Fibroblast Growth Factor Receptor Inhibitors as a Cancer Treatment: From a Biologic Rationale to Medical Perspectives

被引:351
作者
Dieci, Maria Vittoria [1 ,3 ,5 ]
Arnedos, Monica [1 ,3 ]
Andre, Fabrice [1 ,3 ,4 ]
Soria, Jean Charles [2 ,3 ,4 ]
机构
[1] Inst Gustave Roussy, Breast Canc Unit, F-94800 Villejuif, France
[2] Inst Gustave Roussy, Early Drug Dev Unit SITEP, Dept Med Oncol, F-94800 Villejuif, France
[3] Inst Gustave Roussy, INSERM, Unit U981, F-94800 Villejuif, France
[4] Univ Paris 11, Orsay, France
[5] Univ Hosp, Dept Oncol Hematol & Resp Dis, Modena, Italy
关键词
TRIPLE ANGIOKINASE INHIBITOR; TYROSINE KINASE INHIBITOR; PHASE-I; SELECTIVE INHIBITOR; MULTIPLE-MYELOMA; FGFR3; MUTATIONS; BREAST-CANCER; CELL-LINES; BIBF; 1120; ACTIVATING MUTATIONS;
D O I
10.1158/2159-8290.CD-12-0362
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The fibroblast growth factor/fibroblast growth factor receptor (FGF/FGFR) signaling pathway plays a fundamental role in many physiologic processes, including embryogenesis, adult tissue homeostasis, and wound healing, by orchestrating angiogenesis. Ligand-independent and ligand-dependent activation have been implicated in a broad range of human malignancies and promote cancer progression in tumors driven by FGF/FGFR oncogenic mutations or amplifications, tumor neoangiogenesis, and targeted treatment resistance, thereby supporting a strong rationale for anti-FGF/FGFR agent development. Efforts are being pursued to develop selective approaches for use against this pathway by optimizing the management of emerging, class-specific toxicity profiles and correctly designing clinical trials to address these different issues. Significance: FGF/FGFR pathway deregulations are increasingly recognized across different human cancers. Understanding the mechanisms at the basis of these alterations and their multiple roles in cancer promotion and drug resistance is a fundamental step for further implementation of targeted therapies and research strategies. Cancer Discov; 3(3); 264-79. (C) 2012 AACR.
引用
收藏
页码:264 / 279
页数:16
相关论文
共 94 条
[31]   Discovery of 3-(2,6-Dichloro-3,5-dimethoxy-phenyl)-1-{6-[4-(4-ethyl-piperazin-1-yl)-phenylamino]-pyrimidin-4-yl}-1-methyl-urea (NVP-BGJ398), A Potent and Selective Inhibitor of the Fibroblast Growth Factor Receptor Family of Receptor Tyrosine Kinase [J].
Guagnano, Vito ;
Furet, Pascal ;
Spanka, Carsten ;
Bordas, Vincent ;
Le Douget, Mickael ;
Stamm, Christelle ;
Brueggen, Josef ;
Jensen, Michael R. ;
Schnell, Christian ;
Schmid, Herbert ;
Wartmann, Markus ;
Berghausen, Joerg ;
Drueckes, Peter ;
Zimmerlin, Alfred ;
Bussiere, Dirksen ;
Murray, Jeremy ;
Porta, Diana Graus .
JOURNAL OF MEDICINAL CHEMISTRY, 2011, 54 (20) :7066-7083
[32]   Prospective study of FGFR3 mutations as a prognostic factor in nonmuscle invasive urothelial bladder carcinomas [J].
Hernandez, Silvia ;
Lopez-Knowles, Elena ;
Lloreta, Josep ;
Kogevinas, Manolis ;
Amoros, Alex ;
Tardon, Adonina ;
Carrato, Alfredo ;
Serra, Consol ;
Malats, Nuria ;
Real, Francisco X. .
JOURNAL OF CLINICAL ONCOLOGY, 2006, 24 (22) :3664-3671
[33]   FGFR3 mutations in prostate cancer: association with low-grade tumors [J].
Hernandez, Silvia ;
de Muga, Silvia ;
Agell, Laia ;
Juanpere, Nuria ;
Esgueva, Raquel ;
Lorente, Jose A. ;
Mojal, Sergi ;
Serrano, Sergio ;
Lloreta, Josep .
MODERN PATHOLOGY, 2009, 22 (06) :848-856
[34]   BIBF 1120: Triple angiokinase inhibitor with sustained receptor blockade and good antitumor efficacy [J].
Hilberg, Frank ;
Roth, Gerald J. ;
Krssak, Martin ;
Kautschitsch, Susanna ;
Sommergruber, Wolfgang ;
Tontsch-Grunt, Ulrike ;
Garin-Chesa, Pilar ;
Bader, Gerd ;
Zoephel, Andreas ;
Quant, Jens ;
Heckel, Armin ;
Rettig, Wolfgang J. .
CANCER RESEARCH, 2008, 68 (12) :4774-4782
[35]   Alternative Splicing of Fibroblast Growth Factor Receptor IgIII Loops in Cancer [J].
Holzmann, Klaus ;
Grunt, Thomas ;
Heinzle, Christine ;
Sampl, Sandra ;
Steinhoff, Heinrich ;
Reichmann, Nicole ;
Kleiter, Miriam ;
Hauck, Marlene ;
Marian, Brigitte .
JOURNAL OF NUCLEIC ACIDS, 2012, 2012
[36]   A genome-wide association study identifies alleles in FGFR2 associated with risk of sporadic postmenopausal breast cancer [J].
Hunter, David J. ;
Kraft, Peter ;
Jacobs, Kevin B. ;
Cox, David G. ;
Yeager, Meredith ;
Hankinson, Susan E. ;
Wacholder, Sholom ;
Wang, Zhaoming ;
Welch, Robert ;
Hutchinson, Amy ;
Wang, Junwen ;
Yu, Kai ;
Chatterjee, Nilanjan ;
Orr, Nick ;
Willett, Walter C. ;
Colditz, Graham A. ;
Ziegler, Regina G. ;
Berg, Christine D. ;
Buys, Saundra S. ;
McCarty, Catherine A. ;
Feigelson, Heather Spencer ;
Calle, Eugenia E. ;
Thun, Michael J. ;
Hayes, Richard B. ;
Tucker, Margaret ;
Gerhard, Daniela S. ;
Fraumeni, Joseph F., Jr. ;
Hoover, Robert N. ;
Thomas, Gilles ;
Chanock, Stephen J. .
NATURE GENETICS, 2007, 39 (07) :870-874
[37]   Gene amplification profiling of esophageal squamous cell carcinomas by DNA array CGH [J].
Ishizuka, T ;
Tanabe, C ;
Sakamoto, H ;
Aoyagi, K ;
Maekawa, M ;
Matsukura, N ;
Tokunaga, A ;
Tajiri, T ;
Yoshida, T ;
Terada, M ;
Sasaki, H .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2002, 296 (01) :152-155
[38]   8p11 myeloproliferative syndrome: a review [J].
Jackson, Courtney C. ;
Medeiros, L. Jeffrey ;
Miranda, Roberto N. .
HUMAN PATHOLOGY, 2010, 41 (04) :461-476
[39]  
Jang JH, 2001, CANCER RES, V61, P3541
[40]   A phase I study to determine the safety, pharmacokinetics and pharmacodynamics of a dual VEGFR and FGFR inhibitor, brivanib, in patients with advanced or metastatic solid tumors [J].
Jonker, D. J. ;
Rosen, L. S. ;
Sawyer, M. B. ;
de Braud, F. ;
Wilding, G. ;
Sweeney, C. J. ;
Jayson, G. C. ;
McArthur, G. A. ;
Rustin, G. ;
Goss, G. ;
Kantor, J. ;
Velasquez, L. ;
Syed, S. ;
Mokliatchouk, O. ;
Feltquate, D. M. ;
Kollia, G. ;
Nuyten, D. S. A. ;
Galbraith, S. .
ANNALS OF ONCOLOGY, 2011, 22 (06) :1413-1419