Adenosine signaling: Next checkpoint for gastric cancer immunotherapy?

被引:11
|
作者
Shi, Linsen [1 ,3 ]
Yang, Lin [4 ]
Wu, Zhaoyin [4 ]
Xu, Wei [1 ]
Song, Jun [1 ]
Guan, Wenxian [2 ]
机构
[1] Xuzhou Med Univ, Dept Gastrointestinal Surg, Affiliated Hosp, 99 West Huaihai Rd, Xuzhou 221006, Jiangsu, Peoples R China
[2] NanJing Med Univ, Affiliated Drum Tower Hosp, Dept Gastrointestinal Surg, Nanjing, Jiangsu, Peoples R China
[3] NanJing Med Univ, Affiliated Drum Tower Clin Coll, Nanjing, Jiangsu, Peoples R China
[4] XuZhou Med Univ, Xuzhou, Jiangsu, Peoples R China
关键词
Adenosine; gastric cancer; A2aR signaling; immunotherapy; REGULATORY T-CELLS; POOR-PROGNOSIS; DEAMINASE ACTIVITY; CD73; EXPRESSION; DOUBLE-BLIND; CD39; RECEPTOR; INFLAMMATION; ACTIVATION; EFFICACY;
D O I
10.1016/j.intimp.2018.07.023
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Adenosine (ADO), generated by the ectonucleotidase CD39 and CD73 from ATP, interacts with its specific G protein-coupled receptors, which can impair anti-tumor immune responses inhibiting the infiltration and function of CD8(+) T cell and natural killer cell. Recent studies have also identified that ADO pathway plays a critical role in tumor immune surveillance, especially for some non-solid cancers. In addition, although immune checkpoint therapy targeting ADO pathway in gastric cancer is still in an early phase, encouraging results have come out from some drugs targeting ADO pathway. Therefore, target ADO signaling may be a new promising strategy to treat gastric cancer. In this review, we summarized recent works on the role of ADO in cancer immunotherapy and also discussed relative mechanisms underlying the function of ADO signaling in cancer immune responses.
引用
收藏
页码:58 / 65
页数:8
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