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A new class of molecular targeted radioprotectors: GSK-3beta inhibitors.
- Source :
-
International journal of radiation oncology, biology, physics [Int J Radiat Oncol Biol Phys] 2010 Feb 01; Vol. 76 (2), pp. 557-65. - Publication Year :
- 2010
-
Abstract
- 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 3beta (GSK-3beta)-SB216763 or SB415286-as radioprotective agents to attenuate intestinal injury.<br />Methods and Materials: A survival study was done by use of C57BL/6J mice to evaluate the radioprotective effect of GSK-3beta 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 beta-catenin, Bcl-2, Bax, and caspase 3 were done by use of Rat intestinal epithelial cell line IEC-6 cells.<br />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-3beta 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.<br />Conclusions: Glycogen synthase kinase 3beta 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-3beta inhibitors reduce deleterious consequences of intestinal irradiation and thereby improve quality of life during radiation therapy.<br /> (Copyright 2010 Elsevier Inc. All rights reserved.)
- Subjects :
- Animals
Apoptosis
Caspase 3 analysis
Cell Line
Cell Survival
Glycogen Synthase Kinase 3 beta
In Situ Nick-End Labeling methods
Mice
Mice, Inbred C57BL
Radiation Injuries, Experimental metabolism
Rats
bcl-2-Associated X Protein analysis
beta Catenin analysis
Aminophenols pharmacology
Glycogen Synthase Kinase 3 antagonists & inhibitors
Indoles pharmacology
Intestines radiation effects
Maleimides pharmacology
Radiation Injuries, Experimental prevention & control
Radiation-Protective Agents pharmacology
Subjects
Details
- Language :
- English
- ISSN :
- 1879-355X
- Volume :
- 76
- Issue :
- 2
- Database :
- MEDLINE
- Journal :
- International journal of radiation oncology, biology, physics
- Publication Type :
- Academic Journal
- Accession number :
- 20117291
- Full Text :
- https://doi.org/10.1016/j.ijrobp.2009.09.024