1 ]
Wang, Jingchao [1 ]
Long, Cong [1 ]
Guo, Wei [2 ]
Sun, Xiaoping [1 ,3 ]
机构
[1] Wuhan Univ, Sch Basic Med Sci, Dept Pathogen Biol, Stat Key Lab Virol, 185 Eastlake Rd, Wuhan 430071, Hubei, Peoples R China
[2] Wuhan Univ, Sch Basic Med Sci, Dept Pathol & Physiol, Wuhan 430071, Hubei, Peoples R China
[3] Wuhan Univ, State Key Lab Virol, Wuhan 430072, Hubei, Peoples R China
基金
中国国家自然科学基金;
关键词
Epstein-Barr virus; EBNA1; Nasopharyngeal carcinoma; Baicalein; NUCLEAR ANTIGEN 1; CONVENTIONAL 2-DIMENSIONAL RADIOTHERAPY; INTENSITY-MODULATED RADIOTHERAPY; TRANSCRIPTION FACTOR SP1; EFFUSION LYMPHOMA-CELLS; CANCER-CELLS; CPG METHYLATION; IN-VIVO; GENE-TRANSCRIPTION; DOWN-REGULATION;
D O I
10.1016/j.biopha.2018.03.114
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Epstein-Barr virus (EBV) can establish a life-long latent infection in the host and is associated with various human malignancies, including nasopharyngeal carcinoma (NPC), the most common cancer originated from nasopharynx. EBV nuclear antigen 1 (EBNA1) is the only viral protein absolutely demanded for segregation, replication, transcription and maintenance of EBV viral genome in host cells. Baicalein, a bioactive flavonoid compound purified from the root of Scutellariae baicaleinsis, displays anti-inflammatory, immunosuppressive, and anti-tumor properties. In this study, the therapeutic effects and functional mechanism of baicalein on EBV-positive human NPC were determined. Cell Counting Kit-8 assays and cell formation colony were performed to investigate that baicalein can suppress proliferation of EBV-infected human NPC cells. Flow cytometric and hoechst 33258 staining results indicated that baicalein induced cell cycle arrest and apoptosis. Western blotting results demonstrated that baicalein down-regulates EBNA1 expression but not reduces the stability and half-life of EBNA1 in EBV-infected NPC cells. Additionally, the mRNA level of EBNA1 was examined by real time-PCR, the activity of EBNA1 Q promoter (Qp) was determined by dual luciferase reporter assay. Considering that transcription factor specificity protein 1 (Sp1) can maintain EBNA1 Qp active. Further analyses also elucidated that baicalein inhibits the expression of Sp1 while knock-down Sp1 by specific shRNAs decreases the expression and transcription levels of EBNA1. Therefore, the results suggested that baicalein may decrease EBNA1 expression level in EBV-positive NPC cells via inhibiting the activity of EBNA1 Q-promoter while over-expression of EBNA1 attenuate the inhibitory effect of baicalein. Finally, it was found that baicalein may strongly reduce growth of tumor in the mouse xenograft model of EBV-positive NPC. These results indicated that baicalein inhibits growth of EBV-positive NPC by repressing the activity of EBNA1 Q-promoter. Baicalein may be used as a therapeutic agent to treat EBV-positive NPC.
引用
收藏
页码:1003 / 1014
页数:12
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