Antolin Albert A, Workman Paul, Mestres Jordi, Al-Lazikani Bissan
Division of Cancer Therapeutics, The Institute of Cancer Research, London, United Kingdom.
Curr Pharm Des. 2016;22(46):6935-6945. doi: 10.2174/1381612822666160923115828.
Over the past decade, a more comprehensive, large-scale approach to studying cancer genetics and biology has revealed the challenges of tumor heterogeneity, adaption, evolution and drug resistance, while systems-based pharmacology and chemical biology strategies have uncovered a much more complex interaction between drugs and the human proteome than was previously anticipated. In this mini-review we assess the progress and potential of drug polypharmacology in biomarker-driven precision oncology. Polypharmacology not only provides great opportunities for drug repurposing to exploit off-target effects in a new single-target indication but through simultaneous blockade of multiple targets or pathways offers exciting opportunities to slow, overcome or even prevent inherent or adaptive drug resistance. We highlight the many challenges associated with exploiting known or desired polypharmacology in drug design and development, and assess computational and experimental methods to uncover unknown polypharmacology. A comprehensive understanding of the intricate links between polypharmacology, efficacy and safety is urgently needed if we are to tackle the enduring challenge of cancer drug resistance and to fully exploit polypharmacology for the ultimate benefit of cancer patients.
在过去十年中,一种更全面、大规模的研究癌症遗传学和生物学的方法揭示了肿瘤异质性、适应性、进化和耐药性等挑战,而基于系统的药理学和化学生物学策略则发现,药物与人类蛋白质组之间的相互作用比之前预期的要复杂得多。在这篇小型综述中,我们评估了药物多药理学在生物标志物驱动的精准肿瘤学中的进展和潜力。多药理学不仅为药物再利用提供了巨大机会,以在新的单靶点适应症中利用脱靶效应,而且通过同时阻断多个靶点或通路,为减缓、克服甚至预防内在或适应性耐药性提供了令人兴奋的机会。我们强调了在药物设计和开发中利用已知或期望的多药理学所面临的诸多挑战,并评估了揭示未知多药理学的计算和实验方法。如果我们要应对癌症耐药性这一持久挑战,并充分利用多药理学为癌症患者带来最终益处,那么迫切需要全面了解多药理学、疗效和安全性之间的复杂联系。