School of Pharmacy, College of Pharmacy, Taipei Medical University, 250 Wuxing Street, Taipei, 11031, Taiwan.
Biomedical Commercialization Center, Taipei Medical University, Taipei, 11031, Taiwan.
J Biomed Sci. 2021 Apr 12;28(1):27. doi: 10.1186/s12929-021-00721-x.
Epigenetic drug discovery field has evidenced significant advancement in the recent times. A plethora of small molecule inhibitors have progressed to clinical stage investigations and are being explored exhaustively to ascertain conclusive benefits in diverse malignancies. Literature precedents indicates that substantial amount of efforts were directed towards the use of epigenetic tools in monotherapy as well as in combination regimens at the clinical level, however, the preclinical/preliminary explorations were inclined towards the identification of prudent approaches that can leverage the anticancer potential of small molecule epigenetic inhibitors as single agents only. This review article presents an update of FDA approved epigenetic drugs along with the epigenetic inhibitors undergoing clinical stage investigations in different cancer types. A detailed discussion of the pragmatic strategies that are expected to steer the progress of the epigenetic therapy through the implementation of emerging approaches such as PROTACS and CRISPR/Cas9 along with logical ways for scaffold fabrication to selectively approach the enzyme isoforms in pursuit of garnering amplified antitumor effects has been covered. In addition, the compilation also presents the rational strategies for the construction of multi-targeting scaffold assemblages employing previously identified pharmacophores as potential alternatives to the combination therapy.
表观遗传学药物发现领域在最近取得了重大进展。大量的小分子抑制剂已经进入临床阶段的研究,并正在进行广泛的探索,以确定在各种恶性肿瘤中的明确获益。文献先例表明,大量的努力都集中在临床水平上使用表观遗传学工具进行单药治疗以及联合治疗方案上,然而,临床前/初步探索倾向于确定谨慎的方法,这些方法可以利用小分子表观遗传学抑制剂作为单一药物的抗癌潜力。本文综述了 FDA 批准的表观遗传学药物以及不同癌症类型中正在进行临床阶段研究的表观遗传学抑制剂。详细讨论了预计通过实施新兴方法(如 PROTACS 和 CRISPR/Cas9)来推动表观遗传学治疗进展的实用策略,以及为选择性接近酶同工型以获得放大的抗肿瘤效果而进行支架设计的合理方法。此外,该汇编还提出了构建多靶点支架组合的合理策略,利用以前确定的药效团作为联合治疗的潜在替代品。