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CASP8 D302H and meningioma risk: an analysis of five case-control series
Authors: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
Affiliation:Section of Cancer Genetics, Institute of Cancer Research, 15 Cotswold Road, Sutton, Surrey SM2 5NG, UK.
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.
Keywords:Caspase 8   Polymorphism   Meningioma   Risk
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