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NF-κB的协同因子导致放射抗性。

The Accomplices of NF-κB Lead to Radioresistance.

作者信息

Bai Miaomiao, Ma Xiaoxing, Li Xiaolei, Wang Xiaohui, Mei Qian, Li Xiang, Wu Zhiqiang, Han Weidong

机构信息

Department of Molecular Biology, Institute of Basic Medicine, School of Life Sciences, Chinese PLA General Hospital, Beijing 100853, China.

出版信息

Curr Protein Pept Sci. 2015;16(4):279-94. doi: 10.2174/138920371604150429152328.

DOI:10.2174/138920371604150429152328
PMID:25929862
Abstract

Ionizing radiation (IR) plays an important role in the treatment of epithelial tumors, such as lung and prostate cancer, by wounding and killing cancer cells. However, IR also activates sophisticated anti-apoptotic transcriptional factors such that cancer cells fail to repair DNA damage and obtain resistance to apoptosis under conditions of radiotherapy. Among these transcription factors, the transcription factor nuclear factor kappa B (NF-κB) is recognized as a key feature for protecting cells from apoptosis in most cell types. Moreover, the induction of radioresistance is mediated by several genes that are regulated by NF- κB. The primary purpose of this review is to introduce the studies of the signaling mechanisms of IR in NF-κB activation, such as ROS/NF-κB, ATM or DNA-PK/MAPKK/ p90rsk, PI3K/AKT/IKK and k-ras/c-raf/ MEKK/ NF-κB pathways. Moreover, we describe how the expression of the target genes (e.g., XIAP, A20, FLIP, Bcl-xL) are induced by NF-κB to regulate the activation of survival signaling pathways and to inhibit apoptotic signaling pathways. In addition, IR activates NF-κB to express cell cycle-specific genes, for example cyclin D1, which is associated with reinforcing radioresistance. We exhibit the signaling pathways that are induced by IR stimulation of NF-κB and illustrate the molecular mechanisms of radioresistance.

摘要

电离辐射(IR)通过损伤和杀死癌细胞,在肺癌和前列腺癌等上皮肿瘤的治疗中发挥着重要作用。然而,IR也会激活复杂的抗凋亡转录因子,导致癌细胞在放疗条件下无法修复DNA损伤并获得抗凋亡能力。在这些转录因子中,转录因子核因子κB(NF-κB)被认为是大多数细胞类型中保护细胞免于凋亡的关键因素。此外,辐射抗性的诱导是由几个受NF-κB调控的基因介导的。本综述的主要目的是介绍IR在NF-κB激活中的信号传导机制研究,如ROS/NF-κB、ATM或DNA-PK/MAPKK/p90rsk、PI3K/AKT/IKK和k-ras/c-raf/MEKK/NF-κB途径。此外,我们描述了NF-κB如何诱导靶基因(如XIAP、A20、FLIP、Bcl-xL)的表达,以调节生存信号通路的激活并抑制凋亡信号通路。此外,IR激活NF-κB以表达细胞周期特异性基因,例如细胞周期蛋白D1,这与增强辐射抗性有关。我们展示了由IR刺激NF-κB诱导的信号通路,并阐明了辐射抗性的分子机制。

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