Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2019 Jul:25:101084.
doi: 10.1016/j.redox.2018.101084. Epub 2018 Dec 21.

ROS and the DNA damage response in cancer

Affiliations
Review

ROS and the DNA damage response in cancer

Upadhyayula Sai Srinivas et al. Redox Biol. 2019 Jul.

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: Chemotherapy; DDR; DNA damage response; ROS; Radiotherapy; Reactive Oxygen Species.

PubMed Disclaimer

Figures

Fig. 1
Fig. 1
An overview of interactions between ROS and the DDR.

References

    1. Curtin N.J. DNA repair dysregulation from cancer driver to therapeutic target. Nat. Rev. Cancer. 2012;12(12):801–817. - PubMed
    1. Sancar A., Lindsey-Boltz L.A., Unsal-Kacmaz K., Linn S. Molecular mechanisms of mammalian DNA repair and the DNA damage checkpoints. Annu. Rev. Biochem. 2004;73:39–85. - PubMed
    1. Goldstein M., Kastan M.B. The DNA damage response: implications for tumor responses to radiation and chemotherapy. Annu. Rev. Med. 2015;66:129–143. - PubMed
    1. Ciccia A., Elledge S.J. The DNA damage response: making it safe to play with knives. Mol. Cell. 2010;40(2):179–204. - PMC - PubMed
    1. McNally J.P., Millen S.H., Chaturvedi V., Lakes N., Terrell C.E., Elfers E.E., Carroll K.R., Hogan S.P., Andreassen P.R., Kanter J. Manipulating DNA damage-response signaling for the treatment of immune-mediated diseases. Proc. Natl. Acad. Sci. USA. 2017;114(24):E4782–E4791. - PMC - PubMed

Publication types

Substances

LinkOut - more resources