Rexinoids modulate steroid and xenobiotic receptor activity by increasing its protein turnover in a calpain-dependent manner

Journal of Biological Chemistry

Volumn 283, Issue 32, 2008, Pages 21945-21952

  Pettersson, Filippa ^a   Hanna, Nessrine ^a   Lagodich, Marina ^a   Dupéré Richer, Daphné ^a   Couture, Marie Claude ^a   Choi, Catherine ^a   Miller Jr , Wilson H ^a  

^a MCGILL UNIVERSITY   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

CHEMICAL ACTIVATION; DETOXIFICATION; LIGANDS; PROTEINS;

NUCLEAR RECEPTORS; PREGNANE X RECEPTORS; PROTEIN DEGRADATION; PROTEIN STABILITY; PROTEIN TURNOVERS; RESPONSE ELEMENTS; RETINOID X RECEPTOR; SELECTIVE LIGANDS;

TRANSCRIPTION;

6 [1 (5,6,7,8 TETRAHYDRO 3,5,5,8,8 PENTAMETHYL 2 NAPHTHYL)CYCLOPROPYL]NICOTINIC ACID; BENZYLOXYCARBONYLLEUCYLLEUCYLLEUCINAL; BEXAROTENE; CALPAIN; CALPASTATIN; COMPLEMENTARY DNA; CYCLOHEXIMIDE; LIGAND; LIVER X RECEPTOR; MESSENGER RNA; MICRORNA; PREGNANE X RECEPTOR; RETINOIC ACID RECEPTOR; RETINOID; RETINOID X RECEPTOR; RIFAMPICIN; SR 12813; STEROID AND XENOBIOTIC RECEPTOR; STEROID RECEPTOR; SULFUR 35; TRANSCRIPTION FACTOR; UNCLASSIFIED DRUG; XENOBIOTIC AGENT; ANTINEOPLASTIC AGENT; GLYCOPROTEIN P; NICOTINIC ACID DERIVATIVE; NUCLEIC ACID SYNTHESIS INHIBITOR; TETRALIN DERIVATIVE;

ARTICLE; BINDING AFFINITY; CALCIUM SIGNALING; CELL STRAIN MCF 7; CHROMATIN IMMUNOPRECIPITATION; CONTROLLED STUDY; DETOXIFICATION; DRUG METABOLISM; DRUG RECEPTOR BINDING; ENZYME ACTIVITY; GENE EXPRESSION REGULATION; GENETIC TRANSCRIPTION; HEPATOMA CELL; HUMAN; HUMAN CELL; ISOTOPE LABELING; PRIORITY JOURNAL; PROTEIN DEGRADATION; RECEPTOR AFFINITY; RECEPTOR OCCUPANCY; WESTERN BLOTTING; DRUG EFFECT; GENETICS; METABOLISM; PROTEIN BINDING; TUMOR CELL LINE;

ANTICARCINOGENIC AGENTS; CALPAIN; CELL LINE, TUMOR; GENE EXPRESSION REGULATION; HUMANS; NICOTINIC ACIDS; NUCLEIC ACID SYNTHESIS INHIBITORS; P-GLYCOPROTEIN; PROTEIN BINDING; RECEPTORS, STEROID; RETINOID X RECEPTORS; RIFAMPIN; TETRAHYDRONAPHTHALENES;

EID: 52049120855     PISSN: 00219258     EISSN: 1083351X     Source Type: Journal    
DOI: 10.1074/jbc.M710358200     Document Type: Article

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