Medicinal Chemistry, Oncology, R&D, Corporate Sigma-Tau S.p.A, Via Pontina km 30, Pomezia, Italy.
Future Med Chem. 2012 Jul;4(11):1439-60. doi: 10.4155/fmc.12.80.
Histone deacetylase inhibitors (HDACis) are one of the last frontiers in pharmaceutical research. Several classes of HDACi have been identified. Although more than 20 HDACi are under preclinical and clinical investigation as single agents and in combination therapies against different cancers, just two of them were approved by the US FDA: Zolinza(®) and Istodax(®), both licensed for the treatment of cutaneous T-cell lymphoma, the latter also of peripheral T-cell lymphoma. Since HDAC enzymes act by forming multiprotein complexes (clusters), containing cofactors, the main problem in designing new HDACi is that the inhibition activity evaluated on isolated enzyme isoforms does not match the in vivo outcomes. In the coming years, the research will be oriented toward a better understanding of the functioning of these protein complexes as well as the development of new screening assays, with the final goal to obtain new drug candidates for the treatment of cancer.
组蛋白去乙酰化酶抑制剂(HDACi)是药物研究的最后一个前沿领域之一。已经确定了几类 HDACi。尽管有 20 多种 HDACi 作为单一药物和联合治疗不同癌症正在进行临床前和临床研究,但只有两种获得了美国 FDA 的批准:Zolinza(®)和 Istodax(®),两者均被批准用于治疗皮肤 T 细胞淋巴瘤,后者也用于治疗外周 T 细胞淋巴瘤。由于 HDAC 酶通过形成包含辅因子的多蛋白复合物(簇)发挥作用,因此在设计新型 HDACi 时的主要问题是,在分离的酶同工型上评估的抑制活性与体内结果不匹配。在未来几年,研究将侧重于更好地了解这些蛋白复合物的功能,以及开发新的筛选测定方法,最终目标是获得用于癌症治疗的新药候选物。