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
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