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dc.contributor.authorBooth, Catherine
dc.contributor.authorBooth, Dawn
dc.contributor.authorWilliamson, S
dc.contributor.authorDemchyshyn, L L
dc.contributor.authorPotten, Christopher S
dc.date.accessioned2009-08-21T10:33:38Z
dc.date.available2009-08-21T10:33:38Z
dc.date.issued2004-12
dc.identifier.citationTeduglutide ([Gly2]GLP-2) protects small intestinal stem cells from radiation damage. 2004, 37 (6):385-400 Cell Prolif.en
dc.identifier.issn0960-7722
dc.identifier.pmid15548172
dc.identifier.doi10.1111/j.1365-2184.2004.00320.x
dc.identifier.urihttp://hdl.handle.net/10541/78153
dc.description.abstractGlucagon-like peptide-2 and its dipeptidyl peptidase (DP-IV) resistant analogue teduglutide are trophic for the gastrointestinal epithelium. Exposure increases villus height and crypt size and results in increased overall intestinal weight. As these effects may be mediated through stimulation of the stem cell compartment, they may promote intestinal healing and act as potential anti-mucositis agents in patients undergoing cancer chemotherapy. A study was initiated to investigate the protective effects of teduglutide on the murine small intestinal epithelium following gamma-irradiation using the crypt microcolony assay as a measure of stem cell survival and functional competence. Teduglutide demonstrated intestinotrophic effects in both CD1 and BDF1 mouse strains. In BDF1 mice, subcutaneous injection of GLP-2 or teduglutide (0.2 mg/kg/day, b.i.d.) for 14 days increased intestinal weight by 28% and resulted in comparable increases in crypt size, villus height and area. Teduglutide given daily for 6 or 14 days prior to whole body, gamma-irradiation significantly increased crypt stem cell survival when compared with vehicle-treated controls. The mean levels of protection over a range of doses provided protection factors from 1.3 to 1.5. A protective effect was only observed when teduglutide was given before irradiation. These results suggest that teduglutide has the ability to modulate clonogenic stem cell survival in the small intestine and this may have a useful clinical application in the prevention of cancer therapy-induced mucositis.
dc.language.isoenen
dc.subject.meshAnimals
dc.subject.meshBiological Assay
dc.subject.meshCell Survival
dc.subject.meshCytoprotection
dc.subject.meshDose-Response Relationship, Drug
dc.subject.meshEpithelial Cells
dc.subject.meshGamma Rays
dc.subject.meshGlucagon-Like Peptide 2
dc.subject.meshGlucagon-Like Peptides
dc.subject.meshIntestine, Small
dc.subject.meshMale
dc.subject.meshMice
dc.subject.meshOrgan Size
dc.subject.meshPeptides
dc.subject.meshRadiation Injuries, Experimental
dc.subject.meshRadiation-Protective Agents
dc.subject.meshRadiotherapy
dc.subject.meshStem Cells
dc.titleTeduglutide ([Gly2]GLP-2) protects small intestinal stem cells from radiation damage.en
dc.typeArticleen
dc.contributor.departmentPaterson Institute for Cancer Research, Christie Hospital NHS Trust, Manchester, UK.en
dc.identifier.journalCell Proliferationen
html.description.abstractGlucagon-like peptide-2 and its dipeptidyl peptidase (DP-IV) resistant analogue teduglutide are trophic for the gastrointestinal epithelium. Exposure increases villus height and crypt size and results in increased overall intestinal weight. As these effects may be mediated through stimulation of the stem cell compartment, they may promote intestinal healing and act as potential anti-mucositis agents in patients undergoing cancer chemotherapy. A study was initiated to investigate the protective effects of teduglutide on the murine small intestinal epithelium following gamma-irradiation using the crypt microcolony assay as a measure of stem cell survival and functional competence. Teduglutide demonstrated intestinotrophic effects in both CD1 and BDF1 mouse strains. In BDF1 mice, subcutaneous injection of GLP-2 or teduglutide (0.2 mg/kg/day, b.i.d.) for 14 days increased intestinal weight by 28% and resulted in comparable increases in crypt size, villus height and area. Teduglutide given daily for 6 or 14 days prior to whole body, gamma-irradiation significantly increased crypt stem cell survival when compared with vehicle-treated controls. The mean levels of protection over a range of doses provided protection factors from 1.3 to 1.5. A protective effect was only observed when teduglutide was given before irradiation. These results suggest that teduglutide has the ability to modulate clonogenic stem cell survival in the small intestine and this may have a useful clinical application in the prevention of cancer therapy-induced mucositis.


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