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Updated: May 15, 2026

Visualizing and Quantifying Endonuclease-Based Site-Specific DNA Damage
Published on: August 21, 2021
Melatonin enhances DNA repair capacity possibly by affecting genes involved in DNA damage responsive pathways
Ran Liu1, Alan Fu, Aaron E Hoffman
1Key Laboratory of Environmental Medicine Engineering, Ministry of Education, School of Public Health, Southeast University, Nanjing, China.
Background:
Melatonin, a hormone-like substance involved in the regulation of the circadian rhythm, has been demonstrated to protect cells against oxidative DNA damage and to inhibit tumorigenesis.
Results:
In the current study, we investigated the effect of melatonin on DNA strand breaks using the alkaline DNA comet assay in breast cancer (MCF-7) and colon cancer (HCT-15) cell lines. Our results demonstrated that cells pretreated with melatonin had significantly shorter Olive tail moments compared to non-melatonin treated cells upon mutagen (methyl methanesulfonate, MMS) exposure, indicating an increased DNA repair capacity after melatonin treatment. We further examined the genome-wide gene expression in melatonin pretreated MCF-7 cells upon carcinogen exposure and detected altered expression of many genes involved in multiple DNA damage responsive pathways. Genes exhibiting altered expression were further analyzed for functional interrelatedness using network- and pathway-based bioinformatics analysis. The top functional network was defined as having relevance for "DNA Replication, Recombination, and Repair, Gene Expression, [and] Cancer".
Conclusions:
These findings suggest that melatonin may enhance DNA repair capacity by affecting several key genes involved in DNA damage responsive pathways.
Insights
Melatonin enhances DNA repair capacity in cancer cells. This hormone may boost the body's ability to fix DNA damage, potentially impacting cancer development.
Area of Science:
- Cell Biology
- Molecular Biology
- Cancer Research
Background:
- Melatonin regulates circadian rhythms and exhibits protective effects against oxidative DNA damage.
- Melatonin has demonstrated potential in inhibiting tumorigenesis.
Purpose of the Study:
- To investigate the effect of melatonin on DNA strand breaks in breast and colon cancer cell lines.
- To explore melatonin's impact on DNA repair mechanisms and gene expression following carcinogen exposure.
Main Methods:
- Alkaline DNA comet assay used to assess DNA strand breaks in MCF-7 and HCT-15 cells.
- Genome-wide gene expression analysis performed on melatonin-pretreated MCF-7 cells.
- Bioinformatics analysis to identify functional networks related to DNA damage response.
Main Results:
- Melatonin pretreatment significantly reduced DNA strand breaks (shorter Olive tail moments) after exposure to methyl methanesulfonate (MMS).
- Altered expression of numerous genes involved in DNA damage responsive pathways was observed in melatonin-treated cells.
- Bioinformatics analysis highlighted a key functional network related to DNA replication, recombination, repair, gene expression, and cancer.
Conclusions:
- Melatonin appears to enhance DNA repair capacity in cancer cells.
- The hormone's effect is mediated by influencing key genes within DNA damage responsive pathways.
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