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Tumour associated glycans: A route to boost immunotherapy?
被引:24
作者:
Scott, Emma
[1
]
Elliott, David J.
[1
]
Munkley, Jennifer
[1
]
机构:
[1] Newcastle Univ, Inst Genet Med, Newcastle Upon Tyne NE1 3BZ, Tyne & Wear, England
关键词:
Glycans;
Lectins;
Immunotherapy;
Cancer glycosylation;
RENAL-CELL CARCINOMA;
T-CELLS;
ANTITUMOR IMMUNITY;
CANCER-CELLS;
CORE FUCOSYLATION;
CTLA-4;
BLOCKADE;
DENDRITIC CELLS;
SINGLE-AGENT;
PHASE-I;
GLYCOSYLATION;
D O I:
10.1016/j.cca.2019.12.015
中图分类号:
R446 [实验室诊断];
R-33 [实验医学、医学实验];
学科分类号:
1001 ;
摘要:
While the development of immunotherapies for cancer treatment offer significant promise across several cancers, still only a small subset of patients respond to immune based monotherapies. As such, attention has turned to the development of combination therapies. These use conventional cancer treatments such as chemotherapy to sensitise tumours to immunotherapy. Here, we summarise key research, highlighting the exciting potential of tumour associated glycans as therapeutic targets to sensitise tumours to immunotherapy. When cells undergo carcinogenesis they reprogram their glyco-code. Several cancer associated glycans have been identified, and therapies targeting them are under development. Proteins containing carbohydrate binding domains (lectins) are expressed by many immune cell subtypes, and upon glycan binding, transduce immune modulatory signals that regulate the tumour immune microenvironment.
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页码:167 / 173
页数:7
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