Anti-Histone Acetyltransferase Activity from Allspice Extracts Inhibits Androgen Receptor-Dependent Prostate Cancer Cell Growth
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概要
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Histone acetylation depends on the activity of two enzyme families, histone acetyltransferase (HAT) and deacetylase (HDAC). In this study, we screened various plant extracts to find potent HAT inhibitors. Hot water extracts of allspice inhibited HAT activity, especially p300 and CBP (40% at 100 μg/ml). The mRNA levels of two androgen receptor (AR) regulated genes, PSA and TSC22, decreased with allspice treatment (100 μg/ml). Importantly, in IP western analysis, AR acetylation was dramatically decreased by allspice treatment.Furthermore, chromatin immunoprecipitation indicated that the acetylation of histone H3 in the PSA and B2M promoter regions was also repressed. Finally, allspice treatment reduced the growth of human prostate cancer cells, LNCaP (50% growth inhibition at 200 μg/ml). Taken together, our data indicate that the potent HAT inhibitory activity of allspice reduced AR and histone acetylation and led to decreased transcription of AR target genes, resulting in inhibition of prostate cancer cell growth.
著者
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Hong Soon
Department of Fire Administration, Chodang University
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CHO Hong
Department of Food and Biotechnology, Korea University
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Yoon Ho-Geun
Department of Biochemistry and Molecular Biology, Center for Chronic Metabolic Disease Research, Col
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Kim Chang-hoon
Department Of Aquaculture Pukyong National University
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LEE Yoo-Hyun
Department of Food Technology, Graduate School of Life Sciences and Biotechnology, Korea University
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JUN Woojin
Department of Food and Nutrition, Chonnam National University
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KIM Han-Cheon
Department of Biochemistry and Molecular Biology, Center for Chronic Metabolic Disease Research, Col
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JUNG Myung
Department of Biochemistry and Molecular Biology, Center for Chronic Metabolic Disease Research, Col
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WONG Jiemin
Institute of Biomedical Sciences, College of Life Science, East China Normal University
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KIM Ha-Il
Department of Biochemistry and Molecular Biology, Center for Chronic Metabolic Disease Research, Col
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