-
1
-
-
0034693799
-
The protein tyrosine kinase family of the human genome
-
Robinson, D. R.; Wu, Y. M.; Lin, S. F. The protein tyrosine kinase family of the human genome. Oncogene, 2000, 19(49), 5548-5557.
-
(2000)
Oncogene
, vol.19
, Issue.49
, pp. 5548-5557
-
-
Robinson, D.R.1
Wu, Y.M.2
Lin, S.F.3
-
2
-
-
27544479318
-
Role of tyrosine kinase inhibitors in cancer therapy
-
Arora, A.; Scholar, E. M. Role of tyrosine kinase inhibitors in cancer therapy. J. Pharmacol. Exp. Ther., 2005, 315(3), 971-979.
-
(2005)
J. Pharmacol. Exp. Ther.
, vol.315
, Issue.3
, pp. 971-979
-
-
Arora, A.1
Scholar, E.M.2
-
3
-
-
0037032835
-
The protein kinase complement of the human genome
-
Manning, G.; Whyte, D. B.; Martinez, R.; Hunter, T.; Sudarsanam, S. The protein kinase complement of the human genome. Science, 2002, 298(5600), 1912-1934.
-
(2002)
Science
, vol.298
, Issue.5600
, pp. 1912-1934
-
-
Manning, G.1
Whyte, D.B.2
Martinez, R.3
Hunter, T.4
Sudarsanam, S.5
-
4
-
-
20444393495
-
Tyrosine kinase inhibitor resistance in cancer: Role of ABC multidrug transporters
-
Ozvegy-Laczka, C.; Cserepes, J.; Elkind, N. B.; Sarkadi, B. Tyrosine kinase inhibitor resistance in cancer: role of ABC multidrug transporters. Drug Resist. Updat., 2005, 8 (1-2), 15-26.
-
(2005)
Drug Resist. Updat.
, vol.8
, Issue.1-2
, pp. 15-26
-
-
Ozvegy-Laczka, C.1
Cserepes, J.2
Elkind, N.B.3
Sarkadi, B.4
-
5
-
-
2342591455
-
The discovery of receptor tyrosine kinases: Targets for cancer therapy
-
Gschwind, A.; Fischer, O. M.; Ullrich, A. The discovery of receptor tyrosine kinases: targets for cancer therapy. Nat. Rev. Cance, 2004, 4(5), 361-370. (Pubitemid 38579482)
-
(2004)
Nature Reviews Cancer
, vol.4
, Issue.5
, pp. 361-370
-
-
Gschwind, A.1
Fischer, O.M.2
Ullrich, A.3
-
6
-
-
0029947186
-
Effects of a selective inhibitor of the Abl tyrosine kinase on the growth of Bcr-Abl positive cells
-
Druker, B. J.; Tamura, S.; Buchdunger, E.; Ohno, S.; Segal, G. M.; Fanning, S.; Zimmermann, J.; Lydon, N. B. Effects of a selective inhibitor of the Abl tyrosine kinase on the growth of Bcr-Abl positive cells. Nat. Med., 1996, 2(5), 561-566.
-
(1996)
Nat. Med.
, vol.2
, Issue.5
, pp. 561-566
-
-
Druker, B.J.1
Tamura, S.2
Buchdunger, E.3
Ohno, S.4
Segal, G.M.5
Fanning, S.6
Zimmermann, J.7
Lydon, N.B.8
-
7
-
-
0031409736
-
Inhibition of the ABL kinase activity blocks the proliferation of BCR/ABL+ leukemic cells and induces apoptosis
-
Gambacorti-Passerini, C.; le Coutre, P.; Mologni, L.; Fanelli, M.; Bertazzoli, C.; Marchesi, E.; Di Nicola, M.; Biondi, A.; Corneo, G. M.; Belotti, D.; Pogliani, E.; Lydon, N. B. Inhibition of the ABL kinase activity blocks the proliferation of BCR/ABL+ leukemic cells and induces apoptosis. Blood Cells, Mol. Dis., 1997, 23(3), 380-394.
-
(1997)
Blood Cells, Mol. Dis.
, vol.23
, Issue.3
, pp. 380-394
-
-
Gambacorti-Passerini, C.1
Coutre, P.2
Mologni, L.3
Fanelli, M.4
Bertazzoli, C.5
Marchesi, E.6
Di Nicola, M.7
Biondi, A.8
Corneo, G.M.9
Belotti, D.10
Pogliani, E.11
Lydon, N.B.12
-
8
-
-
69049092008
-
Exploiting the promiscuity of imatinib
-
Lee, S. J.; Wang, J. Y. Exploiting the promiscuity of imatinib. J. Biol., 2009, 8(3), 30.
-
(2009)
J. Biol.
, vol.8
, Issue.3
, pp. 30
-
-
Lee, S.J.1
Wang, J.Y.2
-
9
-
-
58149398623
-
Translation of the Philadelphia chromosome into therapy for CML
-
Druker, B. J. Translation of the Philadelphia chromosome into therapy for CML. Blood, 2008, 112(13), 4808-4817.
-
(2008)
Blood
, vol.112
, Issue.13
, pp. 4808-4817
-
-
Druker, B.J.1
-
10
-
-
33745863150
-
Imatinib mesylate in the treatment of systemic mastocytosis: A phase II trial
-
Droogendijk, H. J.; Kluin-Nelemans, H. J.; van Doormaal, J. J.; Oranje, A. P.; van de Loosdrecht, A. A.; van Daele, P. L. Imatinib mesylate in the treatment of systemic mastocytosis: a phase II trial. Cancer, 2006, 107(2), 345-351.
-
(2006)
Cancer
, vol.107
, Issue.2
, pp. 345-351
-
-
Droogendijk, H.J.1
Kluin-Nelemans, H.J.2
Van Doormaal, J.J.3
Oranje, A.P.4
Van De Loosdrecht, A.A.5
Van Daele, P.L.6
-
11
-
-
57349186496
-
Imatinib as a novel therapeutic approach for fibrotic disorders
-
Distler, J. H.; Distler, O. Imatinib as a novel therapeutic approach for fibrotic disorders. Rheumatology (Oxford, England), 2009, 48(1), 2-4.
-
(2009)
Rheumatology (Oxford, England)
, vol.48
, Issue.1
, pp. 2-4
-
-
Distler, J.H.1
Distler, O.2
-
12
-
-
21144451094
-
In vitro activity of Bcr-Abl inhibitors AMN107 and BMS-354825 against clinically relevant imatinibresistant Abl kinase domain mutants
-
O'Hare, T.; Walters, D. K.; Stoffregen, E. P.; Jia, T.; Manley, P. W.; Mestan, J.; Cowan-Jacob, S. W.; Lee, F. Y.; Heinrich, M. C.; Deininger, M. W.; Druker, B. J. In vitro activity of Bcr-Abl inhibitors AMN107 and BMS-354825 against clinically relevant imatinibresistant Abl kinase domain mutants. Cancer Res., 2005, 65(11), 4500-4505.
-
(2005)
Cancer Res.
, vol.65
, Issue.11
, pp. 4500-4505
-
-
O'Hare, T.1
Walters, D.K.2
Stoffregen, E.P.3
Jia, T.4
Manley, P.W.5
Mestan, J.6
Cowan-Jacob, S.W.7
Lee, F.Y.8
Heinrich, M.C.9
Deininger, M.W.10
Druker, B.J.11
-
13
-
-
3142676436
-
Overriding imatinib resistance with a novel ABL kinase inhibitor
-
Shah, N. P.; Tran, C.; Lee, F. Y.; Chen, P.; Norris, D.; Sawyers, C. L. Overriding imatinib resistance with a novel ABL kinase inhibitor. Science, 2004, 305(5682), 399-401.
-
(2004)
Science
, vol.305
, Issue.5682
, pp. 399-401
-
-
Shah, N.P.1
Tran, C.2
Lee, F.Y.3
Chen, P.4
Norris, D.5
Sawyers, C.L.6
-
14
-
-
13844251975
-
Characterization of AMN107, a selective inhibitor of native and mutant Bcr-Abl
-
Weisberg, E.; Manley, P. W.; Breitenstein, W.; Bruggen, J.; Cowan-Jacob, S. W.; Ray, A.; Huntly, B.; Fabbro, D.; Fendrich, G.; Hall-Meyers, E.; Kung, A. L.; Mestan, J.; Daley, G. Q.; Callahan, L.; Catley, L.; Cavazza, C.; Azam, M.; Neuberg, D.; Wright, R. D.; Gilliland, D. G.; Griffin, J. D. Characterization of AMN107, a selective inhibitor of native and mutant Bcr-Abl. Cancer Cell, 2005, 7(2), 129-141.
-
(2005)
Cancer Cell.
, vol.7
, Issue.2
, pp. 129-141
-
-
Weisberg, E.1
Manley, P.W.2
Breitenstein, W.3
Bruggen, J.4
Cowan-Jacob, S.W.5
Ray, A.6
Huntly, B.7
Fabbro, D.8
Fendrich, G.9
Hall-Meyers, E.10
Kung, A.L.11
Mestan, J.12
Daley, G.Q.13
Callahan, L.14
Catley, L.15
Cavazza, C.16
Azam, M.17
Neuberg, D.18
Wright, R.D.19
Gilliland, D.G.20
Griffin, J.D.21
more..
-
15
-
-
41349083969
-
Nilotinib (formerly AMN107), a highly selective BCR-ABL tyrosine kinase inhibitor, is active in patients with imatinib-resistant or-intolerant accelerated-phase chronic myelogenous leukemia
-
le Coutre, P.; Ottmann, O. G.; Giles, F.; Kim, D. W.; Cortes, J.; Gattermann, N.; Apperley, J. F.; Larson, R. A.; Abruzzese, E.; O'Brien, S. G.; Kuliczkowski, K.; Hochhaus, A.; Mahon, F. X.; Saglio, G.; Gobbi, M.; Kwong, Y. L.; Baccarani, M.; Hughes, T.; Martinelli, G.; Radich, J. P.; Zheng, M.; Shou, Y.; Kantarjian, H. Nilotinib (formerly AMN107), a highly selective BCR-ABL tyrosine kinase inhibitor, is active in patients with imatinib-resistant or-intolerant accelerated-phase chronic myelogenous leukemia. Blood, 2008, 111(4), 1834-1839.
-
(2008)
Blood
, vol.111
, Issue.4
, pp. 1834-1839
-
-
Coutre, P.1
Ottmann, O.G.2
Giles, F.3
Kim, D.W.4
Cortes, J.5
Gattermann, N.6
Apperley, J.F.7
Larson, R.A.8
Abruzzese, E.9
O'Brien, S.G.10
Kuliczkowski, K.11
Hochhaus, A.12
Mahon, F.X.13
Saglio, G.14
Gobbi, M.15
Kwong, Y.L.16
Baccarani, M.17
Hughes, T.18
Martinelli, G.19
Radich, J.P.20
Zheng, M.21
Shou, Y.22
Kantarjian, H.23
more..
-
16
-
-
68949174991
-
Nilotinib in the treatment of advanced gastrointestinal stromal tumours resistant to both imatinib and sunitinib
-
Montemurro, M.; Schoffski, P.; Reichardt, P.; Gelderblom, H.; Schutte, J.; Hartmann, J. T.; von Moos, R.; Seddon, B.; Joensuu, H.; Wendtner, C. M.; Weber, E.; Grunwald, V.; Roth, A.; Leyvraz, S. Nilotinib in the treatment of advanced gastrointestinal stromal tumours resistant to both imatinib and sunitinib. Eur. J. Cancer, 2009, 45(13), 2293-2297.
-
(2009)
Eur. J. Cancer
, vol.45
, Issue.13
, pp. 2293-2297
-
-
Montemurro, M.1
Schoffski, P.2
Reichardt, P.3
Gelderblom, H.4
Schutte, J.5
Hartmann, J.T.6
Von Moos, R.7
Seddon, B.8
Joensuu, H.9
Wendtner, C.M.10
Weber, E.11
Grunwald, V.12
Roth, A.13
Leyvraz, S.14
-
17
-
-
33745283618
-
The structure of Dasatinib (BMS-354825) bound to activated ABL kinase domain elucidates its inhibitory activity against imatinib-resistant ABL mutants
-
Tokarski, J. S.; Newitt, J. A.; Chang, C. Y.; Cheng, J. D.; Wittekind, M.; Kiefer, S. E.; Kish, K.; Lee, F. Y.; Borzillerri, R.; Lombardo, L. J.; Xie, D.; Zhang, Y.; Klei, H. E. The structure of Dasatinib (BMS-354825) bound to activated ABL kinase domain elucidates its inhibitory activity against imatinib-resistant ABL mutants. Cancer Res., 2006, 66(11), 5790-5797.
-
(2006)
Cancer Res.
, vol.66
, Issue.11
, pp. 5790-5797
-
-
Tokarski, J.S.1
Newitt, J.A.2
Chang, C.Y.3
Cheng, J.D.4
Wittekind, M.5
Kiefer, S.E.6
Kish, K.7
Lee, F.Y.8
Borzillerri, R.9
Lombardo, L.J.10
Xie, D.11
Zhang, Y.12
Klei, H.E.13
-
18
-
-
33745102555
-
Dasatinib in imatinib-resistant Philadelphia chromosome-positive leukemias
-
DOI 10.1056/NEJMoa055229
-
Talpaz, M.; Shah, N. P.; Kantarjian, H.; Donato, N.; Nicoll, J.; Paquette, R.; Cortes, J.; O'Brien, S.; Nicaise, C.; Bleickardt, E.; Blackwood-Chirchir, M. A.; Iyer, V.; Chen, T. T.; Huang, F.; Decillis, A. P.; Sawyers, C. L. Dasatinib in imatinib-resistant Philadelphia chromosome-positive leukemias. N. Engl. J. Med., 2006, 354(24), 2531-2541. (Pubitemid 43882349)
-
(2006)
New England Journal of Medicine
, vol.354
, Issue.24
, pp. 2531-2541
-
-
Talpaz, M.1
Shah, N.P.2
Kantarjian, H.3
Donato, N.4
Nicoll, J.5
Paquette, R.6
Cortes, J.7
O'Brien, S.8
Nicaise, C.9
Bleickardt, E.10
Blackwood-Chirchir, M.A.11
Iyer, V.12
Chen, T.-T.13
Huang, F.14
Decillis, A.P.15
Sawyers, C.L.16
-
19
-
-
70249141675
-
Dasatinib in the treatment of chronic myeloid leukemia in accelerated phase after imatinib failure: The START a trial
-
Apperley, J. F.; Cortes, J. E.; Kim, D. W.; Roy, L.; Roboz, G. J.; Rosti, G.; Bullorsky, E. O.; Abruzzese, E.; Hochhaus, A.; Heim, D.; de Souza, C. A.; Larson, R. A.; Lipton, J. H.; Khoury, H. J.; Kim, H. J.; Sillaber, C.; Hughes, T. P.; Erben, P.; Van Tornout, J.; Stone, R. M. Dasatinib in the treatment of chronic myeloid leukemia in accelerated phase after imatinib failure: the START a trial. J. Clin. Oncol., 2009, 27(21), 3472-3479.
-
(2009)
J. Clin. Oncol.
, vol.27
, Issue.21
, pp. 3472-3479
-
-
Apperley, J.F.1
Cortes, J.E.2
Kim, D.W.3
Roy, L.4
Roboz, G.J.5
Rosti, G.6
Bullorsky, E.O.7
Abruzzese, E.8
Hochhaus, A.9
Heim, D.10
Souza, C.A.11
Larson, R.A.12
Lipton, J.H.13
Khoury, H.J.14
Kim, H.J.15
Sillaber, C.16
Hughes, T.P.17
Erben, P.18
Van Tornout, J.19
Stone, R.M.20
more..
-
20
-
-
19944428353
-
Discovery of N-(2-chloro-6-methyl-phenyl)-2-(6-(4-(2-hydroxyethyl)- piperazin-1-yl)-2-methylpyrimidin-4-ylamino) thiazole-5-carboxamide (BMS-354825), a dual Src/Abl kinase inhibitor with potent antitumor activity in preclinical assays
-
Lombardo, L. J.; Lee, F. Y.; Chen, P.; Norris, D.; Barrish, J. C.; Behnia, K.; Castaneda, S.; Cornelius, L. A.; Das, J.; Doweyko, A. M.; Fairchild, C.; Hunt, J. T.; Inigo, I.; Johnston, K.; Kamath, A.; Kan, D.; Klei, H.; Marathe, P.; Pang, S.; Peterson, R.; Pitt, S.; Schieven, G. L.; Schmidt, R. J.; Tokarski, J.; Wen, M. L.; Wityak, J.; Borzilleri, R. M. Discovery of N-(2-chloro-6-methyl-phenyl)-2-(6-(4-(2-hydroxyethyl)-piperazin-1-yl) -2-methylpyrimidin-4-ylamino) thiazole-5-carboxamide (BMS-354825), a dual Src/Abl kinase inhibitor with potent antitumor activity in preclinical assays. J. Med. Chem., 2004, 47(27), 6658-6661.
-
(2004)
J. Med. Chem.
, vol.47
, Issue.27
, pp. 6658-6661
-
-
Lombardo, L.J.1
Lee, F.Y.2
Chen, P.3
Norris, D.4
Barrish, J.C.5
Behnia, K.6
Castaneda, S.7
Cornelius, L.A.8
Das, J.9
Doweyko, A.M.10
Fairchild, C.11
Hunt, J.T.12
Inigo, I.13
Johnston, K.14
Kamath, A.15
Kan, D.16
Klei, H.17
Marathe, P.18
Pang, S.19
Peterson, R.20
Pitt, S.21
Schieven, G.L.22
Schmidt, R.J.23
Tokarski, J.24
Wen, M.L.25
Wityak, J.26
Borzilleri, R.M.27
more..
-
21
-
-
77956072809
-
Dasatinib: A potent SRC inhibitor in clinical development for the treatment of solid tumors
-
Available from
-
Araujo, J.; Logothetis, C. Dasatinib: A potent SRC inhibitor in clinical development for the treatment of solid tumors. Cancer Treat. Rev., 2010, Available from: http://www.sciencedirect.com/science/article/B6WC8-4YK897K-1/2/ ddb186ce3d3ef352c9c18eee 1594fc7a
-
(2010)
Cancer Treat. Rev.
-
-
Araujo, J.1
Logothetis, C.2
-
22
-
-
76949099015
-
Dasatinib in solid tumors
-
Kim, L. C.; Rix, U.; Haura, E. B. Dasatinib in solid tumors. Expert Opin. Investig. Drugs., 2010, 19(3), 415-425.
-
(2010)
Expert Opin. Investig. Drugs.
, vol.19
, Issue.3
, pp. 415-425
-
-
Kim, L.C.1
Rix, U.2
Haura, E.B.3
-
23
-
-
77955750697
-
The tyrosine kinase inhibitor dasatinib dysregulates bone remodelling through inhibition of osteoclasts in vivo
-
Vandyke, K.; Dewar, A. L.; Diamond, P.; Fitter, S.; Schultz, C. G.; Sims, N. A.; Zannettino, A. C. The tyrosine kinase inhibitor dasatinib dysregulates bone remodelling through inhibition of osteoclasts in vivo. J. Bone. Miner. Res., 2010, 25(8), 1759-1770.
-
(2010)
J. Bone. Miner. Res.
, vol.25
, Issue.8
, pp. 1759-1770
-
-
Vandyke, K.1
Dewar, A.L.2
Diamond, P.3
Fitter, S.4
Schultz, C.G.5
Sims, N.A.6
Zannettino, A.C.7
-
24
-
-
77953229623
-
Src family kinase/abl inhibitor dasatinib suppresses proliferation and enhances differentiation of osteoblasts
-
Lee, Y. C.; Huang, C. F.; Murshed, M.; Chu, K.; Araujo, J. C.; Ye, X.; Decrombrugghe, B.; Yu-Lee, L. Y.; Gallick, G. E.; Lin, S. H. Src family kinase/abl inhibitor dasatinib suppresses proliferation and enhances differentiation of osteoblasts. Oncogene, 2010, 29(22), 3196-3207
-
(2010)
Oncogene
, vol.29
, Issue.22
, pp. 3196-3207
-
-
Lee, Y.C.1
Huang, C.F.2
Murshed, M.3
Chu, K.4
Araujo, J.C.5
Ye, X.6
Decrombrugghe, B.7
Yu-Lee, L.Y.8
Gallick, G.E.9
Lin, S.H.10
-
25
-
-
0038204144
-
SU11248 is a novel FLT3 tyrosine kinase inhibitor with potent activity in vitro and in vivo
-
O'Farrell, A. M.; Abrams, T. J.; Yuen, H. A.; Ngai, T. J.; Louie, S. G.; Yee, K. W.; Wong, L. M.; Hong, W.; Lee, L. B.; Town, A.; Smolich, B. D.; Manning, W. C.; Murray, L. J.; Heinrich, M. C.; Cherrington, J. M. SU11248 is a novel FLT3 tyrosine kinase inhibitor with potent activity in vitro and in vivo. Blood, 2003, 101(9), 3597-3605.
-
(2003)
Blood
, vol.101
, Issue.9
, pp. 3597-3605
-
-
O'Farrell, A.M.1
Abrams, T.J.2
Yuen, H.A.3
Ngai, T.J.4
Louie, S.G.5
Yee, K.W.6
Wong, L.M.7
Hong, W.8
Lee, L.B.9
Town, A.10
Smolich, B.D.11
Manning, W.C.12
Murray, L.J.13
Heinrich, M.C.14
Cherrington, J.M.15
-
26
-
-
78650874372
-
SU11248 inhibits KIT and platelet-derived growth factor receptor beta in preclinical models of human small cell lung cancer
-
Abrams, T. J.; Lee, L. B.; Murray, L. J.; Pryer, N. K.; Cherrington, J. M. SU11248 inhibits KIT and platelet-derived growth factor receptor beta in preclinical models of human small cell lung cancer. Mol. Cancer Ther., 2003, 2(5), 471-478.
-
(2003)
Mol. Cancer Ther.
, vol.2
, Issue.5
, pp. 471-478
-
-
Abrams, T.J.1
Lee, L.B.2
Murray, L.J.3
Pryer, N.K.4
Cherrington, J.M.5
-
27
-
-
33947504730
-
Sunitinib: From rational design to clinical efficacy
-
Chow, L. Q.; Eckhardt, S. G. Sunitinib: from rational design to clinical efficacy. J. Clin. Oncol., 2007, 25(7), 884-896.
-
(2007)
J. Clin. Oncol.
, vol.25
, Issue.7
, pp. 884-896
-
-
Chow, L.Q.1
Eckhardt, S.G.2
-
28
-
-
70349329441
-
Novel antiangiogenic agents in the treatment of refractory renal cell carcinoma
-
Sonpavde, G.; Hutson, T. E. Novel antiangiogenic agents in the treatment of refractory renal cell carcinoma. Clin. Genitourin. Cancer, 2008, 6 (Suppl 1), S29-36.
-
(2008)
Clin. Genitourin. Cancer
, vol.6
, Issue.1 SUPPL.
-
-
Sonpavde, G.1
Hutson, T.E.2
-
29
-
-
84886943002
-
Sunitinib for the treatment of gastrointestinal stromal tumours: A critique of the submission from Pfizer
-
Bond, M.; Hoyle, M.; Moxham, T.; Napier, M.; Anderson, R. Sunitinib for the treatment of gastrointestinal stromal tumours: a critique of the submission from Pfizer. Health Technol. Assess., 2009, 13 (Suppl 2), 69-74.
-
(2009)
Health Technol. Assess.
, vol.13
, Issue.2 SUPPL.
, pp. 69-74
-
-
Bond, M.1
Hoyle, M.2
Moxham, T.3
Napier, M.4
Anderson, R.5
-
30
-
-
33749505836
-
Efficacy and safety of sunitinib in patients with advanced gastrointestinal stromal tumour after failure of imatinib: A randomised controlled trial
-
Demetri, G. D.; van Oosterom, A. T.; Garrett, C. R.; Blackstein, M. E.; Shah, M. H.; Verweij, J.; McArthur, G.; Judson, I. R.; Heinrich, M. C.; Morgan, J. A.; Desai, J.; Fletcher, C. D.; George, S.; Bello, C. L.; Huang, X.; Baum, C. M.; Casali, P. G. 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
Blackstein, M.E.4
Shah, M.H.5
Verweij, J.6
McArthur, G.7
Judson, I.R.8
Heinrich, M.C.9
Morgan, J.A.10
Desai, J.11
Fletcher, C.D.12
George, S.13
Bello, C.L.14
Huang, X.15
Baum, C.M.16
Casali, P.G.17
-
31
-
-
0035553174
-
The effects of the novel, reversible epidermal growth factor receptor/ErbB-2 tyrosine kinase inhibitor, GW2016, on the growth of human normal and tumor-derived cell lines in vitro and in vivo
-
Rusnak, D. W.; Lackey, K.; Affleck, K.; Wood, E. R.; Alligood, K. J.; Rhodes, N.; Keith, B. R.; Murray, D. M.; Knight, W. B.; Mullin, R. J.; Gilmer, T. M. The effects of the novel, reversible epidermal growth factor receptor/ErbB-2 tyrosine kinase inhibitor, GW2016, on the growth of human normal and tumor-derived cell lines in vitro and in vivo. Mol. Cancer Ther., 2001, 1(2), 85-94.
-
(2001)
Mol. Cancer Ther.
, vol.1
, Issue.2
, pp. 85-94
-
-
Rusnak, D.W.1
Lackey, K.2
Affleck, K.3
Wood, E.R.4
Alligood, K.J.5
Rhodes, N.6
Keith, B.R.7
Murray, D.M.8
Knight, W.B.9
Mullin, R.J.10
Gilmer, T.M.11
-
32
-
-
32944461545
-
Activity of the dual kinase inhibitor lapatinib (GW572016) against HER-2-overexpressing and trastuzumab-treated breast cancer cells
-
Konecny, G. E.; Pegram, M. D.; Venkatesan, N.; Finn, R.; Yang, G.; Rahmeh, M.; Untch, M.; Rusnak, D. W.; Spehar, G.; Mullin, R. J.; Keith, B. R.; Gilmer, T. M.; Berger, M.; Podratz, K. C.; Slamon, D. J. Activity of the dual kinase inhibitor lapatinib (GW572016) against HER-2-overexpressing and trastuzumab-treated breast cancer cells. Cancer Res., 2006, 66(3), 1630-1639.
-
(2006)
Cancer Res.
, vol.66
, Issue.3
, pp. 1630-1639
-
-
Konecny, G.E.1
Pegram, M.D.2
Venkatesan, N.3
Finn, R.4
Yang, G.5
Rahmeh, M.6
Untch, M.7
Rusnak, D.W.8
Spehar, G.9
Mullin, R.J.10
Keith, B.R.11
Gilmer, T.M.12
Berger, M.13
Podratz, K.C.14
Slamon, D.J.15
-
33
-
-
33845886440
-
Lapatinib plus capecitabine for HER2-positive advanced breast cancer
-
Geyer, C. E.; Forster, J.; Lindquist, D.; Chan, S.; Romieu, C. G.; Pienkowski, T.; Jagiello-Gruszfeld, A.; Crown, J.; Chan, A.; Kaufman, B.; Skarlos, D.; Campone, M.; Davidson, N.; Berger, M.; Oliva, C.; Rubin, S. D.; Stein, S.; Cameron, D. Lapatinib plus capecitabine for HER2-positive advanced breast cancer. N. Engl. J. Med., 2006, 355(26), 2733-2743.
-
(2006)
N. Engl. J. Med.
, vol.355
, Issue.26
, pp. 2733-2743
-
-
Geyer, C.E.1
Forster, J.2
Lindquist, D.3
Chan, S.4
Romieu, C.G.5
Pienkowski, T.6
Jagiello-Gruszfeld, A.7
Crown, J.8
Chan, A.9
Kaufman, B.10
Skarlos, D.11
Campone, M.12
Davidson, N.13
Berger, M.14
Oliva, C.15
Rubin, S.D.16
Stein, S.17
Cameron, D.18
-
34
-
-
40849102700
-
Activity of lapatinib a novel HER2 and EGFR dual kinase inhibitor in human endometrial cancer cells
-
Konecny, G. E.; Venkatesan, N.; Yang, G.; Dering, J.; Ginther, C.; Finn, R.; Rahmeh, M.; Fejzo, M. S.; Toft, D.; Jiang, S. W.; Slamon, D. J.; Podratz, K. C. Activity of lapatinib a novel HER2 and EGFR dual kinase inhibitor in human endometrial cancer cells. Br. J. Cancer, 2008, 98(6), 1076-1084.
-
(2008)
Br. J. Cancer
, vol.98
, Issue.6
, pp. 1076-1084
-
-
Konecny, G.E.1
Venkatesan, N.2
Yang, G.3
Dering, J.4
Ginther, C.5
Finn, R.6
Rahmeh, M.7
Fejzo, M.S.8
Toft, D.9
Jiang, S.W.10
Slamon, D.J.11
Podratz, K.C.12
-
35
-
-
31544457665
-
Blockade of EGFR and ErbB2 by the novel dual EGFR and ErbB2 tyrosine kinase inhibitor GW572016 sensitizes human colon carcinoma GEO cells to apoptosis
-
Zhou, Y.; Li, S.; Hu, Y. P.; Wang, J.; Hauser, J.; Conway, A. N.; Vinci, M. A.; Humphrey, L.; Zborowska, E.; Willson, J. K.; Brattain, M. G. Blockade of EGFR and ErbB2 by the novel dual EGFR and ErbB2 tyrosine kinase inhibitor GW572016 sensitizes human colon carcinoma GEO cells to apoptosis. Cancer Res., 2006, 66(1), 404-411.
-
(2006)
Cancer Res.
, vol.66
, Issue.1
, pp. 404-411
-
-
Zhou, Y.1
Li, S.2
Hu, Y.P.3
Wang, J.4
Hauser, J.5
Conway, A.N.6
Vinci, M.A.7
Humphrey, L.8
Zborowska, E.9
Willson, J.K.10
Brattain, M.G.11
-
36
-
-
33747125264
-
EGF103009, a phase II trial of lapatinib monotherapy in patients with relapsed/refractory inflammatory breast cancer (IBC): Clinical activity and biologic predictors of response
-
N. L. Spector, K. B., J. Hurley, J. L. Harris, D. Lombardi, S. Bacus, S. B. Ahmed, H. Boussen, M. Frikha and F. B. Ayed EGF103009, a phase II trial of lapatinib monotherapy in patients with relapsed/refractory inflammatory breast cancer (IBC): Clinical activity and biologic predictors of response. J. Clin. Oncol., 2006, 24(18), 502.
-
(2006)
J. Clin. Oncol.
, vol.24
, Issue.18
, pp. 502
-
-
Spector, N.L.1
Hurley, J.2
Harris, J.L.3
Lombardi, D.4
Bacus, S.5
Ahmed, S.B.6
Boussen, H.7
Frikha, M.8
Ayed, F.B.9
-
37
-
-
4944249117
-
BAY 43-9006 exhibits broad spectrum oral antitumor activity and targets the RAF/MEK/ERK pathway and receptor tyrosine kinases involved in tumor progression and angiogenesis
-
Wilhelm, S. M.; Carter, C.; Tang, L.; Wilkie, D.; McNabola, A.; Rong, H.; Chen, C.; Zhang, X.; Vincent, P.; McHugh, M.; Cao, Y.; Shujath, J.; Gawlak, S.; Eveleigh, D.; Rowley, B.; Liu, L.; Adnane, L.; Lynch, M.; Auclair, D.; Taylor, I.; Gedrich, R.; Voznesensky, A.; Riedl, B.; Post, L. E.; Bollag, G.; Trail, P. A. BAY 43-9006 exhibits broad spectrum oral antitumor activity and targets the RAF/MEK/ERK pathway and receptor tyrosine kinases involved in tumor progression and angiogenesis. Cancer Res., 2004, 64(19), 7099-7109.
-
(2004)
Cancer Res.
, vol.64
, Issue.19
, pp. 7099-7109
-
-
Wilhelm, S.M.1
Carter, C.2
Tang, L.3
Wilkie, D.4
McNabola, A.5
Rong, H.6
Chen, C.7
Zhang, X.8
Vincent, P.9
McHugh, M.10
Cao, Y.11
Shujath, J.12
Gawlak, S.13
Eveleigh, D.14
Rowley, B.15
Liu, L.16
Adnane, L.17
Lynch, M.18
Auclair, D.19
Taylor, I.20
Gedrich, R.21
Voznesensky, A.22
Riedl, B.23
Post, L.E.24
Bollag, G.25
Trail, P.A.26
more..
-
38
-
-
33847195060
-
Antitumor activity of sorafenib in FLT3-driven leukemic cells
-
Auclair, D.; Miller, D.; Yatsula, V.; Pickett, W.; Carter, C.; Chang, Y.; Zhang, X.; Wilkie, D.; Burd, A.; Shi, H.; Rocks, S.; Gedrich, R.; Abriola, L.; Vasavada, H.; Lynch, M.; Dumas, J.; Trail, P. A.; Wilhelm, S. M. Antitumor activity of sorafenib in FLT3-driven leukemic cells. Leukemia, 2007, 21(3), 439-445.
-
(2007)
Leukemia
, vol.21
, Issue.3
, pp. 439-445
-
-
Auclair, D.1
Miller, D.2
Yatsula, V.3
Pickett, W.4
Carter, C.5
Chang, Y.6
Zhang, X.7
Wilkie, D.8
Burd, A.9
Shi, H.10
Rocks, S.11
Gedrich, R.12
Abriola, L.13
Vasavada, H.14
Lynch, M.15
Dumas, J.16
Trail, P.A.17
Wilhelm, S.M.18
-
39
-
-
75749119984
-
Sorafenib in the management of metastatic renal cell carcinoma
-
Guevremont, C.; Jeldres, C.; Perrotte, P.; Karakiewicz, P. I. Sorafenib in the management of metastatic renal cell carcinoma. Curr. Oncol., 2009, 16 (Suppl 1), S27-32.
-
(2009)
Curr. Oncol.
, vol.16
, Issue.1 SUPPL.
-
-
Guevremont, C.1
Jeldres, C.2
Perrotte, P.3
Karakiewicz, P.I.4
-
40
-
-
47949116252
-
Sorafenib in advanced hepatocellular carcinoma
-
Llovet, J. M.; Ricci, S.; Mazzaferro, V.; Hilgard, P.; Gane, E.; Blanc, J. F.; de Oliveira, A. C.; Santoro, A.; Raoul, J. L.; Forner, A.; Schwartz, M.; Porta, C.; Zeuzem, S.; Bolondi, L.; Greten, T. F.; Galle, P. R.; Seitz, J. F.; Borbath, I.; Haussinger, D.; Giannaris, T.; Shan, M.; Moscovici, M.; Voliotis, D.; Bruix, J. Sorafenib in advanced hepatocellular carcinoma. N. Engl. J. Med., 2008, 359(4), 378-390.
-
(2008)
N. Engl. J. Med.
, vol.359
, Issue.4
, pp. 378-390
-
-
Llovet, J.M.1
Ricci, S.2
Mazzaferro, V.3
Hilgard, P.4
Gane, E.5
Blanc, J.F.6
De Oliveira, A.C.7
Santoro, A.8
Raoul, J.L.9
Forner, A.10
Schwartz, M.11
Porta, C.12
Zeuzem, S.13
Bolondi, L.14
Greten, T.F.15
Galle, P.R.16
Seitz, J.F.17
Borbath, I.18
Haussinger, D.19
Giannaris, T.20
Shan, M.21
Moscovici, M.22
Voliotis, D.23
Bruix, J.24
more..
-
41
-
-
75349113024
-
Molecular targeting for treatment of advanced hepatocellular carcinoma
-
Song, I. H. Molecular targeting for treatment of advanced hepatocellular carcinoma. Korean J. Hepatol., 2009, 15(3), 299-308.
-
(2009)
Korean J. Hepatol.
, vol.15
, Issue.3
, pp. 299-308
-
-
Song, I.H.1
-
42
-
-
27444436166
-
Apoptosis induced by the kinase inhibitor BAY 43-9006 in human leukemia cells involves down-regulation of Mcl-1 through inhibition of translation
-
Rahmani, M.; Davis, E. M.; Bauer, C.; Dent, P.; Grant, S. Apoptosis induced by the kinase inhibitor BAY 43-9006 in human leukemia cells involves down-regulation of Mcl-1 through inhibition of translation. J. Biol. Chem., 2005, 280(42), 35217-35227.
-
(2005)
J. Biol. Chem.
, vol.280
, Issue.42
, pp. 35217-35227
-
-
Rahmani, M.1
Davis, E.M.2
Bauer, C.3
Dent, P.4
Grant, S.5
-
43
-
-
0034758726
-
Tyrosine kinase inhibitors-ZD1839 (Iressa)
-
Arteaga, C. L.; Johnson, D. H. Tyrosine kinase inhibitors-ZD1839 (Iressa). Curr. Opin. Oncol., 2001, 13(6), 491-498.
-
(2001)
Curr. Opin. Oncol.
, vol.13
, Issue.6
, pp. 491-498
-
-
Arteaga, C.L.1
Johnson, D.H.2
-
44
-
-
70450248381
-
Erlotinib (tarceva) for the treatment of non-small-cell lung cancer and pancreatic cancer
-
Rocha-Lima, C. M.; Raez, L. E. Erlotinib (tarceva) for the treatment of non-small-cell lung cancer and pancreatic cancer. P. T., 2009, 34(10), 554-564.
-
(2009)
P. T.
, vol.34
, Issue.10
, pp. 554-564
-
-
Rocha-Lima, C.M.1
Raez, L.E.2
-
45
-
-
12144287534
-
United States food and drug administration drug approval summary: Gefitinib (ZD1839; Iressa) tablets
-
Cohen, M. H.; Williams, G. A.; Sridhara, R.; Chen, G.; McGuinn, W. D., Jr.; Morse, D.; Abraham, S.; Rahman, A.; Liang, C.; Lostritto, R.; Baird, A.; Pazdur, R. United States Food and Drug Administration Drug Approval summary: Gefitinib (ZD1839; Iressa) tablets. Clin. Cancer Res., 2004, 10(4), 1212-1218.
-
(2004)
Clin. Cancer Res.
, vol.10
, Issue.4
, pp. 1212-1218
-
-
Cohen, M.H.1
Williams, G.A.2
Sridhara, R.3
Chen, G.4
McGuinn Jr., W.D.5
Morse, D.6
Abraham, S.7
Rahman, A.8
Liang, C.9
Lostritto, R.10
Baird, A.11
Pazdur, R.12
-
46
-
-
85047691722
-
Gefitinib (Iressa): A novel treatment for non-small cell lung cancer
-
DOI 10.1586/14787210.4.1.5
-
Vansteenkiste, J. Gefitinib (Iressa): a novel treatment for non-small cell lung cancer. Expert Rev. Anticancer Ther., 2004, 4(1), 5-17. (Pubitemid 38208482)
-
(2004)
Expert Review of Anticancer Therapy
, vol.4
, Issue.1
, pp. 5-17
-
-
Vansteenkiste, J.F.1
-
47
-
-
30644478919
-
A phase II, open-label study of gefitinib (IRESSA) in patients with locally advanced, metastatic, or relapsed renal-cell carcinoma
-
Jermann, M.; Stahel, R. A.; Salzberg, M.; Cerny, T.; Joerger, M.; Gillessen, S.; Morant, R.; Egli, F.; Rhyner, K.; Bauer, J. A.; Pless, M. A phase II, open-label study of gefitinib (IRESSA) in patients with locally advanced, metastatic, or relapsed renal-cell carcinoma. Cancer Chemother. Pharmacol., 2006, 57(4), 533-539.
-
(2006)
Cancer Chemother. Pharmacol.
, vol.57
, Issue.4
, pp. 533-539
-
-
Jermann, M.1
Stahel, R.A.2
Salzberg, M.3
Cerny, T.4
Joerger, M.5
Gillessen, S.6
Morant, R.7
Egli, F.8
Rhyner, K.9
Bauer, J.A.10
Pless, M.11
-
48
-
-
9744240281
-
A phase II trial of gefitinib (Iressa, ZD1839) in stage IV and recurrent renal cell carcinoma
-
Dawson, N. A.; Guo, C.; Zak, R.; Dorsey, B.; Smoot, J.; Wong, J.; Hussain, A. A phase II trial of gefitinib (Iressa, ZD1839) in stage IV and recurrent renal cell carcinoma. Clin. Cancer Res., 2004, 10(23), 7812-7819.
-
(2004)
Clin. Cancer Res.
, vol.10
, Issue.23
, pp. 7812-7819
-
-
Dawson, N.A.1
Guo, C.2
Zak, R.3
Dorsey, B.4
Smoot, J.5
Wong, J.6
Hussain, A.7
-
49
-
-
78650004173
-
Phase I/II trial of sunitinib plus gefitinib in patients with metastatic renal cell carcinoma
-
Epub ahead of print
-
Motzer, R. J.; Hudes, G. R.; Ginsberg, M. S.; Baum, M. S.; Harmon, C. S.; Kim, S. T.; Chen, I.; Redman, B. G. Phase I/II Trial of Sunitinib Plus Gefitinib in Patients With Metastatic Renal Cell Carcinoma. Am. J. Clin. Oncol., 2010, (Epub ahead of print).
-
(2010)
Am. J. Clin. Oncol.
-
-
Motzer, R.J.1
Hudes, G.R.2
Ginsberg, M.S.3
Baum, M.S.4
Harmon, C.S.5
Kim, S.T.6
Chen, I.7
Redman, B.G.8
-
50
-
-
68149105809
-
Clinical efficacy of erlotinib in patients previously treated for advanced non-small cell lung cancer
-
Zhou, S.; Ren, S.; Yan, L.; Zhang, L.; Tang, L.; Zhang, J.; Zhou, C. Clinical efficacy of erlotinib in patients previously treated for advanced non-small cell lung cancer. Respirology, 2009, 14(5), 709-715.
-
(2009)
Respirology
, vol.14
, Issue.5
, pp. 709-715
-
-
Zhou, S.1
Ren, S.2
Yan, L.3
Zhang, L.4
Tang, L.5
Zhang, J.6
Zhou, C.7
-
51
-
-
34249933404
-
Erlotinib plus gemcitabine compared with gemcitabine alone in patients with advanced pancreatic cancer: A phase III trial of the national cancer institute of canada clinical trials group
-
Moore, M. J.; Goldstein, D.; Hamm, J.; Figer, A.; Hecht, J. R.; Gallinger, S.; Au, H. J.; Murawa, P.; Walde, D.; Wolff, R. A.; Campos, D.; Lim, R.; Ding, K.; Clark, G.; Voskoglou-Nomikos, T.; Ptasynski, M.; Parulekar, W. Erlotinib plus gemcitabine compared with gemcitabine alone in patients with advanced pancreatic cancer: a phase III trial of the National Cancer Institute of Canada Clinical Trials Group. J. Clin. Oncol., 2007, 25(15), 1960-1966.
-
(2007)
J. Clin. Oncol.
, vol.25
, Issue.15
, pp. 1960-1966
-
-
Moore, M.J.1
Goldstein, D.2
Hamm, J.3
Figer, A.4
Hecht, J.R.5
Gallinger, S.6
Au, H.J.7
Murawa, P.8
Walde, D.9
Wolff, R.A.10
Campos, D.11
Lim, R.12
Ding, K.13
Clark, G.14
Voskoglou-Nomikos, T.15
Ptasynski, M.16
Parulekar, W.17
-
52
-
-
77949890945
-
Pazopanib in locally advanced or metastatic renal cell carcinoma: Results of a randomized phase III trial
-
Sternberg, C. N.; Davis, I. D.; Mardiak, J.; Szczylik, C.; Lee, E.; Wagstaff, J.; Barrios, C. H.; Salman, P.; Gladkov, O. A.; Kavina, A.; Zarba, J. J.; Chen, M.; McCann, L.; Pandite, L.; Roychowdhury, D. F.; Hawkins, R. E. Pazopanib in locally advanced or metastatic renal cell carcinoma: results of a randomized phase III trial. J. Clin. Oncol., 2010, 28(6), 1061-1068.
-
(2010)
J. Clin. Oncol.
, vol.28
, Issue.6
, pp. 1061-1068
-
-
Sternberg, C.N.1
Davis, I.D.2
Mardiak, J.3
Szczylik, C.4
Lee, E.5
Wagstaff, J.6
Barrios, C.H.7
Salman, P.8
Gladkov, O.A.9
Kavina, A.10
Zarba, J.J.11
Chen, M.12
McCann, L.13
Pandite, L.14
Roychowdhury, D.F.15
Hawkins, R.E.16
-
53
-
-
75749090050
-
Efficacy and safety of pazopanib in patients with metastatic renal cell carcinoma
-
Hutson, T. E.; Davis, I. D.; Machiels, J. P.; De Souza, P. L.; Rottey, S.; Hong, B. F.; Epstein, R. J.; Baker, K. L.; McCann, L.; Crofts, T.; Pandite, L.; Figlin, R. A. Efficacy and safety of pazopanib in patients with metastatic renal cell carcinoma. J. Clin. Oncol., 2010, 28(3), 475-480.
-
(2010)
J. Clin. Oncol.
, vol.28
, Issue.3
, pp. 475-480
-
-
Hutson, T.E.1
Davis, I.D.2
Machiels, J.P.3
De Souza, P.L.4
Rottey, S.5
Hong, B.F.6
Epstein, R.J.7
Baker, K.L.8
McCann, L.9
Crofts, T.10
Pandite, L.11
Figlin, R.A.12
-
54
-
-
75749151307
-
Pazopanib for the treatment of renal cell carcinoma and other malignancies
-
Sonpavde, G.; Hutson, T. E.; Sternberg, C. N. Pazopanib for the treatment of renal cell carcinoma and other malignancies. Drugs Today (Barc), 2009, 45(9), 651-661.
-
(2009)
Drugs Today (Barc)
, vol.45
, Issue.9
, pp. 651-661
-
-
Sonpavde, G.1
Hutson, T.E.2
Sternberg, C.N.3
-
55
-
-
71249164372
-
Synergistic proapoptotic effects of the two tyrosine kinase inhibitors pazopanib and lapatinib on multiple carcinoma cell lines
-
Olaussen, K. A.; Commo, F.; Tailler, M.; Lacroix, L.; Vitale, I.; Raza, S. Q.; Richon, C.; Dessen, P.; Lazar, V.; Soria, J. C.; Kroemer, G. Synergistic proapoptotic effects of the two tyrosine kinase inhibitors pazopanib and lapatinib on multiple carcinoma cell lines. Oncogene, 2009, 28(48), 4249-4260.
-
(2009)
Oncogene
, vol.28
, Issue.48
, pp. 4249-4260
-
-
Olaussen, K.A.1
Commo, F.2
Tailler, M.3
Lacroix, L.4
Vitale, I.5
Raza, S.Q.6
Richon, C.7
Dessen, P.8
Lazar, V.9
Soria, J.C.10
Kroemer, G.11
-
56
-
-
36549038661
-
Pazopanib (GW786034) is active in women with advanced epithelial ovarian, fallopian tube and peritoneal cancers: Initial results of a phase II study
-
M. Friedlander, K. C. H., B. Benigno, D. Rischin, M. Messing, C. A. Stringer, E. H. Tay, S. Kathman, G. Matthys and J. J. Lager Pazopanib (GW786034) is active in women with advanced epithelial ovarian, fallopian tube and peritoneal cancers: Initial results of a phase II study. J. Clin. Oncol., 2007, 25(18), 5561.
-
(2007)
J. Clin. Oncol.
, vol.25
, Issue.18
, pp. 5561
-
-
Friedlander, M.1
Benigno, B.2
Rischin, D.3
Messing, M.4
Stringer, C.A.5
Tay, E.H.6
Kathman, S.7
Matthys, G.8
Lager Pazopanib, J.J.9
-
57
-
-
77949439646
-
Dasatinib in chronic myeloid leukemia: A review
-
Aguilera, D. G.; Tsimberidou, A. M. Dasatinib in chronic myeloid leukemia: a review. Ther. Clin. Risk. Manag., 2009, 5(2), 281-289.
-
(2009)
Ther. Clin. Risk. Manag.
, vol.5
, Issue.2
, pp. 281-289
-
-
Aguilera, D.G.1
Tsimberidou, A.M.2
-
58
-
-
57849159300
-
Efficacy and safety of dasatinib in imatinib-resistant or-intolerant patients with chronic myeloid leukemia in blast phase
-
Cortes, J.; Kim, D. W.; Raffoux, E.; Martinelli, G.; Ritchie, E.; Roy, L.; Coutre, S.; Corm, S.; Hamerschlak, N.; Tang, J. L.; Hochhaus, A.; Khoury, H. J.; Brummendorf, T. H.; Michallet, M.; Rege-Cambrin, G.; Gambacorti-Passerini, C.; Radich, J. P.; Ernst, T.; Zhu, C.; Van Tornout, J. M.; Talpaz, M. Efficacy and safety of dasatinib in imatinib-resistant or-intolerant patients with chronic myeloid leukemia in blast phase. Leukemia, 2008, 22(12), 2176-2183.
-
(2008)
Leukemia
, vol.22
, Issue.12
, pp. 2176-2183
-
-
Cortes, J.1
Kim, D.W.2
Raffoux, E.3
Martinelli, G.4
Ritchie, E.5
Roy, L.6
Coutre, S.7
Corm, S.8
Hamerschlak, N.9
Tang, J.L.10
Hochhaus, A.11
Khoury, H.J.12
Brummendorf, T.H.13
Michallet, M.14
Rege-Cambrin, G.15
Gambacorti-Passerini, C.16
Radich, J.P.17
Ernst, T.18
Zhu, C.19
Van Tornout, J.M.20
Talpaz, M.21
more..
-
59
-
-
57449120869
-
Differences in hematological and non-hematological toxicity during treatment with imatinib in patients with early and late chronic phase chronic myeloid leukemia
-
Breccia, M.; Stefanizzi, C.; Cannella, L.; Latagliata, R.; Frustaci, A. M.; Carmosino, I.; Santopietro, M.; Alimena, G. Differences in hematological and non-hematological toxicity during treatment with imatinib in patients with early and late chronic phase chronic myeloid leukemia. Leuk. Lymphoma., 2008, 49(12), 2328-2332.
-
(2008)
Leuk. Lymphoma.
, vol.49
, Issue.12
, pp. 2328-2332
-
-
Breccia, M.1
Stefanizzi, C.2
Cannella, L.3
Latagliata, R.4
Frustaci, A.M.5
Carmosino, I.6
Santopietro, M.7
Alimena, G.8
-
60
-
-
4444283314
-
Effectiveness and cost-effectiveness of imatinib for first-line treatment of chronic myeloid leukaemia in chronic phase: A systematic review and economic analysis
-
1-120
-
Dalziel, K.; Round, A.; Stein, K.; Garside, R.; Price, A. Effectiveness and cost-effectiveness of imatinib for first-line treatment of chronic myeloid leukaemia in chronic phase: a systematic review and economic analysis. Health Technol. Assess. (Winchester, England), 2004, 8(28), iii, 1-120.
-
(2004)
Health Technol. Assess. (Winchester, England)
, vol.8
, Issue.28
-
-
Dalziel, K.1
Round, A.2
Stein, K.3
Garside, R.4
Price, A.5
-
61
-
-
34447618418
-
Drug evaluation: Nilotinib - A novel Bcr-Abl tyrosine kinase inhibitor for the treatment of chronic myelocytic leukemia and beyond
-
Jabbour, E.; Cortes, J.; Giles, F.; O'Brien, S.; Kantarijan, H. Drug evaluation: Nilotinib - a novel Bcr-Abl tyrosine kinase inhibitor for the treatment of chronic myelocytic leukemia and beyond. IDrugs, 2007, 10(7), 468-479.
-
(2007)
IDrugs
, vol.10
, Issue.7
, pp. 468-479
-
-
Jabbour, E.1
Cortes, J.2
Giles, F.3
O'Brien, S.4
Kantarijan, H.5
-
62
-
-
36849023013
-
Cardiotoxicity associated with tyrosine kinase inhibitor sunitinib
-
DOI 10.1016/S0140-6736(07)61865-0, PII S0140673607618650
-
Chu, T. F.; Rupnick, M. A.; Kerkela, R.; Dallabrida, S. M.; Zurakowski, D.; Nguyen, L.; Woulfe, K.; Pravda, E.; Cassiola, F.; Desai, J.; George, S.; Morgan, J. A.; Harris, D. M.; Ismail, N. S.; Chen, J. H.; Schoen, F. J.; Van den Abbeele, A. D.; Demetri, G. D.; Force, T.; Chen, M. H. Cardiotoxicity associated with tyrosine kinase inhibitor sunitinib. Lancet, 2007, 370(9604), 2011-2019. (Pubitemid 350236338)
-
(2007)
Lancet
, vol.370
, Issue.9604
, pp. 2011-2019
-
-
Chu, T.F.1
Rupnick, M.A.2
Kerkela, R.3
Dallabrida, S.M.4
Zurakowski, D.5
Nguyen, L.6
Woulfe, K.7
Pravda, E.8
Cassiola, F.9
Desai, J.10
George, S.11
Morgan, J.A.12
Harris, D.M.13
Ismail, N.S.14
Chen, J.-H.15
Schoen, F.J.16
Van den Abbeele, A.D.17
Demetri, G.D.18
Force, T.19
Chen, M.H.20
more..
-
63
-
-
33751205030
-
Lapatinib: Current status and future directions in breast cancer
-
Moy, B.; Goss, P. E. Lapatinib: current status and future directions in breast cancer. Oncologist, 2006, 11(10), 1047-1057.
-
(2006)
Oncologist
, vol.11
, Issue.10
, pp. 1047-1057
-
-
Moy, B.1
Goss, P.E.2
-
64
-
-
76549116248
-
Potent, transient inhibition of BCR-ABL with dasatinib 100 mg daily achieves rapid and durable cytogenetic responses and high transformation-free survival rates in chronic phase chronic myeloid leukemia patients with resistance, suboptimal response or intolerance to imatinib
-
Shah, N. P.; Kim, D. W.; Kantarjian, H.; Rousselot, P.; Llacer, P. E.; Enrico, A.; Vela-Ojeda, J.; Silver, R. T.; Khoury, H. J.; Muller, M. C.; Lambert, A.; Matloub, Y.; Hochhaus, A. Potent, transient inhibition of BCR-ABL with dasatinib 100 mg daily achieves rapid and durable cytogenetic responses and high transformation-free survival rates in chronic phase chronic myeloid leukemia patients with resistance, suboptimal response or intolerance to imatinib. Haematologica, 2010, 95(2), 232-240.
-
(2010)
Haematologica
, vol.95
, Issue.2
, pp. 232-240
-
-
Shah, N.P.1
Kim, D.W.2
Kantarjian, H.3
Rousselot, P.4
Llacer, P.E.5
Enrico, A.6
Vela-Ojeda, J.7
Silver, R.T.8
Khoury, H.J.9
Muller, M.C.10
Lambert, A.11
Matloub, Y.12
Hochhaus, A.13
-
65
-
-
0026621245
-
ABC transporters: From microorganisms to man
-
Higgins, C. F. ABC transporters: from microorganisms to man. Annu. Rev. Cell Biol., 1992, 8, 67-113.
-
(1992)
Annu. Rev. Cell. Biol.
, vol.8
, pp. 67-113
-
-
Higgins, C.F.1
-
66
-
-
65549121495
-
Human ATP-binding cassette (ABC) transporter family
-
Vasiliou, V.; Vasiliou, K.; Nebert, D. W. Human ATP-binding cassette (ABC) transporter family. Hum. Genomics, 2009, 3(3), 281-290.
-
(2009)
Hum. Genomics
, vol.3
, Issue.3
, pp. 281-290
-
-
Vasiliou, V.1
Vasiliou, K.2
Nebert, D.W.3
-
67
-
-
0034917716
-
The human ATP-binding cassette (ABC) transporter superfamily
-
DOI 10.1101/gr.GR-1649R
-
Dean, M.; Rzhetsky, A.; Allikmets, R. The human ATP-binding cassette (ABC) transporter superfamily. Genome Res., 2001, 11(7), 1156-1166. (Pubitemid 32677289)
-
(2001)
Genome Research
, vol.11
, Issue.7
, pp. 1156-1166
-
-
Dean, M.1
Rzhetsky, A.2
Allikmets, R.3
-
68
-
-
40949121607
-
ABC multidrug transporters: Structure, function and role in chemoresistance
-
Sharom, F. J. ABC multidrug transporters: structure, function and role in chemoresistance. Pharmacogenomics, 2008, 9(1), 105-127.
-
(2008)
Pharmacogenomics
, vol.9
, Issue.1
, pp. 105-127
-
-
Sharom, F.J.1
-
69
-
-
33745748312
-
The functions and structure of ABC transporters: Implications for the design of new inhibitors of Pgp and MRP1 to control multidrug resistance (MDR)
-
Teodori, E.; Dei, S.; Martelli, C.; Scapecchi, S.; Gualtieri, F. The functions and structure of ABC transporters: implications for the design of new inhibitors of Pgp and MRP1 to control multidrug resistance (MDR). Curr. Drug Targets, 2006, 7(7), 893-909.
-
(2006)
Curr. Drug Targets
, vol.7
, Issue.7
, pp. 893-909
-
-
Teodori, E.1
Dei, S.2
Martelli, C.3
Scapecchi, S.4
Gualtieri, F.5
-
70
-
-
25844487733
-
Evolution of the ATP-binding cassette (ABC) transporter superfamily in vertebrates
-
Dean, M.; Annilo, T. Evolution of the ATP-binding cassette (ABC) transporter superfamily in vertebrates. Annu. Rev. Genomics Hum. Genet., 2005, 6, 123-142.
-
(2005)
Annu. Rev. Genomics Hum. Genet.
, vol.6
, pp. 123-142
-
-
Dean, M.1
Annilo, T.2
-
71
-
-
0036176510
-
Mechanisms of cancer drug resistance
-
Gottesman, M. M. Mechanisms of cancer drug resistance. Annu. Rev. Med., 2002, 53, 615-627.
-
(2002)
Annu. Rev. Med.
, vol.53
, pp. 615-627
-
-
Gottesman, M.M.1
-
72
-
-
34248594839
-
The emerging pharmacotherapeutic significance of the breast cancer resistance protein (ABCG2)
-
Hardwick, L. J.; Velamakanni, S.; van Veen, H. W. The emerging pharmacotherapeutic significance of the breast cancer resistance protein (ABCG2). Br. J. Pharmacol., 2007, 151(2), 163-174.
-
(2007)
Br. J. Pharmacol.
, vol.151
, Issue.2
, pp. 163-174
-
-
Hardwick, L.J.1
Velamakanni, S.2
Van Veen, H.W.3
-
73
-
-
33947381412
-
ABCG2: Determining its relevance in clinical drug resistance
-
Robey, R. W.; Polgar, O.; Deeken, J.; To, K. W.; Bates, S. E. ABCG2: determining its relevance in clinical drug resistance. Cancer Metastasis. Rev., 2007, 26(1), 39-57.
-
(2007)
Cancer Metastasis. Rev.
, vol.26
, Issue.1
, pp. 39-57
-
-
Robey, R.W.1
Polgar, O.2
Deeken, J.3
To, K.W.4
Bates, S.E.5
-
74
-
-
44649084920
-
Transport proteins of the ABC family and multidrug resistance of tumor cells
-
Stavrovskaya, A. A.; Stromskaya, T. P. Transport proteins of the ABC family and multidrug resistance of tumor cells. Biochemistry, 2008, 73(5), 592-604.
-
(2008)
Biochemistry
, vol.73
, Issue.5
, pp. 592-604
-
-
Stavrovskaya, A.A.1
Stromskaya, T.P.2
-
75
-
-
33646078329
-
ABC A-subfamily transporters: Structure, function and disease
-
Kaminski, W. E.; Piehler, A.; Wenzel, J. J. ABC A-subfamily transporters: structure, function and disease. Biochim. Biophys. Acta., 2006, 1762(5), 510-524.
-
(2006)
Biochim. Biophys. Acta.
, vol.1762
, Issue.5
, pp. 510-524
-
-
Kaminski, W.E.1
Piehler, A.2
Wenzel, J.J.3
-
76
-
-
0035870262
-
Cloning and characterization of human adenosine 5'-triphosphate-binding cassette, sub-family A, transporter 2 (ABCA2)
-
Vulevic, B.; Chen, Z.; Boyd, J. T.; Davis, W., Jr.; Walsh, E. S.; Belinsky, M. G.; Tew, K. D. Cloning and characterization of human adenosine 5'-triphosphate-binding cassette, sub-family A, transporter 2 (ABCA2). Cancer Res., 2001, 61(8), 3339-3347.
-
(2001)
Cancer Res.
, vol.61
, Issue.8
, pp. 3339-3347
-
-
Vulevic, B.1
Chen, Z.2
Boyd, J.T.3
Davis Jr., W.4
Walsh, E.S.5
Belinsky, M.G.6
Tew, K.D.7
-
77
-
-
0032900953
-
Biochemical, cellular, and pharmacological aspects of the multidrug transporter
-
Ambudkar, S. V.; Dey, S.; Hrycyna, C. A.; Ramachandra, M.; Pastan, I.; Gottesman, M. M. Biochemical, cellular, and pharmacological aspects of the multidrug transporter. Annu. Rev. Pharmacol. Toxicol., 1999, 39, 361-398.
-
(1999)
Annu. Rev. Pharmacol. Toxicol.
, vol.39
, pp. 361-398
-
-
Ambudkar, S.V.1
Dey, S.2
Hrycyna, C.A.3
Ramachandra, M.4
Pastan, I.5
Gottesman, M.M.6
-
78
-
-
24344439264
-
Transporters and drug therapy: Implications for drug disposition and disease
-
Ho, R. H.; Kim, R. B. Transporters and drug therapy: implications for drug disposition and disease. Clin. Pharmacol. Ther., 2005, 78(3), 260-277.
-
(2005)
Clin. Pharmacol. Ther.
, vol.78
, Issue.3
, pp. 260-277
-
-
Ho, R.H.1
Kim, R.B.2
-
79
-
-
3042696864
-
Mitoxantrone resistance in a small cell lung cancer cell line is associated with ABCA2 upregulation
-
Boonstra, R.; Timmer-Bosscha, H.; van Echten-Arends, J.; van der Kolk, D. M.; van den Berg, A.; de Jong, B.; Tew, K. D.; Poppema, S.; de Vries, E. G. Mitoxantrone resistance in a small cell lung cancer cell line is associated with ABCA2 upregulation. Br. J. Cancer, 2004, 90(12), 2411-2417.
-
(2004)
Br. J. Cancer
, vol.90
, Issue.12
, pp. 2411-2417
-
-
Boonstra, R.1
Timmer-Bosscha, H.2
Van Echten-Arends, J.3
Van Der Kolk, D.M.4
Van Den Berg, A.5
De Jong, B.6
Tew, K.D.7
Poppema, S.8
De Vries, E.G.9
-
80
-
-
0032054730
-
Amplification of the ATP-binding cassette 2 transporter gene is functionally linked with enhanced efflux of estramustine in ovarian carcinoma cells
-
Laing, N. M.; Belinsky, M. G.; Kruh, G. D.; Bell, D. W.; Boyd, J. T.; Barone, L.; Testa, J. R.; Tew, K. D. Amplification of the ATP-binding cassette 2 transporter gene is functionally linked with enhanced efflux of estramustine in ovarian carcinoma cells. Cancer Res., 1998, 58(7), 1332-1337.
-
(1998)
Cancer Res.
, vol.58
, Issue.7
, pp. 1332-1337
-
-
Laing, N.M.1
Belinsky, M.G.2
Kruh, G.D.3
Bell, D.W.4
Boyd, J.T.5
Barone, L.6
Testa, J.R.7
Tew, K.D.8
-
81
-
-
10844235689
-
Microarray-based detection of multidrug resistance in human tumor cells by expression profiling of ATP-binding cassette transporter genes
-
Gillet, J. P.; Efferth, T.; Steinbach, D.; Hamels, J.; de Longueville, F.; Bertholet, V.; Remacle, J. Microarray-based detection of multidrug resistance in human tumor cells by expression profiling of ATP-binding cassette transporter genes. Cancer Res., 2004, 64(24), 8987-8993.
-
(2004)
Cancer Res.
, vol.64
, Issue.24
, pp. 8987-8993
-
-
Gillet, J.P.1
Efferth, T.2
Steinbach, D.3
Hamels, J.4
De Longueville, F.5
Bertholet, V.6
Remacle, J.7
-
82
-
-
62549108159
-
ABC transporters, drug resistance, and cancer stem cells
-
Dean, M. ABC transporters, drug resistance, and cancer stem cells. J. Mammary Gland Biol. Neoplasia., 2009, 14(1), 3-9.
-
(2009)
J. Mammary Gland Biol. Neoplasia.
, vol.14
, Issue.1
, pp. 3-9
-
-
Dean, M.1
-
83
-
-
33745831231
-
Structure, function, expression, genomic organization, and single nucleotide polymorphisms of human ABCB1 (MDR1), ABCC (MRP), and ABCG2 (BCRP) efflux transporters
-
Choudhuri, S.; Klaassen, C. D. Structure, function, expression, genomic organization, and single nucleotide polymorphisms of human ABCB1 (MDR1), ABCC (MRP), and ABCG2 (BCRP) efflux transporters. Int. J. Toxicol., 2006, 25(4), 231-259.
-
(2006)
Int. J. Toxicol.
, vol.25
, Issue.4
, pp. 231-259
-
-
Choudhuri, S.1
Klaassen, C.D.2
-
84
-
-
0031949071
-
P-glycoprotein functions and substrates: Possible roles of MDR1 gene in the kidney
-
Ernest, S.; Bello-Reuss, E. P-glycoprotein functions and substrates: possible roles of MDR1 gene in the kidney. Kidney Int., 1998, 65, S11-17.
-
(1998)
Kidney Int.
, vol.65
-
-
Ernest, S.1
Bello-Reuss, E.2
-
85
-
-
33749488939
-
Human multidrug resistance ABCB and ABCG transporters: Participation in a chemoimmunity defense system
-
Sarkadi, B.; Homolya, L.; Szakacs, G.; Varadi, A. Human multidrug resistance ABCB and ABCG transporters: participation in a chemoimmunity defense system. Physiol. Rev., 2006, 86(4), 1179-1236.
-
(2006)
Physiol. Rev.
, vol.86
, Issue.4
, pp. 1179-1236
-
-
Sarkadi, B.1
Homolya, L.2
Szakacs, G.3
Varadi, A.4
-
86
-
-
33646741238
-
The ATP-binding cassette transporters and their implication in drug disposition: A special look at the heart
-
Couture, L.; Nash, J. A.; Turgeon, J. The ATP-binding cassette transporters and their implication in drug disposition: a special look at the heart. Pharmacol. Rev., 2006, 58(2), 244-258.
-
(2006)
Pharmacol. Rev.
, vol.58
, Issue.2
, pp. 244-258
-
-
Couture, L.1
Nash, J.A.2
Turgeon, J.3
-
87
-
-
0020605073
-
Daunorubicinresistant Chinese hamster ovary cells expressing multidrug resistance and a cell-surface P-glycoprotein
-
Kartner, N.; Shales, M.; Riordan, J. R.; Ling, V. Daunorubicinresistant Chinese hamster ovary cells expressing multidrug resistance and a cell-surface P-glycoprotein. Cancer Res., 1983, 43(9), 4413-4419.
-
(1983)
Cancer Res.
, vol.43
, Issue.9
, pp. 4413-4419
-
-
Kartner, N.1
Shales, M.2
Riordan, J.R.3
Ling, V.4
-
88
-
-
0008632564
-
Expression of a full-length cDNA for the human "MDR1" gene confers resistance to colchicine, doxorubicin, and vinblastine
-
Ueda, K.; Cardarelli, C.; Gottesman, M. M.; Pastan, I. Expression of a full-length cDNA for the human "MDR1" gene confers resistance to colchicine, doxorubicin, and vinblastine. Proc. Natl. Acad. Sci. U. S. A., 1987, 84(9), 3004-3008.
-
(1987)
Proc. Natl. Acad. Sci. U. S. A.
, vol.84
, Issue.9
, pp. 3004-3008
-
-
Ueda, K.1
Cardarelli, C.2
Gottesman, M.M.3
Pastan, I.4
-
89
-
-
0027146389
-
Transport of celiprolol across human intestinal epithelial (Caco-2) cells: Mediation of secretion by multiple transporters including P-glycoprotein
-
Karlsson, J.; Kuo, S. M.; Ziemniak, J.; Artursson, P. Transport of celiprolol across human intestinal epithelial (Caco-2) cells: mediation of secretion by multiple transporters including P-glycoprotein. Br. J. Pharmacol., 1993, 110(3), 1009-1016.
-
(1993)
Br. J. Pharmacol.
, vol.110
, Issue.3
, pp. 1009-1016
-
-
Karlsson, J.1
Kuo, S.M.2
Ziemniak, J.3
Artursson, P.4
-
90
-
-
12644278301
-
Limited oral bioavailability and active epithelial excretion of paclitaxel (Taxol) caused by P-glycoprotein in the intestine
-
Sparreboom, A.; van Asperen, J.; Mayer, U.; Schinkel, A. H.; Smit, J. W.; Meijer, D. K.; Borst, P.; Nooijen, W. J.; Beijnen, J. H.; van Tellingen, O. Limited oral bioavailability and active epithelial excretion of paclitaxel (Taxol) caused by P-glycoprotein in the intestine. Proc. Natl. Acad. Sci. U. S. A., 1997, 94(5), 2031-2035.
-
(1997)
Proc. Natl. Acad. Sci. U. S. A.
, vol.94
, Issue.5
, pp. 2031-2035
-
-
Sparreboom, A.1
Van Asperen, J.2
Mayer, U.3
Schinkel, A.H.4
Smit, J.W.5
Meijer, D.K.6
Borst, P.7
Nooijen, W.J.8
Beijnen, J.H.9
Van Tellingen, O.10
-
91
-
-
0032518290
-
The drug transporter P-glycoprotein limits oral absorption and brain entry of HIV-1 protease inhibitors
-
Kim, R. B.; Fromm, M. F.; Wandel, C.; Leake, B.; Wood, A. J.; Roden, D. M.; Wilkinson, G. R. The drug transporter P-glycoprotein limits oral absorption and brain entry of HIV-1 protease inhibitors. J. Clin. Invest., 1998, 101(2), 289-294.
-
(1998)
J. Clin. Invest.
, vol.101
, Issue.2
, pp. 289-294
-
-
Kim, R.B.1
Fromm, M.F.2
Wandel, C.3
Leake, B.4
Wood, A.J.5
Roden, D.M.6
Wilkinson, G.R.7
-
92
-
-
0034604707
-
MDR3 P-glycoprotein, a phosphatidylcholine translocase, transports several cytotoxic drugs and directly interacts with drugs as judged by interference with nucleotide trapping
-
Smith, A. J.; van Helvoort, A.; van Meer, G.; Szabo, K.; Welker, E.; Szakacs, G.; Varadi, A.; Sarkadi, B.; Borst, P. MDR3 P-glycoprotein, a phosphatidylcholine translocase, transports several cytotoxic drugs and directly interacts with drugs as judged by interference with nucleotide trapping. J. Biol. Chem., 2000, 275(31), 23530-23539.
-
(2000)
J. Biol. Chem.
, vol.275
, Issue.31
, pp. 23530-23539
-
-
Smith, A.J.1
Van Helvoort, A.2
Van Meer, G.3
Szabo, K.4
Welker, E.5
Szakacs, G.6
Varadi, A.7
Sarkadi, B.8
Borst, P.9
-
93
-
-
0033989134
-
Cloning and expression of murine sister of P-glycoprotein reveals a more discriminating transporter than MDR1/P-glycoprotein
-
Lecureur, V.; Sun, D.; Hargrove, P.; Schuetz, E. G.; Kim, R. B.; Lan, L. B.; Schuetz, J. D. Cloning and expression of murine sister of P-glycoprotein reveals a more discriminating transporter than MDR1/P-glycoprotein. Mol. Pharmacol., 2000, 57(1), 24-35.
-
(2000)
Mol. Pharmacol.
, vol.57
, Issue.1
, pp. 24-35
-
-
Lecureur, V.1
Sun, D.2
Hargrove, P.3
Schuetz, E.G.4
Kim, R.B.5
Lan, L.B.6
Schuetz, J.D.7
-
94
-
-
0033984873
-
Drug-and estrogen-induced cholestasis through inhibition of the hepatocellular bile salt export pump (Bsep) of rat liver
-
Stieger, B.; Fattinger, K.; Madon, J.; Kullak-Ublick, G. A.; Meier, P. J. Drug-and estrogen-induced cholestasis through inhibition of the hepatocellular bile salt export pump (Bsep) of rat liver. Gastroenterology, 2000, 118(2), 422-430.
-
(2000)
Gastroenterology
, vol.118
, Issue.2
, pp. 422-430
-
-
Stieger, B.1
Fattinger, K.2
Madon, J.3
Kullak-Ublick, G.A.4
Meier, P.J.5
-
95
-
-
0027960078
-
Pharmacological characterization of multidrug resistant MRP-transfected human tumor cells
-
Cole, S. P.; Sparks, K. E.; Fraser, K.; Loe, D. W.; Grant, C. E.; Wilson, G. M.; Deeley, R. G. Pharmacological characterization of multidrug resistant MRP-transfected human tumor cells. Cancer Res., 1994, 54(22), 5902-5910.
-
(1994)
Cancer Res.
, vol.54
, Issue.22
, pp. 5902-5910
-
-
Cole, S.P.1
Sparks, K.E.2
Fraser, K.3
Loe, D.W.4
Grant, C.E.5
Wilson, G.M.6
Deeley, R.G.7
-
96
-
-
9244261944
-
Tissue distribution of the multidrug resistance protein
-
Flens, M. J.; Zaman, G. J.; van der Valk, P.; Izquierdo, M. A.; Schroeijers, A. B.; Scheffer, G. L.; van der Groep, P.; de Haas, M.; Meijer, C. J.; Scheper, R. J. Tissue distribution of the multidrug resistance protein. Am. J. Pathol., 1996, 148(4), 1237-1247. (Pubitemid 26111082)
-
(1996)
American Journal of Pathology
, vol.148
, Issue.4
, pp. 1237-1247
-
-
Flens, M.J.1
Zaman, G.J.R.2
Van Der Valk, P.3
Izquierdo, M.A.4
Schroeijers, A.B.5
Scheffer, G.L.6
Van Der Groep, P.7
De Haas, M.8
Meijer, C.J.L.M.9
Scheper, R.J.10
-
97
-
-
0033815392
-
Limited distribution of new quinolone antibacterial agents into brain caused by multiple efflux transporters at the blood-brain barrier
-
Tamai, I.; Yamashita, J.; Kido, Y.; Ohnari, A.; Sai, Y.; Shima, Y.; Naruhashi, K.; Koizumi, S.; Tsuji, A. Limited distribution of new quinolone antibacterial agents into brain caused by multiple efflux transporters at the blood-brain barrier. J. Pharmacol. Exp. Ther., 2000, 295(1), 146-152.
-
(2000)
J. Pharmacol. Exp. Ther.
, vol.295
, Issue.1
, pp. 146-152
-
-
Tamai, I.1
Yamashita, J.2
Kido, Y.3
Ohnari, A.4
Sai, Y.5
Shima, Y.6
Naruhashi, K.7
Koizumi, S.8
Tsuji, A.9
-
98
-
-
0033936291
-
Vinblastine and sulfinpyrazone export by the multidrug resistance protein MRP2 is associated with glutathione export
-
Evers, R.; de Haas, M.; Sparidans, R.; Beijnen, J.; Wielinga, P. R.; Lankelma, J.; Borst, P. Vinblastine and sulfinpyrazone export by the multidrug resistance protein MRP2 is associated with glutathione export. Br. J. Cancer, 2000, 83(3), 375-383.
-
(2000)
Br. J. Cancer
, vol.83
, Issue.3
, pp. 375-383
-
-
Evers, R.1
De Haas, M.2
Sparidans, R.3
Beijnen, J.4
Wielinga, P.R.5
Lankelma, J.6
Borst, P.7
-
99
-
-
0033152212
-
Antifolate resistance mediated by the multidrug resistance proteins MRP1 and MRP2
-
Hooijberg, J. H.; Broxterman, H. J.; Kool, M.; Assaraf, Y. G.; Peters, G. J.; Noordhuis, P.; Scheper, R. J.; Borst, P.; Pinedo, H. M.; Jansen, G. Antifolate resistance mediated by the multidrug resistance proteins MRP1 and MRP2. Cancer Res., 1999, 59(11), 2532-2535.
-
(1999)
Cancer Res.
, vol.59
, Issue.11
, pp. 2532-2535
-
-
Hooijberg, J.H.1
Broxterman, H.J.2
Kool, M.3
Assaraf, Y.G.4
Peters, G.J.5
Noordhuis, P.6
Scheper, R.J.7
Borst, P.8
Pinedo, H.M.9
Jansen, G.10
-
100
-
-
0037159933
-
Multidrug resistance protein 2 (MRP2) transports HIV protease inhibitors, and transport can be enhanced by other drugs
-
Huisman, M. T.; Smit, J. W.; Crommentuyn, K. M.; Zelcer, N.; Wiltshire, H. R.; Beijnen, J. H.; Schinkel, A. H. Multidrug resistance protein 2 (MRP2) transports HIV protease inhibitors, and transport can be enhanced by other drugs. AIDS. (London, England), 2002, 16(17), 2295-2301.
-
(2002)
AIDS. (London, England)
, vol.16
, Issue.17
, pp. 2295-2301
-
-
Huisman, M.T.1
Smit, J.W.2
Crommentuyn, K.M.3
Zelcer, N.4
Wiltshire, H.R.5
Beijnen, J.H.6
Schinkel, A.H.7
-
101
-
-
0034765470
-
Nucleoside phosphonate interactions with multiple organic anion transporters in renal proximal tubule
-
Miller, D. S. Nucleoside phosphonate interactions with multiple organic anion transporters in renal proximal tubule. J. Pharmacol. Exp. Ther., 2001, 299(2), 567-574.
-
(2001)
J. Pharmacol. Exp. Ther.
, vol.299
, Issue.2
, pp. 567-574
-
-
Miller, D.S.1
-
102
-
-
0033407050
-
Expression of multidrug resistance protein-3 (multispecific organic anion transporter-D) in human embryonic kidney 293 cells confers resistance to anticancer agents
-
Zeng, H.; Bain, L. J.; Belinsky, M. G.; Kruh, G. D. Expression of multidrug resistance protein-3 (multispecific organic anion transporter-D) in human embryonic kidney 293 cells confers resistance to anticancer agents. Cancer Res., 1999, 59(23), 5964-5967.
-
(1999)
Cancer Res.
, vol.59
, Issue.23
, pp. 5964-5967
-
-
Zeng, H.1
Bain, L.J.2
Belinsky, M.G.3
Kruh, G.D.4
-
103
-
-
0035824674
-
Characterization of drug transport by the human multidrug resistance protein 3 (ABCC3)
-
Zelcer, N.; Saeki, T.; Reid, G.; Beijnen, J. H.; Borst, P. Characterization of drug transport by the human multidrug resistance protein 3 (ABCC3). J. Biol. Chem., 2001, 276(49), 46400-46407.
-
(2001)
J. Biol. Chem.
, vol.276
, Issue.49
, pp. 46400-46407
-
-
Zelcer, N.1
Saeki, T.2
Reid, G.3
Beijnen, J.H.4
Borst, P.5
-
104
-
-
0033681486
-
Expression of members of the multidrug resistance protein family in human term placenta
-
St-Pierre, M. V.; Serrano, M. A.; Macias, R. I.; Dubs, U.; Hoechli, M.; Lauper, U.; Meier, P. J.; Marin, J. J. Expression of members of the multidrug resistance protein family in human term placenta. Am. J. Physiol. Regul. Integr. Comp. Physiol., 2000, 279(4), R1495-1503.
-
(2000)
Am. J. Physiol. Regul. Integr. Comp. Physiol.
, vol.279
, Issue.4
-
-
St-Pierre, M.V.1
Serrano, M.A.2
Macias, R.I.3
Dubs, U.4
Hoechli, M.5
Lauper, U.6
Meier, P.J.7
Marin, J.J.8
-
105
-
-
0036606023
-
Analysis of methotrexate and folate transport by multidrug resistance protein 4 (ABCC4): MRP4 is a component of the methotrexate efflux system
-
Chen, Z. S.; Lee, K.; Walther, S.; Raftogianis, R. B.; Kuwano, M.; Zeng, H.; Kruh, G. D. Analysis of methotrexate and folate transport by multidrug resistance protein 4 (ABCC4): MRP4 is a component of the methotrexate efflux system. Cancer Res., 2002, 62(11), 3144-3150.
-
(2002)
Cancer Res.
, vol.62
, Issue.11
, pp. 3144-3150
-
-
Chen, Z.S.1
Lee, K.2
Walther, S.3
Raftogianis, R.B.4
Kuwano, M.5
Zeng, H.6
Kruh, G.D.7
-
106
-
-
0034614112
-
Analysis of the MRP4 drug resistance profile in transfected NIH3T3 cells
-
Lee, K.; Klein-Szanto, A. J.; Kruh, G. D. Analysis of the MRP4 drug resistance profile in transfected NIH3T3 cells. J. Natl. Cancer. Inst., 2000, 92(23), 1934-1940.
-
(2000)
J. Natl. Cancer. Inst.
, vol.92
, Issue.23
, pp. 1934-1940
-
-
Lee, K.1
Klein-Szanto, A.J.2
Kruh, G.D.3
-
107
-
-
0032879904
-
MRP4: A previously unidentified factor in resistance to nucleoside-based antiviral drugs
-
Schuetz, J. D.; Connelly, M. C.; Sun, D.; Paibir, S. G.; Flynn, P. M.; Srinivas, R. V.; Kumar, A.; Fridland, A. MRP4: A previously unidentified factor in resistance to nucleoside-based antiviral drugs. Nat. Med., 1999, 5(9), 1048-1051.
-
(1999)
Nat. Med.
, vol.5
, Issue.9
, pp. 1048-1051
-
-
Schuetz, J.D.1
Connelly, M.C.2
Sun, D.3
Paibir, S.G.4
Flynn, P.M.5
Srinivas, R.V.6
Kumar, A.7
Fridland, A.8
-
108
-
-
1242335471
-
The MRP-related and BCRP/ABCG2 multidrug resistance proteins: Biology, substrate specificity and regulation
-
Haimeur, A.; Conseil, G.; Deeley, R. G.; Cole, S. P. The MRP-related and BCRP/ABCG2 multidrug resistance proteins: biology, substrate specificity and regulation. Curr. Drug Metab., 2004, 5(1), 21-53.
-
(2004)
Curr. Drug Metab.
, vol.5
, Issue.1
, pp. 21-53
-
-
Haimeur, A.1
Conseil, G.2
Deeley, R.G.3
Cole, S.P.4
-
109
-
-
0033020785
-
MOAT-E (ARA) is a full-length MRP/cMOAT subfamily transporter expressed in kidney and liver
-
Belinsky, M. G.; Kruh, G. D. MOAT-E (ARA) is a full-length MRP/cMOAT subfamily transporter expressed in kidney and liver. Br. J. Cancer, 1999, 80(9), 1342-1349.
-
(1999)
Br. J. Cancer
, vol.80
, Issue.9
, pp. 1342-1349
-
-
Belinsky, M.G.1
Kruh, G.D.2
-
110
-
-
0036829109
-
Characterization of the drug resistance and transport properties of multidrug resistance protein 6 (MRP6, ABCC6)
-
Belinsky, M. G.; Chen, Z. S.; Shchaveleva, I.; Zeng, H.; Kruh, G. D. Characterization of the drug resistance and transport properties of multidrug resistance protein 6 (MRP6, ABCC6). Cancer Res., 2002, 62(21), 6172-6177.
-
(2002)
Cancer Res.
, vol.62
, Issue.21
, pp. 6172-6177
-
-
Belinsky, M.G.1
Chen, Z.S.2
Shchaveleva, I.3
Zeng, H.4
Kruh, G.D.5
-
111
-
-
0037139535
-
CDNA cloning and genomic organization of the murine MRP7, a new ATP-binding cassette transporter
-
Kao, H. H.; Huang, J. D.; Chang, M. S. cDNA cloning and genomic organization of the murine MRP7, a new ATP-binding cassette transporter. Gene, 2002, 286(2), 299-306.
-
(2002)
Gene
, vol.286
, Issue.2
, pp. 299-306
-
-
Kao, H.H.1
Huang, J.D.2
Chang, M.S.3
-
112
-
-
3142752689
-
Analysis of the drug resistance profile of multidrug resistance protein 7 (ABCC10): Resistance to docetaxel
-
Hopper-Borge, E.; Chen, Z. S.; Shchaveleva, I.; Belinsky, M. G.; Kruh, G. D. Analysis of the drug resistance profile of multidrug resistance protein 7 (ABCC10): resistance to docetaxel. Cancer Res., 2004, 64(14), 4927-4930.
-
(2004)
Cancer Res.
, vol.64
, Issue.14
, pp. 4927-4930
-
-
Hopper-Borge, E.1
Chen, Z.S.2
Shchaveleva, I.3
Belinsky, M.G.4
Kruh, G.D.5
-
113
-
-
2442451598
-
MRP8, a new member of ABC transporter superfamily, identified by EST database mining and gene prediction program, is highly expressed in breast cancer
-
Bera, T. K.; Lee, S.; Salvatore, G.; Lee, B.; Pastan, I. MRP8, a new member of ABC transporter superfamily, identified by EST database mining and gene prediction program, is highly expressed in breast cancer. Mol. Med. (Cambridge, Mass), 2001, 7(8), 509-516.
-
(2001)
Mol. Med. (Cambridge, Mass)
, vol.7
, Issue.8
, pp. 509-516
-
-
Bera, T.K.1
Lee, S.2
Salvatore, G.3
Lee, B.4
Pastan, I.5
-
114
-
-
0037076375
-
MRP9, an unusual truncated member of the ABC transporter superfamily, is highly expressed in breast cancer
-
Bera, T. K.; Iavarone, C.; Kumar, V.; Lee, S.; Lee, B.; Pastan, I. MRP9, an unusual truncated member of the ABC transporter superfamily, is highly expressed in breast cancer. Proc. Natl. Acad. Sci. U. S. A., 2002, 99(10), 6997-7002.
-
(2002)
Proc. Natl. Acad. Sci. U. S. A.
, vol.99
, Issue.10
, pp. 6997-7002
-
-
Bera, T.K.1
Iavarone, C.2
Kumar, V.3
Lee, S.4
Lee, B.5
Pastan, I.6
-
115
-
-
0037218382
-
Breast cancer resistance protein (BCRP/ABCG2) induces cellular resistance to HIV-1 nucleoside reverse transcriptase inhibitors
-
Wang, X.; Furukawa, T.; Nitanda, T.; Okamoto, M.; Sugimoto, Y.; Akiyama, S.; Baba, M. Breast cancer resistance protein (BCRP/ABCG2) induces cellular resistance to HIV-1 nucleoside reverse transcriptase inhibitors. Mol. Pharmacol., 2003, 63(1), 65-72.
-
(2003)
Mol. Pharmacol.
, vol.63
, Issue.1
, pp. 65-72
-
-
Wang, X.1
Furukawa, T.2
Nitanda, T.3
Okamoto, M.4
Sugimoto, Y.5
Akiyama, S.6
Baba, M.7
-
116
-
-
66649132535
-
Breast cancer resistance protein interacts with various compounds in vitro, but plays a minor role in substrate efflux at the blood-brain barrier
-
Zhao, R.; Raub, T. J.; Sawada, G. A.; Kasper, S. C.; Bacon, J. A.; Bridges, A. S.; Pollack, G. M. Breast cancer resistance protein interacts with various compounds in vitro, but plays a minor role in substrate efflux at the blood-brain barrier. Drug Metab. Dispos.: the biological fate of chemicals, 2009, 37(6), 1251-1258.
-
(2009)
Drug Metab. Dispos.: The Biological Fate of Chemicals
, vol.37
, Issue.6
, pp. 1251-1258
-
-
Zhao, R.1
Raub, T.J.2
Sawada, G.A.3
Kasper, S.C.4
Bacon, J.A.5
Bridges, A.S.6
Pollack, G.M.7
-
117
-
-
16844368698
-
Tumour stem cells and drug resistance
-
Dean, M.; Fojo, T.; Bates, S. Tumour stem cells and drug resistance. Nat. Rev. Cancer, 2005, 5(4), 275-284.
-
(2005)
Nat. Rev. Cancer
, vol.5
, Issue.4
, pp. 275-284
-
-
Dean, M.1
Fojo, T.2
Bates, S.3
-
118
-
-
0345724724
-
The MRP family of drug efflux pumps
-
Kruh, G. D.; Belinsky, M. G. The MRP family of drug efflux pumps. Oncogene, 2003, 22(47), 7537-7552.
-
(2003)
Oncogene
, vol.22
, Issue.47
, pp. 7537-7552
-
-
Kruh, G.D.1
Belinsky, M.G.2
-
119
-
-
31844444140
-
The molecular basis of multidrug resistance in cancer: The early years of P-glycoprotein research
-
Gottesman, M. M.; Ling, V. The molecular basis of multidrug resistance in cancer: the early years of P-glycoprotein research. FEBS Lett., 2006, 580(4), 998-1009.
-
(2006)
FEBS Lett.
, vol.580
, Issue.4
, pp. 998-1009
-
-
Gottesman, M.M.1
Ling, V.2
-
120
-
-
33745835398
-
Transmembrane transport of endo-and xenobiotics by mammalian ATP-binding cassette multidrug resistance proteins
-
Deeley, R. G.; Westlake, C.; Cole, S. P. Transmembrane transport of endo-and xenobiotics by mammalian ATP-binding cassette multidrug resistance proteins. Physiol. Rev., 2006, 86(3), 849-899.
-
(2006)
Physiol. Rev.
, vol.86
, Issue.3
, pp. 849-899
-
-
Deeley, R.G.1
Westlake, C.2
Cole, S.P.3
-
121
-
-
0034254368
-
Selection and characterization of BCR-ABL positive cell lines with differential sensitivity to the tyrosine kinase inhibitor STI571: Diverse mechanisms of resistance
-
Mahon, F. X.; Deininger, M. W.; Schultheis, B.; Chabrol, J.; Reiffers, J.; Goldman, J. M.; Melo, J. V. Selection and characterization of BCR-ABL positive cell lines with differential sensitivity to the tyrosine kinase inhibitor STI571: diverse mechanisms of resistance. Blood, 2000, 96(3), 1070-1079.
-
(2000)
Blood
, vol.96
, Issue.3
, pp. 1070-1079
-
-
Mahon, F.X.1
Deininger, M.W.2
Schultheis, B.3
Chabrol, J.4
Reiffers, J.5
Goldman, J.M.6
Melo, J.V.7
-
122
-
-
0037443754
-
MDR1 gene overexpression confers resistance to imatinib mesylate in leukemia cell line models
-
Mahon, F. X.; Belloc, F.; Lagarde, V.; Chollet, C.; Moreau-Gaudry, F.; Reiffers, J.; Goldman, J. M.; Melo, J. V. MDR1 gene overexpression confers resistance to imatinib mesylate in leukemia cell line models. Blood, 2003, 101(6), 2368-2373.
-
(2003)
Blood
, vol.101
, Issue.6
, pp. 2368-2373
-
-
Mahon, F.X.1
Belloc, F.2
Lagarde, V.3
Chollet, C.4
Moreau-Gaudry, F.5
Reiffers, J.6
Goldman, J.M.7
Melo, J.V.8
-
123
-
-
57149098598
-
Evidence that resistance to nilotinib may be due to BCR-ABL, Pgp, or Src kinase overexpression
-
Mahon, F. X.; Hayette, S.; Lagarde, V.; Belloc, F.; Turcq, B.; Nicolini, F.; Belanger, C.; Manley, P. W.; Leroy, C.; Etienne, G.; Roche, S.; Pasquet, J. M. Evidence that resistance to nilotinib may be due to BCR-ABL, Pgp, or Src kinase overexpression. Cancer Res., 2008, 68(23), 9809-9816.
-
(2008)
Cancer Res.
, vol.68
, Issue.23
, pp. 9809-9816
-
-
Mahon, F.X.1
Hayette, S.2
Lagarde, V.3
Belloc, F.4
Turcq, B.5
Nicolini, F.6
Belanger, C.7
Manley, P.W.8
Leroy, C.9
Etienne, G.10
Roche, S.11
Pasquet, J.M.12
-
124
-
-
2442638937
-
Highaffinity interaction of tyrosine kinase inhibitors with the ABCG2 multidrug transporter
-
Ozvegy-Laczka, C.; Hegedus, T.; Varady, G.; Ujhelly, O.; Schuetz, J. D.; Varadi, A.; Keri, G.; Orfi, L.; Nemet, K.; Sarkadi, B. Highaffinity interaction of tyrosine kinase inhibitors with the ABCG2 multidrug transporter. Mol. Pharmacol., 2004, 65(6), 1485-1495.
-
(2004)
Mol. Pharmacol.
, vol.65
, Issue.6
, pp. 1485-1495
-
-
Ozvegy-Laczka, C.1
Hegedus, T.2
Varady, G.3
Ujhelly, O.4
Schuetz, J.D.5
Varadi, A.6
Keri, G.7
Orfi, L.8
Nemet, K.9
Sarkadi, B.10
-
125
-
-
20144389530
-
Multidrug transporter ABCG2 prevents tumor cell death induced by the epidermal growth factor receptor inhibitor Iressa (ZD1839, Gefitinib)
-
Elkind, N. B.; Szentpetery, Z.; Apati, A.; Ozvegy-Laczka, C.; Varady, G.; Ujhelly, O.; Szabo, K.; Homolya, L.; Varadi, A.; Buday, L.; Keri, G.; Nemet, K.; Sarkadi, B. Multidrug transporter ABCG2 prevents tumor cell death induced by the epidermal growth factor receptor inhibitor Iressa (ZD1839, Gefitinib). Cancer Res., 2005, 65(5), 1770-1777.
-
(2005)
Cancer Res.
, vol.65
, Issue.5
, pp. 1770-1777
-
-
Elkind, N.B.1
Szentpetery, Z.2
Apati, A.3
Ozvegy-Laczka, C.4
Varady, G.5
Ujhelly, O.6
Szabo, K.7
Homolya, L.8
Varadi, A.9
Buday, L.10
Keri, G.11
Nemet, K.12
Sarkadi, B.13
-
126
-
-
4644329144
-
Gefitinib reverses breast cancer resistance proteinmediated drug resistance
-
Yanase, K.; Tsukahara, S.; Asada, S.; Ishikawa, E.; Imai, Y.; Sugimoto, Y. Gefitinib reverses breast cancer resistance proteinmediated drug resistance. Mol. Cancer Ther., 2004, 3(9), 1119-1125.
-
(2004)
Mol. Cancer Ther.
, vol.3
, Issue.9
, pp. 1119-1125
-
-
Yanase, K.1
Tsukahara, S.2
Asada, S.3
Ishikawa, E.4
Imai, Y.5
Sugimoto, Y.6
-
127
-
-
7244232706
-
Imatinib mesylate (STI571) is a substrate for the breast cancer resistance protein (BCRP)/ABCG2 drug pump
-
Burger, H.; van Tol, H.; Boersma, A. W.; Brok, M.; Wiemer, E. A.; Stoter, G.; Nooter, K. Imatinib mesylate (STI571) is a substrate for the breast cancer resistance protein (BCRP)/ABCG2 drug pump. Blood, 2004, 104(9), 2940-2942.
-
(2004)
Blood
, vol.104
, Issue.9
, pp. 2940-2942
-
-
Burger, H.1
Van Tol, H.2
Boersma, A.W.3
Brok, M.4
Wiemer, E.A.5
Stoter, G.6
Nooter, K.7
-
128
-
-
70350132811
-
Interaction of nilotinib, dasatinib and bosutinib with ABCB1 and ABCG2: Implications for altered anti-cancer effects and pharmacological properties
-
Hegedus, C.; Ozvegy-Laczka, C.; Apati, A.; Magocsi, M.; Nemet, K.; Orfi, L.; Keri, G.; Katona, M.; Takats, Z.; Varadi, A.; Szakacs, G.; Sarkadi, B. Interaction of nilotinib, dasatinib and bosutinib with ABCB1 and ABCG2: implications for altered anti-cancer effects and pharmacological properties. Br. J. Pharmacol., 2009, 158(4), 1153-1164.
-
(2009)
Br. J. Pharmacol.
, vol.158
, Issue.4
, pp. 1153-1164
-
-
Hegedus, C.1
Ozvegy-Laczka, C.2
Apati, A.3
Magocsi, M.4
Nemet, K.5
Orfi, L.6
Keri, G.7
Katona, M.8
Takats, Z.9
Varadi, A.10
Szakacs, G.11
Sarkadi, B.12
-
129
-
-
67650477192
-
Pharmacokinetic assessment of multiple ATP-binding cassette transporters: The power of combination knockout mice
-
Lagas, J. S.; Vlaming, M. L.; Schinkel, A. H. Pharmacokinetic assessment of multiple ATP-binding cassette transporters: the power of combination knockout mice. Mol. Interv., 2009, 9(3), 136-145.
-
(2009)
Mol. Interv.
, vol.9
, Issue.3
, pp. 136-145
-
-
Lagas, J.S.1
Vlaming, M.L.2
Schinkel, A.H.3
-
130
-
-
77953783419
-
Distribution of gefitinib to the brain is limited by P-glycoprotein (ABCB1) and breast cancer resistance protein (ABCG2)-mediated active efflux
-
Agarwal, S.; Sane, R.; Gallardo, J. L.; Ohlfest, J. R.; Elmquist, W. F. Distribution of gefitinib to the brain is limited by P-glycoprotein (ABCB1) and breast cancer resistance protein (ABCG2)-mediated active efflux. J. Pharmacol. Exp. Ther., 2010, 334(1), 147-155.
-
(2010)
J. Pharmacol. Exp. Ther.
, vol.334
, Issue.1
, pp. 147-155
-
-
Agarwal, S.1
Sane, R.2
Gallardo, J.L.3
Ohlfest, J.R.4
Elmquist, W.F.5
-
131
-
-
59049091078
-
The effect of P-gp (Mdr1a/1b), BCRP (Bcrp1) and P-gp/BCRP inhibitors on the in vivo absorption, distribution, metabolism and excretion of imatinib
-
Oostendorp, R. L.; Buckle, T.; Beijnen, J. H.; van Tellingen, O.; Schellens, J. H. The effect of P-gp (Mdr1a/1b), BCRP (Bcrp1) and P-gp/BCRP inhibitors on the in vivo absorption, distribution, metabolism and excretion of imatinib. Invest. New Drugs, 2009, 27(1), 31-40.
-
(2009)
Invest. New Drugs
, vol.27
, Issue.1
, pp. 31-40
-
-
Oostendorp, R.L.1
Buckle, T.2
Beijnen, J.H.3
Van Tellingen, O.4
Schellens, J.H.5
-
132
-
-
17144381630
-
Pharmacokinetic resistance to imatinib mesylate: Role of the ABC drug pumps ABCG2 (BCRP) and ABCB1 (MDR1) in the oral bioavailability of imatinib
-
Burger, H.; Nooter, K. Pharmacokinetic resistance to imatinib mesylate: role of the ABC drug pumps ABCG2 (BCRP) and ABCB1 (MDR1) in the oral bioavailability of imatinib. Cell Cycle (Georgetown, Tex), 2004, 3(12), 1502-1505.
-
(2004)
Cell. Cycle (Georgetown, Tex)
, vol.3
, Issue.12
, pp. 1502-1505
-
-
Burger, H.1
Nooter, K.2
-
133
-
-
70349142722
-
P-glycoprotein and breast cancer resistance protein influence brain distribution of dasatinib
-
Chen, Y.; Agarwal, S.; Shaik, N. M.; Chen, C.; Yang, Z.; Elmquist, W. F.
-
(2009)
J. Pharmacol. Exp. Ther.
, vol.330
, Issue.3
, pp. 956-963
-
-
Chen, Y.1
Agarwal, S.2
Shaik, N.M.3
Chen, C.4
Yang, Z.5
Elmquist, W.F.6
-
134
-
-
0026584396
-
Cyclosporins as drug resistance modifiers
-
Twentyman, P. R. Cyclosporins as drug resistance modifiers. Biochem. Pharmacol., 1992, 43(1), 109-117.
-
(1992)
Biochem. Pharmacol.
, vol.43
, Issue.1
, pp. 109-117
-
-
Twentyman, P.R.1
-
135
-
-
0345084436
-
The multidrug resistance modulator valspodar (PSC 833) is metabolized by human cytochrome P450 3A. Implications for drug-drug interactions and pharmacological activity of the main metabolite
-
Fischer, V.; Rodriguez-Gascon, A.; Heitz, F.; Tynes, R.; Hauck, C.; Cohen, D.; Vickers, A. E. The multidrug resistance modulator valspodar (PSC 833) is metabolized by human cytochrome P450 3A. Implications for drug-drug interactions and pharmacological activity of the main metabolite. Drug Metab. Dispos.: the biological fate of chemicals, 1998, 26(8), 802-811.
-
(1998)
Drug Metab. Dispos.: The Biological Fate of Chemicals
, vol.26
, Issue.8
, pp. 802-811
-
-
Fischer, V.1
Rodriguez-Gascon, A.2
Heitz, F.3
Tynes, R.4
Hauck, C.5
Cohen, D.6
Vickers, A.E.7
-
136
-
-
0036644903
-
Increased oral bioavailability of topotecan in combination with the breast cancer resistance protein and P-glycoprotein inhibitor GF120918
-
Kruijtzer, C. M.; Beijnen, J. H.; Rosing, H.; ten Bokkel Huinink, W. W.; Schot, M.; Jewell, R. C.; Paul, E. M.; Schellens, J. H. Increased oral bioavailability of topotecan in combination with the breast cancer resistance protein and P-glycoprotein inhibitor GF120918. J. Clin. Oncol., 2002, 20(13), 2943-2950.
-
(2002)
J. Clin. Oncol.
, vol.20
, Issue.13
, pp. 2943-2950
-
-
Kruijtzer, C.M.1
Beijnen, J.H.2
Rosing, H.3
Ten Bokkel Huinink, W.W.4
Schot, M.5
Jewell, R.C.6
Paul, E.M.7
Schellens, J.H.8
-
137
-
-
1942506722
-
Imatinib mesylate is a potent inhibitor of the ABCG2 (BCRP) transporter and reverses resistance to topotecan and SN-38 in vitro
-
Houghton, P. J.; Germain, G. S.; Harwood, F. C.; Schuetz, J. D.; Stewart, C. F.; Buchdunger, E.; Traxler, P. Imatinib mesylate is a potent inhibitor of the ABCG2 (BCRP) transporter and reverses resistance to topotecan and SN-38 in vitro. Cancer Res., 2004, 64(7), 2333-2337.
-
(2004)
Cancer Res.
, vol.64
, Issue.7
, pp. 2333-2337
-
-
Houghton, P.J.1
Germain, G.S.2
Harwood, F.C.3
Schuetz, J.D.4
Stewart, C.F.5
Buchdunger, E.6
Traxler, P.7
-
138
-
-
10744221573
-
Reversal of the resistance to STI571 in human chronic myelogenous leukemia K562 cells
-
Mukai, M.; Che, X. F.; Furukawa, T.; Sumizawa, T.; Aoki, S.; Ren, X. Q.; Haraguchi, M.; Sugimoto, Y.; Kobayashi, M.; Takamatsu, H.; Akiyama, S. Reversal of the resistance to STI571 in human chronic myelogenous leukemia K562 cells. Cancer Sci., 2003, 94(6), 557-563.
-
(2003)
Cancer Sci.
, vol.94
, Issue.6
, pp. 557-563
-
-
Mukai, M.1
Che, X.F.2
Furukawa, T.3
Sumizawa, T.4
Aoki, S.5
Ren, X.Q.6
Haraguchi, M.7
Sugimoto, Y.8
Kobayashi, M.9
Takamatsu, H.10
Akiyama, S.11
-
139
-
-
0037130294
-
Interaction of tyrosine kinase inhibitors with the human multidrug transporter proteins, MDR1 and MRP1
-
Hegedus, T.; Orfi, L.; Seprodi, A.; Varadi, A.; Sarkadi, B.; Keri, G. Interaction of tyrosine kinase inhibitors with the human multidrug transporter proteins, MDR1 and MRP1. Biochim. Biophys. Acta., 2002, 1587 (2-3), 318-325.
-
(2002)
Biochim. Biophys. Acta.
, vol.1587
, Issue.2-3
, pp. 318-325
-
-
Hegedus, T.1
Orfi, L.2
Seprodi, A.3
Varadi, A.4
Sarkadi, B.5
Keri, G.6
-
140
-
-
20344366052
-
The tyrosine kinase inhibitors imatinib and AG957 reverse multidrug resistance in a chronic myelogenous leukemia cell line
-
Yeheskely-Hayon, D.; Regev, R.; Eytan, G. D.; Dann, E. J. The tyrosine kinase inhibitors imatinib and AG957 reverse multidrug resistance in a chronic myelogenous leukemia cell line. Leukemia Res., 2005, 29(7), 793-802.
-
(2005)
Leukemia Res.
, vol.29
, Issue.7
, pp. 793-802
-
-
Yeheskely-Hayon, D.1
Regev, R.2
Eytan, G.D.3
Dann, E.J.4
-
141
-
-
70449564331
-
Imatinib and nilotinib reverse multidrug resistance in cancer cells by inhibiting the efflux activity of the MRP7 (ABCC10)
-
Shen, T.; Kuang, Y. H.; Ashby, C. R.; Lei, Y.; Chen, A.; Zhou, Y.; Chen, X.; Tiwari, A. K.; Hopper-Borge, E.; Ouyang, J.; Chen, Z. S. Imatinib and nilotinib reverse multidrug resistance in cancer cells by inhibiting the efflux activity of the MRP7 (ABCC10). PloS One, 2009, 4(10), e7520.
-
(2009)
PloS One
, vol.4
, Issue.10
-
-
Shen, T.1
Kuang, Y.H.2
Ashby, C.R.3
Lei, Y.4
Chen, A.5
Zhou, Y.6
Chen, X.7
Tiwari, A.K.8
Hopper-Borge, E.9
Ouyang, J.10
Chen, Z.S.11
-
142
-
-
23744502215
-
Gefitinib, an EGFR tyrosine kinase inhibitor, directly inhibits the function of P-glycoprotein in multidrug resistant cancer cells
-
Kitazaki, T.; Oka, M.; Nakamura, Y.; Tsurutani, J.; Doi, S.; Yasunaga, M.; Takemura, M.; Yabuuchi, H.; Soda, H.; Kohno, S. Gefitinib, an EGFR tyrosine kinase inhibitor, directly inhibits the function of P-glycoprotein in multidrug resistant cancer cells. Lung Cancer (Amsterdam, Netherlands), 2005, 49(3), 337-343.
-
(2005)
Lung Cancer (Amsterdam, Netherlands)
, vol.49
, Issue.3
, pp. 337-343
-
-
Kitazaki, T.1
Oka, M.2
Nakamura, Y.3
Tsurutani, J.4
Doi, S.5
Yasunaga, M.6
Takemura, M.7
Yabuuchi, H.8
Soda, H.9
Kohno, S.10
-
143
-
-
13944269488
-
Gefitinib ("Iressa", ZD1839), an epidermal growth factor receptor tyrosine kinase inhibitor, reverses breast cancer resistance protein/ABCG2-mediated drug resistance
-
Nakamura, Y.; Oka, M.; Soda, H.; Shiozawa, K.; Yoshikawa, M.; Itoh, A.; Ikegami, Y.; Tsurutani, J.; Nakatomi, K.; Kitazaki, T.; Doi, S.; Yoshida, H.; Kohno, S. Gefitinib ("Iressa", ZD1839), an epidermal growth factor receptor tyrosine kinase inhibitor, reverses breast cancer resistance protein/ABCG2-mediated drug resistance. Cancer Res., 2005, 65(4), 1541-1546.
-
(2005)
Cancer Res.
, vol.65
, Issue.4
, pp. 1541-1546
-
-
Nakamura, Y.1
Oka, M.2
Soda, H.3
Shiozawa, K.4
Yoshikawa, M.5
Itoh, A.6
Ikegami, Y.7
Tsurutani, J.8
Nakatomi, K.9
Kitazaki, T.10
Doi, S.11
Yoshida, H.12
Kohno, S.13
-
144
-
-
52649118041
-
Gefitinib induction of in vivo detectable signals by Bcl-2/Bcl-xL modulation of inositol trisphosphate receptor type 3
-
Zannetti, A.; Iommelli, F.; Fonti, R.; Papaccioli, A.; Sommella, J.; Lettieri, A.; Pirozzi, G.; Bianco, R.; Tortora, G.; Salvatore, M.; Del Vecchio, S. Gefitinib induction of in vivo detectable signals by Bcl-2/Bcl-xL modulation of inositol trisphosphate receptor type 3. Clin. Cancer Res,, 2008, 14(16), 5209-5219.
-
(2008)
Clin. Cancer Res.
, vol.14
, Issue.16
, pp. 5209-5219
-
-
Zannetti, A.1
Iommelli, F.2
Fonti, R.3
Papaccioli, A.4
Sommella, J.5
Lettieri, A.6
Pirozzi, G.7
Bianco, R.8
Tortora, G.9
Salvatore, M.10
Del Vecchio, S.11
-
145
-
-
59649129538
-
Sunitinib (Sutent, SU11248), a small-molecule receptor tyrosine kinase inhibitor, blocks function of the ATP-binding cassette (ABC) transporters P-glycoprotein (ABCB1) and ABCG2
-
Shukla, S.; Robey, R. W.; Bates, S. E.; Ambudkar, S. V. Sunitinib (Sutent, SU11248), a small-molecule receptor tyrosine kinase inhibitor, blocks function of the ATP-binding cassette (ABC) transporters P-glycoprotein (ABCB1) and ABCG2. Drug Metab. Dispos.: the biological fate of chemicals, 2009, 37(2), 359-365.
-
(2009)
Drug Metab. Dispos.: The Biological Fate of Chemicals
, vol.37
, Issue.2
, pp. 359-365
-
-
Shukla, S.1
Robey, R.W.2
Bates, S.E.3
Ambudkar, S.V.4
-
146
-
-
70149084335
-
Substrate-dependent bidirectional modulation of P-glycoprotein-mediated drug resistance by erlotinib
-
Noguchi, K.; Kawahara, H.; Kaji, A.; Katayama, K.; Mitsuhashi, J.; Sugimoto, Y. Substrate-dependent bidirectional modulation of P-glycoprotein-mediated drug resistance by erlotinib. Cancer Sci., 2009, 100(9), 1701-1707.
-
(2009)
Cancer Sci.
, vol.100
, Issue.9
, pp. 1701-1707
-
-
Noguchi, K.1
Kawahara, H.2
Kaji, A.3
Katayama, K.4
Mitsuhashi, J.5
Sugimoto, Y.6
-
147
-
-
36348967305
-
Erlotinib (Tarceva, OSI-774) antagonizes ATP-binding cassette subfamily B member 1 and ATP-binding cassette subfamily G member 2-mediated drug resistance
-
Shi, Z.; Peng, X. X.; Kim, I. W.; Shukla, S.; Si, Q. S.; Robey, R. W.; Bates, S. E.; Shen, T.; Ashby, C. R., Jr.; Fu, L. W.; Ambudkar, S. V.; Chen, Z. S. Erlotinib (Tarceva, OSI-774) antagonizes ATP-binding cassette subfamily B member 1 and ATP-binding cassette subfamily G member 2-mediated drug resistance. Cancer Res., 2007, 67(22), 11012-11020.
-
(2007)
Cancer Res.
, vol.67
, Issue.22
, pp. 11012-11020
-
-
Shi, Z.1
Peng, X.X.2
Kim, I.W.3
Shukla, S.4
Si, Q.S.5
Robey, R.W.6
Bates, S.E.7
Shen, T.8
Ashby Jr., C.R.9
Fu, L.W.10
Ambudkar, S.V.11
Chen, Z.S.12
-
148
-
-
54249157033
-
Lapatinib (Tykerb, GW572016) reverses multidrug resistance in cancer cells by inhibiting the activity of ATP-binding cassette subfamily B member 1 and G member 2
-
Dai, C. L.; Tiwari, A. K.; Wu, C. P.; Su, X. D.; Wang, S. R.; Liu, D. G.; Ashby, C. R., Jr.; Huang, Y.; Robey, R. W.; Liang, Y. J.; Chen, L. M.; Shi, C. J.; Ambudkar, S. V.; Chen, Z. S.; Fu, L. W. Lapatinib (Tykerb, GW572016) reverses multidrug resistance in cancer cells by inhibiting the activity of ATP-binding cassette subfamily B member 1 and G member 2. Cancer Res., 2008, 68(19), 7905-7914.
-
(2008)
Cancer Res.
, vol.68
, Issue.19
, pp. 7905-7914
-
-
Dai, C.L.1
Tiwari, A.K.2
Wu, C.P.3
Su, X.D.4
Wang, S.R.5
Liu, D.G.6
Ashby Jr., C.R.7
Huang, Y.8
Robey, R.W.9
Liang, Y.J.10
Chen, L.M.11
Shi, C.J.12
Ambudkar, S.V.13
Chen, Z.S.14
Fu, L.W.15
-
149
-
-
65649084180
-
Nilotinib (AMN107, Tasigna) reverses multidrug resistance by inhibiting the activity of the ABCB1/Pgp and ABCG2/BCRP/MXR transporters
-
Tiwari, A. K.; Sodani, K.; Wang, S. R.; Kuang, Y. H.; Ashby, C. R., Jr.; Chen, X.; Chen, Z. S. Nilotinib (AMN107, Tasigna) reverses multidrug resistance by inhibiting the activity of the ABCB1/Pgp and ABCG2/BCRP/MXR transporters. Biochem. Pharmacol., 2009, 78(2), 153-161.
-
(2009)
Biochem. Pharmacol.
, vol.78
, Issue.2
, pp. 153-161
-
-
Tiwari, A.K.1
Sodani, K.2
Wang, S.R.3
Kuang, Y.H.4
Ashby Jr., C.R.5
Chen, X.6
Chen, Z.S.7
-
150
-
-
71749112181
-
Lapatinib and erlotinib are potent reversal agents for MRP7 (ABCC10)-mediated multidrug resistance
-
Kuang, Y. H.; Shen, T.; Chen, X.; Sodani, K.; Hopper-Borge, E.; Tiwari, A. K.; Lee, J. W.; Fu, L. W.; Chen, Z. S. Lapatinib and erlotinib are potent reversal agents for MRP7 (ABCC10)-mediated multidrug resistance. Biochem. Pharmacol., 2010, 79(2), 154-161.
-
(2010)
Biochem. Pharmacol.
, vol.79
, Issue.2
, pp. 154-161
-
-
Kuang, Y.H.1
Shen, T.2
Chen, X.3
Sodani, K.4
Hopper-Borge, E.5
Tiwari, A.K.6
Lee, J.W.7
Fu, L.W.8
Chen, Z.S.9
-
151
-
-
62849124784
-
The epidermal growth factor tyrosine kinase inhibitor AG1478 and erlotinib reverse ABCG2-mediated drug resistance
-
Shi, Z.; Parmar, S.; Peng, X. X.; Shen, T.; Robey, R. W.; Bates, S. E.; Fu, L. W.; Shao, Y.; Chen, Y. M.; Zang, F.; Chen, Z. S. The epidermal growth factor tyrosine kinase inhibitor AG1478 and erlotinib reverse ABCG2-mediated drug resistance. Oncol. Rep., 2009, 21(2), 483-489.
-
(2009)
Oncol. Rep.
, vol.21
, Issue.2
, pp. 483-489
-
-
Shi, Z.1
Parmar, S.2
Peng, X.X.3
Shen, T.4
Robey, R.W.5
Bates, S.E.6
Fu, L.W.7
Shao, Y.8
Chen, Y.M.9
Zang, F.10
Chen, Z.S.11
-
152
-
-
65449152867
-
Vandetanib (Zactima, ZD6474) antagonizes ABCC1-and ABCG2-mediated multidrug resistance by inhibition of their transport function
-
Zheng, L. S.; Wang, F.; Li, Y. H.; Zhang, X.; Chen, L. M.; Liang, Y. J.; Dai, C. L.; Yan, Y. Y.; Tao, L. Y.; Mi, Y. J.; Yang, A. K.; To, K. K.; Fu, L. W. Vandetanib (Zactima, ZD6474) antagonizes ABCC1-and ABCG2-mediated multidrug resistance by inhibition of their transport function. PloS One, 2009, 4(4), e5172.
-
(2009)
PloS One
, vol.4
, Issue.4
-
-
Zheng, L.S.1
Wang, F.2
Li, Y.H.3
Zhang, X.4
Chen, L.M.5
Liang, Y.J.6
Dai, C.L.7
Yan, Y.Y.8
Tao, L.Y.9
Mi, Y.J.10
Yang, A.K.11
To, K.K.12
Fu, L.W.13
-
153
-
-
33745953739
-
Complex interaction of BCRP/ABCG2 and imatinib in BCR-ABL-expressing cells: BCRP-mediated resistance to imatinib is attenuated by imatinib-induced reduction of BCRP expression
-
Nakanishi, T.; Shiozawa, K.; Hassel, B. A.; Ross, D. D. Complex interaction of BCRP/ABCG2 and imatinib in BCR-ABL-expressing cells: BCRP-mediated resistance to imatinib is attenuated by imatinib-induced reduction of BCRP expression. Blood, 2006, 108(2), 678-684.
-
(2006)
Blood
, vol.108
, Issue.2
, pp. 678-684
-
-
Nakanishi, T.1
Shiozawa, K.2
Hassel, B.A.3
Ross, D.D.4
-
154
-
-
77954892297
-
Comparison of ATP-binding cassette transporter interactions with the tyrosine kinase inhibitors imatinib, nilotinib, and dasatinib
-
Dohse, M.; Scharenberg, C.; Shukla, S.; Robey, R. W.; Volkmann, T.; Deeken, J. F.; Brendel, C.; Ambudkar, S. V.; Neubauer, A.; Bates, S. E. Comparison of ATP-binding cassette transporter interactions with the tyrosine kinase inhibitors imatinib, nilotinib, and dasatinib. Drug Metab. Dispos.: the biological fate of chemicals, 2010, 38(8), 1371-1380.
-
(2010)
Drug Metab. Dispos.: The Biological Fate of Chemicals
, vol.38
, Issue.8
, pp. 1371-1380
-
-
Dohse, M.1
Scharenberg, C.2
Shukla, S.3
Robey, R.W.4
Volkmann, T.5
Deeken, J.F.6
Brendel, C.7
Ambudkar, S.V.8
Neubauer, A.9
Bates, S.E.10
-
155
-
-
25144450089
-
Chronic imatinib mesylate exposure leads to reduced intracellular drug accumulation by induction of the ABCG2 (BCRP) and ABCB1 (MDR1) drug transport pumps
-
Burger, H.; van Tol, H.; Brok, M.; Wiemer, E. A.; de Bruijn, E. A.; Guetens, G.; de Boeck, G.; Sparreboom, A.; Verweij, J.; Nooter, K. Chronic imatinib mesylate exposure leads to reduced intracellular drug accumulation by induction of the ABCG2 (BCRP) and ABCB1 (MDR1) drug transport pumps. Cancer Biol. Ther., 2005, 4(7), 747-752.
-
(2005)
Cancer Biol. Ther.
, vol.4
, Issue.7
, pp. 747-752
-
-
Burger, H.1
Van Tol, H.2
Brok, M.3
Wiemer, E.A.4
De Bruijn, E.A.5
Guetens, G.6
De Boeck, G.7
Sparreboom, A.8
Verweij, J.9
Nooter, K.10
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