Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
12
pubmed:dateCreated
2006-11-30
pubmed:abstractText
The CYP2C subfamily of cytochrome P450 monooxygenases is responsible for the metabolism of approximately 20% of therapeutic drugs and many endogenous compounds in humans. These enzymes can be induced by prior treatment with drugs, resulting in changes in drug efficacy. Induction of human CYP2C enzymes by xenobiotics occurs at the transcriptional level and is reported to involve the constitutive androstane receptor (CAR) and the pregnane X receptor (PXR). In the present study, we report that murine CYP2C37 mRNA is induced by phenobarbital and phenytoin. In contrast, the mouse PXR agonist 5-pregnen-3beta-ol-20-one-16alpha-carbonitrile did not induce CYP2C37 mRNA, suggesting that PXR does not regulate this gene. The induction of CYP2C37 mRNA by phenobarbital and phenytoin is essentially abolished in CAR-null mice; thus, induction of Cyp2c37 by these xenobiotics is CAR-dependent. A functional CAR response element (CAR-RE) was identified at -2791 base pairs from the translation start site of the Cyp2c37 gene. Mutation of this CAR-RE abolished mouse CAR transactivation of a Cyp2c37 -2.9-kilobase pair luciferase reporter construct in HepG2 cells.
pubmed:grant
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/16936065-10037683, http://linkedlifedata.com/resource/pubmed/commentcorrection/16936065-10570062, http://linkedlifedata.com/resource/pubmed/commentcorrection/16936065-10749660, http://linkedlifedata.com/resource/pubmed/commentcorrection/16936065-10757780, http://linkedlifedata.com/resource/pubmed/commentcorrection/16936065-10935643, http://linkedlifedata.com/resource/pubmed/commentcorrection/16936065-11181490, http://linkedlifedata.com/resource/pubmed/commentcorrection/16936065-11248085, http://linkedlifedata.com/resource/pubmed/commentcorrection/16936065-11264453, http://linkedlifedata.com/resource/pubmed/commentcorrection/16936065-11437368, http://linkedlifedata.com/resource/pubmed/commentcorrection/16936065-11602523, http://linkedlifedata.com/resource/pubmed/commentcorrection/16936065-11679585, http://linkedlifedata.com/resource/pubmed/commentcorrection/16936065-11752199, http://linkedlifedata.com/resource/pubmed/commentcorrection/16936065-11807162, http://linkedlifedata.com/resource/pubmed/commentcorrection/16936065-12130689, http://linkedlifedata.com/resource/pubmed/commentcorrection/16936065-12130704, http://linkedlifedata.com/resource/pubmed/commentcorrection/16936065-12181440, http://linkedlifedata.com/resource/pubmed/commentcorrection/16936065-12571232, http://linkedlifedata.com/resource/pubmed/commentcorrection/16936065-12869636, http://linkedlifedata.com/resource/pubmed/commentcorrection/16936065-14600250, http://linkedlifedata.com/resource/pubmed/commentcorrection/16936065-15084647, http://linkedlifedata.com/resource/pubmed/commentcorrection/16936065-15102943, http://linkedlifedata.com/resource/pubmed/commentcorrection/16936065-15123723, http://linkedlifedata.com/resource/pubmed/commentcorrection/16936065-15128046, http://linkedlifedata.com/resource/pubmed/commentcorrection/16936065-15155833, http://linkedlifedata.com/resource/pubmed/commentcorrection/16936065-15358766, http://linkedlifedata.com/resource/pubmed/commentcorrection/16936065-15672753, http://linkedlifedata.com/resource/pubmed/commentcorrection/16936065-15933212, http://linkedlifedata.com/resource/pubmed/commentcorrection/16936065-16749864, http://linkedlifedata.com/resource/pubmed/commentcorrection/16936065-2545475, http://linkedlifedata.com/resource/pubmed/commentcorrection/16936065-7704034, http://linkedlifedata.com/resource/pubmed/commentcorrection/16936065-7887901, http://linkedlifedata.com/resource/pubmed/commentcorrection/16936065-9663807, http://linkedlifedata.com/resource/pubmed/commentcorrection/16936065-9742082, http://linkedlifedata.com/resource/pubmed/commentcorrection/16936065-9783588
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Cytochrome P-450 Enzyme System, http://linkedlifedata.com/resource/pubmed/chemical/Phenobarbital, http://linkedlifedata.com/resource/pubmed/chemical/Phenytoin, http://linkedlifedata.com/resource/pubmed/chemical/Pregnenolone Carbonitrile, http://linkedlifedata.com/resource/pubmed/chemical/RNA, Messenger, http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Cytoplasmic and Nuclear, http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Steroid, http://linkedlifedata.com/resource/pubmed/chemical/Transcription Factors, http://linkedlifedata.com/resource/pubmed/chemical/constitutive androstane receptor, http://linkedlifedata.com/resource/pubmed/chemical/cytochrome P-450 CYP2C subfamily, http://linkedlifedata.com/resource/pubmed/chemical/pregnane X receptor
pubmed:status
MEDLINE
pubmed:month
Dec
pubmed:issn
0090-9556
pubmed:author
pubmed:issnType
Print
pubmed:volume
34
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
2003-10
pubmed:dateRevised
2011-9-26
pubmed:meshHeading
pubmed:year
2006
pubmed:articleTitle
Phenytoin induction of the cyp2c37 gene is mediated by the constitutive androstane receptor.
pubmed:affiliation
Laboratory of Pharmacology and Chemistry, National Institute of Environmental Health Sciences, Research Triangle Park, NC 27709, USA.
pubmed:publicationType
Journal Article, Research Support, N.I.H., Intramural