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Impaired nuclear translocation of CAR in hepatic preneoplastic lesions: association with an attenuated CYP2B induction by phenobarbital
Authors:Numazawa Satoshi  Shindo Sawako  Maruyama Keiji  Chibana Fumika  Kawahara Yosuke  Ashino Takashi  Tanaka Sachiko  Yoshida Takemi
Affiliation:Department of Biochemical Toxicology, School of Pharmaceutical Sciences, Showa University, 1-5-8 Hatanodai, Shinagawa, Tokyo 142-8555, Japan
Abstract:Phenobarbital (PB) induction of CYP2B, a representative target gene of constitutive androstane receptor (CAR), has been observed to be attenuated in preneoplastic lesions of rat liver; however, molecular basis for this attenuation is poorly understood. In this report, we provide evidence indicating that the CAR expressed in the hepatic preneoplastic lesions of rats and mice was resistant to nuclear translocation and transactivation of the PB-responsive enhancer module upon PB treatment. These observations suggest that the attenuation of the induction of CYP2B by PB in hepatic preneoplastic lesions is evidently a consequence of impaired nuclear translocation of CAR.
Keywords:2-AAF, 2-acetylaminofluorene   CAR, constitutive androstane receptor   CCRP, cytosolic CAR retention protein   CYP, cytochrome P450   GAPDH, glyceraldehyde-3-phosphate dehydrogenase   GFP, green fluorescent protein   GSTp, placenta form of glutathione S-transferase   PB, phenobarbital   PBREM, PB-responsive enhancer module   PROD, 7-pentoxyresorufin-O-dealkylase   RXR, retinoid X receptor   TCPOBOP, 1,4-bis[2-(3,5-dichloropyridyloxy)]benzene
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