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Sensitization of 5-Fluorouracil-Resistant SNUC5 Colon Cancer Cells to Apoptosis by α-Mangostin
Biomolecules & Therapeutics ; : 604-609, 2016.
Article Dans Anglais | WPRIM | ID: wpr-209973
ABSTRACT
5-fluorouracil (5-FU) is a chemotherapeutic agent commonly used for treatment of solid tumors, including colorectal cancer. However, chemoresistance against 5-fluorouracil (5-FU) often limits its success for chemotherapy and, therefore, finding out appropriate adjuvant(s) that might overcome chemoresistance against 5-FU bears a significant importance. In the present study, we have found that α-mangostin can sensitize 5-FU-resistant SNUC5/5-FUR colon cancer cells to apoptosis. Exposure of α-mangostin induced significant DNA damages and increased the intracellular 8-hydroxyguanosine (8-OH-G) and 4-hydroxynonenal (4-HNE) levels in SNUC5 and SNUC5/5-FUR cells. Western blot analysis illustrated that α-mangostin-induced apoptosis was mediated by the activation of the extrinsic and intrinsic pathways in SNUC5/5-FUR cells. In particular, we observed that Fas receptor (FasR) level was lower in SNUC5/5-FUR cells, compared with SNUC5 cells and that silencing FasR attenuated α-mangostin-mediated apoptosis in SNUC5/5-FUR cells. Together, our study illustrates that α-mangostin might be an efficient apoptosis sensitizer that can overcome chemoresistance against 5-FU by activating apoptosis pathway.
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Texte intégral: Disponible Indice: WPRIM (Pacifique occidental) Sujet Principal: Altération de l'ADN / Tumeurs colorectales / Technique de Western / Apoptose / Côlon / Tumeurs du côlon / Antigènes CD95 / Traitement médicamenteux / Fluorouracil langue: Anglais Texte intégral: Biomolecules & Therapeutics Année: 2016 Type: Article

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Texte intégral: Disponible Indice: WPRIM (Pacifique occidental) Sujet Principal: Altération de l'ADN / Tumeurs colorectales / Technique de Western / Apoptose / Côlon / Tumeurs du côlon / Antigènes CD95 / Traitement médicamenteux / Fluorouracil langue: Anglais Texte intégral: Biomolecules & Therapeutics Année: 2016 Type: Article