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Volumn 4, Issue 11, 2006, Pages 831-836

Novel targets in solid tumors: MEK inhibitors

Author keywords

ERK; MAPK; MEK inhibitor

Indexed keywords

1,4 DIAMINO 1,4 BIS(2 AMINOPHENYLTHIO) 2,3 DICYANOBUTADIENE; 2 (2 AMINO 3 METHOXYPHENYL)CHROMONE; 2 (2 CHLORO 4 IODOANILINO) N CYCLOPROPYLMETHOXY 3,4 DIFLUOROBENZAMIDE; 7 HYDROXYSTAUROSPORINE; ANTINEOPLASTIC AGENT; ARRY 142886; AZD 6244; B RAF KINASE; DOCETAXEL; EPIDERMAL GROWTH FACTOR RECEPTOR KINASE INHIBITOR; ERLOTINIB; GEFITINIB; IMATINIB; MAMMALIAN TARGET OF RAPAMYCIN INHIBITOR; MITOGEN ACTIVATED PROTEIN KINASE; MITOGEN ACTIVATED PROTEIN KINASE INHIBITOR; N (2,3 DIHYDROXYPROPOXY) 3,4 DIFLUORO 2 (2 FLUORO 4 IODOANILINO)BENZAMIDE; PD 184362; PHOSPHATIDYLINOSITOL 3 KINASE INHIBITOR; TAMOXIFEN;

EID: 33845353775     PISSN: 15430790     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (36)

References (44)
  • 1
    • 2442615800 scopus 로고    scopus 로고
    • MEK inhibitors: A therapeutic approach to targeting the Ras-MAP kinase pathway in tumors
    • Sebolt-Leopold JS. MEK inhibitors: a therapeutic approach to targeting the Ras-MAP kinase pathway in tumors. Curr Pharm Des. 2004;10:1907-1914.
    • (2004) Curr Pharm Des. , vol.10 , pp. 1907-1914
    • Sebolt-Leopold, J.S.1
  • 2
    • 0029011218 scopus 로고
    • The MAPK signaling cascade
    • Seger R, Krebs EG. The MAPK signaling cascade. Faseb J. 1995;9:726-735.
    • (1995) Faseb J. , vol.9 , pp. 726-735
    • Seger, R.1    Krebs, E.G.2
  • 3
    • 0027212082 scopus 로고
    • Signal transduction. How receptors turn Ras on
    • McCormick F. Signal transduction. How receptors turn Ras on. Nature. 1993; 363:15-16.
    • (1993) Nature , vol.363 , pp. 15-16
    • McCormick, F.1
  • 4
    • 0037264633 scopus 로고    scopus 로고
    • Targeting RAS signalling pathways in cancer therapy
    • Downward J. Targeting RAS signalling pathways in cancer therapy. Nat Rev Cancer. 2003;3:11-22
    • (2003) Nat Rev Cancer , vol.3 , pp. 11-22
    • Downward, J.1
  • 5
    • 5444227865 scopus 로고    scopus 로고
    • Guilty as charged: B-RAF is a human oncogene
    • Garnett MJ, Marais R. Guilty as charged: B-RAF is a human oncogene. Cancer Cell. 2004;6:313-319
    • (2004) Cancer Cell. , vol.6 , pp. 313-319
    • Garnett, M.J.1    Marais, R.2
  • 6
    • 0032718656 scopus 로고    scopus 로고
    • Mitogen-activated protein kinase cascade in breast cancer
    • Maemura M, Iino Y, Koibuchi Y, Yokoe T, Morishita Y. Mitogen-activated protein kinase cascade in breast cancer. Oncology. 1999;57(suppl 2):37-44.
    • (1999) Oncology , vol.57 , Issue.SUPPL. 2 , pp. 37-44
    • Maemura, M.1    Iino, Y.2    Koibuchi, Y.3    Yokoe, T.4    Morishita, Y.5
  • 7
    • 0034691562 scopus 로고    scopus 로고
    • Potential prognostic value of mitogen-activated protein kinase activity for disease-free survival of primary breast cancer patients
    • Mueller H, Flury N, Eppenberger-Castori S, Kueng W, David F, Eppenberger U. Potential prognostic value of mitogen-activated protein kinase activity for disease-free survival of primary breast cancer patients Int J Cancer. 2000;89:384-388.
    • (2000) Int J Cancer , vol.89 , pp. 384-388
    • Mueller, H.1    Flury, N.2    Eppenberger-Castori, S.3    Kueng, W.4    David, F.5    Eppenberger, U.6
  • 8
    • 0030946366 scopus 로고    scopus 로고
    • Hyperexpression of mitogen-activated protein kinase in human breast cancer
    • Sivaraman VS, Wang H, Nuovo GJ, Malbon CC. Hyperexpression of mitogen-activated protein kinase in human breast cancer. J Clin Invest. 1997;99:1478-1483.
    • (1997) J Clin Invest. , vol.99 , pp. 1478-1483
    • Sivaraman, V.S.1    Wang, H.2    Nuovo, G.J.3    Malbon, C.C.4
  • 9
    • 0033590636 scopus 로고    scopus 로고
    • Constitutive activation of the 41-/43-kDa mitogen-activated protein kinase signaling pathway in human tumors
    • Hoshino R, Chatani Y, Yamori T, et al. Constitutive activation of the 41-/43-kDa mitogen-activated protein kinase signaling pathway in human tumors. Oncogene. 1999;18:813-822
    • (1999) Oncogene , vol.18 , pp. 813-822
    • Hoshino, R.1    Chatani, Y.2    Yamori, T.3
  • 10
    • 0028228616 scopus 로고
    • Activation of MAP kinase kinase is necessary and sufficient for PC12 differentiation and for transformation of NIH 3T3 cells
    • Cowley S, Paterson H, Kemp P, Marshall CJ. Activation of MAP kinase kinase is necessary and sufficient for PC12 differentiation and for transformation of NIH 3T3 cells. Cell. 1994;77:841-852.
    • (1994) Cell , vol.77 , pp. 841-852
    • Cowley, S.1    Paterson, H.2    Kemp, P.3    Marshall, C.J.4
  • 11
    • 0028141496 scopus 로고
    • Transformation of mammalian cells by constitutively active MAP kinase kinase
    • Minster SJ, Matten WT, Hermann AS, et al. Transformation of mammalian cells by constitutively active MAP kinase kinase. Science. 1994;265:966-970.
    • (1994) Science , vol.265 , pp. 966-970
    • Minster, S.J.1    Matten, W.T.2    Hermann, A.S.3
  • 12
    • 0027692679 scopus 로고
    • MEK2 is a kinase related to MEK1 and is differentially expressed in murine tissues
    • Brott BK, Alessandrini A, Largaespada DA, et al. MEK2 is a kinase related to MEK1 and is differentially expressed in murine tissues. Cell Growth Differ. 1993;4:921-929.
    • (1993) Cell Growth Differ. , vol.4 , pp. 921-929
    • Brott, B.K.1    Alessandrini, A.2    Largaespada, D.A.3
  • 13
    • 15744380263 scopus 로고    scopus 로고
    • Structures of human MAP kinase kinase 1 (MEK1) and MEK2 describe novel noncompetitive kinase inhibition
    • Ohren JF, Chen H, Pavlovsky A, et al. Structures of human MAP kinase kinase 1 (MEK1) and MEK2 describe novel noncompetitive kinase inhibition. Nat Struct Mol Biol. 2004;11:1192-1197.
    • (2004) Nat Struct Mol Biol. , vol.11 , pp. 1192-1197
    • Ohren, J.F.1    Chen, H.2    Pavlovsky, A.3
  • 14
    • 0026690922 scopus 로고
    • Purification and characterization of mitogen-activated protein kinase activator(s) from epidermal growth factor-stimulated A431 cells
    • Seger R, Ahn NG, Posada J, et al. Purification and characterization of mitogen-activated protein kinase activator(s) from epidermal growth factor-stimulated A431 cells. J Biol Chem 1992;267:14373-14381.
    • (1992) J Biol Chem , vol.267 , pp. 14373-14381
    • Seger, R.1    Ahn, N.G.2    Posada, J.3
  • 15
    • 0027217533 scopus 로고
    • Cloning and characterization of two distinct human extra-cellular signal-regulated kinase activator kinases, MEK1 and MEK2
    • Zheng CF, Guan KL. Cloning and characterization of two distinct human extra-cellular signal-regulated kinase activator kinases, MEK1 and MEK2. J Biol Chem. 1993;268:11435-11439
    • (1993) J Biol Chem. , vol.268 , pp. 11435-11439
    • Zheng, C.F.1    Guan, K.L.2
  • 16
    • 0033535584 scopus 로고    scopus 로고
    • Embryonic death of Mek1-deficient mice reveals a role for this kinase in angiogenesis in the labyrinthine region of the placenta
    • Giroux S, Tremblay M, Bernard D, et al. Embryonic death of Mek1-deficient mice reveals a role for this kinase in angiogenesis in the labyrinthine region of the placenta. Curr Biol 1999;9:369-372.
    • (1999) Curr Biol , vol.9 , pp. 369-372
    • Giroux, S.1    Tremblay, M.2    Bernard, D.3
  • 17
    • 1242290740 scopus 로고    scopus 로고
    • Mek2 is dispensable for mouse growth and development
    • Belanger LF, Roy S, Tremblay M, et al. Mek2 is dispensable for mouse growth and development. Mol Cell Biol. 2003;23:4778-4787.
    • (2003) Mol Cell Biol. , vol.23 , pp. 4778-4787
    • Belanger, L.F.1    Roy, S.2    Tremblay, M.3
  • 19
    • 17144418558 scopus 로고    scopus 로고
    • Progress towards therapeutic small molecule MEK inhibitors for use in cancer therapy
    • Wallace EM, Lyssikatos JP, Yeh T, Winkler JD, Koch K. Progress towards therapeutic small molecule MEK inhibitors for use in cancer therapy. Curr Top Med Chem. 2005;5:215-229
    • (2005) Curr Top Med Chem. , vol.5 , pp. 215-229
    • Wallace, E.M.1    Lyssikatos, J.P.2    Yeh, T.3    Winkler, J.D.4    Koch, K.5
  • 20
    • 0028884033 scopus 로고
    • PD 098059 is a specific inhibitor of the activation of mitogen-activated protein kinase kinase in vitro and in vivo
    • Alessi DR, Cuenda A, Cohen P, Dudley DT, Saltiel AR. PD 098059 is a specific inhibitor of the activation of mitogen-activated protein kinase kinase in vitro and in vivo. J Biol Chem 1995;270:27489-27494.
    • (1995) J Biol Chem , vol.270 , pp. 27489-27494
    • Alessi, D.R.1    Cuenda, A.2    Cohen, P.3    Dudley, D.T.4    Saltiel, A.R.5
  • 22
    • 0034306450 scopus 로고    scopus 로고
    • Specificity and mechanism of action of some commonly used protein kinase inhibitors
    • Davies SP, Reddy H, Caivano M, Cohen P. Specificity and mechanism of action of some commonly used protein kinase inhibitors. Biochem J. 2000;351(pt 1):95-105.
    • (2000) Biochem J. , vol.351 , Issue.PART 1 , pp. 95-105
    • Davies, S.P.1    Reddy, H.2    Caivano, M.3    Cohen, P.4
  • 23
    • 14444279192 scopus 로고    scopus 로고
    • Identification of a novel inhibitor of mitogen-activated protein kinase kinase
    • Favata MF, Horiuchi KY, Manos EJ, et al. Identification of a novel inhibitor of mitogen-activated protein kinase kinase. J Biol Chem. 1998;273:18623-18632.
    • (1998) J Biol Chem. , vol.273 , pp. 18623-18632
    • Favata, M.F.1    Horiuchi, K.Y.2    Manos, E.J.3
  • 24
    • 0242468891 scopus 로고    scopus 로고
    • CI-1040 (PD184352), a targeted signal transduction inhibitor of MEK (MAPKK)
    • Oct
    • Allen LF, Sebolt-Leopold J, Meyer MB. CI-1040 (PD184352), a targeted signal transduction inhibitor of MEK (MAPKK). Semin Oncol. Oct 2003;30 (5 suppl 16):105-116.
    • (2003) Semin Oncol. , vol.30 , Issue.5 SUPPL. 16 , pp. 105-116
    • Allen, L.F.1    Sebolt-Leopold, J.2    Meyer, M.B.3
  • 25
    • 23944439944 scopus 로고    scopus 로고
    • Phase I and pharmacodynamic study of the oral MEK inhibitor CI-1040 in patients with advanced malignancies
    • Lorusso PM, Adjei AA, Varterasian M, et al. Phase I and pharmacodynamic study of the oral MEK inhibitor CI-1040 in patients with advanced malignancies. J Clin Oncol. 2005;23:5281-5293.
    • (2005) J Clin Oncol. , vol.23 , pp. 5281-5293
    • Lorusso, P.M.1    Adjei, A.A.2    Varterasian, M.3
  • 26
    • 14844285975 scopus 로고    scopus 로고
    • Multicenter phase II study of the oral MEK inhibitor, CI-1040, in patients with advanced non-small-cell lung, breast, colon, and pancreatic cancer
    • Rinehart J, Adjei AA, Lorusso PM, et al. Multicenter phase II study of the oral MEK inhibitor, CI-1040, in patients with advanced non-small-cell lung, breast, colon, and pancreatic cancer. J Clin Oncol. 2004;22:4456-4462.
    • (2004) J Clin Oncol. , vol.22 , pp. 4456-4462
    • Rinehart, J.1    Adjei, A.A.2    Lorusso, P.M.3
  • 27
    • 10344258041 scopus 로고    scopus 로고
    • Targeting the mitogen-activated protein kinase cascade to treat cancer
    • Sebolt-Leopold JS, Herrera R. Targeting the mitogen-activated protein kinase cascade to treat cancer. Nat Rev Cancer. 2004;4:937-947.
    • (2004) Nat Rev Cancer , vol.4 , pp. 937-947
    • Sebolt-Leopold, J.S.1    Herrera, R.2
  • 28
    • 31544450194 scopus 로고    scopus 로고
    • A phase 1-2 clinical study of a second generation oral MEK inhibitor, PD 0325901 in patients with advanced cancer
    • Lorusso PM, Krishnamurthy S, Rinehart J, et al A phase 1-2 clinical study of a second generation oral MEK inhibitor, PD 0325901 in patients with advanced cancer. J Clin Oncol. 2005;23(16S):3011.
    • (2005) J Clin Oncol. , vol.23 , Issue.16 S , pp. 3011
    • Lorusso, P.M.1    Krishnamurthy, S.2    Rinehart, J.3
  • 29
    • 33646402805 scopus 로고    scopus 로고
    • Pharmacokinetics (PK) and pharmaco-dynamics (PD) of PD 0325901, a second generation MEK inhibitor after multiple oral doses of PD 0325901 to advanced cancer patients
    • Menon SS, Whitfield LR, Sadis SS, et al. Pharmacokinetics (PK) and pharmaco-dynamics (PD) of PD 0325901, a second generation MEK inhibitor after multiple oral doses of PD 0325901 to advanced cancer patients. J Clin Oncol. 2005;23(16S):3066.
    • (2005) J Clin Oncol. , vol.23 , Issue.16 S , pp. 3066
    • Menon, S.S.1    Whitfield, L.R.2    Sadis, S.S.3
  • 30
    • 31544446922 scopus 로고    scopus 로고
    • Potent and selective mitogen-activated protein kinase kinase (MEK) 1,2 inhibitors. 1. 4-(4-bromo-2-fluorophenylamino)-1-methylpyridin-2(1H)-ones
    • Wallace EM, Lyssikatos J, Blake JF, et al. Potent and selective mitogen-activated protein kinase kinase (MEK) 1,2 inhibitors. 1. 4-(4-bromo-2-fluorophenylamino)-1-methylpyridin-2(1H)-ones. J Med Chem. 2006;49:441-444.
    • (2006) J Med Chem. , vol.49 , pp. 441-444
    • Wallace, E.M.1    Lyssikatos, J.2    Blake, J.F.3
  • 31
    • 33845357462 scopus 로고    scopus 로고
    • A first in human dose-ranging study to assess the pharmacokinetics, pharmacodynamics, and toxicities of the MEK inhibitor, ARRY-142886 (AZD6244) in patients with advanced solid malignancies
    • Chow L, Eckhardt SG, Reid J, et al, A first in human dose-ranging study to assess the pharmacokinetics, pharmacodynamics, and toxicities of the MEK inhibitor, ARRY-142886 (AZD6244) in patients with advanced solid malignancies. Proc AACR-EORTC-NCI Targeted Ther Conference. 2005:C162.
    • (2005) Proc AACR-EORTC-NCI Targeted Ther Conference
    • Chow, L.1    Eckhardt, S.G.2    Reid, J.3
  • 32
    • 31144453233 scopus 로고    scopus 로고
    • BRAF mutation predicts sensitivity to MEK inhibition
    • Solit DB, Garraway LA, Pratilas CA, et al. BRAF mutation predicts sensitivity to MEK inhibition. Nature. 2006;439:358-362.
    • (2006) Nature , vol.439 , pp. 358-362
    • Solit, D.B.1    Garraway, L.A.2    Pratilas, C.A.3
  • 33
    • 33645652766 scopus 로고    scopus 로고
    • The MEK/MAPK pathway is involved in the resistance of breast cancer cells to the EGFR tyrosine kinase inhibitor gefitinib
    • Normanno N, De Luca A, Maiello MR, et al. The MEK/MAPK pathway is involved in the resistance of breast cancer cells to the EGFR tyrosine kinase inhibitor gefitinib. J Cell Physiol 2006;207:420-427.
    • (2006) J Cell Physiol , vol.207 , pp. 420-427
    • Normanno, N.1    De Luca, A.2    Maiello, M.R.3
  • 34
    • 33845359730 scopus 로고    scopus 로고
    • Therapeutic doses of Tamoxifen only partially inhibit the non-genomic effects of Estrogen: Evidence for additive antiproliferative effect of Tamoxifen with MEK inhibitor
    • Djahansouzi S, Heimerzheim T, Reinhardt M, et al. Therapeutic doses of Tamoxifen only partially inhibit the non-genomic effects of Estrogen: Evidence for additive antiproliferative effect of Tamoxifen with MEK inhibitor. J Clin Oncol. 2005;23(16S):3195.
    • (2005) J Clin Oncol. , vol.23 , Issue.16 S , pp. 3195
    • Djahansouzi, S.1    Heimerzheim, T.2    Reinhardt, M.3
  • 35
    • 33745075558 scopus 로고    scopus 로고
    • Multiple signaling pathways must be targeted to overcome drug resistance in cell lines derived from melanoma metastases
    • Smalley KS, Haass NK, Brafford PA, Lioni M, Flaherty KT, Herlyn M. Multiple signaling pathways must be targeted to overcome drug resistance in cell lines derived from melanoma metastases. Mol Cancer Ther. 2006;5:1136-1144.
    • (2006) Mol Cancer Ther. , vol.5 , pp. 1136-1144
    • Smalley, K.S.1    Haass, N.K.2    Brafford, P.A.3    Lioni, M.4    Flaherty, K.T.5    Herlyn, M.6
  • 36
    • 36349006801 scopus 로고    scopus 로고
    • Chemosensitization by dual pharmacological inhibition of MEK and MTRO signaling pathways in human non-small cell lung cancer (NSCLC)
    • Abstract 4867
    • Legrier ME DSS, Yan HG, et al, Chemosensitization by dual pharmacological inhibition of MEK and MTRO signaling pathways in human non-small cell lung cancer (NSCLC). Proc Amer Assoc Can Res. 2006: Abstract 4867.
    • (2006) Proc Amer Assoc Can Res.
    • Legrier, M.E.D.S.S.1    Yan, H.G.2
  • 37
    • 16844386676 scopus 로고    scopus 로고
    • Enhancement of the therapeutic efficacy of taxol by the mitogen-activated protein kinase kinase inhibitor CI-1040 in nude mice bearing human heterotransplants
    • McDaid HM, Lopez-Barcons L, Grossman A, et al. Enhancement of the therapeutic efficacy of taxol by the mitogen-activated protein kinase kinase inhibitor CI-1040 in nude mice bearing human heterotransplants. Cancer Res. 2005;65:2854-2860.
    • (2005) Cancer Res. , vol.65 , pp. 2854-2860
    • McDaid, H.M.1    Lopez-Barcons, L.2    Grossman, A.3
  • 38
    • 1942456523 scopus 로고    scopus 로고
    • Specific roles for the PI3K and the MEK-ERK pathway in IGF-1-stimulated chemotaxis, VEGF secretion and proliferation of multiple myeloma cells: Study in the 5T33MM model
    • Menu E, Kooijman R, Van Valckenborgh E, et al. Specific roles for the PI3K and the MEK-ERK pathway in IGF-1-stimulated chemotaxis, VEGF secretion and proliferation of multiple myeloma cells: study in the 5T33MM model. Br J Cancer. 2004;90:1076-1083
    • (2004) Br J Cancer , vol.90 , pp. 1076-1083
    • Menu, E.1    Kooijman, R.2    Van Valckenborgh, E.3
  • 39
    • 0038649977 scopus 로고    scopus 로고
    • Targeting of mitogen-activated protein kinases and phosphatidylinositol 3 kinase inhibits hepatocyte growth factor/scatter factor-induced angiogenesis
    • Sengupta S, Sellers LA, Li RC, et al. Targeting of mitogen-activated protein kinases and phosphatidylinositol 3 kinase inhibits hepatocyte growth factor/scatter factor-induced angiogenesis. Circulation. 2003;107:2955-2961.
    • (2003) Circulation , vol.107 , pp. 2955-2961
    • Sengupta, S.1    Sellers, L.A.2    Li, R.C.3
  • 40
    • 33845360080 scopus 로고    scopus 로고
    • Targeted inhibition of the MEK-ERK signaling cascade by the selective MEK1/2 inhibitor AZD6244 (ARRY-142886) for the treatment of hepatocellular carcinoma
    • Abstract 5470
    • Tran E SK, Chow P, and Huynh H, Targeted inhibition of the MEK-ERK signaling cascade by the selective MEK1/2 inhibitor AZD6244 (ARRY-142886) for the treatment of hepatocellular carcinoma. Amer Assoc Can Res. 2006: Abstract 5470.
    • (2006) Amer Assoc Can Res.
    • Tran, E.S.K.1    Chow, P.2    Huynh, H.3
  • 41
    • 0034823632 scopus 로고    scopus 로고
    • Therapeutic targeting of the MEK/MAPK signal transduction module in acute myeloid leukemia
    • Milella M, Kornblau SM, Estrov Z, et al. Therapeutic targeting of the MEK/MAPK signal transduction module in acute myeloid leukemia. J Clin Invest. 2001; 108:851-859.
    • (2001) J Clin Invest. , vol.108 , pp. 851-859
    • Milella, M.1    Kornblau, S.M.2    Estrov, Z.3
  • 42
    • 0035393498 scopus 로고    scopus 로고
    • Pharmacological inhibitors of the mitogen-activated protein kinase (MAPK) kinase/MAPK cascade interact synergistically with UCN-01 to induce mitochondrial dysfunction and apoptosis in human leukemia cells
    • Dai Y, Yu C, Singh V, et al. Pharmacological inhibitors of the mitogen-activated protein kinase (MAPK) kinase/MAPK cascade interact synergistically with UCN-01 to induce mitochondrial dysfunction and apoptosis in human leukemia cells. Cancer Res. 2001;61:5106-5115
    • (2001) Cancer Res. , vol.61 , pp. 5106-5115
    • Dai, Y.1    Yu, C.2    Singh, V.3
  • 43
    • 0036142963 scopus 로고    scopus 로고
    • Pharmacologic mitogen-activated protein/extracellular signal-regulated kinase kinase/mitogen-activated protein kinase inhibitors interact synergistically with STI571 to induce apoptosis in Bcr/Abl-expressing human leukemia cells
    • Yu C, Krystal G, Varticovksi L, et al. Pharmacologic mitogen-activated protein/extracellular signal-regulated kinase kinase/mitogen-activated protein kinase inhibitors interact synergistically with STI571 to induce apoptosis in Bcr/Abl-expressing human leukemia cells. Cancer Res. 2002;62:188-199.
    • (2002) Cancer Res. , vol.62 , pp. 188-199
    • Yu, C.1    Krystal, G.2    Varticovksi, L.3
  • 44
    • 20544432488 scopus 로고    scopus 로고
    • Successful implementation of the randomized discontinuation trial design: An application to the study of the putative antiangiogenic agent carboxyaminoimidazole in renal cell carcinoma - CALGB 69901
    • Stadler WM, Rosner G, Small E, et al. Successful implementation of the randomized discontinuation trial design: an application to the study of the putative antiangiogenic agent carboxyaminoimidazole in renal cell carcinoma - CALGB 69901. J Clin Oncol. 2005;23:3726-3732
    • (2005) J Clin Oncol. , vol.23 , pp. 3726-3732
    • Stadler, W.M.1    Rosner, G.2    Small, E.3


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