Cancer Mutations Converge on a Collection of Protein Assemblies to Predict Resistance to Replication Stress

• Published in: Cancer discovery Vol. 14; no. 3; pp. 508 - 523
• Main Authors: Zhao, Xiaoyu, Singhal, Akshat, Park, Sungjoon, Kong, JungHo, Bachelder, Robin, Ideker, Trey
• Format: Journal Article
• Language: English
• Published: United States 01.03.2024
• Subjects: Cisplatin - pharmacology; Cisplatin - therapeutic use; Female; Humans; Machine Learning; Mutation; Signal Transduction; Uterine Cervical Neoplasms
• ISSN: 2159-8274; 2159-8290
• DOI: 10.1158/2159-8290.CD-23-0641

Rapid proliferation is a hallmark of cancer associated with sensitivity to therapeutics that cause DNA replication stress (RS). Many tumors exhibit drug resistance, however, via molecular pathways that are incompletely understood. Here, we develop an ensemble of predictive models that elucidate how cancer mutations impact the response to common RS-inducing (RSi) agents. The models implement recent advances in deep learning to facilitate multidrug prediction and mechanistic interpretation. Initial studies in tumor cells identify 41 molecular assemblies that integrate alterations in hundreds of genes for accurate drug response prediction. These cover roles in transcription, repair, cell-cycle checkpoints, and growth signaling, of which 30 are shown by loss-of-function genetic screens to regulate drug sensitivity or replication restart. The model translates to cisplatin-treated cervical cancer patients, highlighting an RTK-JAK-STAT assembly governing resistance. This study defines a compendium of mechanisms by which mutations affect therapeutic responses, with implications for precision medicine. Zhao and colleagues use recent advances in machine learning to study the effects of tumor mutations on the response to common therapeutics that cause RS. The resulting predictive models integrate numerous genetic alterations distributed across a constellation of molecular assemblies, facilitating a quantitative and interpretable assessment of drug response. This article is featured in Selected Articles from This Issue, p. 384.