Author:
Kase Kina,Kondo Satoru,Wakisaka Naohiro,Dochi Hirotomo,Mizokami Harue,Kobayashi Eiji,Kano Makoto,Komori Takeshi,Hirai Nobuyuki,Ueno Takayoshi,Nakanishi Yosuke,Hatano Miyako,Endo Kazuhira,Moriyama-Kita Makiko,Sugimoto Hisashi,Yoshizaki Tomokazu
Abstract
Nasopharyngeal carcinoma (NPC) is an Epstein–Barr virus (EBV)-associated malignancy. The principal oncogene of EBV, latent membrane protein 1 (LMP1), induces the expression of programmed death-ligand 1 (PD-L1), which is an immunosuppressive transmembrane protein and a promising therapeutic target for various malignancies. Recent studies have revealed an association between the level of soluble PD-L1 (sPD-L1) and disease progression. However, the role of sPD-L1 in NPC or its relevance to LMP1 has not been elucidated. This study aimed to examine whether LMP1 induces sPD-L1 in vitro and analyze the clinical relevance of LMP1, PD-L1, and sPD-L1 in NPC patients. Analysis of nasopharyngeal cell lines revealed that LMP1 induces both cellular PD-L1 and sPD-L1. Analysis of biopsy specimens from 32 NPC patients revealed that LMP1 expression was significantly correlated with PD-L1 expression. Finally, the serum sPD-L1 level in NPC patients was higher than that in the controls. Moreover, the sPD-L1 level in the advanced stage was higher than that in the early stage. However, LMP1 expression, PD-L1 expression, and sPD-L1 levels were not associated with prognosis. These results suggest that LMP1 induces both sPD-L1 and PD-L1, which are associated with NPC progression.
Funder
the Ministry of Education, Science, Sports, Culture and Technology of Japan
Subject
Virology,Microbiology (medical),Microbiology
Cited by
12 articles.
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