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Updated: May 28, 2026

Assessment of Global DNA Double-Strand End Resection using BrdU-DNA Labeling coupled with Cell Cycle Discrimination Imaging
Published on: April 28, 2021
Base excision repair targets for cancer therapy
1Gray Institute for Radiation Oncology and Biology, Department of Oncology, University of Oxford, Old Road Campus Research Building Roosevelt Drive, Oxford 0X3 7DQ, UK.
DNA repair maintains genome integrity but also protects cancer cells from treatments. This review examines the base excision repair pathway as a target for improving cancer therapy.
Area of Science:
- Molecular Biology
- Genetics
- Cancer Research
Background:
- Cellular DNA repair is crucial for maintaining genome stability and preventing diseases like cancer.
- DNA repair mechanisms, particularly in cancer cells, can counteract the effectiveness of chemotherapy and radiation therapy.
- The base excision repair (BER) pathway is a key component of cellular DNA repair.
Purpose of the Study:
- To critically examine the base excision repair (BER) pathway.
- To explore the mechanisms regulating BER capacity.
- To identify BER as a potential therapeutic target for enhancing cancer treatment efficacy.
Main Methods:
- Literature review of existing research on DNA repair pathways.
- Analysis of studies focusing on the base excision repair mechanism.
- Examination of regulatory factors influencing BER activity in normal and cancer cells.
Main Results:
- The base excision repair pathway is a significant contributor to DNA lesion repair.
- Dysregulation of BER can impact cancer development and progression.
- BER pathway components and regulatory mechanisms present viable targets for therapeutic intervention.
Conclusions:
- Targeting the base excision repair pathway offers a promising strategy to overcome cancer treatment resistance.
- Modulating BER capacity could enhance the efficacy of chemotherapy and radiotherapy.
- Further research into BER regulation is warranted for novel cancer therapy development.
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