@article{oai:soar-ir.repo.nii.ac.jp:00008028,
 author = {Matsunaga,  Tamihide and Maruyama,  Masataka and Matsubara,  Tsutomu and Nagata,  Kiyoshi and Yamazoe,  Yasushi and Ohmori,  Shigeru},
 issue = {6},
 journal = {DRUG METABOLISM AND PHARMACOKINETICS},
 month = {Dec},
 note = {Human fetal liver (HFL) cells express major drug metabolic enzymes CYP3A4, CYP3A5 and CYP3A7. In the fetal hepatocytes, betamethasone and dexamethasone (DEX) markedly enhanced the expression levels of CYP3A4 and CYP3A7 mRNAs and slightly increased the expression level of CYP3A5 mRNA. Interestingly, a high correlation between the CYP3A induction ability and the intensity of anti-inflammatory effect was observed. Human glucocorticoid receptor (GR) small interfering RNA clearly attenuated the expression level of GR mRNA, and diminished the DEX-stimulated CYP3A4, CYP3A5 and CYP3A7 expression in HFL cells. These findings indicate that GR mediates the induction of CYP3A4 and CYP3A7 expression in human fetal hepatocytes as well as the CYP3A5., Article, DRUG METABOLISM AND PHARMACOKINETICS. 27(6):653-657 (2012)},
 pages = {653--657},
 title = {Mechanisms of CYP3A Induction by Glucocorticoids in Human Fetal Liver Cells},
 volume = {27},
 year = {2012}
}