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NF-κB 信号转导中的受体近端激酶作为癌症和炎症治疗靶点的潜力。

Receptor proximal kinases in NF-κB signaling as potential therapeutic targets in cancer and inflammation.

机构信息

Inflammation Research Center, Unit of Molecular Signal Transduction in Inflammation, VIB, Ghent, Belgium; Department of Biomedical Molecular Biology, Ghent University, Ghent, Belgium.

Inflammation Research Center, Unit of Molecular Signal Transduction in Inflammation, VIB, Ghent, Belgium; Department of Biomedical Molecular Biology, Ghent University, Ghent, Belgium.

出版信息

Biochem Pharmacol. 2014 Dec 15;92(4):519-29. doi: 10.1016/j.bcp.2014.10.017. Epub 2014 Nov 7.

Abstract

Many signaling pathways leading to activation of transcription factors and gene expression are characterized by phosphorylation events mediated by specific kinases. The transcription factor NF-κB plays a key role in multiple cellular processes, including immune signaling, inflammation, development, proliferation and survival. Dysregulated NF-κB activation is associated with autoimmunity, chronic inflammation and cancer. Activation of NF-κB requires IκB kinase (IKK)α or β, the activity of which is regulated via phosphorylation by specific IKK kinases and by autophosphorylation. Receptor specificity is further obtained by the use of multiple upstream receptor proximal kinases. We review the identities of several IKK regulatory kinases as well as the proposed molecular mechanisms. In addition, we discuss the potential for therapeutic targeting of some of these kinases in the context of inflammatory diseases and cancer.

摘要

许多导致转录因子激活和基因表达的信号通路的特征是由特定激酶介导的磷酸化事件。转录因子 NF-κB 在多种细胞过程中发挥关键作用,包括免疫信号、炎症、发育、增殖和存活。NF-κB 激活失调与自身免疫、慢性炎症和癌症有关。NF-κB 的激活需要 IκB 激酶 (IKK)α 或β,其活性通过特定的 IKK 激酶和自身磷酸化的磷酸化来调节。受体特异性还通过使用多个上游受体近端激酶来获得。我们回顾了几种 IKK 调节激酶的身份以及提出的分子机制。此外,我们还讨论了在炎症性疾病和癌症的背景下靶向这些激酶的治疗潜力。

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