Learning chemical sensitivity reveals mechanisms of cellular response
Open accessPublished version of a preprint
Abstract
Chemical probes interrogate disease mechanisms at the molecular level by linking genetic changes to observable traits. However, comprehensive chemical screens in diverse biological models are impractical. To address this challenge, we develop ChemProbe, a model that predicts cellular sensitivity to hundreds of molecular probes and drugs by learning to combine transcriptomes and chemical structures. Using ChemProbe, we infer the chemical sensitivity of cancer cell lines and tumor samples and analyze how the model makes predictions. We retrospectively evaluate drug response predictions for precision breast cancer treatment and prospectively validate chemical sensitivity predictions in new cellular models, including a genetically modified cell line. Our model interpretation analysis identifies transcriptome features reflecting compound targets and protein network modules, identifying genes that drive ferroptosis. ChemProbe is an interpretable in silico screening tool that allows researchers to measure cellular response to diverse compounds, facilitating research into molecular mechanisms of chemical sensitivity.
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Cites
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Ribosome stalling during selenoprotein translation exposes a ferroptosis vulnerability
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- Authors
- Connell, W., Garcia, K., Goodarzi, H., & Keiser, M. J.
- Affiliations
- University of California, San Francisco (US)
- Corresponding author
- Keiser, Michael J.
- Venue
- Communications Biology
- Published
- 2024-09-15
- Volume
- 7
- Issue
- 1
- Pages
- 1149-1149
- ISSN
- 2399-3642 (ISSN-L)
- PMC
- PMC11402971
- OpenAlex
- W4402552237
- Cited by
- 4
- References
- 6
- Citations by year
- 2026: 2 · 2025: 2
- FWCI
- 0.85
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Locations
- Communications Biology (publishedVersion, cc-by)
- bioRxiv (Cold Spring Harbor Laboratory) (acceptedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- eScholarship (California Digital Library) (submittedVersion, cc-by)
- PubMed Central (submittedVersion, cc-by)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion)
- Funders
- U.S. Department of Health and Human Services (U01 MH115747-02)
- Silicon Valley Community Foundation (DAF2018-191905, 10.13039/100014989)
- Chan Zuckerberg Initiative (DAF2018-191905)
- National Institutes of Health
- National Institute of Mental Health (U01MH115747)
- National Institute of General Medical Sciences (P41GM103504)
- Topics
- Physical Sciences › Computer Science › Computational Theory and Mathematics › Computational Drug Discovery Methods
- Health Sciences › Medicine › Pulmonary and Respiratory Medicine › Ferroptosis and cancer prognosis
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Gene expression and cancer classification
- Keywords
- chemosensitivity, drug response prediction, cancer cell lines, tumor samples, ferroptosis, model interpretability, compound targets, virtual screening
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