Identifying gene regulation modules associated with tumor metastasis using a network decomposition approach and combinatorial fusion analysis
Aninda Astuti,
Christina Schweikert,
Chia-Wei Weng,
Derbiau Frank Hsu and
Ka-Lok Ng
PLOS ONE, 2026, vol. 21, issue 6, 1-22
Abstract:
We systematically evaluated whether modular decomposition of molecular networks into gene regulatory modules (GRMs) enables the identification of metastasis‑associated genes. We developed an efficient bioinformatics framework that integrates subgraph extraction with combinatorial fusion analysis (CFA) to identify and prioritize metastasis‑associated GRMs in cancer networks. We validated top‑ranked GRMs using cancer hallmark annotations, enrichment analysis, drug–target associations, and survival data, and assessed GRM cooperativity through comparisons with prior metastasis studies. The proposed approach consistently outperformed existing methods in identifying metastasis‑associated GRMs. Robustness analyses across ten feature combinations and comparisons between three‑node and four‑node GRMs confirmed stable performance under diverse settings. Application to three independent KIRC metastasis cohorts further demonstrated improved identification of metastasis‑related GRMs. Overall, this integrated GRM‑based framework reliably captures coordinated regulatory patterns linked to metastasis and shows potential for identifying clinically relevant target genes and therapeutic drug candidates.
Date: 2026
References: Add references at CitEc
Citations:
Downloads: (external link)
https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0337873 (text/html)
https://journals.plos.org/plosone/article/file?id= ... 37873&type=printable (application/pdf)
Related works:
This item may be available elsewhere in EconPapers: Search for items with the same title.
Export reference: BibTeX
RIS (EndNote, ProCite, RefMan)
HTML/Text
Persistent link: https://EconPapers.repec.org/RePEc:plo:pone00:0337873
DOI: 10.1371/journal.pone.0337873
Access Statistics for this article
More articles in PLOS ONE from Public Library of Science
Bibliographic data for series maintained by plosone ().