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National Institute of Environmental Health Sciences

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Publication Detail

Title: Irradiated esophageal cells are protected from radiation-induced recombination by MnSOD gene therapy.

Authors: Niu, Yunyun; Wang, Hong; Wiktor-Brown, Dominika; Rugo, Rebecca; Shen, Hongmei; Huq, M Saiful; Engelward, Bevin; Epperly, Michael; Greenberger, Joel S

Published In Radiat Res, (2010 Apr)

Abstract: Radiation-induced DNA damage is a precursor to mutagenesis and cytotoxicity. During radiotherapy, exposure of healthy tissues can lead to severe side effects. We explored the potential of mitochondrial SOD (MnSOD) gene therapy to protect esophageal, pancreatic and bone marrow cells from radiation-induced genomic instability. Specifically, we measured the frequency of homologous recombination (HR) at an integrated transgene in the Fluorescent Yellow Direct Repeat (FYDR) mice, in which an HR event can give rise to a fluorescent signal. Mitochondrial SOD plasmid/liposome complex (MnSOD-PL) was administered to esophageal cells 24 h prior to 29 Gy upper-body irradiation. Single cell suspensions from FYDR, positive control FYDR-REC, and negative control C57BL/6NHsd (wild-type) mouse esophagus, pancreas and bone marrow were evaluated by flow cytometry. Radiation induced a statistically significant increase in HR 7 days after irradiation compared to unirradiated FYDR mice. MnSOD-PL significantly reduced the induction of HR by radiation at day 7 and also reduced the level of HR in the pancreas. Irradiation of the femur and tibial marrow with 8 Gy also induced a significant increase in HR at 7 days. Radioprotection by intraesophageal administration of MnSOD-PL was correlated with a reduced level of radiation-induced HR in esophageal cells. These results demonstrate the efficacy of MnSOD-PL for suppressing radiation-induced HR in vivo.

PubMed ID: 20334517 Exiting the NIEHS site

MeSH Terms: Animals; Body Burden; Esophagus/drug effects; Esophagus/physiopathology*; Esophagus/radiation effects*; Female; Genetic Therapy/methods; Genomic Instability/drug effects*; Genomic Instability/radiation effects*; Male; Mice; Mitochondria/enzymology*; Radiation Injuries/etiology; Radiation Injuries/genetics; Radiation Injuries/prevention & control; Radiation Tolerance/drug effects; Superoxide Dismutase/genetics; Superoxide Dismutase/therapeutic use*; Treatment Outcome; Whole-Body Irradiation/adverse effects

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