Rethinking Cancer Gene Identification through Graph Anomaly Analysis

Fuente: arXiv
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Main Authors: Zang, Yilong, Ren, Lingfei, Li, Yue, Wang, Zhikang, Selby, David Antony, Wang, Zheng, Vollmer, Sebastian Josef, Yin, Hongzhi, Song, Jiangning, Wu, Junhang
Format: Preprint
Published: 2024
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author Zang, Yilong
Ren, Lingfei
Li, Yue
Wang, Zhikang
Selby, David Antony
Wang, Zheng
Vollmer, Sebastian Josef
Yin, Hongzhi
Song, Jiangning
Wu, Junhang
author_facet Zang, Yilong
Ren, Lingfei
Li, Yue
Wang, Zhikang
Selby, David Antony
Wang, Zheng
Vollmer, Sebastian Josef
Yin, Hongzhi
Song, Jiangning
Wu, Junhang
contents Graph neural networks (GNNs) have shown promise in integrating protein-protein interaction (PPI) networks for identifying cancer genes in recent studies. However, due to the insufficient modeling of the biological information in PPI networks, more faithfully depiction of complex protein interaction patterns for cancer genes within the graph structure remains largely unexplored. This study takes a pioneering step toward bridging biological anomalies in protein interactions caused by cancer genes to statistical graph anomaly. We find a unique graph anomaly exhibited by cancer genes, namely weight heterogeneity, which manifests as significantly higher variance in edge weights of cancer gene nodes within the graph. Additionally, from the spectral perspective, we demonstrate that the weight heterogeneity could lead to the "flattening out" of spectral energy, with a concentration towards the extremes of the spectrum. Building on these insights, we propose the HIerarchical-Perspective Graph Neural Network (HIPGNN) that not only determines spectral energy distribution variations on the spectral perspective, but also perceives detailed protein interaction context on the spatial perspective. Extensive experiments are conducted on two reprocessed datasets STRINGdb and CPDB, and the experimental results demonstrate the superiority of HIPGNN.
format Preprint
id arxiv_https___arxiv_org_abs_2412_17240
institution arXiv
publishDate 2024
record_format arxiv
spellingShingle Rethinking Cancer Gene Identification through Graph Anomaly Analysis
Zang, Yilong
Ren, Lingfei
Li, Yue
Wang, Zhikang
Selby, David Antony
Wang, Zheng
Vollmer, Sebastian Josef
Yin, Hongzhi
Song, Jiangning
Wu, Junhang
Computational Engineering, Finance, and Science
Artificial Intelligence
Machine Learning
Graph neural networks (GNNs) have shown promise in integrating protein-protein interaction (PPI) networks for identifying cancer genes in recent studies. However, due to the insufficient modeling of the biological information in PPI networks, more faithfully depiction of complex protein interaction patterns for cancer genes within the graph structure remains largely unexplored. This study takes a pioneering step toward bridging biological anomalies in protein interactions caused by cancer genes to statistical graph anomaly. We find a unique graph anomaly exhibited by cancer genes, namely weight heterogeneity, which manifests as significantly higher variance in edge weights of cancer gene nodes within the graph. Additionally, from the spectral perspective, we demonstrate that the weight heterogeneity could lead to the "flattening out" of spectral energy, with a concentration towards the extremes of the spectrum. Building on these insights, we propose the HIerarchical-Perspective Graph Neural Network (HIPGNN) that not only determines spectral energy distribution variations on the spectral perspective, but also perceives detailed protein interaction context on the spatial perspective. Extensive experiments are conducted on two reprocessed datasets STRINGdb and CPDB, and the experimental results demonstrate the superiority of HIPGNN.
title Rethinking Cancer Gene Identification through Graph Anomaly Analysis
topic Computational Engineering, Finance, and Science
Artificial Intelligence
Machine Learning
url https://arxiv.org/abs/2412.17240