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Mathematical Modelling of the Function of Ubiquitylation in TNFR1-Mediated NF-kappaB Signalling

机译:TNFR1介导的NF-κB信号传导中泛力的数学建模

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The tumor necrosis factor receptor 1 (TNFR1) pathway plays a crucial role in immune signalling and development by controlling cell growth and death [7]. The binding of tumor necrosis factor-alpha (TNFalpha) to TNFR1 can either trigger two different forms of cell death - apoptosis and necroptosis - or promote cell survival due to the activation of the transcription factor nuclear factor-kappaB (NF-kappaB) [5]. A dysregulation of this pathway can result in chronic diseases and cancer-related inflammation and features a strictly controlled regulatory network [6]. Therefore, the logic of the pathway regulation is of interest for cancer research to recognise the mechanisms that determine the outcome of death receptor stimulation.
机译:肿瘤坏死因子受体1(TNFR1)途径通过控制细胞生长和死亡对免疫信号传导和发育起到至关重要的作用[7]。肿瘤坏死因子-α-α(TNFalpha)与TNFr1的结合可以引发两种不同形式的细胞死亡 - 细胞凋亡和死亡,或促进由于转录因子核因子-κB(NF-Kappab)的激活而促进细胞存活[5 ]。该途径的疑虑可能导致慢性疾病和癌症相关的炎症,并具有严格控制的监管网络[6]。因此,途径调节的逻辑对癌症研究感兴趣,以识别确定死亡受体刺激结果的机制。

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