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.
Original language | English |
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Pages (from-to) | 604-609 |
Number of pages | 6 |
Journal | Biomolecules and Therapeutics |
Volume | 24 |
Issue number | 6 |
DOIs | |
State | Published - Nov 2016 |
Keywords
- 5-fluorouracil (5-FU)
- Apoptosis
- Oxidative damages
- α-mangostin