Quantifying tumor specificity using Bayesian probabilistic modeling for drug and immunotherapeutic target discovery

In diseases such as cancer, the design of new therapeutic strategies requires extensive, costly, and unfortunately sometimes deadly testing to reveal life threatening off-target effects. We hypothesized that the disease specificity of targets can be systematically learned for all genes by jointly evaluating complementary molecular measurements of healthy tissues using a hierarchical Bayesian modeling approach. Our method, BayesTS, integrates protein and gene expression evidence and includes tunable parameters to moderate tissue essentiality. Applied to all protein coding genes, BayesTS outperforms alternative strategies to define therapeutic targets and nominates previously unknown targets while allowing for incorporation of new types of modalities. To expand target repertoires, we show that extension of BayesTS to splicing antigens and combinatorial target pairs results in more specific targets for therapy. We expect that BayesTS will facilitate improved target prioritization for oncology drug development, ultimately leading to the discovery of more effective and safer treatments.

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Publication Details

Journal
Cell Reports Methods
Published
2024-11-01
DOI
https://doi.org/10.1016/j.crmeth.2024.100900
Citations
3
Primary Topic
Computational Drug Discovery Methods
Type
article
Field-Weighted Citation Impact
1.08

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article

Quantifying tumor specificity using Bayesian probabilistic modeling for drug and immunotherapeutic target discovery

Mark Yarmarkovich, Daniel Schnell, Anukana Bhattacharjee, Nathan Salomonis et al.
3 citations
Cell Reports Methods
Computational Drug Discovery Methods
1.08
article

Quantifying tumor specificity using Bayesian probabilistic modeling for drug and immunotherapeutic target discovery

Mark Yarmarkovich, Daniel Schnell, Anukana Bhattacharjee, Nathan Salomonis, Guangyuan Li
article en
3 citations

Abstract

In diseases such as cancer, the design of new therapeutic strategies requires extensive, costly, and unfortunately sometimes deadly testing to reveal life threatening off-target effects. We hypothesized that the disease specificity of targets can be systematically learned for all genes by jointly evaluating complementary molecular measurements of healthy tissues using a hierarchical Bayesian modeling approach. Our method, BayesTS, integrates protein and gene expression evidence and includes tunable parameters to moderate tissue essentiality. Applied to all protein coding genes, BayesTS outperforms alternative strategies to define therapeutic targets and nominates previously unknown targets while allowing for incorporation of new types of modalities. To expand target repertoires, we show that extension of BayesTS to splicing antigens and combinatorial target pairs results in more specific targets for therapy. We expect that BayesTS will facilitate improved target prioritization for oncology drug development, ultimately leading to the discovery of more effective and safer treatments.

Cell Reports MethodsVol. 4(11)
Cincinnati Children's Hospital Medical Center (US), New York University (US), University of Cincinnati (US), University of Cincinnati Medical Center (US)
Cincinnati Children's Hospital Medical Center, National Institutes of Health
Openalex Percentile: Top 19%
Computational Drug Discovery Methods
1.08
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