Network-driven cancer cell avatars for combination discovery and biomarker identification for DNA damage response inhibitors.
Orsolya PappViktória JordánSzabolcs HeteyRóbert BalázsValér KaszásÁrpád BarthaNóra N OrdasiSebestyén KampBálint FarkasJay MettetalJonathan R DryDuncan YoungBen SiddersKrishna C BulusuDaniel V VeresPublished in: NPJ systems biology and applications (2024)
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.
Keyphrases
- human health
- risk assessment
- dna damage response
- combination therapy
- single cell
- randomized controlled trial
- dna repair
- small molecule
- stem cells
- mass spectrometry
- squamous cell carcinoma
- cancer therapy
- dna damage
- bone marrow
- papillary thyroid
- network analysis
- young adults
- squamous cell
- study protocol
- oxidative stress
- childhood cancer