IκB激酶
生物
癌变
癌症研究
癌症
分子肿瘤学
激酶
坦克结合激酶1
克拉斯
先天免疫系统
炎症
NF-κB
免疫学
细胞生物学
遗传学
结直肠癌
细胞周期
免疫系统
细胞周期蛋白依赖激酶2
作者
Rhine R. Shen,William C. Hahn
出处
期刊:Oncogene
[Springer Nature]
日期:2010-11-01
卷期号:30 (6): 631-641
被引量:124
摘要
The IκB Kinase (IKK)-related kinases TBK1 and IKKɛ have essential roles as regulators of innate immunity by modulating interferon and NF-κB signaling. Recent work has also implicated these non-canonical IKKs in malignant transformation. IKKɛ is amplified in ∼30% of breast cancers and transforms cells through the activation of NF-κB. TBK1 participates in RalB-mediated inflammatory responses and cell survival, and is essential for the survival of non-small cell lung cancers driven by oncogenic KRAS. The delineation of target substrates and downstream activities for TBK1 and IKKɛ has begun to define their role(s) in promoting tumorigenesis. In this review, we will highlight the mechanisms by which IKKɛ and TBK1 orchestrate pathways involved in inflammation and cancer.
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