Chidamide Induces Epstein-Barr Virus (EBV) Lytic Infection and Acts Synergistically with Tenofovir to Eliminate EBV-Positive Burkitt Lymphoma

被引:3
|
作者
Xu, Linyan [1 ,2 ,3 ]
Zhang, Meng [1 ,2 ,3 ]
Tu, Dongyun [1 ,2 ,3 ]
Lu, Ziyi [1 ,2 ,3 ]
Lu, Tianyi [1 ,2 ,3 ]
Ma, Dongshen [4 ]
Zhou, Yi [1 ,2 ,3 ]
Zhang, Shuo [1 ,2 ,3 ]
Ma, Yuhan [1 ,2 ,3 ]
Yan, Dongmei [1 ,2 ,3 ]
Wang, Xiangmin [1 ,2 ,3 ,5 ]
Sang, Wei [1 ,2 ,3 ,5 ]
机构
[1] Xuzhou Med Univ, Blood Dis Inst, Xuzhou, Peoples R China
[2] Xuzhou Med Univ, Key Lab Bone Marrow Stem Cell, Xuzhou, Peoples R China
[3] Xuzhou Med Univ, Dept Hematol, Affiliated Hosp, Xuzhou, Peoples R China
[4] Xuzhou Med Univ, Dept Oncol, Affiliated Hosp, Xuzhou, Peoples R China
[5] 84 West Huaihai Rd, Xuzhou, Peoples R China
来源
JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS | 2023年 / 387卷 / 03期
关键词
HISTONE DEACETYLASE INHIBITOR; CELL-CYCLE ARREST; PHASE I/II TRIAL; SIGNALING PATHWAY; GENE-EXPRESSION; HDAC INHIBITOR; VIRAL GENOME; CANCER CELLS; APOPTOSIS; COMBINATION;
D O I
10.1124/jpet.123.001583
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Epstein-Barr virus (EBV) is a type of human c-herpesvirus, and its reactivation plays an important role in the development of EBVdriven Burkitt lymphoma (BL). Despite intensive chemotherapy, the prognosis of relapsed/refractory BL patients remains unfavorable, and a definitive method to completely eliminate latent EBV infection is lacking. Previous studies have demonstrated that his tone deacetylase (HDAC) inhibitors can induce the transition of EBV from latency to the lytic phase. The lytic activation of EBV can be inhibited by tenofovir, a potent inhibitor of DNA replication. Herein, we explored the antitumor effect and EBV clearance potential of a novel HDAC inhibitor called chidamide, combined with tenofovir, in the treatment of EBV-positive BL. In the study, chidamide exhibited inhibitory activity against HDAC. Moreover, chidamide inhibited BL cell proliferation, arrested cell cycle progression, and induced BL cell apoptosis primarily by regulating the MAPK pathways. Additionally, chidamide promoted the transcription of lytic genes, including BZLF1, BMRF1, and BMLF1. Compared with chidamide alone, the addition of tenofovir further induced growth arrest and apoptosis in EBV-positive BL cells and inhibited the transcriptions of EBV lytic genes induced by chidamide alone. Furthermore, our in vivo data demonstrated that the combination of chidamide and tenofovir had superior tumor-suppressive effects in a mouse model of BL cell tumors. The aforementioned findings confirm the synergistic effect of chidamide combined with tenofovir in inducing growth inhibition and apoptosis in EBV-positive BL cells and provide an effective strategy for eliminating EBV and EBV-associated malignancies. SIGNIFICANCE STATEMENT High levels of Epstein-Barr virus (EBV)-DNA have consistently been associated with unfavorable progression-free survival and overall survival in EBV-associated lymphomas. Therefore, identifying novel strategies to effectively eradicate tumor cells and eliminate EBV is crucial for lymphoma patients. This study confirmed, for the first time, the synergistic effect of chidamide combined with tenofovir in the treatment of Burkitt lymphoma and the eradication of EBV virus.
引用
收藏
页码:288 / 298
页数:11
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