曲古抑菌素A
组蛋白脱乙酰基酶
组蛋白脱乙酰酶抑制剂
化学
MCF-7型
生长抑制
HDAC11型
组蛋白脱乙酰基酶5
细胞生长
癌症研究
组蛋白
乙酰化
癌细胞
顺铂
人体乳房
癌症
生物化学
生物
医学
内科学
化疗
DNA
基因
作者
K Schmidt,Ronald Gust,Manfred Jung
标识
DOI:10.1002/(sici)1521-4184(199910)332:10<353::aid-ardp353>3.0.co;2-x
摘要
Inhibitors of histone deacetylase are attracting increasing interest due to their influence on transcription, differentiation, and apoptosis. We have investigated two synthetic inhibitors 3 and 4 of histone deacetylase and the natural product inhibitor trichostatin A for their ability to suppress the growth of MCF-7 breast cancer cells and here present complete and improved synthetic procedures. The compounds show a dose dependent inhibition of growth with activities in the low micromolar and nanomolar range. Trichostatin shows cytocidal effects at 100 nM and still has activity comparable to cisplatin (0.5 μM) at 10 nM. Whereas the synthetic inhibitor 3 has cytocidal activity at 10 μM compound 4 shows a maximum of 40% growth suppression at that concentration.
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