-
1
-
-
0036635291
-
Glivec (STI571, imatinib), a rationally developed, targeted anticancer drug
-
Capdeville R, Buchdunger E, Zimmermann J, et al., Glivec (STI571, imatinib), a rationally developed, targeted anticancer drug. Nat Rev Drug Discov 2002; 1 (7): 493-502.
-
(2002)
Nat Rev Drug Discov
, vol.1
, Issue.7
, pp. 493-502
-
-
Capdeville, R.1
Buchdunger, E.2
Zimmermann, J.3
-
2
-
-
0000286732
-
Minute chromosome in human chronic granulocytic leukemia
-
Nowell P, Hungerford D,. Minute chromosome in human chronic granulocytic leukemia. Science 1960; 1497.
-
(1960)
Science
, pp. 1497
-
-
Nowell, P.1
Hungerford, D.2
-
3
-
-
0015694748
-
Letter: A new consistent chromosomal abnormality in chronic myelogenous leukaemia identified by quinacrine fluorescence and Giemsa staining
-
Rowley JD,. Letter: a new consistent chromosomal abnormality in chronic myelogenous leukaemia identified by quinacrine fluorescence and Giemsa staining. Nature 1973; 243 (5405): 290-293.
-
(1973)
Nature
, vol.243
, Issue.5405
, pp. 290-293
-
-
Rowley, J.D.1
-
5
-
-
0034665713
-
Structural mechanism for STI-571 inhibition of Abelson tyrosine kinase
-
Schindler T., Structural mechanism for STI-571 inhibition of Abelson tyrosine kinase. Science 2000; 289 (5486): 1938-1942.
-
(2000)
Science
, vol.289
, Issue.5486
, pp. 1938-1942
-
-
Schindler, T.1
-
6
-
-
77951961590
-
Imatinib treatment for gastrointestinal stromal tumour (GIST)
-
Lopes LF, Bacchi CE,. Imatinib treatment for gastrointestinal stromal tumour (GIST). J Cell Mol Med 2010; 14 (1-2): 42-50.
-
(2010)
J Cell Mol Med
, vol.14
, Issue.12
, pp. 42-50
-
-
Lopes, L.F.1
Bacchi, C.E.2
-
7
-
-
78651337547
-
Seeking the causes and solutions to imatinib-resistance in chronic myeloid leukemia
-
Bixby D, Talpaz M,. Seeking the causes and solutions to imatinib-resistance in chronic myeloid leukemia. Leukemia 2011; 25 (1): 7-22.
-
(2011)
Leukemia
, vol.25
, Issue.1
, pp. 7-22
-
-
Bixby, D.1
Talpaz, M.2
-
8
-
-
43749107912
-
Acquired resistance to tyrosine kinase inhibitors during cancer therapy
-
Engelman JA, Settleman J,. Acquired resistance to tyrosine kinase inhibitors during cancer therapy. Curr Opin Genet Dev 2008; 18 (1): 73-79.
-
(2008)
Curr Opin Genet Dev
, vol.18
, Issue.1
, pp. 73-79
-
-
Engelman, J.A.1
Settleman, J.2
-
9
-
-
0035800507
-
Clinical resistance to STI-571 cancer therapy caused by BCR-ABL gene mutation or amplification
-
New York, NY
-
Gorre ME, Mohammed M, Ellwood K, et al., Clinical resistance to STI-571 cancer therapy caused by BCR-ABL gene mutation or amplification. Science (New York, NY) 2001; 293 (5531): 876-880.
-
(2001)
Science
, vol.293
, Issue.5531
, pp. 876-880
-
-
Gorre, M.E.1
Mohammed, M.2
Ellwood, K.3
-
10
-
-
33746934638
-
Kinase domain mutants of Bcr-Abl exhibit altered transformation potency, kinase activity, and substrate utilization, irrespective of sensitivity to imatinib
-
Griswold IJ, MacPartlin M, Bumm T, et al., Kinase domain mutants of Bcr-Abl exhibit altered transformation potency, kinase activity, and substrate utilization, irrespective of sensitivity to imatinib. Mol Cell Biol 2006; 26 (16): 6082-6093.
-
(2006)
Mol Cell Biol
, vol.26
, Issue.16
, pp. 6082-6093
-
-
Griswold, I.J.1
MacPartlin, M.2
Bumm, T.3
-
11
-
-
34548316976
-
Molecular basis for sunitinib efficacy and future clinical development
-
Faivre S, Demetri G, Sargent W, et al., Molecular basis for sunitinib efficacy and future clinical development. Nat Rev Drug Discov 2007; 6 (9): 734-745.
-
(2007)
Nat Rev Drug Discov
, vol.6
, Issue.9
, pp. 734-745
-
-
Faivre, S.1
Demetri, G.2
Sargent, W.3
-
12
-
-
33749238553
-
Discovery and development of sorafenib: A multikinase inhibitor for treating cancer
-
Wilhelm S, Carter C, Lynch M, et al., Discovery and development of sorafenib: a multikinase inhibitor for treating cancer. Nat Rev Drug Discov 2006; 5 (10): 835-844.
-
(2006)
Nat Rev Drug Discov
, vol.5
, Issue.10
, pp. 835-844
-
-
Wilhelm, S.1
Carter, C.2
Lynch, M.3
-
13
-
-
12144289677
-
Mechanism of activation of the RAF-ERK signaling pathway by oncogenic mutations of B-RAF
-
Wan PTC, Garnett MJ, Roe SM, et al., Mechanism of activation of the RAF-ERK signaling pathway by oncogenic mutations of B-RAF. Cell 2004; 116 (6): 855-867.
-
(2004)
Cell
, vol.116
, Issue.6
, pp. 855-867
-
-
Wan, P.T.C.1
Garnett, M.J.2
Roe, S.M.3
-
14
-
-
60549098640
-
Sorafenib: A review of its use in advanced hepatocellular carcinoma
-
Keating GM, Santoro A,. Sorafenib: a review of its use in advanced hepatocellular carcinoma. Drugs 2009; 69 (2): 223-240.
-
(2009)
Drugs
, vol.69
, Issue.2
, pp. 223-240
-
-
Keating, G.M.1
Santoro, A.2
-
15
-
-
2442669093
-
Preclinical evaluation of the tyrosine kinase inhibitor SU11248 as a single agent and in combination with 'standard of care' therapeutic agents for the treatment of breast cancer
-
Abrams TJ, Murray LJ, Pesenti E, et al., Preclinical evaluation of the tyrosine kinase inhibitor SU11248 as a single agent and in combination with 'standard of care' therapeutic agents for the treatment of breast cancer. Mol Cancer Therap 2003; 2 (10): 1011-1021.
-
(2003)
Mol Cancer Therap
, vol.2
, Issue.10
, pp. 1011-1021
-
-
Abrams, T.J.1
Murray, L.J.2
Pesenti, E.3
-
16
-
-
0347480511
-
Quantitation of SU1 1248, an oral multi-target tyrosine kinase inhibitor, and its metabolite in monkey tissues by liquid chromatograph with tandem mass spectrometry following semi-automated liquid-liquid extraction
-
Barattè S, Sarati S, Frigerio E, et al., Quantitation of SU1 1248, an oral multi-target tyrosine kinase inhibitor, and its metabolite in monkey tissues by liquid chromatograph with tandem mass spectrometry following semi-automated liquid-liquid extraction. J Chromatogr A 2004; 1024 (1-2): 87-94.
-
(2004)
J Chromatogr A
, vol.1024
, Issue.12
, pp. 87-94
-
-
Barattè, S.1
Sarati, S.2
Frigerio, E.3
-
17
-
-
34250020187
-
Sunitinib: A novel tyrosine kinase inhibitor. A brief review of its therapeutic potential in the treatment of renal carcinoma and gastrointestinal stromal tumors (GIST). Therap Clin
-
Le Tourneau C, Raymond E, Faivre S,. Sunitinib: a novel tyrosine kinase inhibitor. A brief review of its therapeutic potential in the treatment of renal carcinoma and gastrointestinal stromal tumors (GIST). Therap Clin Risk Manage 2007; 3 (2): 341-348.
-
(2007)
Risk Manage
, vol.3
, Issue.2
, pp. 341-348
-
-
Le Tourneau, C.1
Raymond, E.2
Faivre, S.3
-
18
-
-
12244301581
-
In vivo antitumor activity of SU11248, a novel tyrosine kinase inhibitor targeting vascular endothelial growth factor and platelet-derived growth factor receptors: Determination of a pharmacokinetic/pharmacodynamic relationship
-
Mendel DB, Laird AD, Xin X, et al., In vivo antitumor activity of SU11248, a novel tyrosine kinase inhibitor targeting vascular endothelial growth factor and platelet-derived growth factor receptors: determination of a pharmacokinetic/pharmacodynamic relationship. Clin Cancer Res 2003; 9 (1): 327-337.
-
(2003)
Clin Cancer Res
, vol.9
, Issue.1
, pp. 327-337
-
-
Mendel, D.B.1
Laird, A.D.2
Xin, X.3
-
19
-
-
0345359585
-
An innovative phase i clinical study demonstrates inhibition of FLT3 phosphorylation by SU11248 in acute myeloid leukemia patients
-
O'Farrell AM, Foran JM, Fiedler W, et al., An innovative phase I clinical study demonstrates inhibition of FLT3 phosphorylation by SU11248 in acute myeloid leukemia patients. Clin Cancer Res 2003; 9 (15): 5465-5476.
-
(2003)
Clin Cancer Res
, vol.9
, Issue.15
, pp. 5465-5476
-
-
O'Farrell, A.M.1
Foran, J.M.2
Fiedler, W.3
-
20
-
-
33749505836
-
Efficacy and safety of sunitinib in patients with advanced gastrointestinal stromal tumour after failure of imatinib: A randomised controlled trial
-
Demetri GD, van Oosterom AT, Garrett CR, et al., Efficacy and safety of sunitinib in patients with advanced gastrointestinal stromal tumour after failure of imatinib: a randomised controlled trial. Lancet 2006; 368 (9544): 1329-1338.
-
(2006)
Lancet
, vol.368
, Issue.9544
, pp. 1329-1338
-
-
Demetri, G.D.1
Van Oosterom, A.T.2
Garrett, C.R.3
-
21
-
-
47949099628
-
Modes of resistance to anti-angiogenic therapy
-
Bergers G, Hanahan D,. Modes of resistance to anti-angiogenic therapy. Nat Rev Cancer 2008; 8 (8): 592-603.
-
(2008)
Nat Rev Cancer
, vol.8
, Issue.8
, pp. 592-603
-
-
Bergers, G.1
Hanahan, D.2
-
22
-
-
82555189379
-
Lysosomal sequestration of sunitinib: A novel mechanism of drug resistance
-
Gotink KJ, Broxterman HJ, Labots M, et al., Lysosomal sequestration of sunitinib: a novel mechanism of drug resistance. Clin Cancer Res 2011; 17 (23): 7337-7346.
-
(2011)
Clin Cancer Res
, vol.17
, Issue.23
, pp. 7337-7346
-
-
Gotink, K.J.1
Broxterman, H.J.2
Labots, M.3
-
23
-
-
78650339354
-
HGF/c-Met acts as an alternative angiogenic pathway in sunitinib-resistant tumors
-
Shojaei F, Lee JH, Simmons BH, et al., HGF/c-Met acts as an alternative angiogenic pathway in sunitinib-resistant tumors. Cancer Res 2010; 70 (24): 10090-10100.
-
(2010)
Cancer Res
, vol.70
, Issue.24
, pp. 10090-10100
-
-
Shojaei, F.1
Lee, J.H.2
Simmons, B.H.3
-
24
-
-
0025776523
-
Targets for cell cycle arrest by the immunosuppressant rapamycin in yeast
-
(New York, NY);.
-
Heitman J, Movva NR, Hall MN,. Targets for cell cycle arrest by the immunosuppressant rapamycin in yeast. Science (New York, NY) 1991; 253 (5022): 905-909.
-
(1991)
Science
, vol.253
, Issue.5022
, pp. 905-909
-
-
Heitman, J.1
Movva, N.R.2
Hall, M.N.3
-
25
-
-
77952007543
-
Mammalian target of rapamycin (mTOR): Conducting the cellular signaling symphony
-
Foster KG, Fingar DC,. Mammalian target of rapamycin (mTOR): conducting the cellular signaling symphony. J Biol Chem 2010; 285 (19): 14071-14077.
-
(2010)
J Biol Chem
, vol.285
, Issue.19
, pp. 14071-14077
-
-
Foster, K.G.1
Fingar, D.C.2
-
27
-
-
0346362997
-
Rapamycins: Mechanism of action and cellular resistance
-
Huang S, Bjornsti M-A, Houghton PJ,. Rapamycins: mechanism of action and cellular resistance. Cancer Biol Ther. 2003; 2 (3): 222-232.
-
(2003)
Cancer Biol Ther.
, vol.2
, Issue.3
, pp. 222-232
-
-
Huang, S.1
Bjornsti, M.-A.2
Houghton, P.J.3
-
28
-
-
80055027842
-
Mammalian target of rapamycin: A central node of complex signaling cascades
-
Dobashi Y, Watanabe Y, Miwa C, et al., Mammalian target of rapamycin: a central node of complex signaling cascades. Int J Clin Exp Pathol 2011; 4 (5): 476-495.
-
(2011)
Int J Clin Exp Pathol
, vol.4
, Issue.5
, pp. 476-495
-
-
Dobashi, Y.1
Watanabe, Y.2
Miwa, C.3
-
29
-
-
2342559981
-
The TOR pathway: A target for cancer therapy
-
Bjornsti M-A, Houghton PJ,. The TOR pathway: a target for cancer therapy. Nat Rev Cancer 2004; 4 (5): 335-348.
-
(2004)
Nat Rev Cancer
, vol.4
, Issue.5
, pp. 335-348
-
-
Bjornsti, M.-A.1
Houghton, P.J.2
-
30
-
-
33746637660
-
Current development of mTOR inhibitors as anticancer agents
-
Faivre S, Kroemer G, Raymond E,. Current development of mTOR inhibitors as anticancer agents. Nat Rev Drug Discov 2006; 5 (8): 671-688.
-
(2006)
Nat Rev Drug Discov
, vol.5
, Issue.8
, pp. 671-688
-
-
Faivre, S.1
Kroemer, G.2
Raymond, E.3
-
31
-
-
72849150434
-
Targeting tumorigenesis: Development and use of mTOR inhibitors in cancer therapy
-
Yuan R, Kay A, Berg WJ, et al., Targeting tumorigenesis: development and use of mTOR inhibitors in cancer therapy. J Hematol Oncol 2009; 2 (1): 45.
-
(2009)
J Hematol Oncol
, vol.2
, Issue.1
, pp. 45
-
-
Yuan, R.1
Kay, A.2
Berg, W.J.3
-
32
-
-
0029004755
-
Dominant mutations confer resistance to the immunosuppressant, rapamycin, in variants of a T cell lymphoma
-
Dumont FJ, Staruch MJ, Grammer T, et al., Dominant mutations confer resistance to the immunosuppressant, rapamycin, in variants of a T cell lymphoma. Cell Immunol 1995; 163 (1): 70-79.
-
(1995)
Cell Immunol
, vol.163
, Issue.1
, pp. 70-79
-
-
Dumont, F.J.1
Staruch, M.J.2
Grammer, T.3
-
33
-
-
0028923877
-
FK506 binding protein 12 mediates sensitivity to both FK506 and rapamycin in murine mast cells
-
Fruman DA, Wood MA, Gjertson CK, et al., FK506 binding protein 12 mediates sensitivity to both FK506 and rapamycin in murine mast cells. Eur J Immunol 1995; 25 (2): 563-571.
-
(1995)
Eur J Immunol
, vol.25
, Issue.2
, pp. 563-571
-
-
Fruman, D.A.1
Wood, M.A.2
Gjertson, C.K.3
-
34
-
-
0028825698
-
TOR mutations confer rapamycin resistance by preventing interaction with FKBP12-rapamycin
-
Lorenz MC, Heitman J,. TOR mutations confer rapamycin resistance by preventing interaction with FKBP12-rapamycin. J Biol Chem 1995; 270 (46): 27531-27537.
-
(1995)
J Biol Chem
, vol.270
, Issue.46
, pp. 27531-27537
-
-
Lorenz, M.C.1
Heitman, J.2
-
35
-
-
51349164790
-
Inhibition of mTORC1 leads to MAPK pathway activation through a PI3K-dependent feedback loop in human cancer
-
Carracedo A, Ma L, Teruya-Feldstein J, et al., Inhibition of mTORC1 leads to MAPK pathway activation through a PI3K-dependent feedback loop in human cancer. J Clin Invest 2008; 118 (9): 3065-3074.
-
(2008)
J Clin Invest
, vol.118
, Issue.9
, pp. 3065-3074
-
-
Carracedo, A.1
Ma, L.2
Teruya-Feldstein, J.3
-
36
-
-
27644534999
-
Mammalian target of rapamycin inhibitors activate the AKT kinase in multiple myeloma cells by up-regulating the insulin-like growth factor receptor/insulin receptor substrate-1/phosphatidylinositol 3-kinase cascade
-
Shi Y, Yan H, Frost P, et al., Mammalian target of rapamycin inhibitors activate the AKT kinase in multiple myeloma cells by up-regulating the insulin-like growth factor receptor/insulin receptor substrate-1/ phosphatidylinositol 3-kinase cascade. Mol Cancer Therap 2005; 4 (10): 1533-1540.
-
(2005)
Mol Cancer Therap
, vol.4
, Issue.10
, pp. 1533-1540
-
-
Shi, Y.1
Yan, H.2
Frost, P.3
-
37
-
-
78249287240
-
B55β-associated PP2A complex controls PDK1-directed myc signaling and modulates rapamycin sensitivity in colorectal cancer
-
Tan J, Lee PL, Li Z, et al., B55β-associated PP2A complex controls PDK1-directed myc signaling and modulates rapamycin sensitivity in colorectal cancer. Cancer Cell 2010; 18 (5): 459-471.
-
(2010)
Cancer Cell
, vol.18
, Issue.5
, pp. 459-471
-
-
Tan, J.1
Lee, P.L.2
Li, Z.3
-
38
-
-
13844312400
-
Phosphorylation and regulation of Akt/PKB by the rictor-mTOR complex
-
(New York, NY);.
-
Sarbassov DD, Guertin DA, Ali SM, et al., Phosphorylation and regulation of Akt/PKB by the rictor-mTOR complex. Science (New York, NY) 2005; 307 (5712): 1098-1101.
-
(2005)
Science
, vol.307
, Issue.5712
, pp. 1098-1101
-
-
Sarbassov, D.D.1
Guertin, D.A.2
Ali, S.M.3
-
39
-
-
0037134480
-
4E-binding proteins, the suppressors of eukaryotic initiation factor 4E, are down-regulated in cells with acquired or intrinsic resistance to rapamycin
-
Dilling MB, Germain GS, Dudkin L, et al., 4E-binding proteins, the suppressors of eukaryotic initiation factor 4E, are down-regulated in cells with acquired or intrinsic resistance to rapamycin. J Biol Chem 2002; 277 (16): 13907-13917.
-
(2002)
J Biol Chem
, vol.277
, Issue.16
, pp. 13907-13917
-
-
Dilling, M.B.1
Germain, G.S.2
Dudkin, L.3
-
40
-
-
38849180436
-
Targeting the eukaryotic translation initiation factor 4E for cancer therapy
-
Graff JR, Konicek BW, Carter JH, et al., Targeting the eukaryotic translation initiation factor 4E for cancer therapy. Cancer Res 2008; 68 (3): 631-634.
-
(2008)
Cancer Res
, vol.68
, Issue.3
, pp. 631-634
-
-
Graff, J.R.1
Konicek, B.W.2
Carter, J.H.3
-
41
-
-
74949089953
-
Vorinostat enhances the activity of temsirolimus in renal cell carcinoma through suppression of survivin levels
-
Mahalingam D, Medina EC, Esquivel JA, et al., Vorinostat enhances the activity of temsirolimus in renal cell carcinoma through suppression of survivin levels. Clin Cancer Res 2010; 16 (1): 141-153.
-
(2010)
Clin Cancer Res
, vol.16
, Issue.1
, pp. 141-153
-
-
Mahalingam, D.1
Medina, E.C.2
Esquivel, J.A.3
-
42
-
-
2942724235
-
MTOR inhibition reverses Akt-dependent prostate intraepithelial neoplasia through regulation of apoptotic and HIF-1-dependent pathways
-
Majumder PK, Febbo PG, Bikoff R, et al., mTOR inhibition reverses Akt-dependent prostate intraepithelial neoplasia through regulation of apoptotic and HIF-1-dependent pathways. Nat Med 2004; 10 (6): 594-601.
-
(2004)
Nat Med
, vol.10
, Issue.6
, pp. 594-601
-
-
Majumder, P.K.1
Febbo, P.G.2
Bikoff, R.3
-
43
-
-
0036174289
-
Rapamycin inhibits primary and metastatic tumor growth by antiangiogenesis: Involvement of vascular endothelial growth factor
-
Guba M, von Breitenbuch P, Steinbauer M, et al., Rapamycin inhibits primary and metastatic tumor growth by antiangiogenesis: involvement of vascular endothelial growth factor. Nat Med 2002; 8 (2): 128-135.
-
(2002)
Nat Med
, vol.8
, Issue.2
, pp. 128-135
-
-
Guba, M.1
Von Breitenbuch, P.2
Steinbauer, M.3
-
44
-
-
77957994045
-
Perspectives on inhibiting mTOR as a future treatment strategy for hematological malignancies
-
Chapuis N, Tamburini J, Green AS, et al., Perspectives on inhibiting mTOR as a future treatment strategy for hematological malignancies. Leukemia 2010; 24 (10): 1686-1699.
-
(2010)
Leukemia
, vol.24
, Issue.10
, pp. 1686-1699
-
-
Chapuis, N.1
Tamburini, J.2
Green, A.S.3
-
46
-
-
0035819546
-
Identification of a new multigene four-transmembrane family (MS4A) related to CD20, HTm4 and β subunit of the high-affinity IgE receptor
-
Ishibashi K, Suzuki M, Sasaki S, et al., Identification of a new multigene four-transmembrane family (MS4A) related to CD20, HTm4 and β subunit of the high-affinity IgE receptor. Gene 2001; 264 (1): 87-93.
-
(2001)
Gene
, vol.264
, Issue.1
, pp. 87-93
-
-
Ishibashi, K.1
Suzuki, M.2
Sasaki, S.3
-
47
-
-
0019448991
-
A unique cell surface antigen identifying lymphoid malignancies of B cell origin
-
Nadler LM, Ritz J, Hardy R, et al., A unique cell surface antigen identifying lymphoid malignancies of B cell origin. J Clin Invest 1981; 67 (1): 134-140.
-
(1981)
J Clin Invest
, vol.67
, Issue.1
, pp. 134-140
-
-
Nadler, L.M.1
Ritz, J.2
Hardy, R.3
-
48
-
-
0028108050
-
CD20: A regulator of cell-cycle progression of B lymphocytes
-
Tedder TF, Engel P,. CD20: a regulator of cell-cycle progression of B lymphocytes. Immunol Today 1994; 15 (9): 450-454.
-
(1994)
Immunol Today
, vol.15
, Issue.9
, pp. 450-454
-
-
Tedder, T.F.1
Engel, P.2
-
49
-
-
0020584077
-
Further biochemical studies of the human B-cell differentiation antigens B1 and B2
-
Oettgen HC, Bayard PJ, Van Ewijk W, et al., Further biochemical studies of the human B-cell differentiation antigens B1 and B2. Hybridoma 1983; 2 (1): 17-28.
-
(1983)
Hybridoma
, vol.2
, Issue.1
, pp. 17-28
-
-
Oettgen, H.C.1
Bayard, P.J.2
Van Ewijk, W.3
-
50
-
-
0032740187
-
Overview of the clinical development of rituximab: First monoclonal antibody approved for the treatment of lymphoma
-
Grillo-Lõpez AJ, White CA, Varns C, et al., Overview of the clinical development of rituximab: first monoclonal antibody approved for the treatment of lymphoma. Semin Oncol 1999; 26 (5, suppl 14): 66-73.
-
(1999)
Semin Oncol
, vol.26
, Issue.5
, pp. 66-73
-
-
Grillo-Lõpez, A.J.1
White, C.A.2
Varns, C.3
-
51
-
-
84881073251
-
Rituximab causes a polarisation of B cells which augments its therapeutic function in NK cell-mediated antibody-dependent cellular cytotoxicity
-
Rudnicka D, Oszmiana A, Finch DK, et al., Rituximab causes a polarisation of B cells which augments its therapeutic function in NK cell-mediated antibody-dependent cellular cytotoxicity. Blood 2013; 121: 4694-4702.
-
(2013)
Blood
, vol.121
, pp. 4694-4702
-
-
Rudnicka, D.1
Oszmiana, A.2
Finch, D.K.3
-
52
-
-
34548221347
-
Mechanisms of killing by anti-CD20 monoclonal antibodies
-
Glennie MJ, French RR, Cragg MS, et al., Mechanisms of killing by anti-CD20 monoclonal antibodies. Mol Immunol 2007; 44 (16): 3823-3837.
-
(2007)
Mol Immunol
, vol.44
, Issue.16
, pp. 3823-3837
-
-
Glennie, M.J.1
French, R.R.2
Cragg, M.S.3
-
53
-
-
0036464719
-
Therapeutic activity of humanized anti-CD20 monoclonal antibody and polymorphism in IgG Fc receptor FcγRIIIa gene
-
Cartron G, Dacheux L, Salles G, et al., Therapeutic activity of humanized anti-CD20 monoclonal antibody and polymorphism in IgG Fc receptor FcγRIIIa gene. Blood 2002; 99 (3): 754-758.
-
(2002)
Blood
, vol.99
, Issue.3
, pp. 754-758
-
-
Cartron, G.1
Dacheux, L.2
Salles, G.3
-
54
-
-
0034076307
-
Inhibitory Fc receptors modulate in vivo cytotoxicity against tumor targets
-
Clynes RA, Towers TL, Presta LG, et al., Inhibitory Fc receptors modulate in vivo cytotoxicity against tumor targets. Nat Med 2000; 6 (4): 443-446.
-
(2000)
Nat Med
, vol.6
, Issue.4
, pp. 443-446
-
-
Clynes, R.A.1
Towers, T.L.2
Presta, L.G.3
-
55
-
-
79958273506
-
Rituximab resistance. Best practice and research
-
Rezvani AR, Maloney DG,. Rituximab resistance. Best practice and research. Clin Haematol 2011; 24 (2): 203-216.
-
(2011)
Clin Haematol
, vol.24
, Issue.2
, pp. 203-216
-
-
Rezvani, A.R.1
Maloney, D.G.2
-
56
-
-
77950332103
-
Rituximab: Mechanism of action
-
Weiner GJ,. Rituximab: mechanism of action. Semin Hematol 2010; 47 (2): 115-123.
-
(2010)
Semin Hematol
, vol.47
, Issue.2
, pp. 115-123
-
-
Weiner, G.J.1
-
57
-
-
33847014608
-
Development of rituximab-resistant lymphoma clones with altered cell signaling and cross-resistance to chemotherapy
-
Jazirehi AR, Vega MI, Bonavida B,. Development of rituximab-resistant lymphoma clones with altered cell signaling and cross-resistance to chemotherapy. Cancer Res 2007; 67 (3): 1270-1281.
-
(2007)
Cancer Res
, vol.67
, Issue.3
, pp. 1270-1281
-
-
Jazirehi, A.R.1
Vega, M.I.2
Bonavida, B.3
-
58
-
-
84875287730
-
Genetic predisposition syndromes and their management
-
Euhus DM, Robinson L,. Genetic predisposition syndromes and their management. Surg Clin N Am 2013; 93 (2): 341-362.
-
(2013)
Surg Clin N Am
, vol.93
, Issue.2
, pp. 341-362
-
-
Euhus, D.M.1
Robinson, L.2
-
59
-
-
0031990269
-
Involvement of Brca2 in DNA repair
-
Patel K., Involvement of Brca2 in DNA repair. Mol Cell 1998; 1 (3): 347-357.
-
(1998)
Mol Cell
, vol.1
, Issue.3
, pp. 347-357
-
-
Patel, K.1
-
60
-
-
0035099044
-
BRCA2 is required for homology-directed repair of chromosomal breaks
-
Moynahan ME, Pierce AJ, Jasin M,. BRCA2 is required for homology-directed repair of chromosomal breaks. Mol Cell 2001; 7 (2): 263-272.
-
(2001)
Mol Cell
, vol.7
, Issue.2
, pp. 263-272
-
-
Moynahan, M.E.1
Pierce, A.J.2
Jasin, M.3
-
61
-
-
0033213392
-
Brca1 controls homology-directed DNA repair
-
Moynahan ME, Chiu JW, Koller BH, et al., Brca1 controls homology-directed DNA repair. Mol Cell 1999; 4 (4): 511-518.
-
(1999)
Mol Cell
, vol.4
, Issue.4
, pp. 511-518
-
-
Moynahan, M.E.1
Chiu, J.W.2
Koller, B.H.3
-
62
-
-
0347991859
-
Stabilization of stalled DNA replication forks by the BRCA2 breast cancer susceptibility protein
-
Lomonosov M, Anand S, Sangrithi M, et al., Stabilization of stalled DNA replication forks by the BRCA2 breast cancer susceptibility protein. Genes Dev 2003; 17 (24): 3017-3022.
-
(2003)
Genes Dev
, vol.17
, Issue.24
, pp. 3017-3022
-
-
Lomonosov, M.1
Anand, S.2
Sangrithi, M.3
-
63
-
-
0025232413
-
The second zinc-finger domain of poly(ADP-ribose) polymerase determines specificity for single-stranded breaks in DNA
-
Gradwohl G, Ménissier de Murcia JM, Molinete M, et al., The second zinc-finger domain of poly(ADP-ribose) polymerase determines specificity for single-stranded breaks in DNA. Proc Natl Acad Sci USA 1990; 87 (8): 2990-2994.
-
(1990)
Proc Natl Acad Sci USA
, vol.87
, Issue.8
, pp. 2990-2994
-
-
Gradwohl, G.1
Ménissier De Murcia, J.M.2
Molinete, M.3
-
64
-
-
0036844340
-
Recombinational repair and restart of damaged replication forks
-
McGlynn P, Lloyd RG,. Recombinational repair and restart of damaged replication forks. Nat Rev Mol Cell Biol 2002; 3 (11): 859-870.
-
(2002)
Nat Rev Mol Cell Biol
, vol.3
, Issue.11
, pp. 859-870
-
-
McGlynn, P.1
Lloyd, R.G.2
-
65
-
-
77950023283
-
PARP inhibition: PARP1 and beyond
-
Rouleau M, Patel A, Hendzel MJ, et al., PARP inhibition: PARP1 and beyond. Nat Rev Cancer 2010; 10 (4): 293-301.
-
(2010)
Nat Rev Cancer
, vol.10
, Issue.4
, pp. 293-301
-
-
Rouleau, M.1
Patel, A.2
Hendzel, M.J.3
-
66
-
-
23344444636
-
Spontaneous homologous recombination is induced by collapsed replication forks that are caused by endogenous DNA single-strand breaks
-
Saleh-Gohari N, Bryant HE, Schultz N, et al., Spontaneous homologous recombination is induced by collapsed replication forks that are caused by endogenous DNA single-strand breaks. Mol Cell Biol 2005; 25 (16): 7158-7169.
-
(2005)
Mol Cell Biol
, vol.25
, Issue.16
, pp. 7158-7169
-
-
Saleh-Gohari, N.1
Bryant, H.E.2
Schultz, N.3
-
67
-
-
84865620494
-
Recognition, signaling, and repair of DNA double-strand breaks produced by ionizing radiation in mammalian cells: The molecular choreography
-
Thompson LH,. Recognition, signaling, and repair of DNA double-strand breaks produced by ionizing radiation in mammalian cells: the molecular choreography. Mutat Res 751 (2): 158-246.
-
Mutat Res
, vol.751
, Issue.2
, pp. 158-246
-
-
Thompson, L.H.1
-
68
-
-
39749166975
-
DNA repair pathways as targets for cancer therapy
-
Helleday T, Petermann E, Lundin C, et al., DNA repair pathways as targets for cancer therapy. Nat Rev Cancer 2008; 8 (3): 193-204.
-
(2008)
Nat Rev Cancer
, vol.8
, Issue.3
, pp. 193-204
-
-
Helleday, T.1
Petermann, E.2
Lundin, C.3
-
69
-
-
84868221110
-
Trapping of PARP1 and PARP2 by clinical PARP inhibitors
-
Murai J, Huang SN, Das BB, et al., Trapping of PARP1 and PARP2 by clinical PARP inhibitors. Cancer Res 2012; 72 (21): 5588-5599.
-
(2012)
Cancer Res
, vol.72
, Issue.21
, pp. 5588-5599
-
-
Murai, J.1
Huang, S.N.2
Das, B.B.3
-
70
-
-
57749113074
-
Drug resistance caused by reversion mutation
-
Ashworth A., Drug resistance caused by reversion mutation. Cancer Res 2008; 68 (24): 10021-10023.
-
(2008)
Cancer Res
, vol.68
, Issue.24
, pp. 10021-10023
-
-
Ashworth, A.1
-
71
-
-
39849097680
-
Resistance to therapy caused by intragenic deletion in BRCA2
-
Edwards SL, Brough R, Lord CJ, et al., Resistance to therapy caused by intragenic deletion in BRCA2. Nature 2008; 451 (7182): 1111-1115.
-
(2008)
Nature
, vol.451
, Issue.7182
, pp. 1111-1115
-
-
Edwards, S.L.1
Brough, R.2
Lord, C.J.3
-
72
-
-
79955738892
-
PARP-1 expression in breast cancer including BRCA1-associated, triple negative and basal-like tumors: Possible implications for PARP-1 inhibitor therapy
-
Domagala P, Huzarski T, Lubinski J, et al., PARP-1 expression in breast cancer including BRCA1-associated, triple negative and basal-like tumors: possible implications for PARP-1 inhibitor therapy. Breast Cancer Res Treat 2011; 127 (3): 861-869.
-
(2011)
Breast Cancer Res Treat
, vol.127
, Issue.3
, pp. 861-869
-
-
Domagala, P.1
Huzarski, T.2
Lubinski, J.3
-
73
-
-
77953291328
-
53BP1 loss rescues BRCA1 deficiency and is associated with triple-negative and BRCA-mutated breast cancers
-
Bouwman P, Aly A, Escandell JM, et al., 53BP1 loss rescues BRCA1 deficiency and is associated with triple-negative and BRCA-mutated breast cancers. Nat Struct Mol Biol 2010; 17 (6): 688-695.
-
(2010)
Nat Struct Mol Biol
, vol.17
, Issue.6
, pp. 688-695
-
-
Bouwman, P.1
Aly, A.2
Escandell, J.M.3
-
74
-
-
77950958141
-
53BP1 inhibits homologous recombination in Brca1-deficient cells by blocking resection of DNA breaks
-
Bunting SF, Callén E, Wong N, et al., 53BP1 inhibits homologous recombination in Brca1-deficient cells by blocking resection of DNA breaks. Cell 2010; 141 (2): 243-254.
-
(2010)
Cell
, vol.141
, Issue.2
, pp. 243-254
-
-
Bunting, S.F.1
Callén, E.2
Wong, N.3
-
75
-
-
0344333420
-
Prognostic and predictive value of c-erbB-2 overexpression in primary breast cancer, alone and in combination with other prognostic markers
-
Sjögren S, Inganäs M, Lindgren A, et al., Prognostic and predictive value of c-erbB-2 overexpression in primary breast cancer, alone and in combination with other prognostic markers. J Clin Oncol 1998; 16 (2): 462-469.
-
(1998)
J Clin Oncol
, vol.16
, Issue.2
, pp. 462-469
-
-
Sjögren, S.1
Inganäs, M.2
Lindgren, A.3
-
76
-
-
0024337144
-
Studies of the HER-2/neu proto-oncogene in human breast and ovarian cancer
-
(New York, NY);.
-
Slamon DJ, Godolphin W, Jones LA, et al., Studies of the HER-2/neu proto-oncogene in human breast and ovarian cancer. Science (New York, NY) 1989; 244 (4905): 707-712.
-
(1989)
Science
, vol.244
, Issue.4905
, pp. 707-712
-
-
Slamon, D.J.1
Godolphin, W.2
Jones, L.A.3
-
77
-
-
0035874898
-
Down-regulation of the erbB-2 receptor by trastuzumab (herceptin) enhances tumor necrosis factor-related apoptosis-inducing ligand-mediated apoptosis in breast and ovarian cancer cell lines that overexpress erbB-2
-
Cuello M, Ettenberg SA, Clark AS, et al., Down-regulation of the erbB-2 receptor by trastuzumab (herceptin) enhances tumor necrosis factor-related apoptosis-inducing ligand-mediated apoptosis in breast and ovarian cancer cell lines that overexpress erbB-2. Cancer Res 2001; 61 (12): 4892-4900.
-
(2001)
Cancer Res
, vol.61
, Issue.12
, pp. 4892-4900
-
-
Cuello, M.1
Ettenberg, S.A.2
Clark, A.S.3
-
78
-
-
0035874981
-
Trastuzumab (herceptin), a humanized anti-Her2 receptor monoclonal antibody, inhibits basal and activated Her2 ectodomain cleavage in breast cancer cells
-
Molina MA, Codony-Servat J, Albanell J, et al., Trastuzumab (herceptin), a humanized anti-Her2 receptor monoclonal antibody, inhibits basal and activated Her2 ectodomain cleavage in breast cancer cells. Cancer Res 2001; 61 (12): 4744-4749.
-
(2001)
Cancer Res
, vol.61
, Issue.12
, pp. 4744-4749
-
-
Molina, M.A.1
Codony-Servat, J.2
Albanell, J.3
-
79
-
-
0035037366
-
Molecular targets for breast cancer therapy and prevention
-
Bange J, Zwick E, Ullrich A,. Molecular targets for breast cancer therapy and prevention. Nat Med 2001; 7 (5): 548-552.
-
(2001)
Nat Med
, vol.7
, Issue.5
, pp. 548-552
-
-
Bange, J.1
Zwick, E.2
Ullrich, A.3
-
80
-
-
65349101151
-
Ligand-independent HER2/HER3/PI3K complex is disrupted by trastuzumab and is effectively inhibited by the PI3K inhibitor GDC-0941
-
Junttila TT, Akita RW, Parsons K, et al., Ligand-independent HER2/HER3/PI3K complex is disrupted by trastuzumab and is effectively inhibited by the PI3K inhibitor GDC-0941. Cancer Cell 2009; 15 (5): 429-440.
-
(2009)
Cancer Cell
, vol.15
, Issue.5
, pp. 429-440
-
-
Junttila, T.T.1
Akita, R.W.2
Parsons, K.3
-
81
-
-
84873579032
-
Update on clinical trials: Genetic targets in breast cancer
-
Lim B, Cream L V, Harvey HA,. Update on clinical trials: genetic targets in breast cancer. Adv Exp Med Biol 2013; 779: 35-54.
-
(2013)
Adv Exp Med Biol
, vol.779
, pp. 35-54
-
-
Lim, B.1
Cream, L.V.2
Harvey, H.A.3
-
82
-
-
84868191543
-
The role of targeted therapy and biomarkers in breast cancer treatment
-
Stopeck AT, Brown-Glaberman U, Wong HY, et al., The role of targeted therapy and biomarkers in breast cancer treatment. Clin Exp Metast 2012; 29 (7): 807-819.
-
(2012)
Clin Exp Metast
, vol.29
, Issue.7
, pp. 807-819
-
-
Stopeck, A.T.1
Brown-Glaberman, U.2
Wong, H.Y.3
-
83
-
-
16644393213
-
The PIK3CA gene is mutated with high frequency in human breast cancers
-
Bachman KE, Argani P, Samuels Y, et al., The PIK3CA gene is mutated with high frequency in human breast cancers. Cancer Biol Therap 2004; 3 (8): 772-775.
-
(2004)
Cancer Biol Therap
, vol.3
, Issue.8
, pp. 772-775
-
-
Bachman, K.E.1
Argani, P.2
Samuels, Y.3
-
84
-
-
35148854641
-
PI3 kinase activation and response to trastuzumab therapy: What's neu with herceptin resistance?
-
Park BH, Davidson NE,. PI3 kinase activation and response to trastuzumab therapy: what's neu with herceptin resistance? Cancer Cell 2007; 12 (4): 297-299.
-
(2007)
Cancer Cell
, vol.12
, Issue.4
, pp. 297-299
-
-
Park, B.H.1
Davidson, N.E.2
-
86
-
-
5144226211
-
PTEN activation contributes to tumor inhibition by trastuzumab, and loss of PTEN predicts trastuzumab resistance in patients
-
Nagata Y, Lan KH, Zhou X, et al., PTEN activation contributes to tumor inhibition by trastuzumab, and loss of PTEN predicts trastuzumab resistance in patients. Cancer Cell 2004; 6 (2): 117-127.
-
(2004)
Cancer Cell
, vol.6
, Issue.2
, pp. 117-127
-
-
Nagata, Y.1
Lan, K.H.2
Zhou, X.3
-
87
-
-
35148885729
-
A functional genetic approach identifies the PI3K pathway as a major determinant of trastuzumab resistance in breast cancer
-
Berns K, Horlings HM, Hennessy BT, et al., A functional genetic approach identifies the PI3K pathway as a major determinant of trastuzumab resistance in breast cancer. Cancer Cell 2007; 12 (4): 395-402.
-
(2007)
Cancer Cell
, vol.12
, Issue.4
, pp. 395-402
-
-
Berns, K.1
Horlings, H.M.2
Hennessy, B.T.3
-
88
-
-
18344390418
-
ERBB receptors and cancer: The complexity of targeted inhibitors
-
Hynes NE, Lane HA,. ERBB receptors and cancer: the complexity of targeted inhibitors. Nat Rev Cancer 2005; 5 (5): 341-354.
-
(2005)
Nat Rev Cancer
, vol.5
, Issue.5
, pp. 341-354
-
-
Hynes, N.E.1
Lane, H.A.2
-
89
-
-
48649092620
-
A central role for HER3 in HER2-amplified breast cancer: Implications for targeted therapy
-
Lee-Hoeflich ST, Crocker L, Yao E, et al., A central role for HER3 in HER2-amplified breast cancer: implications for targeted therapy. Cancer Res 2008; 68 (14): 5878-5887.
-
(2008)
Cancer Res
, vol.68
, Issue.14
, pp. 5878-5887
-
-
Lee-Hoeflich, S.T.1
Crocker, L.2
Yao, E.3
-
90
-
-
33846552656
-
Escape from HER-family tyrosine kinase inhibitor therapy by the kinase-inactive HER3
-
Sergina N V, Rausch M, Wang D, et al., Escape from HER-family tyrosine kinase inhibitor therapy by the kinase-inactive HER3. Nature 2007; 445 (7126): 437-441.
-
(2007)
Nature
, vol.445
, Issue.7126
, pp. 437-441
-
-
Sergina, N.V.1
Rausch, M.2
Wang, D.3
-
91
-
-
34548071359
-
Human breast cancer cells selected for resistance to trastuzumab in vivo overexpress epidermal growth factor receptor and ErbB ligands and remain dependent on the ErbB receptor network
-
Ritter CA, Perez-Torres M, Rinehart C, et al., Human breast cancer cells selected for resistance to trastuzumab in vivo overexpress epidermal growth factor receptor and ErbB ligands and remain dependent on the ErbB receptor network. Clin Cancer Res 2007; 13 (16): 4909-4919.
-
(2007)
Clin Cancer Res
, vol.13
, Issue.16
, pp. 4909-4919
-
-
Ritter, C.A.1
Perez-Torres, M.2
Rinehart, C.3
-
92
-
-
0035915421
-
Insulin-like growth factor-I receptor signaling and resistance to trastuzumab (Herceptin)
-
Lu Y, Zi X, Zhao Y, et al., Insulin-like growth factor-I receptor signaling and resistance to trastuzumab (Herceptin). J Natl Cancer Inst 2001; 93 (24): 1852-1857.
-
(2001)
J Natl Cancer Inst
, vol.93
, Issue.24
, pp. 1852-1857
-
-
Lu, Y.1
Zi, X.2
Zhao, Y.3
-
93
-
-
28244432561
-
Insulin-like growth factor-I receptor/human epidermal growth factor receptor 2 heterodimerization contributes to trastuzumab resistance of breast cancer cells
-
Nahta R, Yuan LXH, Zhang B, et al., Insulin-like growth factor-I receptor/human epidermal growth factor receptor 2 heterodimerization contributes to trastuzumab resistance of breast cancer cells. Cancer Res 2005; 65 (23): 11118-11128.
-
(2005)
Cancer Res
, vol.65
, Issue.23
, pp. 11118-11128
-
-
Nahta, R.1
Yuan, L.X.H.2
Zhang, B.3
-
94
-
-
31544465529
-
P95HER-2 predicts worse outcome in patients with HER-2-positive breast cancer
-
Sáez R, Molina MA, Ramsey EE, et al., p95HER-2 predicts worse outcome in patients with HER-2-positive breast cancer. Clin Cancer Res 2006; 12 (2): 424-431.
-
(2006)
Clin Cancer Res
, vol.12
, Issue.2
, pp. 424-431
-
-
Sáez, R.1
Molina, M.A.2
Ramsey, E.E.3
-
95
-
-
1842605531
-
Insights into ErbB signaling from the structure of the ErbB2-pertuzumab complex
-
Franklin MC, Carey KD, Vajdos FF, et al., Insights into ErbB signaling from the structure of the ErbB2-pertuzumab complex. Cancer Cell 2004; 5 (4): 317-328.
-
(2004)
Cancer Cell
, vol.5
, Issue.4
, pp. 317-328
-
-
Franklin, M.C.1
Carey, K.D.2
Vajdos, F.F.3
-
96
-
-
33644600485
-
Humanization of a recombinant monoclonal antibody to produce a therapeutic HER dimerization inhibitor, pertuzumab
-
Adams CW, Allison DE, Flagella K, et al., Humanization of a recombinant monoclonal antibody to produce a therapeutic HER dimerization inhibitor, pertuzumab. Cancer Immunol Immunother 2006; 55 (6): 717-727.
-
(2006)
Cancer Immunol Immunother
, vol.55
, Issue.6
, pp. 717-727
-
-
Adams, C.W.1
Allison, D.E.2
Flagella, K.3
-
97
-
-
34249075147
-
MET amplification leads to gefitinib resistance in lung cancer by activating ERBB3 signaling
-
Engelman JA, Zejnullahu K, Mitsudomi T, et al., MET amplification leads to gefitinib resistance in lung cancer by activating ERBB3 signaling. Science (New York, NY) 2007; 316 (5827): 1039-1043.
-
(2007)
Science (New York, NY)
, vol.316
, Issue.5827
, pp. 1039-1043
-
-
Engelman, J.A.1
Zejnullahu, K.2
Mitsudomi, T.3
-
98
-
-
84872971201
-
Spontaneous and pronase-induced HER2 truncation increases the trastuzumab binding capacity of breast cancer tissues and cell lines
-
Recupero D, Daniele L, Marchiò C, et al., Spontaneous and pronase-induced HER2 truncation increases the trastuzumab binding capacity of breast cancer tissues and cell lines. J Pathol 2013; 229 (3): 390-399.
-
(2013)
J Pathol
, vol.229
, Issue.3
, pp. 390-399
-
-
Recupero, D.1
Daniele, L.2
Marchiò, C.3
-
99
-
-
73649149433
-
Strongly enhanced antitumor activity of trastuzumab and pertuzumab combination treatment on HER2-positive human xenograft tumor models
-
Scheuer W, Friess T, Burtscher H, et al., Strongly enhanced antitumor activity of trastuzumab and pertuzumab combination treatment on HER2-positive human xenograft tumor models. Cancer Res 2009; 69 (24): 9330-9336.
-
(2009)
Cancer Res
, vol.69
, Issue.24
, pp. 9330-9336
-
-
Scheuer, W.1
Friess, T.2
Burtscher, H.3
-
100
-
-
56449129810
-
Targeting HER2-positive breast cancer with trastuzumab-DM1, an antibody-cytotoxic drug conjugate
-
Lewis Phillips GD, Li G, Dugger DL, et al., Targeting HER2-positive breast cancer with trastuzumab-DM1, an antibody-cytotoxic drug conjugate. Cancer Res 2008; 68 (22): 9280-9290.
-
(2008)
Cancer Res
, vol.68
, Issue.22
, pp. 9280-9290
-
-
Lewis Phillips, G.D.1
Li, G.2
Dugger, D.L.3
-
101
-
-
79959700509
-
Trastuzumab-DM1 (T-DM1) retains all the mechanisms of action of trastuzumab and efficiently inhibits growth of lapatinib insensitive breast cancer
-
Junttila TT, Li G, Parsons K, et al., Trastuzumab-DM1 (T-DM1) retains all the mechanisms of action of trastuzumab and efficiently inhibits growth of lapatinib insensitive breast cancer. Breast Cancer Res Treat 2011; 128 (2): 347-356.
-
(2011)
Breast Cancer Res Treat
, vol.128
, Issue.2
, pp. 347-356
-
-
Junttila, T.T.1
Li, G.2
Parsons, K.3
-
102
-
-
84873993908
-
Current approaches and future directions in the treatment of HER2-positive breast cancer
-
Hurvitz SA, Hu Y, O'Brien N, et al., Current approaches and future directions in the treatment of HER2-positive breast cancer. Cancer Treat Rev 2013; 39 (3): 219-229.
-
(2013)
Cancer Treat Rev
, vol.39
, Issue.3
, pp. 219-229
-
-
Hurvitz, S.A.1
Hu, Y.2
O'Brien, N.3
-
103
-
-
84873918443
-
Activating HER2 mutations in HER2 gene amplification-negative breast cancer
-
Bose R, Kavuri SM, Searleman AC, et al., Activating HER2 mutations in HER2 gene amplification-negative breast cancer. Cancer Discov 2013; 3 (2): 224-237.
-
(2013)
Cancer Discov
, vol.3
, Issue.2
, pp. 224-237
-
-
Bose, R.1
Kavuri, S.M.2
Searleman, A.C.3
-
104
-
-
70149109569
-
Novel mechanism of lapatinib resistance in HER2-positive breast tumor cells: Activation of AXL
-
Liu L, Greger J, Shi H, et al., Novel mechanism of lapatinib resistance in HER2-positive breast tumor cells: activation of AXL. Cancer Res 2009; 69 (17): 6871-6878.
-
(2009)
Cancer Res
, vol.69
, Issue.17
, pp. 6871-6878
-
-
Liu, L.1
Greger, J.2
Shi, H.3
-
105
-
-
33646746413
-
A model of acquired autoresistance to a potent ErbB2 tyrosine kinase inhibitor and a therapeutic strategy to prevent its onset in breast cancer
-
Xia W, Bacus S, Hegde P, et al., A model of acquired autoresistance to a potent ErbB2 tyrosine kinase inhibitor and a therapeutic strategy to prevent its onset in breast cancer. Proc Natl Acad Sci USA 2006; 103 (20): 7795-7800.
-
(2006)
Proc Natl Acad Sci USA
, vol.103
, Issue.20
, pp. 7795-7800
-
-
Xia, W.1
Bacus, S.2
Hegde, P.3
-
106
-
-
0035939330
-
Studies leading to the identification of ZD1839 (IRESSA): An orally active, selective epidermal growth factor receptor tyrosine kinase inhibitor targeted to the treatment of cancer
-
Barker AJ, Gibson KH, Grundy W, et al., Studies leading to the identification of ZD1839 (IRESSA): an orally active, selective epidermal growth factor receptor tyrosine kinase inhibitor targeted to the treatment of cancer. Bioorg Med Chem Lett 2001; 11 (14): 1911-1914.
-
(2001)
Bioorg Med Chem Lett
, vol.11
, Issue.14
, pp. 1911-1914
-
-
Barker, A.J.1
Gibson, K.H.2
Grundy, W.3
-
107
-
-
0037109014
-
ZD1839 (Iressa): An orally active inhibitor of epidermal growth factor signaling with potential for cancer therapy
-
Wakeling AE, Guy SP, Woodburn JR, et al., ZD1839 (Iressa): an orally active inhibitor of epidermal growth factor signaling with potential for cancer therapy. Cancer Res 2002; 62 (20): 5749-5754.
-
(2002)
Cancer Res
, vol.62
, Issue.20
, pp. 5749-5754
-
-
Wakeling, A.E.1
Guy, S.P.2
Woodburn, J.R.3
-
108
-
-
33847323129
-
Epidermal growth factor receptor mutations in lung cancer
-
Sharma S V, Bell DW, Settleman J, et al., Epidermal growth factor receptor mutations in lung cancer. Nat Rev Cancer 2007; 7 (3): 169-181.
-
(2007)
Nat Rev Cancer
, vol.7
, Issue.3
, pp. 169-181
-
-
Sharma, S.V.1
Bell, D.W.2
Settleman, J.3
-
109
-
-
10844231985
-
Mutations of the epidermal growth factor receptor gene in lung cancer: Biological and clinical implications
-
Kosaka T, Yatabe Y, Endoh H, et al., Mutations of the epidermal growth factor receptor gene in lung cancer: biological and clinical implications. Cancer Res 2004; 64 (24): 8919-8923.
-
(2004)
Cancer Res
, vol.64
, Issue.24
, pp. 8919-8923
-
-
Kosaka, T.1
Yatabe, Y.2
Endoh, H.3
-
110
-
-
13844317894
-
EGFR mutation and resistance of non-small-cell lung cancer to gefitinib
-
Kobayashi S, Boggon TJ, Dayaram T, et al., EGFR mutation and resistance of non-small-cell lung cancer to gefitinib. N Engl J Med 2005; 352 (8): 786-792.
-
(2005)
N Engl J Med
, vol.352
, Issue.8
, pp. 786-792
-
-
Kobayashi, S.1
Boggon, T.J.2
Dayaram, T.3
-
111
-
-
18244371651
-
Acquired resistance of lung adenocarcinomas to gefitinib or erlotinib is associated with a second mutation in the EGFR kinase domain
-
Pao W, Miller VA, Politi KA, et al., Acquired resistance of lung adenocarcinomas to gefitinib or erlotinib is associated with a second mutation in the EGFR kinase domain. PLoS Med 2005; 2 (3): e73.
-
(2005)
PLoS Med
, vol.2
, Issue.3
-
-
Pao, W.1
Miller, V.A.2
Politi, K.A.3
-
112
-
-
40049099220
-
The T790M mutation in EGFR kinase causes drug resistance by increasing the affinity for ATP
-
Yun C-H, Mengwasser KE, Toms A V, et al., The T790M mutation in EGFR kinase causes drug resistance by increasing the affinity for ATP. Proc Natl Acad Sci USA 2008; 105 (6): 2070-2075.
-
(2008)
Proc Natl Acad Sci USA
, vol.105
, Issue.6
, pp. 2070-2075
-
-
Yun, C.-H.1
Mengwasser, K.E.2
Toms, A.V.3
-
113
-
-
21144439000
-
Irreversible inhibitors of the EGF receptor may circumvent acquired resistance to gefitinib
-
Kwak EL, Sordella R, Bell DW, et al., Irreversible inhibitors of the EGF receptor may circumvent acquired resistance to gefitinib. Proc Natl Acad Sci USA 2005; 102 (21): 7665-7670.
-
(2005)
Proc Natl Acad Sci USA
, vol.102
, Issue.21
, pp. 7665-7670
-
-
Kwak, E.L.1
Sordella, R.2
Bell, D.W.3
-
114
-
-
33751292685
-
Novel D761Y and common secondary T790M mutations in epidermal growth factor receptor-mutant lung adenocarcinomas with acquired resistance to kinase inhibitors
-
Balak MN, Gong Y, Riely GJ, et al., Novel D761Y and common secondary T790M mutations in epidermal growth factor receptor-mutant lung adenocarcinomas with acquired resistance to kinase inhibitors. Clin Cancer Res 2006; 12 (21): 6494-6501.
-
(2006)
Clin Cancer Res
, vol.12
, Issue.21
, pp. 6494-6501
-
-
Balak, M.N.1
Gong, Y.2
Riely, G.J.3
-
115
-
-
33744781279
-
Double mutation and gene copy number of EGFR in gefitinib refractory non-small-cell lung cancer
-
Tokumo M, Toyooka S, Ichihara S, et al., Double mutation and gene copy number of EGFR in gefitinib refractory non-small-cell lung cancer. Lung Cancer (Amsterdam, Netherlands) 2006; 53 (1): 117-121.
-
(2006)
Lung Cancer (Amsterdam, Netherlands)
, vol.53
, Issue.1
, pp. 117-121
-
-
Tokumo, M.1
Toyooka, S.2
Ichihara, S.3
-
116
-
-
77953710855
-
Acquired resistance of lung adenocarcinoma to EGFR-tyrosine kinase inhibitors gefitinib and erlotinib
-
Xu Y, Liu H, Chen J, et al., Acquired resistance of lung adenocarcinoma to EGFR-tyrosine kinase inhibitors gefitinib and erlotinib. Cancer Biol Therap Landes Biosci 2010; 9 (8): 572-582.
-
(2010)
Cancer Biol Therap Landes Biosci
, vol.9
, Issue.8
, pp. 572-582
-
-
Xu, Y.1
Liu, H.2
Chen, J.3
-
117
-
-
17444403242
-
Structural basis for inhibition of the epidermal growth factor receptor by cetuximab
-
Li S, Schmitz KR, Jeffrey PD, et al., Structural basis for inhibition of the epidermal growth factor receptor by cetuximab. Cancer Cell 2005; 7 (4): 301-311.
-
(2005)
Cancer Cell
, vol.7
, Issue.4
, pp. 301-311
-
-
Li, S.1
Schmitz, K.R.2
Jeffrey, P.D.3
-
118
-
-
79955513633
-
Molecular mechanisms of resistance to the EGFR monoclonal antibody cetuximab
-
Brand TM, Iida M, Wheeler DL,. Molecular mechanisms of resistance to the EGFR monoclonal antibody cetuximab. Cancer Biol Therap 2011; 11 (9): 777-792.
-
(2011)
Cancer Biol Therap
, vol.11
, Issue.9
, pp. 777-792
-
-
Brand, T.M.1
Iida, M.2
Wheeler, D.L.3
-
119
-
-
34247278727
-
Clinical relevance of KRAS mutation detection in metastatic colorectal cancer treated by Cetuximab plus chemotherapy
-
Di Fiore F, Blanchard F, Charbonnier F, et al., Clinical relevance of KRAS mutation detection in metastatic colorectal cancer treated by Cetuximab plus chemotherapy. Br J Cancer 2007; 96 (8): 1166-1169.
-
(2007)
Br J Cancer
, vol.96
, Issue.8
, pp. 1166-1169
-
-
Di Fiore, F.1
Blanchard, F.2
Charbonnier, F.3
-
120
-
-
40149088765
-
KRAS wild-type state predicts survival and is associated to early radiological response in metastatic colorectal cancer treated with cetuximab
-
De Roock W, Piessevaux H, De Schutter J, et al., KRAS wild-type state predicts survival and is associated to early radiological response in metastatic colorectal cancer treated with cetuximab. Ann Oncol 2008; 19 (3): 508-515.
-
(2008)
Ann Oncol
, vol.19
, Issue.3
, pp. 508-515
-
-
De Roock, W.1
Piessevaux, H.2
De Schutter, J.3
-
121
-
-
42649145667
-
Wild-type KRAS is required for panitumumab efficacy in patients with metastatic colorectal cancer
-
Amado RG, Wolf M, Peeters M, et al., Wild-type KRAS is required for panitumumab efficacy in patients with metastatic colorectal cancer. J Clin Oncol 2008; 26 (10): 1626-1634.
-
(2008)
J Clin Oncol
, vol.26
, Issue.10
, pp. 1626-1634
-
-
Amado, R.G.1
Wolf, M.2
Peeters, M.3
-
122
-
-
84863000299
-
The molecular evolution of acquired resistance to targeted EGFR blockade in colorectal cancers
-
Diaz LA, Williams RT, Wu J, et al., The molecular evolution of acquired resistance to targeted EGFR blockade in colorectal cancers. Nature 2012; 486 (7404): 537-540.
-
(2012)
Nature
, vol.486
, Issue.7404
, pp. 537-540
-
-
Diaz, L.A.1
Williams, R.T.2
Wu, J.3
-
123
-
-
84862999938
-
Emergence of KRAS mutations and acquired resistance to anti-EGFR therapy in colorectal cancer
-
Misale S, Yaeger R, Hobor S, et al., Emergence of KRAS mutations and acquired resistance to anti-EGFR therapy in colorectal cancer. Nature 2012; 486 (7404): 532-536.
-
(2012)
Nature
, vol.486
, Issue.7404
, pp. 532-536
-
-
Misale, S.1
Yaeger, R.2
Hobor, S.3
-
124
-
-
57449095367
-
Wild-type BRAF is required for response to panitumumab or cetuximab in metastatic colorectal cancer
-
Di Nicolantonio F, Martini M, Molinari F, et al., Wild-type BRAF is required for response to panitumumab or cetuximab in metastatic colorectal cancer. J Clin Oncol 2008; 26 (35): 5705-5712.
-
(2008)
J Clin Oncol
, vol.26
, Issue.35
, pp. 5705-5712
-
-
Di Nicolantonio, F.1
Martini, M.2
Molinari, F.3
-
125
-
-
62449302407
-
PIK3CA mutations in colorectal cancer are associated with clinical resistance to EGFR-targeted monoclonal antibodies
-
Sartore-Bianchi A, Martini M, Molinari F, et al., PIK3CA mutations in colorectal cancer are associated with clinical resistance to EGFR-targeted monoclonal antibodies. Cancer Res 2009; 69 (5): 1851-1857.
-
(2009)
Cancer Res
, vol.69
, Issue.5
, pp. 1851-1857
-
-
Sartore-Bianchi, A.1
Martini, M.2
Molinari, F.3
-
126
-
-
84878862323
-
Amplification of the MET receptor drives resistance to anti-EGFR therapies in colorectal cancer
-
Bardelli A, Corso S, Bertotti A, et al., Amplification of the MET receptor drives resistance to anti-EGFR therapies in colorectal cancer. Cancer Discov 2013; 3 (6): 658-673.
-
(2013)
Cancer Discov
, vol.3
, Issue.6
, pp. 658-673
-
-
Bardelli, A.1
Corso, S.2
Bertotti, A.3
-
127
-
-
18444374405
-
Mutations of the BRAF gene in human cancer
-
Davies H, Bignell GR, Cox C, et al., Mutations of the BRAF gene in human cancer. Nature 2002; 417 (6892): 949-954.
-
(2002)
Nature
, vol.417
, Issue.6892
, pp. 949-954
-
-
Davies, H.1
Bignell, G.R.2
Cox, C.3
-
128
-
-
42949149240
-
Discovery of a selective inhibitor of oncogenic B-Raf kinase with potent antimelanoma activity
-
Tsai J, Lee JT, Wang W, et al., Discovery of a selective inhibitor of oncogenic B-Raf kinase with potent antimelanoma activity. Proc Natl Acad Sci USA 2008; 105 (8): 3041-3046.
-
(2008)
Proc Natl Acad Sci USA
, vol.105
, Issue.8
, pp. 3041-3046
-
-
Tsai, J.1
Lee, J.T.2
Wang, W.3
-
129
-
-
77949685981
-
RAF inhibitors prime wild-type RAF to activate the MAPK pathway and enhance growth
-
Hatzivassiliou G, Song K, Yen I, et al., RAF inhibitors prime wild-type RAF to activate the MAPK pathway and enhance growth. Nature 2010; 464 (7287): 431-435.
-
(2010)
Nature
, vol.464
, Issue.7287
, pp. 431-435
-
-
Hatzivassiliou, G.1
Song, K.2
Yen, I.3
-
130
-
-
77956030786
-
Inhibition of mutated, activated BRAF in metastatic melanoma
-
Flaherty KT, Puzanov I, Kim KB, et al., Inhibition of mutated, activated BRAF in metastatic melanoma. N Engl J Med 2010; 363 (9): 809-819.
-
(2010)
N Engl J Med
, vol.363
, Issue.9
, pp. 809-819
-
-
Flaherty, K.T.1
Puzanov, I.2
Kim, K.B.3
-
131
-
-
84868224906
-
Combined BRAF and MEK inhibition in melanoma with BRAF V600 mutations
-
Flaherty KT, Infante JR, Daud A, et al., Combined BRAF and MEK inhibition in melanoma with BRAF V600 mutations. N Engl J Med 2012; 367 (18): 1694-1703.
-
(2012)
N Engl J Med
, vol.367
, Issue.18
, pp. 1694-1703
-
-
Flaherty, K.T.1
Infante, J.R.2
Daud, A.3
-
132
-
-
78650303507
-
Melanomas acquire resistance to B-RAF(V600E) inhibition by RTK or N-RAS upregulation
-
Nazarian R, Shi H, Wang Q, et al., Melanomas acquire resistance to B-RAF(V600E) inhibition by RTK or N-RAS upregulation. Nature 2010; 468 (7326): 973-977.
-
(2010)
Nature
, vol.468
, Issue.7326
, pp. 973-977
-
-
Nazarian, R.1
Shi, H.2
Wang, Q.3
-
133
-
-
84879496934
-
Pharmacodynamic effects and mechanisms of resistance to vemurafenib in patients with metastatic melanoma
-
Trunzer K, Pavlick AC, Schuchter L, et al., Pharmacodynamic effects and mechanisms of resistance to vemurafenib in patients with metastatic melanoma. J Clin Oncol 2013; 31 (14): 1767-1774.
-
(2013)
J Clin Oncol
, vol.31
, Issue.14
, pp. 1767-1774
-
-
Trunzer, K.1
Pavlick, A.C.2
Schuchter, L.3
-
134
-
-
84864285794
-
Tumour micro-environment elicits innate resistance to RAF inhibitors through HGF secretion
-
Straussman R, Morikawa T, Shee K, et al., Tumour micro-environment elicits innate resistance to RAF inhibitors through HGF secretion. Nature 2012; 487 (7408): 500-504.
-
(2012)
Nature
, vol.487
, Issue.7408
, pp. 500-504
-
-
Straussman, R.1
Morikawa, T.2
Shee, K.3
-
135
-
-
84863230465
-
Unresponsiveness of colon cancer to BRAF(V600E) inhibition through feedback activation of EGFR
-
Prahallad A, Sun C, Huang S, et al., Unresponsiveness of colon cancer to BRAF(V600E) inhibition through feedback activation of EGFR. Nature 2012; 483 (7387): 100-103.
-
(2012)
Nature
, vol.483
, Issue.7387
, pp. 100-103
-
-
Prahallad, A.1
Sun, C.2
Huang, S.3
-
136
-
-
34547638047
-
Identification of the transforming EML4-ALK fusion gene in non-small-cell lung cancer
-
Soda M, Choi YL, Enomoto M, et al., Identification of the transforming EML4-ALK fusion gene in non-small-cell lung cancer. Nature 2007; 448 (7153): 561-566.
-
(2007)
Nature
, vol.448
, Issue.7153
, pp. 561-566
-
-
Soda, M.1
Choi, Y.L.2
Enomoto, M.3
-
137
-
-
77953291664
-
The biology and treatment of EML4-ALK non-small cell lung cancer
-
Sasaki T, Rodig SJ, Chirieac LR, et al., The biology and treatment of EML4-ALK non-small cell lung cancer. Eur J Cancer 2010; 46 (10): 1773-1780.
-
(2010)
Eur J Cancer
, vol.46
, Issue.10
, pp. 1773-1780
-
-
Sasaki, T.1
Rodig, S.J.2
Chirieac, L.R.3
-
138
-
-
84879879406
-
Treatment and detection of ALK-rearranged NSCLC
-
Peters S, Taron M, Bubendorf L, et al., Treatment and detection of ALK-rearranged NSCLC. Lung Cancer 2013; 81: 145-154.
-
(2013)
Lung Cancer
, vol.81
, pp. 145-154
-
-
Peters, S.1
Taron, M.2
Bubendorf, L.3
-
139
-
-
37549059613
-
Cytoreductive antitumor activity of PF-2341066, a novel inhibitor of anaplastic lymphoma kinase and c-Met, in experimental models of anaplastic large-cell lymphoma
-
Christensen JG, Zou HY, Arango ME, et al., Cytoreductive antitumor activity of PF-2341066, a novel inhibitor of anaplastic lymphoma kinase and c-Met, in experimental models of anaplastic large-cell lymphoma. Mol Cancer Therap 2007; 6 (12, pt 1): 3314-3322.
-
(2007)
Mol Cancer Therap
, vol.6
, Issue.12
, pp. 3314-3322
-
-
Christensen, J.G.1
Zou, H.Y.2
Arango, M.E.3
-
140
-
-
34249324494
-
An orally available small-molecule inhibitor of c-Met, PF-2341066, exhibits cytoreductive antitumor efficacy through antiproliferative and antiangiogenic mechanisms
-
Zou HY, Li Q, Lee JH, et al., An orally available small-molecule inhibitor of c-Met, PF-2341066, exhibits cytoreductive antitumor efficacy through antiproliferative and antiangiogenic mechanisms. Cancer Res 2007; 67 (9): 4408-4417.
-
(2007)
Cancer Res
, vol.67
, Issue.9
, pp. 4408-4417
-
-
Zou, H.Y.1
Li, Q.2
Lee, J.H.3
-
141
-
-
78049426513
-
EML4-ALK mutations in lung cancer that confer resistance to ALK inhibitors
-
Choi YL, Soda M, Yamashita Y, et al., EML4-ALK mutations in lung cancer that confer resistance to ALK inhibitors. N Engl J Med 2010; 363 (18): 1734-1739.
-
(2010)
N Engl J Med
, vol.363
, Issue.18
, pp. 1734-1739
-
-
Choi, Y.L.1
Soda, M.2
Yamashita, Y.3
-
142
-
-
84856999699
-
Mechanisms of acquired crizotinib resistance in ALK-rearranged lung cancers
-
120ra17.
-
Katayama R, Shaw AT, Khan TM, et al., Mechanisms of acquired crizotinib resistance in ALK-rearranged lung cancers. Sci Translat Med 2012; 4 (120): 120ra17.
-
(2012)
Sci Translat Med
, vol.4
, Issue.120
-
-
Katayama, R.1
Shaw, A.T.2
Khan, T.M.3
-
143
-
-
84869211206
-
Activation of HER family signaling as a mechanism of acquired resistance to ALK inhibitors in EML4-ALK-positive non-small cell lung cancer
-
Tanizaki J, Okamoto I, Okabe T, et al., Activation of HER family signaling as a mechanism of acquired resistance to ALK inhibitors in EML4-ALK-positive non-small cell lung cancer. Clin Cancer Res 2012; 18 (22): 6219-6226.
-
(2012)
Clin Cancer Res
, vol.18
, Issue.22
, pp. 6219-6226
-
-
Tanizaki, J.1
Okamoto, I.2
Okabe, T.3
-
144
-
-
11144358645
-
High frequency of mutations of the PIK3CA gene in human cancers
-
554.
-
Samuels Y, Wang Z, Bardelli A, et al., High frequency of mutations of the PIK3CA gene in human cancers. Science (New York, NY) 2004; 304 (5670): 554.
-
(2004)
Science (New York, NY)
, vol.304
, Issue.5670
-
-
Samuels, Y.1
Wang, Z.2
Bardelli, A.3
-
145
-
-
84871968444
-
PIK3CA mutation H1047R is associated with response to PI3K/AKT/mTOR signaling pathway inhibitors in early-phase clinical trials
-
Janku F, Wheler JJ, Naing A, et al., PIK3CA mutation H1047R is associated with response to PI3K/AKT/mTOR signaling pathway inhibitors in early-phase clinical trials. Cancer Res 2013; 73 (1): 276-284.
-
(2013)
Cancer Res
, vol.73
, Issue.1
, pp. 276-284
-
-
Janku, F.1
Wheler, J.J.2
Naing, A.3
-
146
-
-
84863338519
-
PI3K/AKT/mTOR inhibitors in patients with breast and gynecologic malignancies harboring PIK3CA mutations
-
Janku F, Wheler JJ, Westin SN, et al., PI3K/AKT/mTOR inhibitors in patients with breast and gynecologic malignancies harboring PIK3CA mutations. J Clin Oncol 2012; 30 (8): 777-782.
-
(2012)
J Clin Oncol
, vol.30
, Issue.8
, pp. 777-782
-
-
Janku, F.1
Wheler, J.J.2
Westin, S.N.3
-
147
-
-
38149120449
-
Targeting phosphoinositide 3-kinase: Moving towards therapy
-
Marone R, Cmiljanovic V, Giese B, et al., Targeting phosphoinositide 3-kinase: moving towards therapy. Biochim Biophys Acta 2008; 1784 (1): 159-185.
-
(2008)
Biochim Biophys Acta
, vol.1784
, Issue.1
, pp. 159-185
-
-
Marone, R.1
Cmiljanovic, V.2
Giese, B.3
-
148
-
-
34547172596
-
A transforming mutation in the pleckstrin homology domain of AKT1 in cancer
-
Carpten JD, Faber AL, Horn C, et al., A transforming mutation in the pleckstrin homology domain of AKT1 in cancer. Nature 2007; 448 (7152): 439-444.
-
(2007)
Nature
, vol.448
, Issue.7152
, pp. 439-444
-
-
Carpten, J.D.1
Faber, A.L.2
Horn, C.3
|