Dutta Pritha, Ma Lichun, Ali Yusuf, Sloot Peter M A, Zheng Jie
Interdisciplinary Graduate School, Nanyang Technogical University, Singapore, Republic of Singapore.
Biomedical Informatics Lab, School of Computer Science and Engineering, Nanyang Technological University, Singapore, Republic of Singapore.
BMC Syst Biol. 2019 Apr 5;13(Suppl 2):36. doi: 10.1186/s12918-019-0692-0.
Major alteration in lifestyle of human population has promoted Type 2 diabetes mellitus (T2DM) to the level of an epidemic. This metabolic disorder is characterized by insulin resistance and pancreatic β-cell dysfunction and apoptosis, triggered by endoplasmic reticulum (ER) stress, oxidative stress and cytokines. Computational modeling is necessary to consolidate information from various sources in order to obtain a comprehensive understanding of the pathogenesis of T2DM and to investigate possible interventions by performing in silico simulations.
In this paper, we propose a Boolean network model integrating the insulin resistance pathway with pancreatic β-cell apoptosis pathway which are responsible for T2DM. The model has five input signals, i.e. ER stress, oxidative stress, tumor necrosis factor α (TNF α), Fas ligand (FasL), and interleukin-6 (IL-6). We performed dynamical simulations using random order asynchronous update and with different combinations of the input signals. From the results, we observed that the proposed model made predictions that closely resemble the expression levels of genes in T2DM as reported in the literature.
The proposed model can make predictions about expression levels of genes in T2DM that are in concordance with literature. Although experimental validation of the model is beyond the scope of this study, the model can be useful for understanding the aetiology of T2DM and discovery of therapeutic intervention for this prevalent complex disease. The files of our model and results are available at https://github.com/JieZheng-ShanghaiTech/boolean-t2dm .
人类生活方式的重大改变已将2型糖尿病(T2DM)提升至流行病水平。这种代谢紊乱的特征是胰岛素抵抗以及胰腺β细胞功能障碍和凋亡,由内质网(ER)应激、氧化应激和细胞因子引发。计算建模对于整合来自各种来源的信息是必要的,以便全面了解T2DM的发病机制,并通过进行计算机模拟来研究可能的干预措施。
在本文中,我们提出了一个布尔网络模型,该模型整合了与T2DM相关的胰岛素抵抗途径和胰腺β细胞凋亡途径。该模型有五个输入信号,即ER应激、氧化应激、肿瘤坏死因子α(TNFα)、Fas配体(FasL)和白细胞介素-6(IL-6)。我们使用随机顺序异步更新并结合不同的输入信号组合进行了动态模拟。从结果中,我们观察到所提出的模型做出的预测与文献中报道的T2DM中基因的表达水平非常相似。
所提出的模型可以对T2DM中基因的表达水平做出与文献一致的预测。尽管对该模型进行实验验证超出了本研究的范围,但该模型对于理解T2DM的病因以及发现针对这种常见复杂疾病的治疗干预措施可能是有用的。我们模型和结果的文件可在https://github.com/JieZheng-ShanghaiTech/boolean-t2dm获取。