Evidence map›Paper›PMID 40814227›Full record

ArticleBriefings in bioinformatics2025

DeepGraphMut: a graph-based deep learning method for cancer prognosis using somatic mutation profile.

Aswin Jose, Akansha Srivastava, Ariba Ansari, Palakkad Krishnanunni Vinod

Abstract read
In one paragraph

Article in Briefings in bioinformatics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Aswin JoseCentre for Computational Natural Sciences and Bioinformatics, IIIT Hyderabad, Prof. C R Rao Road, Gachibowli, Hyderabad 500032, India.
Akansha SrivastavaCentre for Computational Natural Sciences and Bioinformatics, IIIT Hyderabad, Prof. C R Rao Road, Gachibowli, Hyderabad 500032, India.
Ariba AnsariCentre for Computational Natural Sciences and Bioinformatics, IIIT Hyderabad, Prof. C R Rao Road, Gachibowli, Hyderabad 500032, India.
Palakkad Krishnanunni VinodCentre for Computational Natural Sciences and Bioinformatics, IIIT Hyderabad, Prof. C R Rao Road, Gachibowli, Hyderabad 500032, India.ORCID 0000-0003-2968-498X

Funding

International Institute of Information Technology, Hyderabad
6 · The paper itself

Abstract

Cancer remains a leading cause of morbidity and mortality worldwide. Despite advances in genomics, identifying clinically relevant subtypes of cancer remains challenging due to its complex and heterogeneous nature. In this work, we propose DeepGraphMut (DGM), a novel graph-based deep-learning pipeline that integrates somatic mutation data with protein-protein interaction (PPI) networks. By employing a graph autoencoder with a graph attention layer and a node-level attention decoder, DGM generates patient-specific clinically relevant encodings for unsupervised and supervised tasks. We demonstrate the effectiveness of DGM across 16 cancer types comprising of 7352 samples from The Cancer Genome Atlas (TCGA). Unsupervised clustering reveals distinct subtypes with significant survival differences in 11 cancer types. In supervised analysis using a Cox regression model, DGM demonstrates excellent performance in predicting survival outcomes, achieving a high concordance index (C-index) value in the range of 0.7 across most cancers, underscoring its robust predictive performance using only somatic mutation data. Furthermore, DGM outperforms its lightweight variant and network-based stratification methods in both unsupervised and supervised analyses. In summary, this study presents a promising approach for cancer subtype identification and prognosis, especially in resource-limited settings where multi-omics data may not be readily available. By leveraging the strengths of graph learning and network biology, DGM offers a valuable tool for advancing personalized medicine.

Indexed as

Deep LearningMutationNeoplasmsComputational BiologyHumansPrognosisProtein Interaction Mapscancer subtype identificationgraph neural networkprotein–protein interaction networksomatic mutationsurvival prediction

Identifiers

PMID40814227
PMCPMC12354957

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.