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通过分子靶向抑制核因子κB激酶抑制剂使肿瘤细胞对癌症治疗敏感化。

Sensitization of tumor cells to cancer therapy by molecularly targeted inhibition of the inhibitor of nuclear factor κB kinase.

作者信息

Shao Lijian, Wu Lixian, Zhou Daohong

机构信息

Division of Radiation Health, Department of Pharmaceutical Sciences, University of Arkansas for Medical Sciences, Little Rock, Arkansas, USA.

出版信息

Transl Cancer Res. 2012 Aug;1(2):100-108. doi: 10.3978/j.issn.2218-676X.2012.05.04.

Abstract

The inhibitor of nuclear factor κB kinase (IKK)-nuclear factor κB (NFκB) pathway is one of the most important cellular signal transduction pathways. It can be activated by diverse stimuli, resulting in liberation of cytoplasmic NFκB from inhibition by inhibitors of NFκB (IκB) after IκB are phosphorylated by IKKβ and IKKα via the canonical and non-canonical pathways, respectively. Activated NFκB then translocates into the nucleus to regulate various NFκB target genes. Through regulation of its target genes, NFκB can regulate various physiologic processes such as cell proliferation, migration and survival. More importantly, activation of the IKK-NFκB pathway has been implicated in carcinogenesis, tumor development, progression and metastasis, and cancer resistance to radiotherapy and chemotherapy. Therefore, molecularly targeted inhibition of the different components of this pathway has been widely explored for treatment of cancer either alone or in combination with other cancer therapies. A growing body of evidence suggests that IKKβ may be a better cancer treatment target in this pathway, because several novel NFκB-independent functions of IKKβ have been identified recently, including promotion of DNA double strand break repair to increase tumor cell resistance to ionizing radiation and chemotherapy in an apoptosis-independent manner. In this review, we highlight some of these new findings and discuss the therapeutic potential of IKKβ specific inhibitors as a novel tumor sensitizer.

摘要

核因子κB激酶(IKK)-核因子κB(NFκB)信号通路抑制剂是最重要的细胞信号转导通路之一。它可被多种刺激激活,分别通过经典途径和非经典途径,在IKKβ和IKKα将核因子κB抑制蛋白(IκB)磷酸化后,使细胞质中的NFκB从IκB的抑制作用中释放出来。激活的NFκB随后转位进入细胞核,调控各种NFκB靶基因。通过调控其靶基因,NFκB可调节多种生理过程,如细胞增殖、迁移和存活。更重要的是,IKK-NFκB信号通路的激活与肿瘤发生、肿瘤发展、进展和转移以及癌症对放疗和化疗的抗性有关。因此,针对该信号通路不同组分的分子靶向抑制已被广泛探索,用于单独治疗癌症或与其他癌症治疗方法联合使用。越来越多的证据表明,IKKβ可能是该信号通路中更好的癌症治疗靶点,因为最近发现了IKKβ一些不依赖NFκB的新功能,包括促进DNA双链断裂修复,以一种不依赖凋亡的方式增加肿瘤细胞对电离辐射和化疗的抗性。在本综述中,我们重点介绍其中一些新发现,并讨论IKKβ特异性抑制剂作为新型肿瘤增敏剂的治疗潜力。

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