组蛋白脱乙酰基酶
组蛋白脱乙酰基酶5
曲古抑菌素A
组蛋白脱乙酰基酶2
HDAC10型
HDAC11型
锡尔图因
组蛋白脱乙酰酶抑制剂
药理学
组蛋白
癌症研究
医学
化学
生物
作者
Simon G. Royce,Katherine Ververis,Tom C. Karagiannis
出处
期刊:PubMed
日期:2012-01-01
卷期号:42 (3): 338-45
被引量:4
摘要
Histone deacetylase inhibitors have emerged as a new class of anti-cancer therapeutics due to their potent anti-proliferative and apoptotic effects in malignant cells. Accumulating evidence is indicating that histone deacetylase inhibitors may also have potential clinical utility in non-oncological applications, including asthma. However, the potential of histone deacetylase inhibitors in asthma remains controversial. For example, the mechanisms of action of the broad-spectrum histone deacetylase inhibitor, Trichostatin A, in animal models of allergic airways disease are conflicting. Further, there is evidence suggesting potential problems associated with histone deacetylase 2 inhibition and conventional glucocorticosteroid therapy. Similarly, disparate findings are emerging following modulation of the class III, sirtuin 1 enzyme. Indeed, it is becoming apparent that the mechanism of action may not be related to histone deacetylase inhibition activity per se. Further, there is only limited evidence that these compounds possess anti-inflammatory effects in models of asthma. In this review, we provide an overview of the biology of the metal-dependent and sirtuin deacetylases in the context of asthma. The controversies surrounding the potential use of histone deacetylase inhibitors in asthma are discussed and future directions involving the investigation of more specific analogues are explored.
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