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Antiproliferative Effects of Fluoxetine on Colon Cancer Cells and in a Colonic Carcinogen Mouse Model

Zitieren Sie bitte immer diese URN: urn:nbn:de:bvb:20-opus-75879
  • The antidepressant fluoxetine has been under discussion because of its potential influence on cancer risk. It was found to inhibit the development of carcinogen-induced preneoplastic lesions in colon tissue, but the mechanisms of action are not well understood. Therefore, we investigated anti-proliferative effects, and used HT29 colon tumor cells in vitro, as well as C57BL/6 mice exposed to intra-rectal treatment with the carcinogen N-methyl-N’-nitro-N-nitrosoguanidine (MNNG) as models. Fluoxetine increased the percentage of HT29 cells in theThe antidepressant fluoxetine has been under discussion because of its potential influence on cancer risk. It was found to inhibit the development of carcinogen-induced preneoplastic lesions in colon tissue, but the mechanisms of action are not well understood. Therefore, we investigated anti-proliferative effects, and used HT29 colon tumor cells in vitro, as well as C57BL/6 mice exposed to intra-rectal treatment with the carcinogen N-methyl-N’-nitro-N-nitrosoguanidine (MNNG) as models. Fluoxetine increased the percentage of HT29 cells in the G0/G1 phase of cell-cycle, and the expression of p27 protein. This was not related to an induction of apoptosis, reactive oxygen species or DNA damage. In vivo, fluoxetine reduced the development of MNNG-induced dysplasia and vascularization-related dysplasia in colon tissue, which was analyzed by histopathological techniques. An anti-proliferative potential of fluoxetine was observed in epithelial and stromal areas. It was accompanied by a reduction of VEGF expression and of the number of cells with angiogenic potential, such as CD133, CD34, and CD31-positive cell clusters. Taken together, our findings suggest that fluoxetine treatment targets steps of early colon carcinogenesis. This confirms its protective potential, explaining at least partially the lower colon cancer risk under antidepressant therapy.zeige mehrzeige weniger

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Metadaten
Autor(en): Vinicius Kannen, Henning Hintzsche, Dalila L. Zanette, Wilson A. Silva Jr., Sergio B. Garcia, Anna Maria Waaga-Gasser, Helga Stopper
URN:urn:nbn:de:bvb:20-opus-75879
Dokumentart:Artikel / Aufsatz in einer Zeitschrift
Institute der Universität:Medizinische Fakultät / Institut für Pharmakologie und Toxikologie
Sprache der Veröffentlichung:Englisch
Erscheinungsjahr:2012
Originalveröffentlichung / Quelle:In: PLoS One (2012) 7: 11, doi:10.1371/journal.pone.0050043
Allgemeine fachliche Zuordnung (DDC-Klassifikation):5 Naturwissenschaften und Mathematik / 54 Chemie / 540 Chemie und zugeordnete Wissenschaften
Normierte Schlagworte (GND):Medizin
Datum der Freischaltung:17.04.2013
Sammlungen:Open-Access-Publikationsfonds / Förderzeitraum 2012
Lizenz (Deutsch):License LogoCC BY: Creative-Commons-Lizenz: Namensnennung