Inhibitory-κB Kinase (IKK) α and Nuclear Factor-κB (NFκB)-Inducing Kinase (NIK) as Anti-Cancer Drug Targets

IκB激酶 激酶 雷布 生物 癌症研究 细胞生物学 NF-κB 信号转导 NFKB1型 转录因子 遗传学 基因
作者
Andrew Paul,Joanne Edwards,Chris Pepper,Simon P. Mackay
出处
期刊:Cells [Multidisciplinary Digital Publishing Institute]
卷期号:7 (10): 176-176 被引量:67
标识
DOI:10.3390/cells7100176
摘要

The cellular kinases inhibitory-κB kinase (IKK) α and Nuclear Factor-κB (NF-κB)-inducing kinase (NIK) are well recognised as key central regulators and drivers of the non-canonical NF-κB cascade and as such dictate the initiation and development of defined transcriptional responses associated with the liberation of p52-RelB and p52-p52 NF-κB dimer complexes. Whilst these kinases and downstream NF-κB complexes transduce pro-inflammatory and growth stimulating signals that contribute to major cellular processes, they also play a key role in the pathogenesis of a number of inflammatory-based conditions and diverse cancer types, which for the latter may be a result of background mutational status. IKKα and NIK, therefore, represent attractive targets for pharmacological intervention. Here, specifically in the cancer setting, we reflect on the potential pathophysiological role(s) of each of these kinases, their associated downstream signalling outcomes and the stimulatory and mutational mechanisms leading to their increased activation. We also consider the downstream coordination of transcriptional events and phenotypic outcomes illustrative of key cancer ‘Hallmarks’ that are now increasingly perceived to be due to the coordinated recruitment of both NF-κB-dependent as well as NF-κB–independent signalling. Furthermore, as these kinases regulate the transition from hormone-dependent to hormone-independent growth in defined tumour subsets, potential tumour reactivation and major cytokine and chemokine species that may have significant bearing upon tumour-stromal communication and tumour microenvironment it reiterates their potential to be drug targets. Therefore, with the emergence of small molecule kinase inhibitors targeting each of these kinases, we consider medicinal chemistry efforts to date and those evolving that may contribute to the development of viable pharmacological intervention strategies to target a variety of tumour types.

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
1秒前
小郭应助单纯的手机采纳,获得10
2秒前
3秒前
phy发布了新的文献求助10
5秒前
57完成签到,获得积分20
5秒前
在水一方应助Eva采纳,获得10
5秒前
5秒前
6秒前
科研通AI6.4应助hjejix采纳,获得10
7秒前
7秒前
黄瑞音完成签到,获得积分10
7秒前
木马木马发布了新的文献求助10
8秒前
2jz发布了新的文献求助10
8秒前
Wenbin发布了新的文献求助10
8秒前
9秒前
ming发布了新的文献求助10
10秒前
lizi发布了新的文献求助10
10秒前
共享精神应助云贝采纳,获得10
11秒前
LIUYU发布了新的文献求助10
11秒前
屯一屯完成签到 ,获得积分10
12秒前
科研通AI6.2应助sunny采纳,获得30
12秒前
路奇发布了新的文献求助10
13秒前
14秒前
17秒前
17秒前
17秒前
18秒前
19秒前
20秒前
十丶年完成签到,获得积分10
21秒前
碧蓝的以彤完成签到 ,获得积分10
21秒前
22秒前
22秒前
碧蓝幻天发布了新的文献求助10
23秒前
初一发布了新的文献求助10
24秒前
25秒前
7h发布了新的文献求助10
26秒前
TaoZhang完成签到,获得积分10
26秒前
27秒前
nine完成签到,获得积分10
27秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
An Introduction to Foreign Language Learning and Teaching 750
China Pluperfect I: Epistemology of Past and Outside in Chinese Art 520
Matrix Methods in Data Mining and Pattern Recognition Second Edition 510
Cosmos as Art Object: Studies in Plato's Timaeus and Other Dialogues 500
What is the Future of Psychotherapy in Digital Age? Technology, AI Bots, and Psychotherapy after Covid 444
煤炭地下气化渗流燃烧方法的研究 400
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 内科学 物理 复合材料 催化作用 细胞生物学 无机化学 光电子学 物理化学 电极 基因
热门帖子
关注 科研通微信公众号,转发送积分 7632541
求助须知:如何正确求助?哪些是违规求助? 9206935
关于积分的说明 19746181
捐赠科研通 7201897
什么是DOI,文献DOI怎么找? 3274871
关于科研通互助平台的介绍 2436759
邀请新用户注册赠送积分活动 2271568