Greten Florian R, Karin Michael
Laboratory of Gene Regulation and Signal Transduction, Department of Pharmacology, School of Medicine, University of California, San Diego, 9500 Gilman Drive, La Jolla, CA 92093-0636, USA.
Cancer Lett. 2004 Apr 8;206(2):193-9. doi: 10.1016/j.canlet.2003.08.029.
The importance of the IkappaB kinase (IKK)/NF-kappaB signaling pathway in immunoregulatory functions is well accepted. However, the relevance of IKK and NF-kappaB in tumor maintenance, tumor promotion and possibly even in tumor initiation is becoming more evident. Activation of the IKK/NF-kappaB signaling pathway leads to the induction of target genes that can interfere with apoptosis, cell cycle regulation, cell invasion and metastatic growth as well as radio- and chemotherapy. By possibly bridging inflammation and cancer NF-kappaB might also contribute to tumorigenesis. Several natural compounds and synthetic drugs that are able to inhibit the IKK/NF-kappaB activation pathway have been shown to either prevent cancer or to inhibit cell growth in animal models. However, these compounds do not selectively inhibit any of the NF-kappaB activation pathways. Furthermore, general inhibition of NF-kappaB might lead to immunodeficiency. The investigation of the different NF-kappaB signaling pathways in different cell types and their role in certain diseases is therefore needed to evaluate the most successful therapeutic strategies.
IκB激酶(IKK)/核因子κB(NF-κB)信号通路在免疫调节功能中的重要性已得到广泛认可。然而,IKK和NF-κB在肿瘤维持、肿瘤促进甚至可能在肿瘤起始中的相关性正变得越来越明显。IKK/NF-κB信号通路的激活会导致靶基因的诱导,这些靶基因可干扰细胞凋亡、细胞周期调控、细胞侵袭和转移生长以及放疗和化疗。通过可能连接炎症和癌症,NF-κB也可能促进肿瘤发生。几种能够抑制IKK/NF-κB激活途径的天然化合物和合成药物已被证明在动物模型中要么预防癌症,要么抑制细胞生长。然而,这些化合物不会选择性地抑制任何一种NF-κB激活途径。此外,对NF-κB的普遍抑制可能导致免疫缺陷。因此,需要研究不同细胞类型中不同的NF-κB信号通路及其在某些疾病中的作用,以评估最成功的治疗策略。