Dipartimento di Scienze della Salute, Università "Magna Græcia" di Catanzaro, Viale Europa, 88100 Catanzaro, Italy.
Net4Science srl, Università 'Magna Græcia' di Catanzaro, Campus Universitario 'S. Venuta', Viale Europa, 88100 Catanzaro, Italy.
Molecules. 2020 Jul 22;25(15):3321. doi: 10.3390/molecules25153321.
The mechanisms of inflammation and cancer are intertwined by complex networks of signaling pathways. Dysregulations in the Janus kinase/signal transducer and activator of transcription (JAK/STAT) pathway underlie several pathogenic conditions related to chronic inflammatory states, autoimmune diseases and cancer. Historically, the potential application of JAK inhibition has been thoroughly explored, thus triggering an escalation of favorable results in this field. So far, five JAK inhibitors have been approved by the Food and Drug Administration (FDA) for the treatment of different diseases. Considering the complexity of JAK-depending processes and their involvement in multiple disorders, JAK inhibitors are the perfect candidates for drug repurposing and for the assessment of multitarget strategies. Herein we reviewed the recent progress concerning JAK inhibition, including the innovations provided by the release of JAKs crystal structures and the improvement of synthetic strategies aimed to simplify of the industrial scale-up.
炎症和癌症的机制通过信号通路的复杂网络相互交织。Janus 激酶/信号转导和转录激活因子(JAK/STAT)通路的失调是与慢性炎症状态、自身免疫性疾病和癌症相关的几种致病条件的基础。从历史上看,JAK 抑制的潜在应用已经得到了彻底的探索,从而在这一领域引发了更多有利结果。迄今为止,已有五种 JAK 抑制剂被美国食品和药物管理局(FDA)批准用于治疗不同的疾病。考虑到 JAK 依赖过程的复杂性及其在多种疾病中的参与,JAK 抑制剂是药物再利用和评估多靶点策略的理想选择。本文综述了 JAK 抑制的最新进展,包括 JAK 晶体结构释放所提供的创新和旨在简化工业规模的合成策略的改进。