Abstract 6423: DNA-encoded chemical library screening for glue discovery for oncology targets

Abstract There is considerable interest in the discovery of novel molecular glues that induce proximity between oncology targets and their modulators. Induced proximity can be used to degrade proteins by a range of mechanisms, including ubiquitination and trafficking to the proteasome. DNA-Encoded Chemical Library screening can readily be adapted to the discovery of glues, and we will describe case studies that exemplify how carefully designed screening campaigns with highly diverse encoded compound libraries can identify small molecules capable of inducing proximity. Case studies will include a small molecule discovered in a DEL screen against ATAD2 that is able to inappropriately dimerize ATAD2 thereby reducing its ability to bind to acetylated histones and an activator of the integrated stress response pathway that only binds to the eIF2b complex, not its isolated components, thereby stabilizing it. Citation Format: Anthony D. Keefe, Paolo A. Centrella, Zhen Chen, Matthew A. Clark, Paige Dickson, Marie-Aude Guie, John P. Guilinger, Ying Zhang. DNA-encoded chemical library screening for glue discovery for oncology targets [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 1 (Regular Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(7 Suppl):Abstract nr 6423.

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Journal
Cancer Research
Published
2026-04-03
DOI
https://doi.org/10.1158/1538-7445.am2026-6423
Primary Topic
Protein Degradation and Inhibitors
Type
article
Field-Weighted Citation Impact
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article

Abstract 6423: DNA-encoded chemical library screening for glue discovery for oncology targets

Anthony D. Keefe, John P. Guilinger, Paige Dickson, Marie-Aude Guié et al.
Cancer Research
Protein Degradation and Inhibitors
article

Abstract 6423: DNA-encoded chemical library screening for glue discovery for oncology targets

Anthony D. Keefe, John P. Guilinger, Paige Dickson, Marie-Aude Guié, Ying Zhang, Zhen Chen, Matthew A. Clark
article en

Abstract

Abstract There is considerable interest in the discovery of novel molecular glues that induce proximity between oncology targets and their modulators. Induced proximity can be used to degrade proteins by a range of mechanisms, including ubiquitination and trafficking to the proteasome. DNA-Encoded Chemical Library screening can readily be adapted to the discovery of glues, and we will describe case studies that exemplify how carefully designed screening campaigns with highly diverse encoded compound libraries can identify small molecules capable of inducing proximity. Case studies will include a small molecule discovered in a DEL screen against ATAD2 that is able to inappropriately dimerize ATAD2 thereby reducing its ability to bind to acetylated histones and an activator of the integrated stress response pathway that only binds to the eIF2b complex, not its isolated components, thereby stabilizing it. Citation Format: Anthony D. Keefe, Paolo A. Centrella, Zhen Chen, Matthew A. Clark, Paige Dickson, Marie-Aude Guie, John P. Guilinger, Ying Zhang. DNA-encoded chemical library screening for glue discovery for oncology targets [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 1 (Regular Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(7 Suppl):Abstract nr 6423.

Cancer ResearchVol. 86(7_Supplement)
Arcon (United States) (US)
Openalex Percentile: Top 9%
Protein Degradation and Inhibitors
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