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| Content Provider | World Health Organization (WHO)-Global Index Medicus |
|---|---|
| Author | Kawaratani, Yasuyuki Matsuoka, Takeshi Hirata, Yoshiyuki Fukata, Naofumi Nagaoka, Yasuo Uesato, Shinichi |
| Description | Author Affiliation: Kawaratani Y ( Department of Life Science and Biotechnology, Faculty of Chemistry, Materials and Bioengineering, Kansai University, Suita, Osaka 564-8680, Japan. Electronic address: hoechst.atanpe@gmail.com.); Matsuoka T ( Department of Life Science and Biotechnology, Faculty of Chemistry, Materials and Bioengineering, Kansai University, Suita, Osaka 564-8680, Japan. Electronic address: audaciapaula@gmail.com.); Hirata Y ( Department of Life Science and Biotechnology, Faculty of Chemistry, Materials and Bioengineering, Kansai University, Suita, Osaka 564-8680, Japan. Electronic address: y.hirata@gly.oups.ac.jp.); Fukata N ( Department of Life Science and Biotechnology, Faculty of Chemistry, Materials and Bioengineering, Kansai University, Suita, Osaka 564-8680, Japan. Electronic address: fukanao0921@gmail.com.); Nagaoka Y ( Department of Life Science and Biotechnology, Faculty of Chemistry, Materials and Bioengineering, Kansai University, Suita, Osaka 564-8680, Japan. Electronic address: ynagaoka@kansai-u.ac.jp.); Uesato S ( Department of Life Science and Biotechnology, Faculty of Chemistry, Materials and Bioengineering, Kansai University, Suita, Osaka 564-8680, Japan. Electronic address: uesato@kansai-u.ac.jp.) |
| Abstract | The carbamate fungicide benomyl reportedly inhibited the growth of the human breast cancer cell line MCF-7 by inducing apoptosis. However, influence of benomyl on the expression and activity of aromatase of MCF-7 cells remains to be examined, since benomyl was identified as an endocrine disruptor. We here confirmed through cell cycle analysis and immunofluorescence staining that benomyl damaged microtubules and caused apoptosis. We also found that benomyl inhibited histone deacetylase (HDAC) 1 and accumulated acetylated histone H3 in MCF-7 cells. Additionally, benomyl enhanced the levels of aromatase protein and mRNA, albeit at high concentrations. It is thus likely that benomyl enhanced the promoter activity of the aromatase gene via acetylation of histone H3 as does the HDAC inhibitor Vorinostat. In conclusion, benomyl remains to be a risk factor as an endocrine disruptor for breast cancer. |
| File Format | HTM / HTML |
| ISSN | 13826689 |
| Issue Number | 1 |
| Volume Number | 39 |
| e-ISSN | 18727077 |
| Journal | Environmental Toxicology and Pharmacology |
| Language | English |
| Publisher | Elsevier |
| Publisher Date | 2015-01-01 |
| Publisher Place | Netherlands |
| Access Restriction | One Nation One Subscription (ONOS) |
| Subject Keyword | Discipline Environmental Health Discipline Pharmacology Aromatase Genetics Metabolism Benomyl Toxicity Fungicides, Industrial Gene Expression Regulation, Enzymologic Drug Effects Histone Deacetylase Inhibitors Breast Neoplasms Enzymology Histone Deacetylase 1 Antagonists & Inhibitors Histones Humans Mcf-7 Cells Journal Article Research Support, Non-u.s. Gov't |
| Content Type | Text |
| Resource Type | Article |
| Subject | Health, Toxicology and Mutagenesis Medicine Toxicology Pharmacology |
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