Abstract
This study investigated the inhibitory effects of 2′- benzoyloxycinnamaldehyde (BCA) on cancer cells, including various drug-resistant cancer cell lines. To observe this activity, the anticancer drug-resistant cell lines were established by continuously exposing the parental cells to 5-fluorouracil (5-FU) and cyclophosphamide (CDDP), and examining the cells with the MTT assay and flow cytometric analysis. The BCA treatment produced similar growth inhibitory effects and apoptotic cell death on the drug-resistant cancer cells as their parental cells. The activation of the p38-mitogen activated protein kinase, an increased level of reactive oxygen species (ROS) generation and downregulation of Bcl-2 were observed in both the drug resistant and non-drug resistant cell lines. The GSH treatment effectively inhibited BCA-induced apoptosis by blocking ROS generation, suggesting that ROS is a major regulator in BCA-induced apoptotic cell death. These results suggest that BCA can be a useful drug candidate for treating drug-resistant cells.
Original language | English |
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Pages (from-to) | 428-437 |
Number of pages | 10 |
Journal | Journal of Chemotherapy |
Volume | 19 |
Issue number | 4 |
DOIs | |
Publication status | Published - 2007 Aug |
Keywords
- 2′-benzoyloxycinnamaldehyde
- Anticancer drugs
- Cancer
- Drug resistance
- Reactive oxygen species
- p38-mitogen activated protein kinase
ASJC Scopus subject areas
- Oncology
- Pharmacology
- Pharmacology (medical)
- Infectious Diseases