Gene context-essentiality assessment supports precision oncology opportunities. The variability of gene effects inference from loss-of-function screenings across models and technologies limits identifying robust hits. We propose a computational framework named PRODE that integrates gene effects with protein-protein interactions to generate neighborhood-informed essential (NIE) and neighborhood-informed context essential (NICE) scores. It outperforms the canonical gene effect approach in recover- ing missed essential genes in shRNA screens and prioritizing context-essential hits from CRISPR-KO screens, as supported by in vitro validations. Applied to Her2 + breast cancer tumor samples, PRODE identifies oxidative phosphorylation genes as vulnerabilities with prognostic value, highlighting new therapeutic opportunities.
PRODE recovers essential and context-essential genes through neighborhood-informed scores / Cantore, Thomas; Gasperini, Paola; Bevilacqua, Riccardo; Ciani, Yari; Sinha, Sanju; Ruppin, Eytan; Demichelis, Francesca. - In: GENOME BIOLOGY. - ISSN 1474-760X. - 26:1(2025). [10.1186/s13059-025-03501-0]
PRODE recovers essential and context-essential genes through neighborhood-informed scores
Cantore, ThomasPrimo
;Gasperini, PaolaSecondo
;Bevilacqua, Riccardo;Ciani, Yari;Demichelis, Francesca
Ultimo
2025-01-01
Abstract
Gene context-essentiality assessment supports precision oncology opportunities. The variability of gene effects inference from loss-of-function screenings across models and technologies limits identifying robust hits. We propose a computational framework named PRODE that integrates gene effects with protein-protein interactions to generate neighborhood-informed essential (NIE) and neighborhood-informed context essential (NICE) scores. It outperforms the canonical gene effect approach in recover- ing missed essential genes in shRNA screens and prioritizing context-essential hits from CRISPR-KO screens, as supported by in vitro validations. Applied to Her2 + breast cancer tumor samples, PRODE identifies oxidative phosphorylation genes as vulnerabilities with prognostic value, highlighting new therapeutic opportunities.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione