Abstract
In this study, we investigated the effect of three synthetic alpha-methylene-gamma-butyrolactones (MBL) on viability of 10 human tumor cell lines and found that these lactones were highly cytotoxic against leukemia cells. Studies performed on HL-60 cells indicate that MBL induce G(2)-M arrest and apoptosis through a caspase-dependent mechanism. Apoptosis was associated to cytochrome c release, cleavage of procaspases-9 and -3, and hydrolysis of PARP. Intracellular reactive oxygen species (ROS) seem to play a key role since high levels of ROS were produced early (<15 min) and apoptosis was completely abrogated by the free radical scavenger N-acetyl-L-cysteine (NAC).
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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4-Butyrolactone / analogs & derivatives*
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4-Butyrolactone / pharmacology
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Antineoplastic Agents / pharmacology*
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Apoptosis / drug effects*
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Caspases / physiology
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Cell Division / drug effects*
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Cell Survival / drug effects
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Cytochromes c / metabolism
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G2 Phase / drug effects*
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HL-60 Cells
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Humans
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Mitogen-Activated Protein Kinases / physiology
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Poly(ADP-ribose) Polymerases / metabolism
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Reactive Oxygen Species / metabolism
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U937 Cells
Substances
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Antineoplastic Agents
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Reactive Oxygen Species
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alpha-methylene gamma-butyrolactone
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Cytochromes c
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Poly(ADP-ribose) Polymerases
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Mitogen-Activated Protein Kinases
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Caspases
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4-Butyrolactone