Regulation of FGF10 Signaling in Development and Disease

被引:48
|
作者
Watson, Joanne [1 ,2 ]
Francavilla, Chiara [1 ]
机构
[1] Univ Manchester, Sch Biol Sci, Fac Biol Med & Hlth, Div Mol & Cellular Funct, Manchester, Lancs, England
[2] Univ Manchester, Sch Biol Sci, Fac Biol Med & Hlth, Div Evolut & Genom Sci, Manchester, Lancs, England
基金
英国惠康基金; 英国生物技术与生命科学研究理事会;
关键词
fibroblast growth factor 10; FGF receptor; signaling; development; cancer; genetic disorders; mass spectrometry; quantitative proteomics; FIBROBLAST-GROWTH-FACTOR; EPITHELIAL-MESENCHYMAL CROSSTALK; BRANCHING MORPHOGENESIS; RECEPTOR SPECIFICITY; CELL-PROLIFERATION; GENE-EXPRESSION; MAP KINASE; LUNG; MUTATIONS; FACTOR-10;
D O I
10.3389/fgene.2018.00500
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Fibroblast Growth Factor 10 (FGF10) is a multifunctional mesenchymal-epithelial signaling growth factor, which is essential for multi-organ development and tissue homeostasis in adults. Furthermore, FGF10 deregulation has been associated with human genetic disorders and certain forms of cancer. Upon binding to FGF receptors with heparan sulfate as co-factor, FGF10 activates several intracellular signaling cascades, resulting in cell proliferation, differentiation, and invasion. FGF10 activity is modulated not only by heparan sulfate proteoglycans in the extracellular matrix, but also by hormones and other soluble factors. Despite more than 20 years of research on FGF10 functions, context-dependent regulation of FGF10 signaling specificity remains poorly understood. Emerging modes of FGF10 signaling regulation will be described, focusing on the role of FGF10 trafficking and sub-cellular localization, heparan sulfate proteoglycans, and miRNAs. Systems biology approaches based on quantitative proteomics will be considered for globally investigating FGF10 signaling specificity. Finally, current gaps in our understanding of FGF10 functions, such as the relative contribution of receptor isoforms to signaling activation, will be discussed in the context of genetic disorders and tumorigenesis.
引用
收藏
页数:10
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