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首页> 外文期刊>Journal of Ethnopharmacology: An Interdisciplinary Journal Devoted to Bioscientific Research on Indigenous Drugs >Effect of anti-histone acetyltransferase activity from Rosa rugosa Thunb. (Rosaceae) extracts on androgen receptor-mediated transcriptional regulation.
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Effect of anti-histone acetyltransferase activity from Rosa rugosa Thunb. (Rosaceae) extracts on androgen receptor-mediated transcriptional regulation.

机译:皱叶蔷薇的抗组蛋白乙酰转移酶活性的影响。 (蔷薇科)提取物对雄激素受体介导的转录调控。

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摘要

ETHNOPHARMACOLOGICAL RELEVANCE: Rosa rugosa Thunb. (Rosaceae) has been traditionally used for treatments of diabetes, chronic inflammatory diseases, pain, and anticancer in Korea. AIM OF STUDY: We investigate the inhibitory effect of histone acetyltransferase activity from the methanol extract of stems of Rosa rugosa on androgen receptor-mediated transcriptional regulation. MATERIALS AND METHODS: For the present study, Rosa rugosa methanol extract (RRME) was obtained from stem part of Rosa rugosa using methanol extraction. Histone acetyltransferase assay were performed to measure the inhibitory effect on acetylation, reporter assay, real-time PCR and ChIP assay were performed to measure androgen receptor-mediated transcriptional regulation, and MTT test were performed to measure cell viability. RESULTS: RRME inhibited both p300 and CBP (60-70% at 100 microg/ml) activity. We show RRME mediates agonist-dependent androgen receptor (AR) activation and suppresses antagonist-dependent inhibition. RRME treatment also decreased transcription of AR regulated genes and also reduced histone H3 and AR acetylation in the promoters of prostate-specific antigen (PSA) and beta-2-microglobulin (B2M). Finally, RRME treatment reduced the growth of LNCaP, a human prostate cancer cell line. CONCLUSION: These results demonstrate RRME is a potent HAT inhibitor, which reduced AR and histone acetylation leading to decreased AR-mediated transcription and reduced LNCaP cell growth.
机译:人类药理学相关性:Rosa rugosa Thunb。 (蔷薇科)在韩国传统上用于治疗糖尿病,慢性炎性疾病,疼痛和抗癌药。研究目的:我们研究玫瑰果茎甲醇提取物中组蛋白乙酰转移酶活性对雄激素受体介导的转录调控的抑制作用。材料与方法:对于本研究,使用甲醇提取从皱叶蔷薇的茎部中获得了皱叶蔷薇的甲醇提取物(RRME)。进行组蛋白乙酰转移酶测定以测定对乙酰化的抑制作用,进行报告基因测定,实时PCR和ChIP测定以测定雄激素受体介导的转录调节,并且进行MTT检验以测定细胞活力。结果:RRME抑制了p300和CBP的活性(在100 microg / ml时为60-70%)。我们显示RRME介导激动剂依赖性雄激素受体(AR)激活并抑制拮抗剂依赖性抑制。 RRME处理还减少了前列腺特异抗原(PSA)和β-2-微球蛋白(B2M)启动子中AR调控基因的转录,并减少了组蛋白H3和AR乙酰化。最后,RRME治疗降低了人类前列腺癌细胞系LNCaP的生长。结论:这些结果表明RRME是一种有效的HAT抑制剂,可减少AR和组蛋白乙酰化,从而减少AR介导的转录并减少LNCaP细胞的生长。

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