Leveraging AI to automate detection and quantification of extrachromosomal DNA to decode drug responses

Introduction: Traditional drug discovery efforts primarily target rapid, reversible protein-mediated adaptations to counteract cancer cell resistance. However, cancer cells also utilize DNA-based strategies, often perceived as slow, irreversible changes like point mutations or drug-resistant clone selection. Extrachromosomal DNA (ecDNA), in contrast, represents a rapid, reversible, and predictable DNA alteration critical for cancer’s adaptive response. Methods: In this study, we developed a novel post-processing pipeline for automated detection and quantification of ecDNA in metaphase Fluorescence in situ Hybridization (FISH) images, leveraging the Microscopy Image Analyzer (MIA) tool. This pipeline is tailored to monitor ecDNA dynamics during drug treatment. Results: Our approach effectively quantified ecDNA changes, providing a robust framework for analyzing the adaptive responses of cancer cells under therapeutic pressure. Discussion: The pipeline not only serves as a valuable resource for automating ecDNA detection in metaphase FISH images but also highlights the role of ecDNA in facilitating swift and reversible adaptation to epigenetic remodeling agents such as JQ1.

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Publication Details

Journal
UNC Libraries
Published
2025-02-12
DOI
https://doi.org/10.17615/yxcy-1395
Primary Topic
Cancer Genomics and Diagnostics
Type
article
Field-Weighted Citation Impact
0.00

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article

Leveraging AI to automate detection and quantification of extrachromosomal DNA to decode drug responses

Elizabeth Brunk, Christina Ford, Oliver Cope, Jingting Chen et al.
UNC Libraries
Cancer Genomics and Diagnostics
article

Leveraging AI to automate detection and quantification of extrachromosomal DNA to decode drug responses

Elizabeth Brunk, Christina Ford, Oliver Cope, Jingting Chen, Kohen Goble, David Cheng, Yue Wang, Kriti Shukla, J H Fessler, William C. Dennis, Aarav Mehta, Nithya Gurumurthy, Damien Guilbaud, William Nenad
article en

Abstract

Introduction: Traditional drug discovery efforts primarily target rapid, reversible protein-mediated adaptations to counteract cancer cell resistance. However, cancer cells also utilize DNA-based strategies, often perceived as slow, irreversible changes like point mutations or drug-resistant clone selection. Extrachromosomal DNA (ecDNA), in contrast, represents a rapid, reversible, and predictable DNA alteration critical for cancer’s adaptive response. Methods: In this study, we developed a novel post-processing pipeline for automated detection and quantification of ecDNA in metaphase Fluorescence in situ Hybridization (FISH) images, leveraging the Microscopy Image Analyzer (MIA) tool. This pipeline is tailored to monitor ecDNA dynamics during drug treatment. Results: Our approach effectively quantified ecDNA changes, providing a robust framework for analyzing the adaptive responses of cancer cells under therapeutic pressure. Discussion: The pipeline not only serves as a valuable resource for automating ecDNA detection in metaphase FISH images but also highlights the role of ecDNA in facilitating swift and reversible adaptation to epigenetic remodeling agents such as JQ1.

UNC Libraries
University of North Carolina at Chapel Hill (US)
University of North Carolina at Chapel Hill, National Institute of General Medical Sciences
Zero hunger
Openalex Percentile: Top 97%
Cancer Genomics and Diagnostics
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