2007 Fiscal Year Final Research Report Summary
Effect of Phthalate Esters on the Expression of Aromatase and Its Action Mechanism
| Project/Area Number |
18590121
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| Research Category |
Grant-in-Aid for Scientific Research (C)
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| Allocation Type | Single-year Grants |
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| Section | 一般 |
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| Research Field |
Environmental pharmacy
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| Research Institution | Hoshi University |
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Principal Investigator |
NAKAJIN Shizuo Hoshi University, School of Pharmacy and Pharmaceutical Sciences, Professor (90101576)
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| Project Period (FY) |
2006 – 2007
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| Keywords | Environment / Gene / Estrogen / Phthalate esters / Enzyme |
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| Research Abstract |
Phthalate esters are widely used as plasticizers for polyvinylchloride and are suspected of functioning as endocrine disrupters. Di-(2-ethylhexyl) phthalate (DEHP), the most important phthalate ester in commercial use, has been reported to act as a rodent reproductive toxicant. In the present study, we investigated the effects of phthalate esters on aromatase(CYP19) activity and on its gene expression in a human adrenocortical carcinoma cell line, NCI-H295R. Mono-(2-ethylhexyl) phthalate(MEHP), a principle metabolite of DEHP, dose-dependently suppressed aromatase activity and its transcription level. Furthermore, MEHP rapidly and transiently induced transcription of the genes which encode nuclear receptor 4A subfamily members(Nur77, Nurr1, and NOR-1), and up-regulated Nur77promoter activation and Nur77 protein expression in the cells. MEHP-induced Nur77 transcription was inhibited by bisindolylmaleimide I(protein kinase C inhibitor) and wortmannin(phosphoinositide 3-kinase inhibitor). Finally, ectopic expression of Nur77 markedly suppressed forskolin-induced transcriptional activation of promoter I.3 and promoter II of the CYP19 gene. These results suggest that the suppression of aromatase activity and its transcription level by MEHP exposure to NCI-H295R cells was regulated through the rapid and transient expression of Nur77 gene.
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Research Products
(8 results)
