Abstract
A single family of proteases, the caspases, has long been considered the pivotal executioner of all programmed cell death. However, recent findings of evolutionarily conserved, caspase-independent controlled death mechanisms have opened new perspectives on the biology of cell demise, with particular implications for neurobiology, cancer research and immunological processes.
MeSH terms
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Animals
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Apoptosis / drug effects
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Apoptosis / physiology*
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Caenorhabditis elegans / physiology
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Caspases / physiology*
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Chromatin / ultrastructure
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Cysteine Proteinase Inhibitors / pharmacology
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Enzyme Activation
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Eukaryotic Cells / cytology
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Eukaryotic Cells / enzymology
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Evolution, Molecular
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Fungal Proteins / physiology
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Helminth Proteins / physiology
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Humans
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Mitochondria / physiology
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Necrosis
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Neoplasms / pathology
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Neoplasms / therapy
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Nervous System / cytology
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Nervous System / embryology
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Nervous System / growth & development
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Receptors, Tumor Necrosis Factor / physiology
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Saccharomyces cerevisiae / physiology
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Signal Transduction
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fas Receptor / physiology
Substances
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Chromatin
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Cysteine Proteinase Inhibitors
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Fungal Proteins
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Helminth Proteins
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Receptors, Tumor Necrosis Factor
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fas Receptor
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Caspases