Han Mingfei, Chen Xiaoqing, Li Xiao, Ma Jie, Chen Tao, Yang Chunyuan, Wang Juan, Li Yingxing, Guo Wenting, Zhu Yunping
State Key Laboratory of Medical Proteomics, Beijing Proteome Research Center, National Center for Protein Sciences (Beijing), Beijing Institute of Lifeomics, No. 38, Life Science Park Road, Changping District, Beijing 102206, China.
Central Research Laboratory, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, No. 1 Shuaifuyuan Wangfujing Dongcheng District, Beijing 100730, China.
Brief Bioinform. 2025 Mar 4;26(2). doi: 10.1093/bib/bbaf081.
Gene expression involves complex interactions between DNA, RNA, proteins, and small molecules. However, most existing molecular networks are built on limited interaction types, resulting in a fragmented understanding of gene regulation. Here, we present MulNet, a framework that organizes diverse molecular interactions underlying gene expression data into a scalable multilayer network. Additionally, MulNet can accurately identify gene modules and key regulators within this network. When applied across diverse cancer datasets, MulNet outperformed state-of-the-art methods in identifying biologically relevant modules. MulNet analysis of RNA-seq data from colon cancer revealed numerous well-established cancer regulators and a promising new therapeutic target, miR-8485, along with several downstream pathways it governs to inhibit tumor growth. MulNet analysis of single-cell RNA-seq data from head and neck cancer revealed intricate communication networks between fibroblasts and malignant cells mediated by transcription factors and cytokines. Overall, MulNet enables high-resolution reconstruction of intra- and intercellular communication from both bulk and single-cell data. The MulNet code and application are available at https://github.com/free1234hm/MulNet.
基因表达涉及DNA、RNA、蛋白质和小分子之间的复杂相互作用。然而,大多数现有的分子网络是基于有限的相互作用类型构建的,导致对基因调控的理解支离破碎。在这里,我们提出了MulNet,这是一个将基因表达数据背后的各种分子相互作用组织成一个可扩展的多层网络的框架。此外,MulNet可以准确识别该网络中的基因模块和关键调节因子。当应用于各种癌症数据集时,MulNet在识别生物学相关模块方面优于现有最先进的方法。对来自结肠癌的RNA-seq数据进行MulNet分析,揭示了许多公认的癌症调节因子和一个有前景的新治疗靶点miR-8485,以及它所调控的几个抑制肿瘤生长的下游通路。对来自头颈癌的单细胞RNA-seq数据进行MulNet分析,揭示了由转录因子和细胞因子介导的成纤维细胞与恶性细胞之间复杂的通讯网络。总体而言,MulNet能够从批量数据和单细胞数据中对细胞内和细胞间通讯进行高分辨率重建。MulNet代码和应用可在https://github.com/free1234hm/MulNet上获取。