نتایج جستجو برای: fgfr

تعداد نتایج: 1529  

Journal: :Molecular and cellular biology 2002
Brian K Yeh Anna V Eliseenkova Alexander N Plotnikov David Green Jared Pinnell Tulay Polat Amel Gritli-Linde Robert J Linhardt Moosa Mohammadi

Sucrose octasulfate (SOS) is believed to stimulate fibroblast growth factor (FGF) signaling by binding and stabilizing FGFs. In this report, we show that SOS induces FGF-dependent dimerization of FGF receptors (FGFRs). The crystal structure of the dimeric FGF2-FGFR1-SOS complex at 2.6-A resolution reveals a symmetric assemblage of two 1:1:1 FGF2-FGFR1-SOS ternary complexes. Within each ternary ...

Journal: :Cancer research 2014
Jeremy H Tchaicha Esra A Akbay Abigail Altabef Oliver R Mikse Eiki Kikuchi Kevin Rhee Rachel G Liao Roderick T Bronson Lynette M Sholl Matthew Meyerson Peter S Hammerman Kwok-Kin Wong

Somatic mutations in FGFR2 are present in 4% to 5% of patients diagnosed with non-small cell lung cancer (NSCLC). Amplification and mutations in FGFR genes have been identified in patients with NSCLCs, and clinical trials are testing the efficacy of anti-FGFR therapies. FGFR2 and other FGFR kinase family gene alterations have been found in both lung squamous cell carcinoma and lung adenocarcino...

2016
Ricardo Costa Benedito A. Carneiro Timothy Taxter Fabio A. Tavora Aparna Kalyan Sachin A. Pai Young Kwang Chae Francis J. Giles

Fibroblast growth factor receptors (FGFR) are transmembrane kinase proteins with growing importance in cancer biology given the frequency of molecular alterations and vast interface with multiple other signaling pathways. Furthermore, numerous FGFR inhibitors in clinical development demonstrate the expanding therapeutic relevance of this pathway. Indeed, results from early phase clinical trials...

Journal: :Cancer research 1994
S W McLeskey I Y Ding M E Lippman F G Kern

Overexpression of some transmembrane tyrosine kinase growth factor receptors in breast and other tumors has been found to correlate with poor prognosis. Following the cloning of the first two members of the fibroblast growth factor family of receptors (FGFRs), amplification of these receptors in breast carcinomas was found. We have examined 23 breast carcinoma cell lines to determine the extent...

Journal: :The Journal of biological chemistry 2011
Kazue Hisaoka Mami Tsuchioka Ryoya Yano Natsuko Maeda Naoto Kajitani Norimitsu Morioka Yoshihiro Nakata Minoru Takebayashi

Recently, both clinical and animal studies demonstrated neuronal and glial plasticity to be important for the therapeutic action of antidepressants. Antidepressants increase glial cell line-derived neurotrophic factor (GDNF) production through monoamine-independent protein-tyrosine kinase, extracellular signal-regulated kinase (ERK), and cAMP responsive element-binding protein (CREB) activation...

Journal: :The Journal of biological chemistry 1992
S Wennström E Landgren P Blume-Jensen L Claesson-Welsh

Signal transduction by tyrosine kinase growth factor receptors involves ligand-induced phosphorylation of substrates for the kinase, resulting in mediation of common or receptor-specific biological signals. We have compared signal transduction pathways for the fibroblast growth factor receptor-1 (FGFR-1), the platelet-derived growth factor beta-receptor (PDGFR-beta), and a chimeric FGFR-1 molec...

2011
Kazue Hisaoka Mami Tsuchioka Ryoya Yano Natsuko Maeda Naoto Kajitani Norimitsu Morioka Yoshihiro Nakata Minoru Takebayashi

Recently, both clinical and animal studies demonstrated neuronal and glial plasticity to be important for the therapeutic action of antidepressants. Antidepressants increase glial cell line-derived neurotrophic factor (GDNF) production through monoamine-independent protein tyrosine kinase (PTK), extracellular signal-regulated kinase (ERK) and cAMP responsive element binding protein (CREB) activ...

Journal: :Journal of cell science 2013
Giulio Auciello Debbie L Cunningham Tulin Tatar John K Heath Joshua Z Rappoport

Fibroblast growth factor receptors (FGFRs) mediate a wide spectrum of cellular responses that are crucial for development and wound healing. However, aberrant FGFR activity leads to cancer. Activated growth factor receptors undergo stimulated endocytosis, but can continue to signal along the endocytic pathway. Endocytic trafficking controls the duration and intensity of signalling, and growth f...

Journal: :Molecular cancer therapeutics 2011
Matthew Squires George Ward Gordan Saxty Valerio Berdini Anne Cleasby Peter King Patrick Angibaud Tim Perera Lynsey Fazal Douglas Ross Charlotte Griffiths Jones Andrew Madin Rajdeep K Benning Emma Vickerstaffe Alistair O'Brien Martyn Frederickson Michael Reader Christopher Hamlett Michael A Batey Sharna Rich Maria Carr Darcey Miller Ruth Feltell Abarna Thiru Susanne Bethell Lindsay A Devine Brent L Graham Andrew Pike Jose Cosme Edward J Lewis Eddy Freyne John Lyons Julie Irving Christopher Murray David R Newell Neil T Thompson

We describe here the identification and characterization of 2 novel inhibitors of the fibroblast growth factor receptor (FGFR) family of receptor tyrosine kinases. The compounds exhibit selective inhibition of FGFR over the closely related VEGFR2 receptor in cell lines and in vivo. The pharmacologic profile of these inhibitors was defined using a panel of human tumor cell lines characterized fo...

2014
Jinjia Chang Xinyang Liu Shanshan Wang Zhe Zhang Zheng Wu Xiaowei Zhang Jin Li

BACKGROUND Fibroblast growth factor receptor (FGFR) gene amplification has been reported in different types of cancer. We performed an up-to-date meta-analysis to further characterize the prognostic value of FGFR gene amplification in patients with cancer. METHODS A search of several databases, including MEDLINE (PubMed), EMBASE, Web of Science, and China National Knowledge Infrastructure, wa...

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