车站3
基因亚型
选择性拼接
生物
调节器
抑制器
STAT蛋白
癌变
细胞生物学
癌基因
斯达
癌症研究
信号转导
计算生物学
癌症
细胞周期
遗传学
基因
作者
Petra Aigner,Valentin Just,Dagmar Stoiber
出处
期刊:Cytokine
[Elsevier BV]
日期:2018-07-20
卷期号:118: 27-34
被引量:70
标识
DOI:10.1016/j.cyto.2018.07.014
摘要
Signal transducer and activator of transcription (STAT) 3 is the main mediator of IL-6-type cytokine signaling and an important transcriptional regulator of cell proliferation, maturation and survival. It has been described as a key player in cancer development and progression. However, under certain circumstances, STAT3 is also considered a potent tumor suppressor. This heterogeneity partially depends on its expression as different isoforms. Alternative splicing gives rise to two STAT3 isoforms, STAT3α and its truncated version STAT3β. Both isoforms are transcriptionally active and display distinct functions under physiological and pathological conditions. In fact, while STAT3α is widely described as an oncogene, STAT3β has gained attention as a potential tumor suppressor. This review provides a concise overview of the current knowledge on STAT3 during tumorigenesis, with special emphasis on the unique and complex roles of its alternatively spliced isoforms.
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