We recently demonstrated that two new prenylflavanones,
propolin A and
propolin B, isolated and characterized from Taiwanese
propolis, induced cytotoxicity effect in human
melanoma A2058 cells and shows a strong capability to scavenge
free radicals. In this study,
propolin A effectively induced a cytotoxic effect on five different
cancer cell lines. Similar results were obtained for
propolin B.
DNA flow cytometric analysis and DNA fragmentation ladder indicated that
propolin A and
propolin B actively induced apoptosis in A2058 cells. To address the mechanism of the apoptosis effect of
propolin A and
propolin B, we evaluated the apoptosis-related
proteins in A2058 cells. The levels of
procaspase-8, Bid,
procaspase-3, DFF45, and PARP were decreased in dose- and time course-dependent manners. Furthermore, also found
propolin A and
propolin B was capable of releasing
cytochrome c from mitochondria to cytosol. The findings suggest that
propolin A and
propolin B may activate a mitochondria-mediated apoptosis pathway. On the other hand, our data show that
propolin B inhibitied
xanthine oxidase activity more efficiently than
propolin A or CAPE. However, CAPE suppressed ROS-induced
DNA strand breakage more efficiently than
propolin A or
propolin B. All these results indicated that
propolin A and
propolin B may trigger apoptosis of A2058 cells through mitochondria-dependent pathways and also shown that
propolin A and
propolin B were strong
antioxidants.