Clinicopathological analysis of PD-L2 expression in colorectal cancer

被引:21
|
作者
Guo, Peng-Da [1 ]
Sun, Zhong-Wen [1 ]
Lai, Hui-Jun [2 ]
Yang, Jie [1 ]
Wu, Ping-Ping [1 ]
Guo, Yun-Di [1 ]
Sun, Jing [1 ]
机构
[1] Suzhou Vocat Hlth Coll, Inst Med Technol, 28 Kehua Rd, Suzhou 215009, Jiangsu, Peoples R China
[2] Suzhou Tradit Chinese Med, Dept Ultrasound, Suzhou 215007, Jiangsu, Peoples R China
来源
ONCOTARGETS AND THERAPY | 2018年 / 11卷
关键词
PD-L2; colorectal cancer; migration; therapeutic; IMMUNE CHECKPOINTS; CELLS; OVEREXPRESSION; LIGANDS; B7-DC;
D O I
10.2147/OTT.S177329
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Background: (PD-L2), a ligand of programmed cell death protein 1 (PD-1), is an inhibitory receptor of T cells and activated B cells. Many studies have focused on PD-L1, another ligand of PD-1, and the prognostic significance of PD-L1 has been reported in many tumors. However, the expression of PD-L2 in relation to clinical outcomes has not been fully investigated in cancer patients. Patients and methods: In this study, we investigated the expression of PD-L2 via immunohistochemistry (IHC) in the pathological specimens of 348 patients treated for colorectal cancer (CRC). Results: Strong PD-L2 expression was found in the cancer tissues from 41% of the CRC patients who also had a high TNM stage and carcinoembryonic antigen (CEA) concentration. We also carried out functional studies in vitro, which showed that PD-L2 did not influence the growth of the CRC cell line HCT116, but increased cell invasion. Conclusion: Collectively, these findings suggest that PD-L2 may be a potential therapeutic target for CRC.
引用
收藏
页码:7635 / 7642
页数:8
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