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成纤维细胞生长因子同源因子:经典和非经典作用机制。

Fibroblast growth factor homologous factors: canonical and non-canonical mechanisms of action.

机构信息

Department of Biological Sciences, Hunter College of City University, New York, New York, USA.

Biology Program, The Graduate Center City University, New York, New York, USA.

出版信息

J Physiol. 2024 Sep;602(17):4097-4110. doi: 10.1113/JP286313. Epub 2024 Jul 31.

Abstract

Since their discovery nearly 30 years ago, fibroblast growth factor homologous factors (FHFs) are now known to control the functionality of excitable tissues through a range of mechanisms. Nervous and cardiac system dysfunctions are caused by loss- or gain-of-function mutations in FHF genes. The best understood 'canonical' targets for FHF action are voltage-gated sodium channels, and recent studies have expanded the repertoire of ways that FHFs modulate sodium channel gating. Additional 'non-canonical' functions of FHFs in excitable and non-excitable cells, including cancer cells, have been reported over the past dozen years. This review summarizes and evaluates reported canonical and non-canonical FHF functions.

摘要

自近 30 年前发现以来,成纤维细胞生长因子同源因子(FHFs)现已被证实通过一系列机制控制兴奋组织的功能。FHF 基因突变导致神经和心脏系统功能障碍,功能丧失或获得。FHF 作用的最佳“经典”靶标是电压门控钠离子通道,最近的研究扩展了 FHF 调节钠离子通道门控的方式。过去十几年间,已有报道称 FHF 在兴奋和非兴奋细胞(包括癌细胞)中具有其他“非经典”功能。本综述总结和评估了报道的经典和非经典 FHF 功能。

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