Instituto de Medicina Molecular, Faculdade de Medicina da Universidade de Lisboa, Av. Prof. Egas Moniz, 1649-028 Lisboa, Portugal.
Instituto de Medicina Molecular, Faculdade de Medicina da Universidade de Lisboa, Av. Prof. Egas Moniz, 1649-028 Lisboa, Portugal and Department of Chemistry, University of Cambridge, Lensfield Road, CB2 1EW Cambridge, UK.
Chem Soc Rev. 2016 Nov 7;45(22):6130-6137. doi: 10.1039/c5cs00916b.
Treatment of cancer is a significant challenge in clinical medicine, and its research is a top priority in chemical biology and drug discovery. Consequently, there is an urgent need for identifying innovative chemotypes capable of modulating unexploited drug targets. The transient receptor potential (TRPs) channels persist scarcely explored as targets, despite intervening in a plethora of pathophysiological events in numerous diseases, including cancer. Both agonists and antagonists have proven capable of evoking phenotype changes leading to either cell death or reduced cell migration. Among these, natural products entail biologically pre-validated and privileged architectures for TRP recognition. Furthermore, several natural products have significantly contributed to our current knowledge on TRP biology. In this Tutorial Review we focus on selected natural products, e.g. capsaicinoids, cannabinoids and terpenes, by highlighting challenges and opportunities in their use as starting points for designing natural product-inspired TRP channel modulators. Importantly, the de-orphanization of natural products as TRP channel ligands may leverage their exploration as viable strategy for developing anticancer therapies. Finally, we foresee that TRP channels may be explored for the selective pharmacodelivery of cytotoxic payloads to diseased tissues, providing an innovative platform in chemical biology and molecular medicine.
癌症治疗是临床医学的重大挑战,其研究是化学生物学和药物发现的重中之重。因此,迫切需要确定能够调节未开发药物靶点的创新化学型。尽管瞬时受体电位 (TRP) 通道在包括癌症在内的许多疾病中的多种病理生理事件中发挥作用,但它们作为靶点仍未得到充分探索。激动剂和拮抗剂都已被证明能够引发表型变化,导致细胞死亡或细胞迁移减少。在这些化合物中,天然产物具有用于 TRP 识别的经过生物预先验证的和有利的结构。此外,几种天然产物极大地促进了我们对 TRP 生物学的现有认识。在本综述中,我们重点关注选定的天然产物,例如辣椒素类、大麻素和萜类化合物,强调了将它们用作设计天然产物启发的 TRP 通道调节剂的起点所面临的挑战和机遇。重要的是,将天然产物去孤儿化作为 TRP 通道配体可能会促进将其作为开发抗癌疗法的可行策略进行探索。最后,我们预计 TRP 通道可能会被探索用于将细胞毒性有效载荷选择性递送至患病组织,为化学生物学和分子医学提供一个创新平台。