CASP8 D302H and meningioma risk: An analysis of five case-control series

Abstract Caspase 8 ( CASP8 ) is a key regulator of apoptosis or programmed cell death, and hence a defence against cancer. The CASP8 polymorphism D302H has recently been shown to influence the risk of breast cancer. We tested the hypothesis that the CASP8 polymorphism D302H may influence risk of men...

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Veröffentlicht in:Cancer letters 2009-01, Vol.273 (2), p.312-315
Hauptverfasser: Bethke, Lara, Sullivan, Kate, Webb, Emily, Murray, Anne, Schoemaker, Minouk, Auvinen, Anssi, Kiuru, Anne, Salminen, Tiina, Johansen, Christoffer, Christensen, Helle Collatz, Muir, Kenneth, McKinney, Patricia, Hepworth, Sarah, Dimitropoulou, Polyxeni, Lophatananon, Artitaya, Feychting, Maria, Lönn, Stefan, Ahlbom, Anders, Malmer, Beatrice, Henriksson, Roger, Swerdlow, Anthony, Houlston, Richard
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Sprache:eng
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Zusammenfassung:Abstract Caspase 8 ( CASP8 ) is a key regulator of apoptosis or programmed cell death, and hence a defence against cancer. The CASP8 polymorphism D302H has recently been shown to influence the risk of breast cancer. We tested the hypothesis that the CASP8 polymorphism D302H may influence risk of meningioma through analysis of five independent series of case patients and controls ( n = 631 and 637, respectively). Carrier status for 302H was not associated with a statistically significantly increased risk (OR = 1.16; 95% CI: 0.87–1.53; P = 0.31) making it unlikely that this variant contributes to the inherited risk of meningioma.
ISSN:0304-3835
1872-7980
1872-7980
DOI:10.1016/j.canlet.2008.08.010