MONet: cancer driver gene identification algorithm based on integrated analysis of multi-omics data and network models.

IF 2.8 4区 医学 Q2 MEDICINE, RESEARCH & EXPERIMENTAL
Experimental Biology and Medicine Pub Date : 2025-02-04 eCollection Date: 2025-01-01 DOI:10.3389/ebm.2025.10399
Yingzan Ren, Tiantian Zhang, Jian Liu, Fubin Ma, Jiaxin Chen, Ponian Li, Guodong Xiao, Chuanqi Sun, Yusen Zhang
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引用次数: 0

Abstract

Cancer progression is orchestrated by the accrual of mutations in driver genes, which endow malignant cells with a selective proliferative advantage. Identifying cancer driver genes is crucial for elucidating the molecular mechanisms of cancer, advancing targeted therapies, and uncovering novel biomarkers. Based on integrated analysis of Multi-Omics data and Network models, we present MONet, a novel cancer driver gene identification algorithm. Our method utilizes two graph neural network algorithms on protein-protein interaction (PPI) networks to extract feature vector representations for each gene. These feature vectors are subsequently concatenated and fed into a multi-layer perceptron model (MLP) to perform semi-supervised identification of cancer driver genes. For each mutated gene, MONet assigns the probability of being potential driver, with genes identified in at least two PPI networks selected as candidate driver genes. When applied to pan-cancer datasets, MONet demonstrated robustness across various PPI networks, outperforming baseline models in terms of both the area under the receiver operating characteristic curve and the area under the precision-recall curve. Notably, MONet identified 37 novel driver genes that were missed by other methods, including 29 genes such as APOBEC2, GDNF, and PRELP, which are corroborated by existing literature, underscoring their critical roles in cancer development and progression. Through the MONet framework, we successfully identified known and novel candidate cancer driver genes, providing biologically meaningful insights into cancer mechanisms.

MONet:基于多组学数据和网络模型集成分析的癌症驱动基因识别算法。
癌症的进展是由驱动基因突变的累积精心策划的,这些突变赋予恶性细胞选择性增殖优势。识别癌症驱动基因对于阐明癌症的分子机制、推进靶向治疗和发现新的生物标志物至关重要。基于多组学数据和网络模型的综合分析,我们提出了一种新的癌症驱动基因识别算法MONet。该方法利用蛋白质-蛋白质相互作用(PPI)网络上的两种图神经网络算法提取每个基因的特征向量表示。这些特征向量随后被连接并输入到多层感知器模型(MLP)中,以执行癌症驱动基因的半监督识别。对于每个突变基因,MONet分配了成为潜在驱动基因的概率,在至少两个PPI网络中识别的基因被选为候选驱动基因。当应用于泛癌症数据集时,MONet在各种PPI网络中表现出鲁棒性,在接受者工作特征曲线下的面积和精确召回率曲线下的面积方面都优于基线模型。值得注意的是,MONet发现了其他方法所遗漏的37个新的驱动基因,包括29个基因,如APOBEC2、GDNF和PRELP,这些基因得到了现有文献的证实,强调了它们在癌症发生和进展中的关键作用。通过MONet框架,我们成功地鉴定了已知的和新的候选癌症驱动基因,为癌症机制提供了具有生物学意义的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Experimental Biology and Medicine
Experimental Biology and Medicine 医学-医学:研究与实验
CiteScore
6.00
自引率
0.00%
发文量
157
审稿时长
1 months
期刊介绍: Experimental Biology and Medicine (EBM) is a global, peer-reviewed journal dedicated to the publication of multidisciplinary and interdisciplinary research in the biomedical sciences. EBM provides both research and review articles as well as meeting symposia and brief communications. Articles in EBM represent cutting edge research at the overlapping junctions of the biological, physical and engineering sciences that impact upon the health and welfare of the world''s population. Topics covered in EBM include: Anatomy/Pathology; Biochemistry and Molecular Biology; Bioimaging; Biomedical Engineering; Bionanoscience; Cell and Developmental Biology; Endocrinology and Nutrition; Environmental Health/Biomarkers/Precision Medicine; Genomics, Proteomics, and Bioinformatics; Immunology/Microbiology/Virology; Mechanisms of Aging; Neuroscience; Pharmacology and Toxicology; Physiology; Stem Cell Biology; Structural Biology; Systems Biology and Microphysiological Systems; and Translational Research.
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