Chen Lijia, Fletcher Steven
a Department of Pharmaceutical Sciences , University of Maryland School of Pharmacy , Baltimore , MD , USA.
Expert Opin Ther Pat. 2017 Feb;27(2):163-178. doi: 10.1080/13543776.2017.1249848. Epub 2016 Nov 17.
The myeloid cell leukemia-1 (MCL-1) protein is one of the key anti-apoptotic members of the B-cell lymphoma-2 (BCL-2) protein family. Over-expression of MCL-1 has been closely related to tumor progression as well as to resistance, not only to traditional chemotherapies but also to targeted therapeutics including BCL-2 inhibitors such as ABT-263. Therefore, there has been extensive research and development in the last decade in both academic and industrial settings to address this unmet medical need. Areas covered: This review covers the research and patent literature of the past 10 years in the field of discovery and development of small-molecule inhibitors of the MCL-1 anti-apoptotic protein. Expert opinion: Small-molecule strategies to disrupt the protein-protein interactions between MCL-1 and its pro-apoptotic counterparts, such as BAK and BIM, have recently emerged. Several small-molecules based on different scaffolds describe promising in vitro data as MCL-1 selective inhibitors. While many lead compounds remain at the in vitro preclinical development stage, the two most recent patent applications describe promising in vivo data, and one small molecule inhibitor has recently entered into clinical development. It is such an exciting moment that the long awaited clinical studies will generate some insight into the therapeutic potential of this anti-cancer approach, and possibly facilitate the further development of other early stage inhibitors.
髓样细胞白血病-1(MCL-1)蛋白是B细胞淋巴瘤-2(BCL-2)蛋白家族中关键的抗凋亡成员之一。MCL-1的过表达不仅与肿瘤进展密切相关,还与包括对传统化疗以及对靶向治疗(如ABT-263等BCL-2抑制剂)的耐药性相关。因此,在过去十年中,学术界和工业界都进行了广泛的研究与开发,以满足这一未被满足的医疗需求。涵盖领域:本综述涵盖了过去10年中MCL-1抗凋亡蛋白小分子抑制剂发现与开发领域的研究和专利文献。专家观点:最近出现了破坏MCL-1与其促凋亡对应物(如BAK和BIM)之间蛋白质-蛋白质相互作用的小分子策略。几种基于不同支架的小分子作为MCL-1选择性抑制剂显示出有前景的体外数据。虽然许多先导化合物仍处于体外临床前开发阶段,但最近的两项专利申请描述了有前景的体内数据,并且一种小分子抑制剂最近已进入临床开发阶段。这是一个令人兴奋的时刻,期待已久的临床研究将对这种抗癌方法的治疗潜力产生一些见解,并可能促进其他早期抑制剂的进一步开发。