Abstract
Both Chk 1 and Chk 2 are critically important checkpoint kinases. Chk 1 is an essential gene that is required for normal cell division and Chk 2 has been found to be mutated in an ever-growing list of human malignancies. Our recent studies indicate that both Chk 1 and Chk 2 have roles to play in the physiological stress of hypoxia/reoxygenation. Loss or inhibition of either kinase sensitizes cells to hypoxia/reoxygenation indicating that either or both could represent significant therapeutic targets.
Publication types
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Research Support, N.I.H., Extramural
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Review
MeSH terms
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Animals
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Cell Hypoxia*
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Checkpoint Kinase 1
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Checkpoint Kinase 2
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DNA Damage
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G2 Phase
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Humans
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Neoplasms / prevention & control
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Oxygen / metabolism*
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Protein Kinases / physiology*
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Protein Serine-Threonine Kinases / antagonists & inhibitors
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Protein Serine-Threonine Kinases / physiology*
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Rad51 Recombinase / physiology
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Signal Transduction
Substances
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Protein Kinases
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Checkpoint Kinase 2
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CHEK2 protein, human
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Checkpoint Kinase 1
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Protein Serine-Threonine Kinases
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RAD51 protein, human
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Rad51 Recombinase
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Oxygen