Department of Medicinal Chemistry, School of Pharmacy, Anhui University of Chinese Medicine, Hefei 230012, China; Department of Medicinal Chemistry, Anhui Academy of Chinese Medicine, Hefei 230012, China.
College of Medicine, Jiaxing University, Jiaxing 314001, China.
Eur J Med Chem. 2018 Jan 1;143:449-463. doi: 10.1016/j.ejmech.2017.11.049. Epub 2017 Nov 21.
Polypharmacology has been increasingly advocated for the therapeutic intervention in complex pathological conditions, exemplified by cancer. Although kinase inhibitors (KIs) have revolutionized the treatment for certain types of malignancies, some major medical needs remain unmet due to the relentless advance of drug resistance and insufficient efficacy of mono-target KIs. Hence, "multiple targets, multi-dimensional activities" represents an emerging paradigm for innovative anti-cancer drug discovery. Over recent years, considerable leaps have been made in pursuit of kinase-centric polypharmacological anti-cancer therapeutics, providing avenues to tackling the limitation of mono-target KIs. In the review, we summarize the clinically important mechanisms inducing KI resistance and depict a landscape of recent medicinal chemistry efforts on exploring kinase-centric polypharmacological anti-cancer agents that targeting multiple cancer-related processes. In parallel, some inevitable challenges are emphasized for the sake of more accurate and efficient drug discovery in the field.
多靶化药物设计策略已被广泛提倡用于治疗复杂病理情况,癌症就是一个很好的例子。虽然激酶抑制剂 (KIs) 的出现已经彻底改变了某些类型恶性肿瘤的治疗方法,但由于耐药性的不断发展和单靶 KIs 的疗效不足,一些主要的医疗需求仍未得到满足。因此,“多靶点、多维度活性”代表了创新抗癌药物发现的新兴范例。近年来,人们在以激酶为中心的多靶化抗癌治疗方面取得了重大进展,为解决单靶 KIs 的局限性提供了途径。在这篇综述中,我们总结了诱导 KI 耐药的临床重要机制,并描绘了近年来探索以激酶为中心的多靶化抗癌药物的药物化学研究进展,这些药物针对多种与癌症相关的过程。同时,为了在该领域更准确、更有效地进行药物发现,我们强调了一些不可避免的挑战。