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Network-driven cancer cell avatars for combination discovery and biomarker identification for DNA damage response inhibitors

Authors :
Orsolya Papp
Viktória Jordán
Szabolcs Hetey
Róbert Balázs
Valér Kaszás
Árpád Bartha
Nóra N. Ordasi
Sebestyén Kamp
Bálint Farkas
Jerome Mettetal
Jonathan R. Dry
Duncan Young
Ben Sidders
Krishna C. Bulusu
Daniel V. Veres
Source :
npj Systems Biology and Applications, Vol 10, Iss 1, Pp 1-15 (2024)
Publication Year :
2024
Publisher :
Nature Portfolio, 2024.

Abstract

Abstract Combination therapy is well established as a key intervention strategy for cancer treatment, with the potential to overcome monotherapy resistance and deliver a more durable efficacy. However, given the scale of unexplored potential target space and the resulting combinatorial explosion, identifying efficacious drug combinations is a critical unmet need that is still evolving. In this paper, we demonstrate a network biology-driven, simulation-based solution, the Simulated Cell™. Integration of omics data with a curated signaling network enables the accurate and interpretable prediction of 66,348 combination-cell line pairs obtained from a large-scale combinatorial drug sensitivity screen of 684 combinations across 97 cancer cell lines (BAC = 0.62, AUC = 0.7). We highlight drug combination pairs that interact with DNA Damage Response pathways and are predicted to be synergistic, and deep network insight to identify biomarkers driving combination synergy. We demonstrate that the cancer cell ‘avatars’ capture the biological complexity of their in vitro counterparts, enabling the identification of pathway-level mechanisms of combination benefit to guide clinical translatability.

Subjects

Subjects :
Biology (General)
QH301-705.5

Details

Language :
English
ISSN :
20567189
Volume :
10
Issue :
1
Database :
Directory of Open Access Journals
Journal :
npj Systems Biology and Applications
Publication Type :
Academic Journal
Accession number :
edsdoj.4b72d20225b452aa4515315182adc6b
Document Type :
article
Full Text :
https://doi.org/10.1038/s41540-024-00394-w