151. Casearin X exhibits cytotoxic effects in leukemia cells triggered by apoptosis
- Author
-
Vanderlan da Silva Bolzani, Letícia V. Costa-Lotufo, Aristeu Gomes Tininis, Raquel Carvalho Montenegro, Manoel Odorico de Moraes, Patrícia Marçal da Costa, Alberto José Cavalheiro, Paulo Michel Pinheiro Ferreira, André Gonzaga dos Santos, and Cláudia Pessoa
- Subjects
Programmed cell death ,Cell Survival ,Stereochemistry ,Apoptosis ,HL-60 Cells ,DNA Fragmentation ,Phosphatidylserines ,Biology ,Toxicology ,Diterpenes, Clerodane ,chemistry.chemical_compound ,Humans ,Cytotoxic T cell ,Fragmentation (cell biology) ,Cytotoxicity ,Caspase 7 ,Leukemia ,Caspase 3 ,Cell Membrane ,Acridine orange ,DNA ,General Medicine ,Flow Cytometry ,Molecular biology ,Mitochondria ,Enzyme Activation ,chemistry ,DNA fragmentation ,Trypan blue ,Diterpenes - Abstract
Clerodane diterpenes have demonstrated cytotoxic, antiplasmodial and anti-ulcer properties. In the present work, we determined the cytotoxic effect of casearin L (Cas L), O (Cas O) and X (Cas X) and (-)-hardwickiic acid isolated from Casearia sylvestris leaves, and investigated the underlying mechanisms involved in in vitro cell death induced by Cas X in HL-60 leukemia cells (0.7, 1.5 and 3.0μM). Cytotoxicity tests demonstrated that Cas X was the most active compound studied, showing greater cytotoxic effects against CEM and HL-60 lines (IC(50) of 0.4μM) and human peripheral blood mononuclear cells (PBMC, IC(50) of 1.2μM). After 24h exposure, Cas X caused a decrease in 5-bromo-20-deoxyuridine (BrdU) incorporation (36.6 and 24.5% labeling at 0.7 and 1.5μM, respectively), reduction in viability, and increase in apoptotic and necrotic leukemia cells in a dose-dependent manner evidenced by the trypan blue and AO/EB (acridine orange/ethidium bromide) assays. Moreover, Cas X-treated cells exhibited nuclear fragmentation and cytoplasmic vacuolization depending on the concentration tested. These characteristics of apoptosis or secondary necrosis were confirmed by flow cytometry which revealed DNA fragmentation, phosphatidylserine externalization, activation of the effector caspases 3/7 and mitochondrial depolarization. We then found evidence that Cas X causes cell death via apoptotic pathways, corroborating the potential of casearins as compounds with promising antitumor-related properties.
- Published
- 2010