Unit for Structural Biology, Laboratory for Protein Biochemistry and Biomolecular Engineering, Ghent University, K.L. Ledeganckstraat 35, 9000 Ghent, Belgium.
Nat Rev Cancer. 2012 Nov;12(11):753-66. doi: 10.1038/nrc3371. Epub 2012 Oct 18.
Intracellular signalling cascades initiated by class III receptor tyrosine kinases (RTK-IIIs) and their cytokine ligands contribute to haematopoiesis and mesenchymal tissue development. They are also implicated in a wide range of inflammatory disorders and cancers. Recent snapshots of RTK-III ectodomains in complex with cognate cytokines have revealed timely insights into the structural determinants of RTK-III activation, evolution and pathology. Importantly, candidate 'driver' and 'passenger' mutations that have been identified in RTK-IIIs can now be collectively mapped for the first time to structural scaffolds of the corresponding RTK-III ectodomains. Such insights will generate a renewed interest in dissecting the mechanistic effects of such mutations and their therapeutic relevance.
由 III 类受体酪氨酸激酶(RTK-III)及其细胞因子配体引发的细胞内信号级联反应有助于造血和间充质组织的发育。它们也与广泛的炎症性疾病和癌症有关。最近,与同源细胞因子结合的 RTK-III 胞外结构域的快照揭示了 RTK-III 激活、进化和病理学的结构决定因素的及时见解。重要的是,现在可以首次将 RTK-III 中鉴定出的候选“驱动”和“乘客”突变集体映射到相应 RTK-III 胞外结构域的结构支架上。这些见解将重新激发人们对剖析此类突变的机制影响及其治疗相关性的兴趣。