Concetti Julia, Wilson Caroline L
Newcastle Fibrosis Research Group, Institute of Cellular Medicine, Newcastle University, Newcastle upon Tyne, Tyne and Wear NE2 4HH, UK.
Cells. 2018 Sep 7;7(9):133. doi: 10.3390/cells7090133.
Current evidence strongly suggests that aberrant activation of the NF-κB signalling pathway is associated with carcinogenesis. A number of key cellular processes are governed by the effectors of this pathway, including immune responses and apoptosis, both crucial in the development of cancer. Therefore, it is not surprising that dysregulated and chronic NF-κB signalling can have a profound impact on cellular homeostasis. Here we discuss NFKB1 (p105/p50), one of the five subunits of NF-κB, widely implicated in carcinogenesis, in some cases driving cancer progression and in others acting as a tumour-suppressor. The complexity of the role of this subunit lies in the multiple dimeric combination possibilities as well as the different interacting co-factors, which dictate whether gene transcription is activated or repressed, in a cell and organ-specific manner. This review highlights the multiple roles of NFKB1 in the development and progression of different cancers, and the considerations to make when attempting to manipulate NF-κB as a potential cancer therapy.
目前的证据有力地表明,NF-κB信号通路的异常激活与癌症发生有关。该信号通路的效应器调控着许多关键的细胞过程,包括免疫反应和细胞凋亡,这两者在癌症发展过程中都至关重要。因此,NF-κB信号失调和长期激活会对细胞稳态产生深远影响也就不足为奇了。在此,我们讨论NFKB1(p105/p50),它是NF-κB的五个亚基之一,在癌症发生过程中广泛涉及,在某些情况下促进癌症进展,而在另一些情况下则起到肿瘤抑制作用。该亚基作用的复杂性在于其多种二聚体组合可能性以及不同的相互作用辅助因子,它们以细胞和器官特异性的方式决定基因转录是被激活还是被抑制。本综述重点介绍了NFKB1在不同癌症发生和发展中的多种作用,以及在尝试将NF-κB作为潜在癌症治疗手段时需要考虑的因素。