Bots Michael, Johnstone Ricky W
Cancer Therapeutics Program, The Peter MacCallum Cancer Centre, East Melbourne Victoria, Australia.
Clin Cancer Res. 2009 Jun 15;15(12):3970-7. doi: 10.1158/1078-0432.CCR-08-2786. Epub 2009 Jun 9.
In addition to well-characterized genetic abnormalities that lead to cancer onset and progression, it is now recognized that alterations to the epigenome may also play a significant role in oncogenesis. As a result, epigenetic-modulating agents such as histone deacetylase inhibitors (HDACi) have attracted enormous attention as anticancer drugs. In numerous in vitro and preclinical settings, these compounds have shown their vast potential as single agent anticancer therapies, but unfortunately equivalent responses have not always been observed in patients. Given the pleiotropic effects HDACi have on malignant cells, their true therapeutic potential most likely lies in combination with other anticancer drugs. In this review we will focus on the anticancer effects of HDACi when combined with other cancer therapeutics with an emphasis on those combinations based on a strong molecular rationale.
除了已充分表征的导致癌症发生和进展的基因异常外,现在人们认识到表观基因组的改变在肿瘤发生中也可能起重要作用。因此,诸如组蛋白去乙酰化酶抑制剂(HDACi)等表观遗传调节剂作为抗癌药物引起了极大关注。在众多体外和临床前研究中,这些化合物已显示出作为单一抗癌疗法的巨大潜力,但不幸的是,在患者中并非总能观察到同等的反应。鉴于HDACi对恶性细胞具有多效性作用,其真正的治疗潜力很可能在于与其他抗癌药物联合使用。在本综述中,我们将重点关注HDACi与其他癌症治疗方法联合使用时的抗癌效果,重点是基于强大分子理论依据的联合用药。