کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
8537034 | 1560926 | 2017 | 82 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
Fibroblast growth factors (FGFs) in cancer: FGF traps as a new therapeutic approach
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کلمات کلیدی
FGFRECMPDGFCAFMMPTSP-1EGFHSPGPTX3GAGMDSCFGFMAPK - MAPKStroma - استروماTAM - تامTumor associated macrophage - تومور مرتبط با ماکروفاژTyrosine kinase - تیروزین کینازCancer - سرطانCancer therapy - سرطان درمانmyeloid-derived suppressor cell - سلول های سرکوب کننده مشتق شده از میلوئیدepidermal growth factor - عامل رشد اپیدرمیVascular endothelial growth factor - فاکتور رشد اندوتلیال عروقیVascular Endothelial Growth Factor (VEGF) - فاکتور رشد اندوتلیال عروقی (VEGF)platelet derived growth factor - فاکتور رشد حاصل از پلاکتfibroblast growth factor - فاکتور رشد فیبروبلاستcancer associated fibroblast - فیبروبلاست وابسته به سرطانExtracellular matrix - ماتریکس خارج سلولیmatrix metallopeptidase - ماتریکس متالوپپتیدازMultiple myeloma - مولتیپل میلوماTumor microenvironment - میکرو محیط زیست تومورHeparan sulfate - هپاران سولفاتmitogen-activated protein kinase - پروتئین کیناز فعال با mitogenheparan sulfate proteoglycans - پروپوگلیکان های سولفات heparanGlycosaminoglycan - گلیکوزآمینوگلیکانfibroblast growth factor receptor - گیرنده فاکتور رشد فیبروبلاست
موضوعات مرتبط
علوم پزشکی و سلامت
داروسازی، سم شناسی و علوم دارویی
داروشناسی
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چکیده انگلیسی
Originally characterized as angiogenic factors, fibroblast growth factors (FGFs) are pleiotropic factors that exert autocrine and paracrine functions on tumor and stromal cells. Thus, they may represent key players in the complex crosstalk among angiogenesis, inflammation, tumor growth, and drug resistance, all contributing to tumor progression. Given the multiple activities of FGFs, inhibitors of the FGF/FGFR system may act as “two compartment” targeting drugs able to exert a deep impact on the growth of FGF/FGFR-driven tumors. To date, the discovery of drugs targeting the FGF/FGFR system has focused mainly on the development of selective and non-selective tyrosine kinase FGFR inhibitors. Recently, a different approach has been emerging, aimed at the development of extracellular “FGF ligand traps” able to bind and sequester FGFs, thus preventing their interaction with cognate signaling receptors. This approach is based on the identification of natural FGF ligands followed by the development of small molecule mimetics endowed with a significant FGF binding/neutralizing capacity. Aim of this review is to provide an overview of the role of the FGF/FGFR system in cancer and a comprehensive analysis of the process, based on the study of the FGF interactome, which has led to the identification and characterization of FGF ligand traps. This approach has allowed the development of promising FGF-targeting molecules with potential implications for the therapy of FGF-driven tumors.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Pharmacology & Therapeutics - Volume 179, November 2017, Pages 171-187
Journal: Pharmacology & Therapeutics - Volume 179, November 2017, Pages 171-187
نویسندگان
Marco Presta, Paola Chiodelli, Arianna Giacomini, Marco Rusnati, Roberto Ronca,