Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
29
pubmed:dateCreated
2011-7-20
pubmed:abstractText
In mice and humans the circadian rhythm of many biochemical reactions, physiology, and behavior is generated by a transcriptional-translation feedback loop (TTFL) made up of the so-called core clock genes/proteins. The circadian system interfaces with most signaling pathways including those involved in cell proliferation and inflammation. Cryptochrome (CRY) is a core clock protein that plays an essential role in the repressive arm of the TTFL. It was recently reported that mutation of CRY in p53-null mice delayed the onset of cancer. It was therefore suggested that CRY mutation may activate p53-independent apoptosis pathways, which eliminate premalignant and malignant cells and thus delay overt tumor formation. Here we show that CRY mutation sensitizes p53 mutant and oncogenically transformed cells to tumor necrosis factor ? (TNF?)-initiated apoptosis by interfacing with the NF-?B signaling pathway through the GSK3? kinase and alleviating prosurvival NF-?B signaling. These findings provide a mechanistic foundation for the delayed onset of tumorigenesis in clock-disrupted p53 mutant mice and suggest unique therapeutic strategies for treating cancers associated with p53 mutation.
pubmed:grant
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/21690409-10518585, http://linkedlifedata.com/resource/pubmed/commentcorrection/21690409-10894547, http://linkedlifedata.com/resource/pubmed/commentcorrection/21690409-12189384, http://linkedlifedata.com/resource/pubmed/commentcorrection/21690409-12198538, http://linkedlifedata.com/resource/pubmed/commentcorrection/21690409-12360211, http://linkedlifedata.com/resource/pubmed/commentcorrection/21690409-12619106, http://linkedlifedata.com/resource/pubmed/commentcorrection/21690409-12887920, http://linkedlifedata.com/resource/pubmed/commentcorrection/21690409-12894240, http://linkedlifedata.com/resource/pubmed/commentcorrection/21690409-15329734, http://linkedlifedata.com/resource/pubmed/commentcorrection/21690409-15371334, http://linkedlifedata.com/resource/pubmed/commentcorrection/21690409-15972822, http://linkedlifedata.com/resource/pubmed/commentcorrection/21690409-16061665, http://linkedlifedata.com/resource/pubmed/commentcorrection/21690409-16253246, http://linkedlifedata.com/resource/pubmed/commentcorrection/21690409-16724054, http://linkedlifedata.com/resource/pubmed/commentcorrection/21690409-17016438, http://linkedlifedata.com/resource/pubmed/commentcorrection/21690409-17251933, http://linkedlifedata.com/resource/pubmed/commentcorrection/21690409-17406473, http://linkedlifedata.com/resource/pubmed/commentcorrection/21690409-18391940, http://linkedlifedata.com/resource/pubmed/commentcorrection/21690409-18802415, http://linkedlifedata.com/resource/pubmed/commentcorrection/21690409-18829575, http://linkedlifedata.com/resource/pubmed/commentcorrection/21690409-19188586, http://linkedlifedata.com/resource/pubmed/commentcorrection/21690409-19202066, http://linkedlifedata.com/resource/pubmed/commentcorrection/21690409-19302050, http://linkedlifedata.com/resource/pubmed/commentcorrection/21690409-19828534, http://linkedlifedata.com/resource/pubmed/commentcorrection/21690409-19847165, http://linkedlifedata.com/resource/pubmed/commentcorrection/21690409-19935677, http://linkedlifedata.com/resource/pubmed/commentcorrection/21690409-20028853, http://linkedlifedata.com/resource/pubmed/commentcorrection/21690409-20042581, http://linkedlifedata.com/resource/pubmed/commentcorrection/21690409-20501836, http://linkedlifedata.com/resource/pubmed/commentcorrection/21690409-21628572, http://linkedlifedata.com/resource/pubmed/commentcorrection/21690409-9670046, http://linkedlifedata.com/resource/pubmed/commentcorrection/21690409-9721089, http://linkedlifedata.com/resource/pubmed/commentcorrection/21690409-9733516
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jul
pubmed:issn
1091-6490
pubmed:author
pubmed:issnType
Electronic
pubmed:day
19
pubmed:volume
108
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
12036-41
pubmed:dateRevised
2011-11-2
pubmed:meshHeading
pubmed-meshheading:21690409-Animals, pubmed-meshheading:21690409-Apoptosis, pubmed-meshheading:21690409-Cell Line, pubmed-meshheading:21690409-Chromatin Immunoprecipitation, pubmed-meshheading:21690409-Circadian Rhythm, pubmed-meshheading:21690409-Cryptochromes, pubmed-meshheading:21690409-DNA Primers, pubmed-meshheading:21690409-Glycogen Synthase Kinase 3, pubmed-meshheading:21690409-Humans, pubmed-meshheading:21690409-Immunoblotting, pubmed-meshheading:21690409-Mice, pubmed-meshheading:21690409-Mice, Inbred C57BL, pubmed-meshheading:21690409-Mice, Knockout, pubmed-meshheading:21690409-Mutation, pubmed-meshheading:21690409-NF-kappa B, pubmed-meshheading:21690409-Positron-Emission Tomography, pubmed-meshheading:21690409-Signal Transduction, pubmed-meshheading:21690409-Tumor Necrosis Factor-alpha, pubmed-meshheading:21690409-Tumor Suppressor Protein p53
pubmed:year
2011
pubmed:articleTitle
Regulation of apoptosis by the circadian clock through NF-kappaB signaling.
pubmed:affiliation
Department of Biochemistry and Biophysics, University of North Carolina School of Medicine, Chapel Hill, NC 27599, USA.
pubmed:publicationType
Journal Article, Research Support, N.I.H., Extramural