-
1
-
-
61649100307
-
The FGF family: Biology, pathophysiology and therapy
-
Beenken A, Mohammadi M. The FGF family: biology, pathophysiology and therapy. Nat Rev Drug Discov 2009; 8: 235-53.
-
(2009)
Nat Rev Drug Discov
, vol.8
, pp. 235-253
-
-
Beenken, A.1
Mohammadi, M.2
-
2
-
-
84868260259
-
Alternative splicing of fi broblast growth factor receptor Ig III loops in cancer
-
Holzmann K, Grunt T, Heinzle C, McKeehan WL. Alternative splicing of fi broblast growth factor receptor Ig III loops in cancer. J Nucleic Acids 2012; 2012: 950508.
-
(2012)
J Nucleic Acids
, vol.2012
, pp. 950508
-
-
Holzmann, K.1
Grunt, T.2
Heinzle, C.3
McKeehan, W.L.4
-
3
-
-
79953718346
-
Biology of FGFRL1, the fi fth fi broblast growth factor receptor
-
Trueb B. Biology of FGFRL1, the fi fth fi broblast growth factor receptor. Cell Mol Life Sci 2011; 68: 951-64.
-
(2011)
Cell Mol Life Sci
, vol.68
, pp. 951-964
-
-
Trueb, B.1
-
4
-
-
75149170979
-
Fibroblast growth factor signaling: From development to cancer
-
Turner N, Grose R. Fibroblast growth factor signaling: from development to cancer. Nat Rev Cancer 2010; 10: 116-29.
-
(2010)
Nat Rev Cancer
, vol.10
, pp. 116-129
-
-
Turner, N.1
Grose, R.2
-
6
-
-
80053493427
-
Beyond VEGF: Inhibition of the fi broblast growth factor pathway and antiangiogenesis
-
Lieu C, Heymach J, Overman M, Tran H, Kopetz S. Beyond VEGF: inhibition of the fi broblast growth factor pathway and antiangiogenesis. Clin Cancer Res 2011; 17: 6130-9.
-
(2011)
Clin Cancer Res
, vol.17
, pp. 6130-6139
-
-
Lieu, C.1
Heymach, J.2
Overman, M.3
Tran, H.4
Kopetz, S.5
-
7
-
-
0027053487
-
Potent synergism between vascular endothelial growth factor and basic fi broblast growth factor in the induction of angiogenesis in vitro
-
Pepper MS, Ferrara N, Orci L, Montesano R. Potent synergism between vascular endothelial growth factor and basic fi broblast growth factor in the induction of angiogenesis in vitro. Biochem Biophys Res Commun 1992; 189: 824-31.
-
(1992)
Biochem Biophys Res Commun
, vol.189
, pp. 824-831
-
-
Pepper, M.S.1
Ferrara, N.2
Orci, L.3
Montesano, R.4
-
8
-
-
33947101019
-
Patterns of somatic mutation in human cancer genomes
-
Greenman C, Stephens P, Smith R, Dalgliesh GL, Hunter C, Bignell G, et al. Patterns of somatic mutation in human cancer genomes. Nature 2007; 446: 153-8.
-
(2007)
Nature
, vol.446
, pp. 153-158
-
-
Greenman, C.1
Stephens, P.2
Smith, R.3
Dalgliesh, G.L.4
Hunter, C.5
Bignell, G.6
-
9
-
-
78650451788
-
Frequent and focal FGFR1 amplifi cation associates with therapeutically tractable FGFR1 dependency in squamous cell lung cancer
-
Weiss J, Sos ML, Seidel D, Peifer M, Zander T, Heuckmann JM, et al. Frequent and focal FGFR1 amplifi cation associates with therapeutically tractable FGFR1 dependency in squamous cell lung cancer. Sci Transl Med 2010; 2: 62ra93.
-
(2010)
Sci Transl Med
, vol.2
, pp. 62-93
-
-
Weiss, J.1
Sos, M.L.2
Seidel, D.3
Peifer, M.4
Zander, T.5
Heuckmann, J.M.6
-
10
-
-
0030845817
-
Mapping of DNA amplifi cations at 15 chromosomal localizations in 1875 breast tumors: Defi nition of phenotypic groups
-
Courjal F, Cuny M, Simony-Lafontaine J, Louason G, Speiser P, Zeillinger R, et al. Mapping of DNA amplifi cations at 15 chromosomal localizations in 1875 breast tumors: defi nition of phenotypic groups. Cancer Res 1997; 57: 4360-7.
-
(1997)
Cancer Res
, vol.57
, pp. 4360-4367
-
-
Courjal, F.1
Cuny, M.2
Simony-Lafontaine, J.3
Louason, G.4
Speiser, P.5
Zeillinger, R.6
-
11
-
-
34548099690
-
High-resolution single nucleotide polymorphism array analysis of epithelial ovarian cancer reveals numerous microdeletions and amplifi cations
-
Gorringe KL, Jacobs S, Thompson ER, Sridhar A, Qiu W, Choong DY, et al. High-resolution single nucleotide polymorphism array analysis of epithelial ovarian cancer reveals numerous microdeletions and amplifi cations. Clin Cancer Res 2007; 13: 4731-9.
-
(2007)
Clin Cancer Res
, vol.13
, pp. 4731-4739
-
-
Gorringe, K.L.1
Jacobs, S.2
Thompson, E.R.3
Sridhar, A.4
Qiu, W.5
Choong, D.Y.6
-
12
-
-
0035361601
-
High-throughput tissue microarray analysis of 3p25 (RAF1) and 8p12 (FGFR1) copy number alterations in urinary bladder cancer
-
Simon R, Richter J, Wagner U, Fijan A, Bruderer J, Schmid U, et al. High-throughput tissue microarray analysis of 3p25 (RAF1) and 8p12 (FGFR1) copy number alterations in urinary bladder cancer. Cancer Res 2001; 61: 4514-9.
-
(2001)
Cancer Res
, vol.61
, pp. 4514-4519
-
-
Simon, R.1
Richter, J.2
Wagner, U.3
Fijan, A.4
Bruderer, J.5
Schmid, U.6
-
13
-
-
33846471623
-
Recurrent FGFR1 amplifi cation and high FGFR1 protein expression in oral squamous cell carcinoma (OSCC)
-
Freier K, Schwaenen C, Sticht C, Flechtenmacher C, Mühling J, Hofele C, et al. Recurrent FGFR1 amplifi cation and high FGFR1 protein expression in oral squamous cell carcinoma (OSCC). Oral Oncol 2007; 43: 60-6.
-
(2007)
Oral Oncol
, vol.43
, pp. 60-66
-
-
Freier, K.1
Schwaenen, C.2
Sticht, C.3
Flechtenmacher, C.4
Mühling, J.5
Hofele, C.6
-
14
-
-
18544379034
-
Gene amplifi cation profi ling of esophageal squamous cell carcinomas by DNA array CGH
-
Ishizuka T, Tanabe C, Sakamoto H, Aoyagi K, Maekawa M, Matsukura N, et al. Gene amplifi cation profi ling of esophageal squamous cell carcinomas by DNA array CGH. Biochem Biophys Res Commun 2002; 296: 152-5.
-
(2002)
Biochem Biophys Res Commun
, vol.296
, pp. 152-155
-
-
Ishizuka, T.1
Tanabe, C.2
Sakamoto, H.3
Aoyagi, K.4
Maekawa, M.5
Matsukura, N.6
-
15
-
-
0242525635
-
Gene amplifi cations associated with the development of hormone-resistant prostate cancer
-
Edwards J, Krishna NS, Witton CJ, Bartlett JM. Gene amplifi cations associated with the development of hormone-resistant prostate cancer. Clin Cancer Res 2003; 9: 5271-81.
-
(2003)
Clin Cancer Res
, vol.9
, pp. 5271-5281
-
-
Edwards, J.1
Krishna, N.S.2
Witton, C.J.3
Bartlett, J.M.4
-
16
-
-
38849166096
-
Modeling genomic diversity and tumor dependency in malignant melanoma
-
Lin WM, Baker AC, Beroukhim R, Winckler W, Feng W, Marmion JM, et al. Modeling genomic diversity and tumor dependency in malignant melanoma. Cancer Res 2008; 68: 664-73.
-
(2008)
Cancer Res
, vol.68
, pp. 664-673
-
-
Lin, W.M.1
Baker, A.C.2
Beroukhim, R.3
Winckler, W.4
Feng, W.5
Marmion, J.M.6
-
17
-
-
26444481568
-
Sequence survey of receptor tyrosine kinases reveals mutations in glioblastomas
-
Rand V, Huang J, Stockwell T, Ferriera S, Buzko O, Levy S, et al. Sequence survey of receptor tyrosine kinases reveals mutations in glioblastomas. Proc Natl Acad Sci U S A 2005; 102: 14344-9.
-
(2005)
Proc Natl Acad Sci U S A
, vol.102
, pp. 14344-14349
-
-
Rand, V.1
Huang, J.2
Stockwell, T.3
Ferriera, S.4
Buzko, O.5
Levy, S.6
-
19
-
-
1642421743
-
Distinct stem cell myeloproliferative/T lymphoma syndromes induced by ZNF198-FGFR1 and BCR-FGFR1 fusion genes from 8p11 translocations
-
Roumiantsev S, Krause DS, Neumann CA, Dimitri CA, Asiedu F, Cross NC, et al. Distinct stem cell myeloproliferative/T lymphoma syndromes induced by ZNF198-FGFR1 and BCR-FGFR1 fusion genes from 8p11 translocations. Cancer Cell 2004; 5: 287-98.
-
(2004)
Cancer Cell
, vol.5
, pp. 287-298
-
-
Roumiantsev, S.1
Krause, D.S.2
Neumann, C.A.3
Dimitri, C.A.4
Asiedu, F.5
Cross, N.C.6
-
20
-
-
42049120475
-
FGFR2-amplifi ed gastric cancer cell lines require FGFR2 and Erbb3 signaling for growth and survival
-
Kunii K, Davis L, Gorenstein J, Hatch H, Yashiro M, Di Bacco A, et al. FGFR2-amplifi ed gastric cancer cell lines require FGFR2 and Erbb3 signaling for growth and survival. Cancer Res 2008; 68: 2340-8.
-
(2008)
Cancer Res
, vol.68
, pp. 2340-2348
-
-
Kunii, K.1
Davis, L.2
Gorenstein, J.3
Hatch, H.4
Yashiro, M.5
Di Bacco, A.6
-
21
-
-
77950866696
-
Integrative molecular profi ling of triple negative breast cancers identifi es amplicon drivers and potential therapeutic targets
-
Turner N, Lambros MB, Horlings HM, Pearson A, Sharpe R, Natrajan R, et al. Integrative molecular profi ling of triple negative breast cancers identifi es amplicon drivers and potential therapeutic targets. Oncogene 2010; 29: 2013-23.
-
(2010)
Oncogene
, vol.29
, pp. 2013-2023
-
-
Turner, N.1
Lambros, M.B.2
Horlings, H.M.3
Pearson, A.4
Sharpe, R.5
Natrajan, R.6
-
22
-
-
47249122523
-
Drug-sensitive FGFR2 mutations in endometrial carcinoma
-
Dutt A, Salvesen HB, Chen TH, Ramos AH, Onofrio RC, Hatton C, et al. Drug-sensitive FGFR2 mutations in endometrial carcinoma. Proc Natl Acad Sci U S A 2008; 105: 8713-7.
-
(2008)
Proc Natl Acad Sci U S A
, vol.105
, pp. 8713-8717
-
-
Dutt, A.1
Salvesen, H.B.2
Chen, T.H.3
Ramos, A.H.4
Onofrio, R.C.5
Hatton, C.6
-
23
-
-
0035328856
-
Mutations in fi broblast growth factor receptor 2 and fi broblast growth factor receptor 3 genes associated with human gastric and colorectal cancers
-
Jang JH, Shin KH, Park JG. Mutations in fi broblast growth factor receptor 2 and fi broblast growth factor receptor 3 genes associated with human gastric and colorectal cancers. Cancer Res 2001; 61: 3541-3.
-
(2001)
Cancer Res
, vol.61
, pp. 3541-3543
-
-
Jang, J.H.1
Shin, K.H.2
Park, J.G.3
-
24
-
-
34250001297
-
A genome-wide association study identifi es alleles in FGFR2 associated with risk of sporadic postmenopausal breast cancer
-
Hunter DJ, Kraft P, Jacobs KB, Cox DG, Yeager M, Hankinson SE, et al. A genome-wide association study identifi es alleles in FGFR2 associated with risk of sporadic postmenopausal breast cancer. Nat Genet 2007; 39: 870-4.
-
(2007)
Nat Genet
, vol.39
, pp. 870-874
-
-
Hunter, D.J.1
Kraft, P.2
Jacobs, K.B.3
Cox, D.G.4
Yeager, M.5
Hankinson, S.E.6
-
25
-
-
74949112352
-
Focal amplifi cations are associated with high-grade and recurrences in stage Ta bladder carcinoma
-
Nord H, Segersten U, Sandgren J, Wester K, Busch C, Menzel U, et al. Focal amplifi cations are associated with high-grade and recurrences in stage Ta bladder carcinoma. Int J Cancer 2010; 126: 1390-402.
-
(2010)
Int J Cancer
, vol.126
, pp. 1390-1402
-
-
Nord, H.1
Segersten, U.2
Sandgren, J.3
Wester, K.4
Busch, C.5
Menzel, U.6
-
26
-
-
34250665448
-
DNA copy number gains at loci of growth factors and their receptors in salivary gland adenoid cystic carcinoma
-
Vékony H, Ylstra B, Wilting SM, Meijer GA, van de Wiel MA, Leemans CR, et al. DNA copy number gains at loci of growth factors and their receptors in salivary gland adenoid cystic carcinoma. Clin Cancer Res 2007; 13: 3133-9.
-
(2007)
Clin Cancer Res
, vol.13
, pp. 3133-3139
-
-
Vékony, H.1
Ylstra, B.2
Wilting, S.M.3
Meijer, G.A.4
van de Wiel, M.A.5
Leemans, C.R.6
-
27
-
-
0036926992
-
Novel fi broblast growth factor receptor 3 (FGFR3) mutations in bladder cancer previously identifi ed in non-lethal skeletal disorders
-
van Rhijn BW, van Tilborg AA, Lurkin I, Bonaventure J, de Vries A, Thiery JP, et al. Novel fi broblast growth factor receptor 3 (FGFR3) mutations in bladder cancer previously identifi ed in non-lethal skeletal disorders. Eur J Hum Genet 2002; 10: 819-24.
-
(2002)
Eur J Hum Genet
, vol.10
, pp. 819-824
-
-
van Rhijn, B.W.1
van Tilborg, A.A.2
Lurkin, I.3
Bonaventure, J.4
de Vries, A.5
Thiery, J.P.6
-
28
-
-
26944455629
-
Clinical and biological characteristics of cervical neoplasias with FGFR3 mutation
-
Rosty C, Aubriot MH, Cappellen D, Bourdin J, Cartier I, Thiery JP, et al. Clinical and biological characteristics of cervical neoplasias with FGFR3 mutation. Mol Cancer 2005; 4: 15.
-
(2005)
Mol Cancer
, vol.4
, pp. 15
-
-
Rosty, C.1
Aubriot, M.H.2
Cappellen, D.3
Bourdin, J.4
Cartier, I.5
Thiery, J.P.6
-
29
-
-
0038156100
-
Mutation, SNP, and isoform analysis of fi broblast growth factor receptor 3 (FGFR3) in 150 newly diagnosed multiple myeloma patients
-
Onwuazor ON, Wen XY, Wang DY, Zhuang L, Masih-Khan E, Claudio J, et al. Mutation, SNP, and isoform analysis of fi broblast growth factor receptor 3 (FGFR3) in 150 newly diagnosed multiple myeloma patients. Blood 2003; 102: 772-3.
-
(2003)
Blood
, vol.102
, pp. 772-773
-
-
Onwuazor, O.N.1
Wen, X.Y.2
Wang, D.Y.3
Zhuang, L.4
Masih-Khan, E.5
Claudio, J.6
-
30
-
-
67349105009
-
FGFR3 mutations in prostate cancer: Association with low-grade tumors
-
Hernández S, de Muga S, Agell L, Juanpere N, Esgueva R, Lorente JA, et al. FGFR3 mutations in prostate cancer: association with low-grade tumors. Mod Pathol 2009; 22: 848-56.
-
(2009)
Mod Pathol
, vol.22
, pp. 848-856
-
-
Hernández, S.1
de Muga, S.2
Agell, L.3
Juanpere, N.4
Esgueva, R.5
Lorente, J.A.6
-
31
-
-
70350646899
-
Activating mutations in FGFR3 and HRAS reveal a shared genetic origin for congenital disorders and testicular tumors
-
Goriely A, Hansen RM, Taylor IB, Olesen IA, Jacobsen GK, McGowan SJ, et al. Activating mutations in FGFR3 and HRAS reveal a shared genetic origin for congenital disorders and testicular tumors. Nat Genet 2009; 41: 1247-52.
-
(2009)
Nat Genet
, vol.41
, pp. 1247-1252
-
-
Goriely, A.1
Hansen, R.M.2
Taylor, I.B.3
Olesen, I.A.4
Jacobsen, G.K.5
McGowan, S.J.6
-
32
-
-
24344468707
-
Constitutive activating mutation of the FGFR3b in oral squamous cell carcinomas
-
Zhang Y, Hiraishi Y, Wang H, Sumi KS, Hayashido Y, Toratani S, et al. Constitutive activating mutation of the FGFR3b in oral squamous cell carcinomas. Int J Cancer 2005; 117: 166-8.
-
(2005)
Int J Cancer
, vol.117
, pp. 166-168
-
-
Zhang, Y.1
Hiraishi, Y.2
Wang, H.3
Sumi, K.S.4
Hayashido, Y.5
Toratani, S.6
-
33
-
-
0030922231
-
Frequent translocation t(4;14) (p16.3;q32.3) in multiple myeloma is associated with increased expression and activating mutations of fi broblast growth factor receptor 3
-
Chesi M, Nardini E, Brents LA, Schröck E, Ried T, Kuehl WM, et al. Frequent translocation t(4;14) (p16.3;q32.3) in multiple myeloma is associated with increased expression and activating mutations of fi broblast growth factor receptor 3. Nat Genet 1997; 16: 260-4.
-
(1997)
Nat Genet
, vol.16
, pp. 260-264
-
-
Chesi, M.1
Nardini, E.2
Brents, L.A.3
Schröck, E.4
Ried, T.5
Kuehl, W.M.6
-
34
-
-
0035577690
-
Fusion of ETV6 to fi broblast growth factor receptor 3 in peripheral T-cell lymphoma with a t(4;12)(p16;p13) chromosomal translocation
-
Yagasaki F, Wakao D, Yokoyama Y, Uchida Y, Murohashi I, Kayano H, et al. Fusion of ETV6 to fi broblast growth factor receptor 3 in peripheral T-cell lymphoma with a t(4;12)(p16;p13) chromosomal translocation. Cancer Res 2001; 61: 8371-4.
-
(2001)
Cancer Res
, vol.61
, pp. 8371-8374
-
-
Yagasaki, F.1
Wakao, D.2
Yokoyama, Y.3
Uchida, Y.4
Murohashi, I.5
Kayano, H.6
-
35
-
-
70449450426
-
Identifi cation of FGFR4-activating mutations in human rhabdomyosarcomas that promote metastasis in xenotransplanted models
-
Taylor JG, Cheuk AT, Tsang PS, Chung JY, Song YK, Desai K, et al. Identifi cation of FGFR4-activating mutations in human rhabdomyosarcomas that promote metastasis in xenotransplanted models. J Clin Invest 2009; 119: 3395-407.
-
(2009)
J Clin Invest
, vol.119
, pp. 3395-3407
-
-
Taylor, J.G.1
Cheuk, A.T.2
Tsang, P.S.3
Chung, J.Y.4
Song, Y.K.5
Desai, K.6
-
36
-
-
79958829857
-
Meta and pooled analyses of FGFR4 Gly388Arg polymorphism as a cancer prognostic factor
-
Frullanti E, Berking C, Harbeck N, Jézéquel P, Haugen A, Mawrin C, et al. Meta and pooled analyses of FGFR4 Gly388Arg polymorphism as a cancer prognostic factor. Eur J Cancer Prev 2011; 20: 340-7.
-
(2011)
Eur J Cancer Prev
, vol.20
, pp. 340-347
-
-
Frullanti, E.1
Berking, C.2
Harbeck, N.3
Jézéquel, P.4
Haugen, A.5
Mawrin, C.6
-
37
-
-
36348943566
-
Activity of TKI258 against primary cells and cell lines with FGFR1 fusion genes associated with the 8p11 myeloproliferative syndrome
-
Chase A, Grand FH, Cross NC. Activity of TKI258 against primary cells and cell lines with FGFR1 fusion genes associated with the 8p11 myeloproliferative syndrome. Blood 2007; 110: 3729-34.
-
(2007)
Blood
, vol.110
, pp. 3729-3734
-
-
Chase, A.1
Grand, F.H.2
Cross, N.C.3
-
38
-
-
59449094654
-
Molecular characterization of breast cancer with high-resolution oligonucleotide comparative genomic hybridization array
-
Andre F, Job B, Dessen P, Tordai A, Michiels S, Liedtke C, et al. Molecular characterization of breast cancer with high-resolution oligonucleotide comparative genomic hybridization array. Clin Cancer Res 2009; 15: 441-51.
-
(2009)
Clin Cancer Res
, vol.15
, pp. 441-451
-
-
Andre, F.1
Job, B.2
Dessen, P.3
Tordai, A.4
Michiels, S.5
Liedtke, C.6
-
39
-
-
34447325266
-
FGFR1 amplifi cation in breast carcinomas: A chromogenic in situ hybridisation analysis
-
Elbauomy ES, Green AR, Lambros MB, Turner NC, Grainge MJ, Powe D, et al. FGFR1 amplifi cation in breast carcinomas: a chromogenic in situ hybridisation analysis. Breast Cancer Res 2007; 9: R23.
-
(2007)
Breast Cancer Res
, vol.9
-
-
Elbauomy, E.S.1
Green, A.R.2
Lambros, M.B.3
Turner, N.C.4
Grainge, M.J.5
Powe, D.6
-
40
-
-
77950278598
-
FGFR1 amplifi cation drives endocrine therapy resistance and is a therapeutic target in breast cancer
-
Turner N, Pearson A, Sharpe R, Lambros M, Geyer F, Lopez-Garcia MA, et al. FGFR1 amplifi cation drives endocrine therapy resistance and is a therapeutic target in breast cancer. Cancer Res es 2010; 70: 2085-94.
-
(2010)
Cancer Res es
, vol.70
, pp. 2085-2094
-
-
Turner, N.1
Pearson, A.2
Sharpe, R.3
Lambros, M.4
Geyer, F.5
Lopez-Garcia, M.A.6
-
41
-
-
33845331706
-
FGFR1 emerges as a potential therapeutic target for lobular breast carcinomas
-
Reis-Filho JS, Simpson PT, Turner NC, Lambros MB, Jones C, Mackay A, et al. FGFR1 emerges as a potential therapeutic target for lobular breast carcinomas. Clin Cancer Res 2006; 12: 6652-62.
-
(2006)
Clin Cancer Res
, vol.12
, pp. 6652-6662
-
-
Reis-Filho, J.S.1
Simpson, P.T.2
Turner, N.C.3
Lambros, M.B.4
Jones, C.5
McKay, A.6
-
42
-
-
79960015997
-
Identifi cation of human triple-negative breast cancer subtypes and preclinical models for selection of targeted therapies
-
Lehmann BD, Bauer JA, Chen X, Sanders ME, Chakravarthy AB, Shyr Y, et al. Identifi cation of human triple-negative breast cancer subtypes and preclinical models for selection of targeted therapies. J Clin Invest 2011; 121: 2750-67.
-
(2011)
J Clin Invest
, vol.121
, pp. 2750-2767
-
-
Lehmann, B.D.1
Bauer, J.A.2
Chen, X.3
Sanders, M.E.4
Chakravarthy, A.B.5
Shyr, Y.6
-
43
-
-
78650875209
-
Small molecule FGF receptor inhibitors block FGFR-dependent urothelial carcinoma growth in vitro and in vivo
-
Lamont FR, Tomlinson DC, Cooper PA, Shnyder SD, Chester JD, Knowles MA, et al. Small molecule FGF receptor inhibitors block FGFR-dependent urothelial carcinoma growth in vitro and in vivo. Br J Cancer 2011; 104: 75-82.
-
(2011)
Br J Cancer
, vol.104
, pp. 75-82
-
-
Lamont, F.R.1
Tomlinson, D.C.2
Cooper, P.A.3
Shnyder, S.D.4
Chester, J.D.5
Knowles, M.A.6
-
44
-
-
33747079040
-
Prospective study of FGFR3 mutations as a prognostic factor in nonmuscle invasive urothelial bladder carcinomas
-
Hernández S, López-Knowles E, Lloreta J, Kogevinas M, Amorós A, Tardón A, et al. Prospective study of FGFR3 mutations as a prognostic factor in nonmuscle invasive urothelial bladder carcinomas. J Clin Oncol 2006; 24: 3664-71.
-
(2006)
J Clin Oncol
, vol.24
, pp. 3664-3671
-
-
Hernández, S.1
López-Knowles, E.2
Lloreta, J.3
Kogevinas, M.4
Amorós, A.5
Tardón, A.6
-
45
-
-
66349135677
-
Antibody-based targeting of FGFR3 in bladder carcinoma and t(4;14)-positive multiple myeloma in mice
-
Qing J, Du X, Chen Y, Chan P, Li H, Wu P, et al. Antibody-based targeting of FGFR3 in bladder carcinoma and t(4;14)-positive multiple myeloma in mice. J Clin Invest 2009; 119: 1216-29.
-
(2009)
J Clin Invest
, vol.119
, pp. 1216-1229
-
-
Qing, J.1
Du, X.2
Chen, Y.3
Chan, P.4
Li, H.5
Wu, P.6
-
46
-
-
79959713140
-
Fibroblast growth factors and their receptors in cancer
-
Wesche J, Haglund K, Haugsten EM. Fibroblast growth factors and their receptors in cancer. Biochem J 2011; 437: 199-213.
-
(2011)
Biochem J
, vol.437
, pp. 199-213
-
-
Wesche, J.1
Haglund, K.2
Haugsten, E.M.3
-
47
-
-
36649025928
-
Inducible FGFR-1 activation leads to irreversible prostate adenocarcinoma and an epithelial-to mesenchymal transition
-
Acevedo VD, Gangula RD, Freeman KW, Li R, Zhang Y, Wang F, et al. Inducible FGFR-1 activation leads to irreversible prostate adenocarcinoma and an epithelial-to mesenchymal transition. Cancer Cell 2007; 12: 559-71.
-
(2007)
Cancer Cell
, vol.12
, pp. 559-571
-
-
Acevedo, V.D.1
Gangula, R.D.2
Freeman, K.W.3
Li, R.4
Zhang, Y.5
Wang, F.6
-
48
-
-
84863940282
-
Targeting fi broblast growth factor receptor signaling inhibits prostate cancer progression
-
Feng S, Shao LJ, Yu W, Gavine PR, Ittmann MM. Targeting fi broblast growth factor receptor signaling inhibits prostate cancer progression. Clin Cancer Res 2012; 18: 3880-8.
-
(2012)
Clin Cancer Res
, vol.18
, pp. 3880-3888
-
-
Feng, S.1
Shao, L.J.2
Yu, W.3
Gavine, P.R.4
Ittmann, M.M.5
-
49
-
-
58849122812
-
Fibroblast growth factor (FGF) and FGF receptor-mediated autocrine signaling in non-small-cell lung cancer cells
-
Marek L, Ware KE, Fritzsche A, Hercule P, Helton WR, Smith JE, et al. Fibroblast growth factor (FGF) and FGF receptor-mediated autocrine signaling in non-small-cell lung cancer cells. Mol Pharmacol 2009; 75: 196-207.
-
(2009)
Mol Pharmacol
, vol.75
, pp. 196-207
-
-
Marek, L.1
Ware, K.E.2
Fritzsche, A.3
Hercule, P.4
Helton, W.R.5
Smith, J.E.6
-
50
-
-
84857407325
-
Fibroblast growth factor signaling in nonsmall-cell lung cancer
-
Semrad TJ, Mack PC. Fibroblast growth factor signaling in nonsmall-cell lung cancer. Clin Lung Cancer 2012; 13: 90-5.
-
(2012)
Clin Lung Cancer
, vol.13
, pp. 90-95
-
-
Semrad, T.J.1
Mack, P.C.2
-
51
-
-
80051685673
-
FGFR signaling promotes the growth of triple-negative and basal-like breast cancer cell lines both in vitro and in vivo
-
Sharpe R, Pearson A, Herrera-Abreu MT, Johnson D, Mackay A, Welti JC, et al. FGFR signaling promotes the growth of triple-negative and basal-like breast cancer cell lines both in vitro and in vivo. Clin Cancer Res 2011; 17: 5275-86.
-
(2011)
Clin Cancer Res
, vol.17
, pp. 5275-5286
-
-
Sharpe, R.1
Pearson, A.2
Herrera-Abreu, M.T.3
Johnson, D.4
McKay, A.5
Welti, J.C.6
-
52
-
-
0034671392
-
Fibroblast growth factors are required for effi cient tumor angiogenesis
-
Compagni A, Wilgenbus P, Impagnatiello M-A, Cotten M, Christofori G. Fibroblast growth factors are required for effi cient tumor angiogenesis. Cancer Res 2000; 60: 7163-9.
-
(2000)
Cancer Res
, vol.60
, pp. 7163-7169
-
-
Compagni, A.1
Wilgenbus, P.2
Impagnatiello, M.-A.3
Cotten, M.4
Christofori, G.5
-
53
-
-
0030855812
-
Antisense targeting of basic fi broblast growth factor and fi broblast growth factor receptor-1 in human melanomas blocks intratumoral angiogenesis and tumor growth
-
Wang Y, Becker D. Antisense targeting of basic fi broblast growth factor and fi broblast growth factor receptor-1 in human melanomas blocks intratumoral angiogenesis and tumor growth. Nat Med 1997; 3: 887-93.
-
(1997)
Nat Med
, vol.3
, pp. 887-893
-
-
Wang, Y.1
Becker, D.2
-
54
-
-
34250200790
-
Whole genome oligonucleotide-based array comparative genomic hybridization analysis identifi ed fi broblast growth factor 1 as a prognostic marker for advanced-stage serous ovarian adenocarcinomas
-
Birrer MJ, Johnson ME, Hao K, Wong KK, Park DC, Bell A, et al. Whole genome oligonucleotide-based array comparative genomic hybridization analysis identifi ed fi broblast growth factor 1 as a prognostic marker for advanced-stage serous ovarian adenocarcinomas. J Clin Oncol 2007; 25: 2281-7.
-
(2007)
J Clin Oncol
, vol.25
, pp. 2281-2287
-
-
Birrer, M.J.1
Johnson, M.E.2
Hao, K.3
Wong, K.K.4
Park, D.C.5
Bell, A.6
-
55
-
-
0037906432
-
Distinct role of fi broblast growth factor-2 and vascular endothelial growth factor on tumor growth and angiogenesis
-
Giavazzi R, Sennino B, Coltrini D, Garofalo A, Dossi R, Ronca R, et al. Distinct role of fi broblast growth factor-2 and vascular endothelial growth factor on tumor growth and angiogenesis. Am J Pathol 2003; 162: 1913-26.
-
(2003)
Am J Pathol
, vol.162
, pp. 1913-1926
-
-
Giavazzi, R.1
Sennino, B.2
Coltrini, D.3
Garofalo, A.4
Dossi, R.5
Ronca, R.6
-
56
-
-
26644471951
-
Drug resistance by evasion of antiangiogenic targeting of VEGF signaling in late-stage pancreatic islet tumors
-
Casanovas O, Hicklin DJ, Bergers G, Hanahan D. Drug resistance by evasion of antiangiogenic targeting of VEGF signaling in late-stage pancreatic islet tumors. Cancer Cell 2005; 8: 299-309.
-
(2005)
Cancer Cell
, vol.8
, pp. 299-309
-
-
Casanovas, O.1
Hicklin, D.J.2
Bergers, G.3
Hanahan, D.4
-
57
-
-
80051690789
-
Brivanib, a dual FGF/VEGF inhibitor, is active both fi rst and second line against mouse pancreatic neuroendocrine tumors developing adaptive/evasive resistance to VEGF inhibition
-
Allen E, Walters I, Hanahan D. Brivanib, a dual FGF/VEGF inhibitor, is active both fi rst and second line against mouse pancreatic neuroendocrine tumors developing adaptive/evasive resistance to VEGF inhibition. Clin Cancer Res 2011; 17: 5299-310.
-
(2011)
Clin Cancer Res
, vol.17
, pp. 5299-5310
-
-
Allen, E.1
Walters, I.2
Hanahan, D.3
-
58
-
-
84864286442
-
Widespread potential for growth-factor-driven resistance to anticancer kinase inhibitors
-
Wilson TR, Fridlyand J, Yan Y, Penuel E, Burton L, Chan E, et al. Widespread potential for growth-factor-driven resistance to anticancer kinase inhibitors. Nature 2012; 487: 505-9.
-
(2012)
Nature
, vol.487
, pp. 505-509
-
-
Wilson, T.R.1
Fridlyand, J.2
Yan, Y.3
Penuel, E.4
Burton, L.5
Chan, E.6
-
59
-
-
84864285794
-
Tumour micro-environment elicits innate resistance to RAF inhibitors through HGF secretion
-
Straussman R, Morikawa T, Shee K, Barzily-Rokni M, Qian ZR, Du J, et al. Tumour micro-environment elicits innate resistance to RAF inhibitors through HGF secretion. Nature 2012; 487: 500-4.
-
(2012)
Nature
, vol.487
, pp. 500-504
-
-
Straussman, R.1
Morikawa, T.2
Shee, K.3
Barzily-Rokni, M.4
Qian, Z.R.5
Du, J.6
-
60
-
-
38849202330
-
Functions of paracrine PDGF signaling in the proangiogenic tumor stroma revealed by pharmacological targeting
-
Pietras K, Pahler J, Bergers G, Hanahan D. Functions of paracrine PDGF signaling in the proangiogenic tumor stroma revealed by pharmacological targeting. PLoS Med 2008; 5: e19.
-
(2008)
PLoS Med
, vol.5
-
-
Pietras, K.1
Pahler, J.2
Bergers, G.3
Hanahan, D.4
-
61
-
-
79955675804
-
Rapidly acquired resistance to EGFR tyrosine kinase inhibitors in NSCLC cell lines through de-repression of FGFR2 and FGFR3 expression
-
Ware KE, Marshall ME, Heasley LR, Marek L, Hinz TK, Hercule P, et al. Rapidly acquired resistance to EGFR tyrosine kinase inhibitors in NSCLC cell lines through de-repression of FGFR2 and FGFR3 expression. PLoS ONE 2010; 5: e14117.
-
(2010)
PLoS ONE
, vol.5
-
-
Ware, K.E.1
Marshall, M.E.2
Heasley, L.R.3
Marek, L.4
Hinz, T.K.5
Hercule, P.6
-
62
-
-
84859652133
-
Cross-suppression of EGFR ligands amphiregulin and epiregulin and de-repression of FGFR3 signalling contribute to cetuximab resistance in wild-type KRAS tumour cells
-
Oliveras-Ferraros C, Cufí S, Queralt B, Vazquez-Martin A, Martin-Castillo B, de Llorens R, et al. Cross-suppression of EGFR ligands amphiregulin and epiregulin and de-repression of FGFR3 signalling contribute to cetuximab resistance in wild-type KRAS tumour cells. Br J Cancer 2012; 106: 1406-14.
-
(2012)
Br J Cancer
, vol.106
, pp. 1406-1414
-
-
Oliveras-Ferraros, C.1
Cufí, S.2
Queralt, B.3
Vazquez-Martin, A.4
Martin-Castillo, B.5
de Llorens, R.6
-
63
-
-
84864994126
-
Reactivation of mitogen-activated protein kinase (MAPK) pathway by FGF receptor 3 (FGFR3)/Ras mediates resistance to vemurafenib in human B-RAF V600E mutant melanoma
-
Yadav V, Zhang X, Liu J, Estrem S, Li S, Gong XQ, et al. Reactivation of mitogen-activated protein kinase (MAPK) pathway by FGF receptor 3 (FGFR3)/Ras mediates resistance to vemurafenib in human B-RAF V600E mutant melanoma. J Biol Chem 2012; 287: 28087-98.
-
(2012)
J Biol Chem
, vol.287
, pp. 28087-28098
-
-
Yadav, V.1
Zhang, X.2
Liu, J.3
Estrem, S.4
Li, S.5
Gong, X.Q.6
-
64
-
-
21044443128
-
In vivo target modulation and biological activity of CHIR-258, a multitargeted growth factor receptor kinase inhibitor, in colon cancer models
-
Lee SH, Lopes de MD, Vora J, Harris A, Ye H, Nordahl L, et al. In vivo target modulation and biological activity of CHIR-258, a multitargeted growth factor receptor kinase inhibitor, in colon cancer models. Clin Cancer Res 2005; 11: 3633-41.
-
(2005)
Clin Cancer Res
, vol.11
, pp. 3633-3641
-
-
Lee, S.H.1
de Lopes, M.D.2
Vora, J.3
Harris, A.4
Ye, H.5
Nordahl, L.6
-
65
-
-
49649123154
-
BIBF 1120: Triple angiokinase inhibitor with sustained receptor blockade and good antitumor effi cacy
-
Hilberg F, Roth GJ, Krssak M, Kautschitsch S, Sommergruber W, Tontsch-Grunt U, et al. BIBF 1120: triple angiokinase inhibitor with sustained receptor blockade and good antitumor effi cacy. Cancer Res 2008; 68: 4774-82.
-
(2008)
Cancer Res
, vol.68
, pp. 4774-4782
-
-
Hilberg, F.1
Roth, G.J.2
Krssak, M.3
Kautschitsch, S.4
Sommergruber, W.5
Tontsch-Grunt, U.6
-
66
-
-
79951826312
-
E-3810 is a potent dual inhibitor of VEGFR and FGFR that exerts antitumor activity in multiple preclinical models
-
Bello E, Colella G, Scarlato V, Oliva P, Berndt A, Valbusa G, et al. E-3810 is a potent dual inhibitor of VEGFR and FGFR that exerts antitumor activity in multiple preclinical models. Cancer Res 2011; 71: 1396-405.
-
(2011)
Cancer Res
, vol.71
, pp. 1396-1405
-
-
Bello, E.1
Colella, G.2
Scarlato, V.3
Oliva, P.4
Berndt, A.5
Valbusa, G.6
-
67
-
-
37349105704
-
E7080, a novel inhibitor that targets multiple kinases, has potent antitumor activities against stem cell factor producing human small cell lung cancer H146, based on angiogenesis inhibition
-
Matsui J, Yamamoto Y, Funahashi Y, Tsuruoka A, Watanabe T, Wakabayashi T, et al. E7080, a novel inhibitor that targets multiple kinases, has potent antitumor activities against stem cell factor producing human small cell lung cancer H146, based on angiogenesis inhibition. Int J Cancer 2008; 122: 664-71.
-
(2008)
Int J Cancer
, vol.122
, pp. 664-671
-
-
Matsui, J.1
Yamamoto, Y.2
Funahashi, Y.3
Tsuruoka, A.4
Watanabe, T.5
Wakabayashi, T.6
-
68
-
-
33645670595
-
Discovery and preclinical studies of (R)-1-(4-(4-fl uoro-2-methyl-1Hindol-5-yloxy)-5-methylpyrrolo[2,1-f][1,2,4]triazin-6-yloxy)propan-2-ol (BMS-540215), an in vivo active potent VEGFR-2 inhibitor
-
Bhide R, Cai Z-W, Zhang Y-Z, Qian L, Wei D, Barbosa S, et al. Discovery and preclinical studies of (R)-1-(4-(4-fl uoro-2-methyl-1Hindol-5-yloxy)-5-methylpyrrolo[2,1-f][1,2,4]triazin-6-yloxy)propan-2-ol (BMS-540215), an in vivo active potent VEGFR-2 inhibitor. J Med Chem 2006; 49: 2143-6.
-
(2006)
J Med Chem
, vol.49
, pp. 2143-2146
-
-
Bhide, R.1
Cai, Z.-W.2
Zhang, Y.-Z.3
Qian, L.4
Wei, D.5
Barbosa, S.6
-
69
-
-
78751492146
-
ENMD-2076 is an orally active kinase inhibitor with antiangiogenic and antiproliferative mechanisms of action
-
Fletcher GC, Brokx RD, Denny TA, Hembrough TA, Plum SM, Fogler WE, et al. ENMD-2076 is an orally active kinase inhibitor with antiangiogenic and antiproliferative mechanisms of action. Mol Cancer Ther 2011; 10: 126-37.
-
(2011)
Mol Cancer Ther
, vol.10
, pp. 126-137
-
-
Fletcher, G.C.1
Brokx, R.D.2
Denny, T.A.3
Hembrough, T.A.4
Plum, S.M.5
Fogler, W.E.6
-
70
-
-
0033883776
-
SU6668 is a potent antiangiogenic and antitumor agent that induces regression of established tumors
-
Laird AD, Vajkoczy P, Shawver LK, Thurnher A, Liang C, Mohammadi M, et al. SU6668 is a potent antiangiogenic and antitumor agent that induces regression of established tumors. Cancer Res 2000; 60: 4152-60.
-
(2000)
Cancer Res
, vol.60
, pp. 4152-4160
-
-
Laird, A.D.1
Vajkoczy, P.2
Shawver, L.K.3
Thurnher, A.4
Liang, C.5
Mohammadi, M.6
-
71
-
-
70350507997
-
AP24534, a pan-BCR-ABL inhibitor for chronic myeloid leukemia, potently inhibits the T315I mutant and overcomes mutation-based resistance
-
O'Hare T, Shakespeare WC, Zhu X, Eide CA, Rivera VM, Wang F, et al. AP24534, a pan-BCR-ABL inhibitor for chronic myeloid leukemia, potently inhibits the T315I mutant and overcomes mutation-based resistance. Cancer Cell 2009; 16: 401-12.
-
(2009)
Cancer Cell
, vol.16
, pp. 401-412
-
-
O'Hare, T.1
Shakespeare, W.C.2
Zhu, X.3
Eide, C.A.4
Rivera, V.M.5
Wang, F.6
-
72
-
-
84860120185
-
AZD4547: An orally bioavailable, potent, and selective inhibitor of the fi broblast growth factor receptor tyrosine kinase family
-
Gavine PR, Mooney L, Kilgour E, Thomas AP, Al-Kadhimi K, Beck S, et al. AZD4547: an orally bioavailable, potent, and selective inhibitor of the fi broblast growth factor receptor tyrosine kinase family. Cancer Res 2012; 72: 2045-56.
-
(2012)
Cancer Res
, vol.72
, pp. 2045-2056
-
-
Gavine, P.R.1
Mooney, L.2
Kilgour, E.3
Thomas, A.P.4
Al-Kadhimi, K.5
Beck, S.6
-
73
-
-
80054900437
-
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 fi broblast growth factor receptor family of receptor tyrosine kinase
-
Guagnano V, Furet P, Spanka C, Bordas V, Le Douget M, Stamm C, et al. 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 fi broblast growth factor receptor family of receptor tyrosine kinase. J Med Chem 2011; 54: 7066-83.
-
(2011)
J Med Chem
, vol.54
, pp. 7066-7083
-
-
Guagnano, V.1
Furet, P.2
Spanka, C.3
Bordas, V.4
Le Douget, M.5
Stamm, C.6
-
74
-
-
81055124246
-
A novel, selective inhibitor of fi broblast growth factor receptors that shows a potent broad spectrum of antitumor activity in several tumor xenograft models
-
Zhao G, Li WY, Chen D, Henry JR, Li HY, Chen Z, et al. A novel, selective inhibitor of fi broblast growth factor receptors that shows a potent broad spectrum of antitumor activity in several tumor xenograft models. Mol Cancer Ther 2011; 10: 2200-10.
-
(2011)
Mol Cancer Ther
, vol.10
, pp. 2200-2210
-
-
Zhao, G.1
Li, W.Y.2
Chen, D.3
Henry, J.R.4
Li, H.Y.5
Chen, Z.6
-
75
-
-
84876045239
-
Antitumor effi cacy of FP-1039, a soluble FGF receptor 1:Fc conjugate, as a single agent or in combination with anticancer drugs [abstract]
-
Apr 17-22; Denver, CO. Philadelphia (PA): AACR; 2009. Abstract nr 2789
-
Long L, Brennan T, Zanghi J, Palencia S, Cheung R, Aguirre M, et al. Antitumor effi cacy of FP-1039, a soluble FGF receptor 1:Fc conjugate, as a single agent or in combination with anticancer drugs [abstract]. In: Proceedings of the 100th Annual Meeting of the American Association for Cancer Research; 2009 Apr 17-22; Denver, CO. Philadelphia (PA): AACR; 2009. Abstract nr 2789.
-
(2009)
Proceedings of the 100th Annual Meeting of the American Association for Cancer Research
-
-
Long, L.1
Brennan, T.2
Zanghi, J.3
Palencia, S.4
Cheung, R.5
Aguirre, M.6
-
76
-
-
42249087301
-
A phase I pharmacokinetic and pharmacodynamic study of TKI258, an oral, multitargeted receptor tyrosine kinase inhibitor in patients with advanced solid tumors
-
Sarker D, Molife R, Evans TR, Hardie M, Marriott C, Butzberger-Zimmerli P, et al. A phase I pharmacokinetic and pharmacodynamic study of TKI258, an oral, multitargeted receptor tyrosine kinase inhibitor in patients with advanced solid tumors. Clin Cancer Res 2008; 14: 2075-81.
-
(2008)
Clin Cancer Res
, vol.14
, pp. 2075-2081
-
-
Sarker, D.1
Molife, R.2
Evans, T.R.3
Hardie, M.4
Marriott, C.5
Butzberger-Zimmerli, P.6
-
77
-
-
82555173128
-
Phase I/II and pharmacodynamic study of dovitinib (TKI258), an inhibitor of fi broblast growth factor receptors and VEGF receptors, in patients with advanced melanoma
-
Kim KB, Chesney J, Robinson D, Gardner H, Shi MM, Kirkwood JM. Phase I/II and pharmacodynamic study of dovitinib (TKI258), an inhibitor of fi broblast growth factor receptors and VEGF receptors, in patients with advanced melanoma. Clin Cancer Res 2011; 17: 7451-61.
-
(2011)
Clin Cancer Res
, vol.17
, pp. 7451-7461
-
-
Kim, K.B.1
Chesney, J.2
Robinson, D.3
Gardner, H.4
Shi, M.M.5
Kirkwood, J.M.6
-
78
-
-
84862763169
-
First-in-man study of E-3810, a novel VEGFR and FGFR inhibitor, in patients with advanced solid tumors
-
abstr L2.5
-
Soria JC, Dienstmann R, de Braud F, Cereda R, Bahleda R, Hollebecque A, et al. First-in-man study of E-3810, a novel VEGFR and FGFR inhibitor, in patients with advanced solid tumors. Ann Oncol 2012;23(Suppl 1):i15-i25, abstr L2.5.
-
(2012)
Ann Oncol
, vol.23
, Issue.SUPPL. 1
-
-
Soria, J.C.1
Dienstmann, R.2
de Braud, F.3
Cereda, R.4
Bahleda, R.5
Hollebecque, A.6
-
79
-
-
74949090791
-
Phase I study of the angiogenesis inhibitor BIBF 1120 in patients with advanced solid tumors
-
Mross K, Stefanic M, Gmehling D, Frost A, Baas F, Unger C, et al. Phase I study of the angiogenesis inhibitor BIBF 1120 in patients with advanced solid tumors. Clin Cancer Res 2010; 16: 311-9.
-
(2010)
Clin Cancer Res
, vol.16
, pp. 311-319
-
-
Mross, K.1
Stefanic, M.2
Gmehling, D.3
Frost, A.4
Baas, F.5
Unger, C.6
-
80
-
-
77958038695
-
Phase I safety, pharmacokinetic, and biomarker study of BIBF 1120, an oral triple tyrosine kinase inhibitor in patients with advanced solid tumors
-
Okamoto I, Kaneda H, Satoh T, Okamoto W, Miyazaki M, Morinaga R, et al. Phase I safety, pharmacokinetic, and biomarker study of BIBF 1120, an oral triple tyrosine kinase inhibitor in patients with advanced solid tumors. Mol Cancer Ther 2010; 9: 2825-33.
-
(2010)
Mol Cancer Ther
, vol.9
, pp. 2825-2833
-
-
Okamoto, I.1
Kaneda, H.2
Satoh, T.3
Okamoto, W.4
Miyazaki, M.5
Morinaga, R.6
-
81
-
-
84859402751
-
Ponatinib (AP24534), a multitargeted pan-FGFR inhibitor with activity in multiple FGFR-amplifi ed or mutated cancer models
-
Gozgit JM, Wong MJ, Moran L, Wardwell S, Mohemmad QK, Narasimhan NI, et al. Ponatinib (AP24534), a multitargeted pan-FGFR inhibitor with activity in multiple FGFR-amplifi ed or mutated cancer models. Mol Cancer Ther 2012; 11: 690-9.
-
(2012)
Mol Cancer Ther
, vol.11
, pp. 690-699
-
-
Gozgit, J.M.1
Wong, M.J.2
Moran, L.3
Wardwell, S.4
Mohemmad, Q.K.5
Narasimhan, N.I.6
-
82
-
-
79952967812
-
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
-
Jonker DJ, Rosen LS, Sawyer MB, de Braud F, Wilding G, Sweeney CJ, et al. 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. Ann Oncol 2011; 22: 1413-9.
-
(2011)
Ann Oncol
, vol.22
, pp. 1413-1419
-
-
Jonker, D.J.1
Rosen, L.S.2
Sawyer, M.B.3
de Braud, F.4
Wilding, G.5
Sweeney, C.J.6
-
83
-
-
79954609271
-
Phase I dose-escalation study and biomarker analysis of E7080 in patients with advanced solid tumors
-
Yamada K, Yamamoto N, Yamada Y, Nokihara H, Fujiwara Y, Hirata T, et al. Phase I dose-escalation study and biomarker analysis of E7080 in patients with advanced solid tumors. Cancer Res 2011; 17: 2528-37.
-
(2011)
Cancer Res
, vol.17
, pp. 2528-2537
-
-
Yamada, K.1
Yamamoto, N.2
Yamada, Y.3
Nokihara, H.4
Fujiwara, Y.5
Hirata, T.6
-
84
-
-
84871527692
-
A phase I dose escalation study of NVP-BGJ398, a selective pan FGFR inhibitor in genetically preselected advanced solid tumors [abstract]
-
Mar 31-Apr 4; Chicago, IL. Philadelphia (PA): AACR; 2012. Abstract nr LB-122
-
Wolf J, LoRusso PM, Camidge RD, Perez JM, Tabernero J, Hidalgo M, et al. A phase I dose escalation study of NVP-BGJ398, a selective pan FGFR inhibitor in genetically preselected advanced solid tumors [abstract]. In: Proceedings of the103rd Annual Meeting of the American Association for Cancer Research; 2012 Mar 31-Apr 4; Chicago, IL. Philadelphia (PA): AACR; 2012. Abstract nr LB-122.
-
(2012)
Proceedings of the103rd Annual Meeting of the American Association for Cancer Research
-
-
Wolf, J.1
LoRusso, P.M.2
Camidge, R.D.3
Perez, J.M.4
Tabernero, J.5
Hidalgo, M.6
-
85
-
-
84858210768
-
A multicenter, open-label phase II trial of dovitinib, an FGFR1 inhibitor, in FGFR1 amplifi ed and non-amplifi ed metastatic breast cancer
-
Andre F, Bachelot D, Campone M, Dalenc F, Perez-Garcia JM, Hurvitz SA, et al. A multicenter, open-label phase II trial of dovitinib, an FGFR1 inhibitor, in FGFR1 amplifi ed and non-amplifi ed metastatic breast cancer. J Clin Oncol 2011; 29 (suppl; abstr 508).
-
(2011)
J Clin Oncol
, vol.29
, Issue.SUPPL.
-
-
Andre, F.1
Bachelot, D.2
Campone, M.3
Dalenc, F.4
Perez-Garcia, J.M.5
Hurvitz, S.A.6
-
86
-
-
84856199835
-
A phase II study of dovitinib (TKI258), an FGFR-and VEGFR-inhibitor, in patients with advanced or metastatic renal cell cancer (mRCC)
-
Angevin E, Grunwald V, Ravaud A, Castellano DE, Lin CC, Gschwend JE, et al. A phase II study of dovitinib (TKI258), an FGFR-and VEGFR-inhibitor, in patients with advanced or metastatic renal cell cancer (mRCC). J Clin Oncol 2011; 29 (suppl; abstr 4551).
-
(2011)
J Clin Oncol
, vol.29
, Issue.SUPPL.
-
-
Angevin, E.1
Grunwald, V.2
Ravaud, A.3
Castellano, D.E.4
Lin, C.C.5
Gschwend, J.E.6
-
87
-
-
84861736119
-
OCEANS: A randomized, double-blind, placebo-controlled phase III trial of chemotherapy with or without bevacizumab in patients with platinum-sensitive recurrent epithelial ovarian, primary peritoneal, or fallopian tube cancer
-
Aghajanian C, Blank SV, Goff BA, Judson PL, Teneriello MG, Husain A, et al. OCEANS: a randomized, double-blind, placebo-controlled phase III trial of chemotherapy with or without bevacizumab in patients with platinum-sensitive recurrent epithelial ovarian, primary peritoneal, or fallopian tube cancer. J Clin Oncol 2012; 30: 2039-45.
-
(2012)
J Clin Oncol
, vol.30
, pp. 2039-2045
-
-
Aghajanian, C.1
Blank, S.V.2
Goff, B.A.3
Judson, P.L.4
Teneriello, M.G.5
Husain, A.6
-
88
-
-
80053561888
-
Randomized phase II placebo-controlled trial of maintenance therapy using the oral triple angiokinase inhibitor BIBF 1120 after chemotherapy for relapsed ovarian cancer
-
Ledermann JA, Hackshaw A, Kaye S, Jayson G, Gabra H, McNeish I, et al. Randomized phase II placebo-controlled trial of maintenance therapy using the oral triple angiokinase inhibitor BIBF 1120 after chemotherapy for relapsed ovarian cancer. J Clin Oncol 2011; 29: 3798-804.
-
(2011)
J Clin Oncol
, vol.29
, pp. 3798-3804
-
-
Ledermann, J.A.1
Hackshaw, A.2
Kaye, S.3
Jayson, G.4
Gabra, H.5
McNeish, I.6
-
89
-
-
84863698793
-
Efficacy and safety of regorafenib in patients with metastatic and/or unresectable GI stromal tumor after failure of imatinib and sunitinib: A multicenter phase II trial
-
George S, Wang Q, Heinrich MC, Corless CL, Zhu M, Butrynski JE, et al. Efficacy and safety of regorafenib in patients with metastatic and/or unresectable GI stromal tumor after failure of imatinib and sunitinib: a multicenter phase II trial. J Clin Oncol 2012; 30: 2401-7.
-
(2012)
J Clin Oncol
, vol.30
, pp. 2401-2407
-
-
George, S.1
Wang, Q.2
Heinrich, M.C.3
Corless, C.L.4
Zhu, M.5
Butrynski, J.E.6
-
90
-
-
33947108356
-
Monoclonal antibody antagonists of hypothalamic FGFR1 cause potent but reversible hypophagia and weight loss in rodents and monkeys
-
Sun HD, Malabunga M, Tonra JR, DiRenzo R, Carrick FE, Zheng H, et al. Monoclonal antibody antagonists of hypothalamic FGFR1 cause potent but reversible hypophagia and weight loss in rodents and monkeys. Am J Physiol Endocrinol Metab 2007; 292: E964-76.
-
(2007)
Am J Physiol Endocrinol Metab
, vol.292
-
-
Sun, H.D.1
Malabunga, M.2
Tonra, J.R.3
DiRenzo, R.4
Carrick, F.E.5
Zheng, H.6
-
91
-
-
79953879710
-
Biology-driven phase II trials: What is the optimal model for molecular selection?
-
Andre F, Delaloge S, Soria JC. Biology-driven phase II trials: what is the optimal model for molecular selection? J Clin Oncol 2011; 29: 1236-8.
-
(2011)
J Clin Oncol
, vol.29
, pp. 1236-1238
-
-
Andre, F.1
Delaloge, S.2
Soria, J.C.3
-
92
-
-
67349202517
-
Co-amplifi ed genes at 8p12 and 11q13 in breast tumors cooperate with two major pathways in oncogenesis
-
Kwek SS, Roy R, Zhou H, Climent J, Martinez-Climent JA, Fridlyand J, et al. Co-amplifi ed genes at 8p12 and 11q13 in breast tumors cooperate with two major pathways in oncogenesis. Oncogene 2009; 28: 1892-903.
-
(2009)
Oncogene
, vol.28
, pp. 1892-1903
-
-
Kwek, S.S.1
Roy, R.2
Zhou, H.3
Climent, J.4
Martinez-Climent, J.A.5
Fridlyand, J.6
-
93
-
-
9644303169
-
Cooperation between fi broblast growth factor receptor-4 and ErbB2 in regulation of cyclin D1 translation
-
Koziczak M, Hynes NE. Cooperation between fi broblast growth factor receptor-4 and ErbB2 in regulation of cyclin D1 translation. J Biol Chem 2004; 279: 50004-11.
-
(2004)
J Biol Chem
, vol.279
, pp. 50004-50011
-
-
Koziczak, M.1
Hynes, N.E.2
-
94
-
-
63449138706
-
Resistance to chemotherapy is associated with fi broblast growth factor receptor 4 up-regulation
-
Roidl A, Berger HJ, Kumar S, Bange J, Knyazev P, Ullrich A. Resistance to chemotherapy is associated with fi broblast growth factor receptor 4 up-regulation. Clin Cancer Res 2009; 15: 2058-66.
-
(2009)
Clin Cancer Res
, vol.15
, pp. 2058-2066
-
-
Roidl, A.1
Berger, H.J.2
Kumar, S.3
Bange, J.4
Knyazev, P.5
Ullrich, A.6
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