| Literature DB >> 29502733 |
Masoud Najafi1, Mohsen Cheki2, Saeed Rezapoor3, Ghazale Geraily4, Elahe Motevaseli5, Carla Carnovale6, Emilio Clementi7, Alireza Shirazi4.
Abstract
The diabetes drug metformin can mitigate the genotoxic effects of cytotoxic agents and has been proposed to prevent or even cure certain cancers. Metformin reduces DNA damage by mechanisms that are only incompletely understood. Metformin scavenges free radicals, including reactive oxygen species and nitric oxide, which are produced by genotoxicants such as ionizing or non-ionizing radiation, heavy metals, and chemotherapeutic agents. The drug may also increase the activities of antioxidant enzymes and inhibit NADPH oxidase, cyclooxygenase-2, and inducible nitric oxide synthase, thereby limiting macrophage recruitment and inflammatory responses. Metformin stimulates the DNA damage response (DDR) in the homologous end-joining, homologous recombination, and nucleotide excision repair pathways. This review focuses on the protective properties of metformin against genomic instability.Entities:
Keywords: DNA damage; Oxidative stress; Reactive oxygen species
Mesh:
Substances:
Year: 2018 PMID: 29502733 DOI: 10.1016/j.mrgentox.2018.01.007
Source DB: PubMed Journal: Mutat Res Genet Toxicol Environ Mutagen ISSN: 1383-5718 Impact factor: 2.873