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Epstein-Barr Virus-Encoded Circular RNA CircBART2.2 Promotes Immune Escape of Nasopharyngeal Carcinoma by Regulating PD-L1.


ABSTRACT: Epstein-Barr virus (EBV) infection is an established cause of nasopharyngeal carcinoma (NPC) and is involved in a variety of malignant phenotypes, including tumor immune escape. EBV can encode a variety of circular RNAs (circRNA), however, little is known regarding the biological functions of these circRNAs in NPC. In this study, EBV-encoded circBART2.2 was found to be highly expressed in NPC where it upregulated PD-L1 expression and inhibited T-cell function in vitro and in vivo. circBART2.2 promoted transcription of PD-L1 by binding the helicase domain of RIG-I and activating transcription factors IRF3 and NF-κB, resulting in tumor immune escape. These results elucidate the biological function of circBART2.2, explain a novel mechanism of immune escape caused by EBV infection, and provide a new immunotherapy target for treating NPC. SIGNIFICANCE: This work demonstrates that circBART2.2 binding to RIG-I is essential for the regulation of PD-L1 and subsequent immune escape in nasopharyngeal carcinoma.

SUBMITTER: Ge J 

PROVIDER: S-EPMC8974435 | biostudies-literature | 2021 Oct

REPOSITORIES: biostudies-literature

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Epstein-Barr Virus-Encoded Circular RNA CircBART2.2 Promotes Immune Escape of Nasopharyngeal Carcinoma by Regulating PD-L1.

Ge Junshang J   Wang Jie J   Xiong Fang F   Jiang Xianjie X   Zhu Kunjie K   Wang Yian Y   Mo Yongzhen Y   Gong Zhaojian Z   Zhang Shanshan S   He Yi Y   Li Xiayu X   Shi Lei L   Guo Can C   Wang Fuyan F   Zhou Ming M   Xiang Bo B   Li Yong Y   Li Guiyuan G   Xiong Wei W   Zeng Zhaoyang Z  

Cancer research 20210728 19


Epstein-Barr virus (EBV) infection is an established cause of nasopharyngeal carcinoma (NPC) and is involved in a variety of malignant phenotypes, including tumor immune escape. EBV can encode a variety of circular RNAs (circRNA), however, little is known regarding the biological functions of these circRNAs in NPC. In this study, EBV-encoded <i>circBART2.2</i> was found to be highly expressed in NPC where it upregulated PD-L1 expression and inhibited T-cell function <i>in vitro</i> and <i>in viv  ...[more]

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