Center for Systems Biology, Department of Bioinformatics, School of Biology and Basic Medical Sciences, Soochow University, Suzhou 215123, China.
State Key Laboratory of Radiation Medicine and Protection, Soochow University, Suzhou 215123, China.
Cells. 2021 Feb 16;10(2):402. doi: 10.3390/cells10020402.
Non-small-cell lung cancer (NSCLC) represents a heterogeneous group of malignancies that are the leading cause of cancer-related death worldwide. Although many NSCLC-related genes and pathways have been identified, there remains an urgent need to mechanistically understand how these genes and pathways drive NSCLC. Here, we propose a knowledge-guided and network-based integration method, called the node and edge Prioritization-based Community Analysis, to identify functional modules and their candidate targets in NSCLC. The protein-protein interaction network was prioritized by performing a random walk with restart algorithm based on NSCLC seed genes and the integrating edge weights, and then a "community network" was constructed by combining Girvan-Newman and Label Propagation algorithms. This systems biology analysis revealed that the -mediated network in the largest community provides a modular biomarker, the second community serves as a drug regulatory module, and the two are connected by some contextual signaling motifs. Moreover, integrating structural information into the signaling network suggested novel protein-protein interactions with therapeutic significance, such as interactions between and , , and . This study provides new mechanistic insights into the landscape of cellular functions in the context of modular networks and will help in developing therapeutic targets for NSCLC.
非小细胞肺癌(NSCLC)是一组异质性恶性肿瘤,是全球癌症相关死亡的主要原因。尽管已经确定了许多与 NSCLC 相关的基因和途径,但仍迫切需要从机制上了解这些基因和途径如何驱动 NSCLC。在这里,我们提出了一种基于知识和网络的整合方法,称为基于节点和边缘优先级的社区分析,以识别 NSCLC 中的功能模块及其候选靶标。通过基于 NSCLC 种子基因和整合边缘权重执行带重启动随机游走算法,对蛋白质-蛋白质相互作用网络进行优先级排序,然后通过结合 Girvan-Newman 和标签传播算法构建“社区网络”。这项系统生物学分析表明,最大社区中的 - 介导网络提供了一个模块化生物标志物,第二个社区充当药物调节模块,这两个模块通过一些上下文信号基序连接。此外,将结构信息整合到信号网络中,提示了具有治疗意义的新型蛋白质-蛋白质相互作用,例如 与 、 、 和 之间的相互作用。本研究为模块化网络背景下细胞功能的全貌提供了新的机制见解,并将有助于为 NSCLC 开发治疗靶点。