Kaltschmidt Barbara, Witte Kaya E, Greiner Johannes F W, Weissinger Florian, Kaltschmidt Christian
Molecular Neurobiology, Faculty of Biology, Bielefeld University, Universitätsstrasse 25, 33615 Bielefeld, Germany.
Forschungsverbund BioMedizin Bielefeld FBMB e.V., Maraweg 21, 33617 Bielefeld, Germany.
Biomedicines. 2022 Jan 25;10(2):261. doi: 10.3390/biomedicines10020261.
Among the cell populations existing within a tumor, cancer stem cells are responsible for metastasis formation and chemotherapeutic resistance. In the present review, we focus on the transcription factor NF-κB, which is present in every cell type including cancer stem cells. NF-κB is involved in pro-tumor inflammation by its target gene interleukin 1 (IL1) and can be activated by a feed-forward loop in an IL1-dependent manner. Here, we summarize current strategies targeting NF-κB by chemicals and biologicals within an integrated cancer therapy. Specifically, we start with a tyrosine kinase inhibitor targeting epidermal growth factor (EGF)-receptor-mediated phosphorylation. Furthermore, we summarize current strategies of multiple myeloma treatment involving lenalidomide, bortezomib, and dexamethasone as potential NF-κB inhibitors. Finally, we discuss programmed death-ligand 1 (PD-L1) as an NF-κB target gene and its role in checkpoint therapy. We conclude, that NF-κB inhibition by specific inhibitors of IκB kinase was of no clinical use but inhibition of upstream and downstream targets with drugs or biologicals might be a fruitful way to treat cancer stem cells.
在肿瘤内存在的细胞群体中,癌症干细胞负责转移的形成和化疗耐药性。在本综述中,我们聚焦于转录因子NF-κB,它存在于包括癌症干细胞在内的每种细胞类型中。NF-κB通过其靶基因白细胞介素1(IL1)参与促肿瘤炎症反应,并能以IL1依赖性方式通过前馈环被激活。在此,我们总结了在综合癌症治疗中通过化学物质和生物制剂靶向NF-κB的当前策略。具体而言,我们首先介绍一种靶向表皮生长因子(EGF)受体介导的磷酸化的酪氨酸激酶抑制剂。此外,我们总结了涉及来那度胺、硼替佐米和地塞米松作为潜在NF-κB抑制剂的多发性骨髓瘤治疗的当前策略。最后,我们讨论程序性死亡配体1(PD-L1)作为NF-κB靶基因及其在检查点治疗中的作用。我们得出结论,IκB激酶的特异性抑制剂对NF-κB的抑制在临床上并无用处,但用药物或生物制剂抑制其上游和下游靶点可能是治疗癌症干细胞的有效方法。