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Dig Dis Sci ; 49(3): 425-33, 2004 Mar.
Article in English | MEDLINE | ID: mdl-15139492

ABSTRACT

A strategy protecting the small intestine against deleterious side effects associated with anti-cancer therapy is arresting epithelial cell cycling temporally. Since endogenous glucagon-like peptide-2 (GLP-2) is a trophic factor specific for intestinal epithelia, the possibility of inhibiting GLP-2-mediated cell proliferation by lactoferrin, thereby protecting the small intestine against deleterious side effects of anticancer therapy, was investigated. In Caco-2 cells, GLP-2-mediated proliferation was reduced in a dose-dependent manner using lactoferrin. Furthermore, in a rat model for methotrexate-induced mucositis, lactoferrin reduced BrdU incorporation in small intestinal epithelial cells, indicating inhibition of epithelial cell proliferation in vivo. Subsequently, protection against methotrexate-induced intestinal damage was found in corresponding regions. These results show, for the first time, that lactoferrin interferes with GLP-2-induced intestinal epithelial proliferation. It may therefore be hypothesized that lactoferrin protects the intestine against anticancer therapy-induced intestinal damage, via inhibition of GLP-2-induced small intestinal epithelial cell proliferation.


Subject(s)
Antimetabolites, Antineoplastic/adverse effects , Cytoprotection/physiology , Intestinal Mucosa/drug effects , Lactoferrin/pharmacology , Methotrexate/adverse effects , Peptides/physiology , Animals , Bromodeoxyuridine/metabolism , Caco-2 Cells , Cell Division , Cells, Cultured , Disease Models, Animal , Dose-Response Relationship, Drug , Epithelial Cells/physiology , Female , Glucagon-Like Peptide 2 , Glucagon-Like Peptides , Humans , Polymerase Chain Reaction , Rats , Rats, Inbred Strains
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