Abstract

Reactive oxygen species (ROS) are a group of short-lived, highly reactive, oxygen-containing molecules that can induce DNA damage and affect the DNA damage response (DDR). There is unequivocal pre-clinical and clinical evidence that ROS influence the genotoxic stress caused by chemotherapeutics agents and ionizing radiation. Recent studies have provided mechanistic insight into how ROS can also influence the cellular response to DNA damage caused by genotoxic therapy, especially in the context of Double Strand Breaks (DSBs). This has led to the clinical evaluation of agents modulating ROS in combination with genotoxic therapy for cancer, with mixed success so far. These studies point to context dependent outcomes with ROS modulator combinations with Chemotherapy and radiotherapy, indicating a need for additional pre-clinical research in the field. In this review, we discuss the current knowledge on the effect of ROS in the DNA damage response, and its clinical relevance.

Keywords

DNA damageReactive oxygen speciesContext (archaeology)Ionizing radiationCancer researchCancerGenotoxicityRadiation therapyDNA repairBiologyDNAOxidative stressCell biologyMedicineGeneticsBiochemistryToxicityInternal medicineIrradiation

MeSH Terms

AnimalsApoptosisDNA DamageDNA RepairHumansNeoplasmsReactive Oxygen SpeciesTumor Suppressor Protein p53

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Publication Info

Year
2018
Type
review
Volume
25
Pages
101084-101084
Citations
1943
Access
Closed

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Social media, news, blog, policy document mentions

Citation Metrics

1943
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26
Influential
1705
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Cite This

Upadhyayula Sai Srinivas, Bryce Wei Quan Tan, Balamurugan Vellayappan et al. (2018). ROS and the DNA damage response in cancer. Redox Biology , 25 , 101084-101084. https://doi.org/10.1016/j.redox.2018.101084

Identifiers

DOI
10.1016/j.redox.2018.101084
PMID
30612957
PMCID
PMC6859528

Data Quality

Data completeness: 90%