Outhwaite Ian R, Kwan Isabelle, Leyte-Vidal Ariel, Shah Neil P, Bahar Ivet, Seeliger Markus A
Department of Pharmacological Sciences, Renaissance School of Medicine, Stony Brook University, Stony Brook, NY 11794, USA.
Laufer Center for Physical and Quantitative Biology, Stony Brook University, Stony Brook, NY 11794, USA.
J Mol Biol. 2025 Oct 15;437(20):169133. doi: 10.1016/j.jmb.2025.169133. Epub 2025 Apr 10.
Allosteric inhibitors have emerged as powerful therapeutic agents capable of overcoming resistance mutations that impair the efficacy of orthosteric inhibitors. However, resistance to allosteric inhibitors can also arise, posing a challenge to their long-term effectiveness. Mechanisms of resistance include altered inhibitor affinity and kinetics, disruption of the allosteric mechanism, changes in receptor recycling and activity, and off-target adaptations such as upregulation of drug efflux pumps or activation of compensatory signaling pathways. Furthermore, the specific mechanism of allosteric regulation induced by inhibitor binding can itself be susceptible to resistance mutations, leading to diminished efficacy. Understanding these diverse resistance mechanisms is crucial for developing strategies to counteract them. One promising approach involves the combination of both allosteric and orthosteric inhibitors, either as separate agents or as linked "bitopic" compounds, to mitigate the impact of resistance mutations. This review explores the molecular basis of resistance to allosteric inhibitors and potential strategies to overcome resistance, offering insights for the development of more resilient therapies.
变构抑制剂已成为强大的治疗药物,能够克服损害正构抑制剂疗效的耐药突变。然而,对变构抑制剂的耐药性也可能出现,这对其长期有效性构成挑战。耐药机制包括抑制剂亲和力和动力学的改变、变构机制的破坏、受体再循环和活性的变化,以及诸如药物外排泵上调或补偿性信号通路激活等脱靶适应性变化。此外,抑制剂结合诱导的变构调节的具体机制本身可能易受耐药突变影响,导致疗效降低。了解这些多样的耐药机制对于制定对抗它们的策略至关重要。一种有前景的方法是将变构抑制剂和正构抑制剂联合使用,无论是作为单独的药物还是作为连接的“双位点”化合物,以减轻耐药突变的影响。本综述探讨了对变构抑制剂耐药的分子基础以及克服耐药性的潜在策略,为开发更具弹性的疗法提供见解。