Literature DB >> 22388515

Molecular pathways: fibroblast growth factor signaling: a new therapeutic opportunity in cancer.

A Nigel Brooks1, Elaine Kilgour, Paul D Smith.   

Abstract

The fibroblast growth factor/fibroblast growth factor receptor (FGF/FGFR) signaling axis plays an important role in normal organ, vascular, and skeletal development. Deregulation of FGFR signaling through genetic modification or overexpression of the receptors (or their ligands) has been observed in numerous tumor settings, whereas the FGF/FGFR axis also plays a key role in driving tumor angiogenesis. A growing body of preclinical data shows that inhibition of FGFR signaling can result in antiproliferative and/or proapoptotic effects, both in vitro and in vivo, thus confirming the validity of the FGF/FGFR axis as a potential therapeutic target. In the past, development of therapeutic approaches to target this axis has been hampered by our inability to develop FGFR-selective agents. With the advent of a number of new modalities for selectively inhibiting FGF/FGFR signaling, we are now in a unique position to test and validate clinically the many hypotheses that have been generated preclinically. ©2012 AACR.

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Year:  2012        PMID: 22388515     DOI: 10.1158/1078-0432.CCR-11-0699

Source DB:  PubMed          Journal:  Clin Cancer Res        ISSN: 1078-0432            Impact factor:   12.531


  153 in total

1.  Overexpression of miR-100 inhibits cancer growth, migration, and chemosensitivity in human NSCLC cells through fibroblast growth factor receptor 3.

Authors:  Jie Luo; Bin Chen; Xian-Xiu Ji; Song-Wen Zhou; Di Zheng
Journal:  Tumour Biol       Date:  2015-08-28

2.  Evaluation of FGFR3 as a Therapeutic Target in Head and Neck Squamous Cell Carcinoma.

Authors:  Anne von Mässenhausen; Mario Deng; Hannah Billig; Angela Queisser; Wenzel Vogel; Glen Kristiansen; Andreas Schröck; Friedrich Bootz; Friederike Göke; Alina Franzen; Lynn Heasley; Jutta Kirfel; Johannes Brägelmann; Sven Perner
Journal:  Target Oncol       Date:  2016-10       Impact factor: 4.493

3.  Loss of FGF21 in diabetic mouse during hepatocellular carcinogenetic transformation.

Authors:  Quan Zhang; Yan Li; Tingting Liang; Xuemian Lu; Xingkai Liu; Chi Zhang; Xin Jiang; Robert C Martin; Mingliang Cheng; Lu Cai
Journal:  Am J Cancer Res       Date:  2015-04-15       Impact factor: 6.166

4.  Phase Ib study of dovitinib in combination with gemcitabine plus cisplatin or gemcitabine plus carboplatin in patients with advanced solid tumors.

Authors:  Matthew D Galsky; Marshall Posner; Randall F Holcombe; Karen M Lee; Krzysztof Misiukiewicz; Che-Kai Tsao; James Godbold; Rothschild Soto; Kiev Gimpel-Tetra; Nancy Lowe; William K Oh
Journal:  Cancer Chemother Pharmacol       Date:  2014-07-15       Impact factor: 3.333

5.  Lineage-specific biomarkers predict response to FGFR inhibition.

Authors:  David C Loch; Pamela M Pollock
Journal:  Cancer Discov       Date:  2012-12       Impact factor: 39.397

Review 6.  New targetable oncogenes in non-small-cell lung cancer.

Authors:  Geoffrey R Oxnard; Adam Binder; Pasi A Jänne
Journal:  J Clin Oncol       Date:  2013-02-11       Impact factor: 44.544

7.  Fibroblast growth factor receptor 3 is a rational therapeutic target in bladder cancer.

Authors:  Kilian M Gust; David J McConkey; Shannon Awrey; Paul K Hegarty; Jing Qing; Jolanta Bondaruk; Avi Ashkenazi; Bogdan Czerniak; Colin P Dinney; Peter C Black
Journal:  Mol Cancer Ther       Date:  2013-05-08       Impact factor: 6.261

8.  Membrane-Type 1 Matrix Metalloproteinase Downregulates Fibroblast Growth Factor-2 Binding to the Cell Surface and Intracellular Signaling.

Authors:  Evelyne Tassone; Cristina Valacca; Paolo Mignatti
Journal:  J Cell Physiol       Date:  2015-02       Impact factor: 6.384

Review 9.  Cyclin D degradation by E3 ligases in cancer progression and treatment.

Authors:  Shuo Qie; J Alan Diehl
Journal:  Semin Cancer Biol       Date:  2020-01-30       Impact factor: 15.707

10.  ARS-interacting multi-functional protein 1 induces proliferation of human bone marrow-derived mesenchymal stem cells by accumulation of β-catenin via fibroblast growth factor receptor 2-mediated activation of Akt.

Authors:  Seo Yoon Kim; Woo Sung Son; Min Chul Park; Chul Min Kim; Byung Hyun Cha; Kang Jun Yoon; Soo-Hong Lee; Sang Gyu Park
Journal:  Stem Cells Dev       Date:  2013-06-25       Impact factor: 3.272

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