Turner Cortney A, Eren-Koçak Emine, Inui Edny G, Watson Stanley J, Akil Huda
Molecular & Behavioral Neuroscience Institute, University of Michigan, Ann Arbor, MI, USA.
Institute of Neurological Sciences and Psychiatry, Hacettepe University, Ankara, Turkey.
Semin Cell Dev Biol. 2016 May;53:136-43. doi: 10.1016/j.semcdb.2015.10.003. Epub 2015 Oct 23.
The role of the fibroblast growth factor (FGF) system in brain-related disorders has received considerable attention in recent years. To understand the role of this system in neurological and psychiatric disorders, it is important to identify the specific members of the FGF family that are implicated, their location and the various mechanisms they can be modulated. Each disorder appears to impact specific molecular players in unique anatomical locations, and all of these could conceivably become targets for treatment. In the last several years, the issue of how to target this system directly has become an area of increasing interest. To date, the most promising therapeutics are small molecule inhibitors and antibodies that modulate FGF receptor (FGFR) function. Beyond attempting to modify the primary players affected by a given brain disorder, it may prove useful to target molecules, such as membrane-bound or extracellular proteins that interact with FGF ligands or FGFRs to modulate signaling.
近年来,成纤维细胞生长因子(FGF)系统在脑相关疾病中的作用受到了广泛关注。为了解该系统在神经和精神疾病中的作用,确定涉及的FGF家族特定成员、它们的位置以及可被调节的各种机制非常重要。每种疾病似乎都在独特的解剖位置影响特定的分子参与者,所有这些都有可能成为治疗靶点。在过去几年中,如何直接靶向该系统的问题已成为一个越来越受关注的领域。迄今为止,最有前景的治疗方法是调节FGF受体(FGFR)功能的小分子抑制剂和抗体。除了试图改变受特定脑部疾病影响的主要参与者外,靶向与FGF配体或FGFR相互作用以调节信号传导的分子,如膜结合或细胞外蛋白质,可能也被证明是有用的。