Title of article :
Up-stream events in the nuclear factor κB activation cascade in response to sparsely ionizing radiation Original Research Article
Author/Authors :
Christine E. Hellweg، نويسنده , , Britta Langen، نويسنده , , Galina Klimow، نويسنده , , Roland Ruscher، نويسنده , , Claudia Schmitz، نويسنده , , Christa Baumstark-Khan، نويسنده , , Günther Reitz، نويسنده ,
Issue Information :
دوهفته نامه با شماره پیاپی سال 2009
Pages :
10
From page :
907
To page :
916
Abstract :
Radiation is a potentially limiting factor for manned long-term space missions. Prolonged exposure to galactic cosmic rays may shorten the healthy life-span after return to Earth due to cancer induction. During the mission, a solar flare can be life threatening. For better risk estimation and development of appropriate countermeasures, the study of the cellular radiation response is necessary. Since apoptosis may be a mechanism the body uses to eliminate damaged cells, the induction by cosmic radiation of the nuclear anti-apoptotic transcription factor nuclear factor κB (NF-κB) could influence the cancer risk of astronauts exposed to cosmic radiation by improving the survival of radiation-damaged cells. In previous studies using a screening assay for the detection of NF-κB-dependent gene induction (HEK-pNF-κB-d2EGFP/Neo cells), the activation of this transcription factor by heavy ions was shown [Baumstark-Khan, C., Hellweg, C.E., Arenz, A., Meier, M.M. Cellular monitoring of the nuclear factor kappa B pathway for assessment of space environmental radiation. Radiat. Res. 164, 527–530, 2005]. Studies with NF-κB inhibitors can map functional details of the NF-κB pathway and the influence of radiation-induced NF-κB activation on various cellular outcomes such as survival or cell cycle arrest.
Keywords :
Nuclear factor ?B inhibitors , Ionizing radiation , Human cells , proteasome , Caffeic acid phenethyl ester , Capsaicin
Journal title :
Advances in Space Research
Serial Year :
2009
Journal title :
Advances in Space Research
Record number :
1132812
Link To Document :
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