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Updated: Oct 20, 2025

Assessment of Global DNA Double-Strand End Resection using BrdU-DNA Labeling coupled with Cell Cycle Discrimination Imaging
Published on: April 28, 2021
DNA double-strand break repair in cancer: A path to achieving precision medicine
Taneisha Gillyard1, Jamaine Davis1
1Department of Biochemistry, Cancer Biology, Neuroscience and Pharmacology, Meharry Medical College, Nashville, TN, United States.
Abstract:
The assessment of DNA damage can be a significant diagnostic for precision medicine. DNA double strand break (DSBs) pathways in cancer are the primary targets in a majority of anticancer therapies, yet the molecular vulnerabilities that underlie each tumor can vary widely making the application of precision medicine challenging. Identifying and understanding these interindividual vulnerabilities enables the design of targeted DSB inhibitors along with evolving precision medicine approaches to selectively kill cancer cells with minimal side effects. A major challenge however, is defining exactly how to target unique differences in DSB repair pathway mechanisms. This review comprises a brief overview of the DSB repair mechanisms in cancer and includes results obtained with revolutionary advances such as CRISPR/Cas9 and machine learning/artificial intelligence, which are rapidly advancing not only our understanding of determinants of DSB repair choice, but also how it can be used to advance precision medicine. Scientific innovation in the methods used to diagnose and treat cancer is converging with advances in basic science and translational research. This revolution will continue to be a critical driver of precision medicine that will enable precise targeting of unique individual mechanisms. This review aims to lay the foundation for achieving this goal.
Insights
Precision medicine uses DNA damage assessments to target cancer. Understanding DNA double-strand break (DSB) repair vulnerabilities advances targeted therapies and selective cancer cell killing.
Area of Science:
- Oncology
- Genetics
- Bioinformatics
Background:
- DNA damage, particularly DNA double-strand breaks (DSBs), is a critical factor in cancer development and a primary target for anticancer therapies.
- Tumor-specific molecular vulnerabilities in DSB repair pathways present challenges for effective precision medicine applications.
- Interindividual differences in DSB repair mechanisms necessitate tailored therapeutic strategies for optimal cancer treatment.
Purpose of the Study:
- To review the mechanisms of DSB repair in cancer.
- To explore how advanced technologies like CRISPR/Cas9 and AI/machine learning enhance understanding of DSB repair choice.
- To lay the foundation for advancing precision medicine through precise targeting of individual cancer vulnerabilities.
Main Methods:
- Review of existing literature on DNA double-strand break repair pathways in cancer.
- Inclusion of recent findings from CRISPR/Cas9 gene editing technologies.
- Integration of insights from machine learning and artificial intelligence applications in cancer research.
Main Results:
- CRISPR/Cas9 and AI/machine learning are revolutionizing the understanding of determinants in DSB repair pathway choice.
- These advancements offer new avenues for identifying and targeting unique tumor vulnerabilities.
- Convergence of scientific innovation in diagnostics and therapeutics is driving precision medicine.
Conclusions:
- Precisely targeting unique individual mechanisms of DNA damage repair is key to advancing precision medicine in oncology.
- A deeper understanding of DSB repair variations enables the design of more effective and selective anticancer therapies.
- Continued innovation in basic and translational research is crucial for realizing the full potential of precision medicine.
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