A New Class of Molecular Targeted Radioprotectors: GSK-3β Inhibitors
Creators
- 1. Department of Radiation Oncology, Vanderbilt University School of Medicine, Nashville, TN (United States)
- 2. Medical Scientist Training Program, Vanderbilt University School of Medicine, Nashville, TN (United States)
- 3. Department of Radiation Oncology, Mallinckrodt Institute of Radiology, Washington University, St Louis, MO (United States)
- 4. Siteman Cancer Center, Washington University, St Louis, MO (United States)
- 5. Vanderbilt-Ingram Cancer Center, Vanderbilt University School of Medicine, Nashville, TN (United States)
Description
Purpose: Development of new treatments is critical to effective protection against radiation-induced injury. We investigate the potential of developing small-molecule inhibitors of glycogen synthase kinase 3β (GSK-3β)-SB216763 or SB415286-as radioprotective agents to attenuate intestinal injury. Methods and Materials: A survival study was done by use of C57BL/6J mice to evaluate the radioprotective effect of GSK-3β inhibitors. Terminal deoxynucleotidyl transferase dUTP nick end labelling (TUNEL) assay and immunohistochemical staining for Bax and Bcl-2 were used to assess apoptosis in the small intestines of the treated mice. A clonogenic survival study, apoptosis assays (staining with annexin V or 4',6-diamidino-2-phenylindole), and immunoblot analysis of β-catenin, Bcl-2, Bax, and caspase 3 were done by use of Rat intestinal epithelial cell line IEC-6 cells. Results: Pretreatment with SB415286 significantly improved survival of mice irradiated with 8 and 12 Gy. Mice pretreated with SB216763 or SB415286 showed a significant reduction in TUNEL- and Bax-positive cells and an increase in Bcl-2-positive cells in intestinal crypts at 4 and/or 12 h after radiation with 4 and/or 8 Gy compared with radiation alone. Pretreatment of irradiated IEC-6 cells with GSK-3β inhibitors significantly increased clonogenic survival compared with cells treated with radiation alone. This increase was due to the attenuation of radiation-induced apoptosis, as shown by annexin V and 4',6-diamidino-2-phenylindole assays, as well as immunoblot analysis of Bcl-2, Bax, and caspase 3. Conclusions: Glycogen synthase kinase 3β small-molecule inhibitors protect mouse intestine from radiation-induced damage in cell culture and in vivo and improve survival of mice. Molecular mechanisms of this protection involve attenuated radiation-induced apoptosis regulated by Bcl-2, Bax, and caspase 3. Therefore GSK-3β inhibitors reduce deleterious consequences of intestinal irradiation and thereby improve quality of life during radiation therapy.
Availability note (English)
Available from http://dx.doi.org/10.1016/j.ijrobp.2009.09.024Additional details
Identifiers
- DOI
- 10.1016/j.ijrobp.2009.09.024;
- PII
- S0360-3016(09)03220-9;
Publishing Information
- Journal Title
- International Journal of Radiation Oncology, Biology and Physics
- Journal Volume
- 76
- Journal Issue
- 2
- Journal Page Range
- p. 557-565
- ISSN
- 0360-3016
- CODEN
- IOBPD3
INIS
- Country of Publication
- United States
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 41102528
- Subject category
- S63: RADIATION, THERMAL, AND OTHER ENVIRONMENTAL POLLUTANT EFFECTS ON LIVING ORGANISMS AND BIOLOGICAL MATERIALS; S62: RADIOLOGY AND NUCLEAR MEDICINE;
- Descriptors DEI
- APOPTOSIS; GLYCOGEN; MICE; RADIATION PROTECTION; RADIOPROTECTIVE SUBSTANCES; RADIOTHERAPY; SMALL INTESTINE; STANDARD OF LIVING
- Descriptors DEC
- ANIMALS; BODY; CARBOHYDRATES; DIGESTIVE SYSTEM; DRUGS; GASTROINTESTINAL TRACT; INTESTINES; MAMMALS; MEDICINE; NUCLEAR MEDICINE; ORGANIC COMPOUNDS; ORGANS; POLYSACCHARIDES; RADIOLOGY; RESPONSE MODIFYING FACTORS; RODENTS; SACCHARIDES; THERAPY; VERTEBRATES
Optional Information
- Copyright
- Copyright (c) 2010 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.