Small-molecule protein kinase inhibitors and their effects on the immune system: implications for cancer treatment

被引:45
|
作者
Ott, Patrick A. [1 ]
Adams, Sylvia [1 ]
机构
[1] NYU, Inst Canc, Div Med Oncol, New York, NY 10016 USA
关键词
cancer immunotherapy; MAPK; PI3K-AKT-mTOR; VEGF-VEGFR; tyrosine kinase inhibitor; ENDOTHELIAL GROWTH-FACTOR; T-CELL RESPONSES; IMATINIB MESYLATE; DENDRITIC CELLS; MAMMALIAN TARGET; KAPPA-B; SIGNALING PATHWAY; FUNCTIONAL MATURATION; METASTATIC MELANOMA; CYCLE PROGRESSION;
D O I
10.2217/IMT.10.99
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Oncogenic signaling pathways have emerged as key targets for the development of small-molecule inhibitors, with several protein kinase inhibitors already in clinical use for cancer patients. In addition to their role in tumorigenesis, many of the molecules and signaling pathways targeted by these inhibitors are also important in the signaling and interaction of immune cells, such as T cells and dendritic cells. Not surprisingly, there is increasing evidence that many of these inhibitors can have a substantial impact on immune function, both stimulating and downregulating an immune response. In order to illustrate the important role of signaling molecule inhibition in the modulation of immune function, we will discuss the exemplary pathways MAPK, AKT-PI3K-mTOR and VEGF-VEGFR, as well as selected small-molecule inhibitors, whose impact on immune cells has been studied more extensively.
引用
收藏
页码:213 / 227
页数:15
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