TYK2: An Upstream Kinase of STATs in Cancer

被引:49
|
作者
Woess, Katharina [1 ]
Simonovic, Natalija [1 ]
Strobl, Birgit [1 ]
Macho-Maschler, Sabine [1 ]
Mueller, Mathias [1 ]
机构
[1] Univ Vet Med Vienna, Inst Anim Breeding & Genet, A-1210 Vienna, Austria
基金
奥地利科学基金会;
关键词
tyrosine kinase 2; JAK family of protein tyrosine kinases; signal transducer and activator of transcription; cytokine receptor signaling; gain-of-function mutation; tumorigenesis; ACUTE LYMPHOBLASTIC-LEUKEMIA; BREAST-CANCER; PROTOONCOGENE PRODUCT; SOMATIC MUTATIONS; JAK INHIBITION; CELL-DEATH; PROTEIN; EXPRESSION; HSP90; GENE;
D O I
10.3390/cancers11111728
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
In this review we concentrate on the recent findings describing the oncogenic potential of the protein tyrosine kinase 2 (TYK2). The overview on the current understanding of TYK2 functions in cytokine responses and carcinogenesis focusses on the activation of the signal transducers and activators of transcription (STAT) 3 and 5. Insight gained from loss-of-function (LOF) gene-modified mice and human patients homozygous for Tyk2/TYK2-mutated alleles established the central role in immunological and inflammatory responses. For the description of physiological TYK2 structure/function relationships in cytokine signaling and of overarching molecular and pathologic properties in carcinogenesis, we mainly refer to the most recent reviews. Dysregulated TYK2 activation, aberrant TYK2 protein levels, and gain-of-function (GOF) TYK2 mutations are found in various cancers. We discuss the molecular consequences thereof and briefly describe the molecular means to counteract TYK2 activity under (patho-)physiological conditions by cellular effectors and by pharmacological intervention. For the role of TYK2 in tumor immune-surveillance we refer to the recent Special Issue of Cancers "JAK-STAT Signaling Pathway in Cancer".
引用
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页数:18
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