PT  - JOURNAL ARTICLE
AU  - Eriko Higashi
AU  - Tatsuki Fukami
AU  - Masahiro Itoh
AU  - Satoru Kyo
AU  - Masaki Inoue
AU  - Tsuyoshi Yokoi
AU  - Miki Nakajima
TI  - Human CYP2A6 Is Induced by Estrogen via Estrogen Receptor
AID  - 10.1124/dmd.107.016568
DP  - 2007 Oct 01
TA  - Drug Metabolism and Disposition
PG  - 1935--1941
VI  - 35
IP  - 10
4099  - http://dmd.aspetjournals.org/content/35/10/1935.short
4100  - http://dmd.aspetjournals.org/content/35/10/1935.full
SO  - Drug Metab Dispos2007 Oct 01; 35
AB  - Human CYP2A6, which is predominantly expressed in liver, is a key enzyme responsible for the metabolism of nicotine, coumarin, and some pharmaceutical drugs. CYP2A6 is also expressed in sex steroid-responsive tissues such as breast, ovary, uterus, testis, and adrenal grand. In this study, we examined the regulation of CYP2A6 gene by estrogen. Reverse transcription-polymerase chain reaction (RT-PCR) assays revealed that CYP2A6 mRNA was induced by estradiol in estrogen receptor (ER)-positive MCF-7 (2.9-fold) and HepG2 (1.3-fold) cells, but not in ER-negative MDA-MB-435 cells. Real-time RT-PCR assays revealed the CYP2A6 induction by estradiol in human hepatocytes (1.2- to 1.5-fold). Computer-assisted homology search identified a putative estrogen response element (ERE) at -2436 on the CYP2A6 gene. Electrophoretic mobility shift assays demonstrated specific binding of ERα to this element. Luciferase assays using MCF-7 cells revealed that the transcriptional activity of the CYP2A6 promoter was significantly activated by estradiol in an ERα-dependent manner, in which ERE was responsible for the activation. Chromatin immunoprecipitation assays verified the in vivo association of ERα with the ERE on the CYP2A6 gene. Immunohistochemical analyses using human endometrial tissues indicated that the CYP2A6 protein level in glandular cells was significantly higher in the proliferative phase than in the secretory phase, concomitant with local estrogen secretion during the menstrual cycle. These findings clearly demonstrated that CYP2A6 is directly induced by estrogen in an ERα-dependent manner, implying a biological role of CYP2A6 in estrogen-responsive tissues. Furthermore, this mechanism can also explain clinical aspects of increased nicotine metabolism under estrogen-rich environments. The American Society for Pharmacology and Experimental Therapeutics