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Volumn 232, Issue 2, 2014, Pages 244-254

Somatic alterations as the basis for resistance to targeted therapies

Author keywords

cancer; drug resistance; somatic alterations; targeted therapies

Indexed keywords

B RAF KINASE; BCR ABL PROTEIN; CRIZOTINIB; DABRAFENIB; EPIDERMAL GROWTH FACTOR RECEPTOR 2; EPIDERMAL GROWTH FACTOR RECEPTOR ANTIBODY; ERLOTINIB; EVEROLIMUS; GEFITINIB; IMATINIB; K RAS PROTEIN; LAPATINIB; MAMMALIAN TARGET OF RAPAMYCIN INHIBITOR; NICOTINAMIDE ADENINE DINUCLEOTIDE ADENOSINE DIPHOSPHATE RIBOSYLTRANSFERASE INHIBITOR; PHOSPHATIDYLINOSITOL 3,4,5 TRISPHOSPHATE 3 PHOSPHATASE; PHOSPHOTRANSFERASE INHIBITOR; PLATELET DERIVED GROWTH FACTOR; PLATELET DERIVED GROWTH FACTOR RECEPTOR; PROTEIN KINASE B; PROTEIN TYROSINE KINASE; RAF PROTEIN; RAPAMYCIN; RIDAFOROLIMUS; RITUXIMAB; SORAFENIB; SUNITINIB; TEMSIROLIMUS; TRAMETINIB; TRASTUZUMAB; VASCULOTROPIN RECEPTOR; VEMURAFENIB;

EID: 84890285771     PISSN: 00223417     EISSN: 10969896     Source Type: Journal    
DOI: 10.1002/path.4278     Document Type: Review
Times cited : (31)

References (148)
  • 1
    • 0036635291 scopus 로고    scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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
  • 26
    • 0028360374 scopus 로고
    • 1-arresting rapamycin-receptor complex
    • 1-arresting rapamycin-receptor complex. Nature 1994; 369 (6483): 756-758.
    • (1994) Nature , vol.369 , Issue.6483 , pp. 756-758
    • Brown, E.J.1    Albers, M.W.2    Bum Shin, T.3
  • 27
    • 0346362997 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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
  • 85
    • 57449083437 scopus 로고    scopus 로고
    • The PIK3CA gene as a mutated target for cancer therapy
    • Gustin JP, Cosgrove DP, Park BH,. The PIK3CA gene as a mutated target for cancer therapy. Curr Cancer Drug Targets 2008; 8 (8): 733-740.
    • (2008) Curr Cancer Drug Targets , vol.8 , Issue.8 , pp. 733-740
    • Gustin, J.P.1    Cosgrove, D.P.2    Park, B.H.3
  • 86
    • 5144226211 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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


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