Parichaya Aimvijarn
1, Teerapat Rodboon
1, Witchuda Payuhakrit
1, Prasit Suwannalert
1*1 Department of Pathobiology, Faculty of Science, Mahidol University, Bangkok 10400, Thailand.
Abstract
Background:
Nymphaea spp., Thai water lilies are aquatic plants. They contain
phenolic pigments that play a major role in free radical scavenging. Melanoma
is strong aggressive skin cancer-associated with oxidative stress. This study,
to determine the effect of Nymphaea spp. extracts on cell apoptosis,
cellular migration and invasion through the role of cellular oxidants in B16
melanoma cells.
Methods:
Free radical scavenging activity and total phenolic were investigated by 1,
1-diphenyl-2 picrylhydrazyl (DPPH) and Ferric reducing anti-oxidant power
(FRAP) methods and Folin-Denis test, respectively. Cytotoxic were assessed by
3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) method. Cell
apoptosis was confirmed by flow cytometry. Cellular oxidants, cellular migration
and invasion were determined with 2,7-dichlorodihydrofluorescein diacetate
(DCFH-DA), wound healing and Boyden chamber assay, respectively.
Results: Nymphaea
pubescens showed higher capacity of scavenging free radical activity than Nymphaea
stellate and also related phenolic content. Nymphaea pubescens
extract was toxic to B16 melanoma cells. High concentrations cell apoptosis was
induced. Contrastingly, low concentrations showed a decrease in cellular
oxidants associated with the suppression of cancer cell progression. In B16
melanoma cell, Nymphaea pubescens extract was able to inhibit B16
melanoma cell migration and invasion through the low doses. Interestingly, the
high doses of extract showed a potential of cytotoxicity to induce melanoma
cell death. At the low doses, Nymphaea pubescens extract might suppress
melanoma cells progression by interfering with both cellular migration and
invasion capacity.
Conclusion:
Hence, Nymphaea pubescens extract induced cellular apoptosis and it also
suppressed cancer cell progression by reducing oxidative stress in B16 melanoma
cells.