-
1
-
-
10744233716
-
Imatinib compared with interferon and low-dose cytarabine for newly diagnosed chronic-phase chronic myeloid leukemia
-
10.1056/NEJMoa022457 12637609
-
O'Brien SG, Guilhot F, Larson RA et al (2003) Imatinib compared with interferon and low-dose cytarabine for newly diagnosed chronic-phase chronic myeloid leukemia. N Engl J Med 348:994-1004
-
(2003)
N Engl J Med
, vol.348
, pp. 994-1004
-
-
O'Brien, S.G.1
Guilhot, F.2
Larson, R.A.3
-
2
-
-
77953725855
-
Dasatinib versus imatinib in newly diagnosed chronicphase chronic myeloid leukemia
-
10.1056/NEJMoa1002315 1:CAS:528:DC%2BC3cXnvVaktbY%3D 20525995
-
Kantarjian H, Shah NP, Hochhaus A et al (2010) Dasatinib versus imatinib in newly diagnosed chronicphase chronic myeloid leukemia. N Engl J Med 362:2260-2270
-
(2010)
N Engl J Med
, vol.362
, pp. 2260-2270
-
-
Kantarjian, H.1
Shah, N.P.2
Hochhaus, A.3
-
3
-
-
77953691179
-
Nilotinib versus imatinib for newly diagnosed chronic myeloid leukemia
-
10.1056/NEJMoa0912614 1:CAS:528:DC%2BC3cXnvVaktbk%3D 20525993
-
Saglio G, Kim DW, Issaragrisil S et al (2010) Nilotinib versus imatinib for newly diagnosed chronic myeloid leukemia. N Engl J Med 362:2251-2259
-
(2010)
N Engl J Med
, vol.362
, pp. 2251-2259
-
-
Saglio, G.1
Kim, D.W.2
Issaragrisil, S.3
-
4
-
-
84875849302
-
Multifaceted mechanisms for cell survival and drug targeting in chronic myelogenous leukemia
-
10.2174/156800913804486638 1:CAS:528:DC%2BC3sXktFersbg%3D
-
Kuroda J, Shimura Y, Yamamoto-Sugitani M, Sasaki N, Taniwaki M (2013) Multifaceted mechanisms for cell survival and drug targeting in chronic myelogenous leukemia. Curr Cancer Drug Targ 13:69-79
-
(2013)
Curr Cancer Drug Targ
, vol.13
, pp. 69-79
-
-
Kuroda, J.1
Shimura, Y.2
Yamamoto-Sugitani, M.3
Sasaki, N.4
Taniwaki, M.5
-
5
-
-
33749510073
-
Bim and Bad mediate imatinib-induced killing of Bcr/Abl+ leukemic cells, and resistance due to their loss is overcome by a BH3 mimetic
-
10.1073/pnas.0606176103 1:CAS:528:DC%2BD28XhtVygsr%2FK 16997913
-
Kuroda J, Puthalakath H, Cragg MS et al (2006) Bim and Bad mediate imatinib-induced killing of Bcr/Abl+ leukemic cells, and resistance due to their loss is overcome by a BH3 mimetic. Proc Natl Acad Sci USA 103:14907-14912
-
(2006)
Proc Natl Acad Sci USA
, vol.103
, pp. 14907-14912
-
-
Kuroda, J.1
Puthalakath, H.2
Cragg, M.S.3
-
6
-
-
34548039481
-
Apoptosis-based dual molecular targeting by INNO-406, a second-generation Bcr-Abl inhibitor, and ABT-737, an inhibitor of antiapoptotic Bcl-2 proteins, against Bcr-Abl-positive leukemia
-
10.1038/sj.cdd.4402168 1:CAS:528:DC%2BD2sXptFymtbs%3D 17510658
-
Kuroda J, Kimura S, Strasser A et al (2007) Apoptosis-based dual molecular targeting by INNO-406, a second-generation Bcr-Abl inhibitor, and ABT-737, an inhibitor of antiapoptotic Bcl-2 proteins, against Bcr-Abl-positive leukemia. Cell Death Differ 14:1667-1677
-
(2007)
Cell Death Differ
, vol.14
, pp. 1667-1677
-
-
Kuroda, J.1
Kimura, S.2
Strasser, A.3
-
7
-
-
33845893074
-
Phosphorylation of the ATP-binding loop directs oncogenicity of drug-resistant BCR-ABL mutants
-
10.1073/pnas.0609239103 1:CAS:528:DC%2BD2sXhs1yrtg%3D%3D 17164333
-
Skaggs BJ, Gorre ME, Ryvkin A et al (2006) Phosphorylation of the ATP-binding loop directs oncogenicity of drug-resistant BCR-ABL mutants. Proc Natl Acad Sci USA 103:19466-19471
-
(2006)
Proc Natl Acad Sci USA
, vol.103
, pp. 19466-19471
-
-
Skaggs, B.J.1
Gorre, M.E.2
Ryvkin, A.3
-
8
-
-
0035800507
-
Clinical resistance to STI-571 cancer therapy caused by BCR-ABL gene mutation or amplification
-
10.1126/science.1062538 1:CAS:528:DC%2BD3MXlvVKrsbs%3D 11423618
-
Gorre ME, Mohammed M, Ellwood K et al (2001) Clinical resistance to STI-571 cancer therapy caused by BCR-ABL gene mutation or amplification. Science 293:876-880
-
(2001)
Science
, vol.293
, pp. 876-880
-
-
Gorre, M.E.1
Mohammed, M.2
Ellwood, K.3
-
9
-
-
80054816404
-
Galectin-3 (Gal-3) induced by leukemia microenvironment promotes drug resistance and bone marrow lodgment in chronic myelogenous leukemia
-
10.1073/pnas.1111138108 1:CAS:528:DC%2BC3MXhtl2ltb3N 21987825
-
Yamamoto-Sugitani M, Kuroda J, Ashihara E et al (2011) Galectin-3 (Gal-3) induced by leukemia microenvironment promotes drug resistance and bone marrow lodgment in chronic myelogenous leukemia. Proc Natl Acad Sci USA 108:17468-17473
-
(2011)
Proc Natl Acad Sci USA
, vol.108
, pp. 17468-17473
-
-
Yamamoto-Sugitani, M.1
Kuroda, J.2
Ashihara, E.3
-
10
-
-
54049135563
-
The Bcr-Abl kinase inhibitor INNO-406 induces autophagy and different modes of cell death execution in Bcr-Abl-positive leukemias
-
10.1038/cdd.2008.107 1:CAS:528:DC%2BD1cXht1aru7zO 18617896
-
Kamitsuji Y, Kuroda J, Kimura S et al (2008) The Bcr-Abl kinase inhibitor INNO-406 induces autophagy and different modes of cell death execution in Bcr-Abl-positive leukemias. Cell Death Differ 15:1712-1722
-
(2008)
Cell Death Differ
, vol.15
, pp. 1712-1722
-
-
Kamitsuji, Y.1
Kuroda, J.2
Kimura, S.3
-
11
-
-
66449122303
-
Targeting autophagy potentiates tyrosine kinase inhibitor-induced cell death in Philadelphia chromosome-positive cells, including primary CML stem cells
-
10.1172/JCI35660 1:CAS:528:DC%2BD1MXlsFyrsLY%3D 19363292
-
Bellodi C, Lidonnici MR, Hamilton A et al (2009) Targeting autophagy potentiates tyrosine kinase inhibitor-induced cell death in Philadelphia chromosome-positive cells, including primary CML stem cells. J Clin Invest 119:1109-1123
-
(2009)
J Clin Invest
, vol.119
, pp. 1109-1123
-
-
Bellodi, C.1
Lidonnici, M.R.2
Hamilton, A.3
-
12
-
-
78650380694
-
Autophagy induction by Bcr-Abl-expressing cells facilitates their recovery from a targeted or nontargeted treatment
-
10.1002/ajh.21914 1:CAS:528:DC%2BC3MXhs1alsbk%3D 21132731
-
Crowley LC, Elzinga BM, O'Sullivan GC, McKenna SL (2011) Autophagy induction by Bcr-Abl-expressing cells facilitates their recovery from a targeted or nontargeted treatment. Am J Hematol 86:38-47
-
(2011)
Am J Hematol
, vol.86
, pp. 38-47
-
-
Crowley, L.C.1
Elzinga, B.M.2
O'Sullivan, G.C.3
McKenna, S.L.4
-
13
-
-
36749033284
-
Characterization of cancer stem cells in chronic myeloid leukaemia
-
10.1042/BST0351347 17956348
-
Jørgensen HG, Holyoake TL (2007) Characterization of cancer stem cells in chronic myeloid leukaemia. Biochem Soc Trans 35:1347-1351
-
(2007)
Biochem Soc Trans
, vol.35
, pp. 1347-1351
-
-
Jørgensen, H.G.1
Holyoake, T.L.2
-
14
-
-
3943088431
-
Granulocyte-macrophage progenitors as candidate leukemic stem cells in blast-crisis CML
-
10.1056/NEJMoa040258 1:CAS:528:DC%2BD2cXms1Oktbg%3D 15306667
-
Jamieson CH, Ailles LE, Dylla SJ et al (2004) Granulocyte-macrophage progenitors as candidate leukemic stem cells in blast-crisis CML. N Engl J Med 351:657-667
-
(2004)
N Engl J Med
, vol.351
, pp. 657-667
-
-
Jamieson, C.H.1
Ailles, L.E.2
Dylla, S.J.3
-
15
-
-
73949142609
-
Molecular and functional analysis of the stem cell compartment of chronic myelogenous leukemia reveals the presence of a CD34- cell population with intrinsic resistance to imatinib
-
10.1182/blood-2008-08-176016 1:CAS:528:DC%2BC3cXls1arug%3D%3D 19855080
-
Lemoli RM, Salvestrini V, Bianchi E et al (2009) Molecular and functional analysis of the stem cell compartment of chronic myelogenous leukemia reveals the presence of a CD34- cell population with intrinsic resistance to imatinib. Blood 114:5191-5200
-
(2009)
Blood
, vol.114
, pp. 5191-5200
-
-
Lemoli, R.M.1
Salvestrini, V.2
Bianchi, E.3
-
16
-
-
33744486584
-
Dasatinib (BMS-354825) targets an earlier progenitor population than imatinib in primary CML but does not eliminate the quiescent fraction
-
10.1182/blood-2005-07-2947 1:CAS:528:DC%2BD28Xlt1CgtrY%3D 16469872
-
Copland M, Hamilton A, Elrick LJ et al (2006) Dasatinib (BMS-354825) targets an earlier progenitor population than imatinib in primary CML but does not eliminate the quiescent fraction. Blood 107:4532-4539
-
(2006)
Blood
, vol.107
, pp. 4532-4539
-
-
Copland, M.1
Hamilton, A.2
Elrick, L.J.3
-
17
-
-
78650949272
-
Human chronic myeloid leukemia stem cells are insensitive to imatinib despite inhibition of BCR-ABL activity
-
10.1172/JCI35721 1:CAS:528:DC%2BC3MXis1yltA%3D%3D 21157039
-
Corbin AS, Agarwal A, Loriaux M, Cortes J, Deininger MW, Druker BJ (2011) Human chronic myeloid leukemia stem cells are insensitive to imatinib despite inhibition of BCR-ABL activity. J Clin Invest 121:396-409
-
(2011)
J Clin Invest
, vol.121
, pp. 396-409
-
-
Corbin, A.S.1
Agarwal, A.2
Loriaux, M.3
Cortes, J.4
Deininger, M.W.5
Druker, B.J.6
-
18
-
-
77953619656
-
Glyoxalase-I is a novel target against Bcr-Abl+ leukemic cells acquiring stem-like characteristics in a hypoxic environment
-
10.1038/cdd.2010.6 1:CAS:528:DC%2BC3cXnsVOgurk%3D 20139893
-
Takeuchi M, Kimura S, Kuroda J et al (2010) Glyoxalase-I is a novel target against Bcr-Abl+ leukemic cells acquiring stem-like characteristics in a hypoxic environment. Cell Death Differ 17:1211-1220
-
(2010)
Cell Death Differ
, vol.17
, pp. 1211-1220
-
-
Takeuchi, M.1
Kimura, S.2
Kuroda, J.3
-
19
-
-
79958732559
-
Loss or inhibition of stromal-derived PlGF prolongs survival of mice with imatinib-resistant Bcr-Abl1(+) leukemia
-
10.1016/j.ccr.2011.05.007 1:CAS:528:DC%2BC3MXnsVClu7s%3D 21665148
-
Schmidt T, Kharabi Masouleh B, Loges S et al (2011) Loss or inhibition of stromal-derived PlGF prolongs survival of mice with imatinib-resistant Bcr-Abl1(+) leukemia. Cancer Cell 19:740-753
-
(2011)
Cancer Cell
, vol.19
, pp. 740-753
-
-
Schmidt, T.1
Kharabi Masouleh, B.2
Loges, S.3
-
20
-
-
0034893416
-
Cell adhesion-mediated drug resistance (CAM-DR) protects the K562 chronic myelogenous leukemia cell line from apoptosis induced by BCR/ABL inhibition, cytotoxic drugs, and gamma-irradiation
-
10.1038/sj.leu.2402179 1:CAS:528:DC%2BD3MXms1Ort7c%3D 11480565
-
Damiano JS, Hazlehurst LA, Dalton WS (2001) Cell adhesion-mediated drug resistance (CAM-DR) protects the K562 chronic myelogenous leukemia cell line from apoptosis induced by BCR/ABL inhibition, cytotoxic drugs, and gamma-irradiation. Leukemia 15:1232-1239
-
(2001)
Leukemia
, vol.15
, pp. 1232-1239
-
-
Damiano, J.S.1
Hazlehurst, L.A.2
Dalton, W.S.3
-
21
-
-
38349086394
-
CXCR4 up-regulation by imatinib induces chronic myelogenous leukemia (CML) cell migration to bone marrow stroma and promotes survival of quiescent CML cells
-
10.1158/1535-7163.MCT-07-0042 1:CAS:528:DC%2BD1cXmsVygug%3D%3D 18202009
-
Jin L, Tabe Y, Konoplev S et al (2008) CXCR4 up-regulation by imatinib induces chronic myelogenous leukemia (CML) cell migration to bone marrow stroma and promotes survival of quiescent CML cells. Mol Cancer Ther 7:48-58
-
(2008)
Mol Cancer Ther
, vol.7
, pp. 48-58
-
-
Jin, L.1
Tabe, Y.2
Konoplev, S.3
-
22
-
-
33847407174
-
Adaptive secretion of granulocyte-macrophage colony-stimulating factor (GM-CSF) mediates imatinib and nilotinib resistance in BCR/ABL+ progenitors via JAK-2/STAT-5 pathway activation
-
10.1182/blood-2006-08-040022 1:CAS:528:DC%2BD2sXjtFequ70%3D 17090651
-
Wang Y, Cai D, Brendel C et al (2007) Adaptive secretion of granulocyte-macrophage colony-stimulating factor (GM-CSF) mediates imatinib and nilotinib resistance in BCR/ABL+ progenitors via JAK-2/STAT-5 pathway activation. Blood 109:2147-2155
-
(2007)
Blood
, vol.109
, pp. 2147-2155
-
-
Wang, Y.1
Cai, D.2
Brendel, C.3
-
23
-
-
84862777672
-
A common BIM deletion polymorphism mediates intrinsic resistance and inferior responses to tyrosine kinase inhibitors in cancer
-
10.1038/nm.2713 1:CAS:528:DC%2BC38XktVaksbk%3D 22426421
-
Ng KP, Hillmer AM, Chuah CT et al (2012) A common BIM deletion polymorphism mediates intrinsic resistance and inferior responses to tyrosine kinase inhibitors in cancer. Nat Med 18:521-528
-
(2012)
Nat Med
, vol.18
, pp. 521-528
-
-
Ng, K.P.1
Hillmer, A.M.2
Chuah, C.T.3
-
24
-
-
79959252521
-
Cancerous inhibitor of PP2A (CIP2A) at diagnosis of chronic myeloid leukemia is a critical determinant of disease progression
-
10.1182/blood-2010-08-304477 1:CAS:528:DC%2BC3MXot1Gqt7o%3D 21490338
-
Lucas CM, Harris RJ, Giannoudis A, Copland M, Slupsky JR, Clark RE (2011) Cancerous inhibitor of PP2A (CIP2A) at diagnosis of chronic myeloid leukemia is a critical determinant of disease progression. Blood 117:6660-6668
-
(2011)
Blood
, vol.117
, pp. 6660-6668
-
-
Lucas, C.M.1
Harris, R.J.2
Giannoudis, A.3
Copland, M.4
Slupsky, J.R.5
Clark, R.E.6
-
25
-
-
78049528573
-
Discontinuation of imatinib in patients with chronic myeloid leukaemia who have maintained complete molecular remission for at least 2 years: The prospective, multicentre stop imatinib (STIM) trial
-
10.1016/S1470-2045(10)70233-3 1:CAS:528:DC%2BC3cXhtlKmtrnP 20965785
-
Mahon FX, Réa D, Guilhot J et al (2010) Discontinuation of imatinib in patients with chronic myeloid leukaemia who have maintained complete molecular remission for at least 2 years: the prospective, multicentre stop imatinib (STIM) trial. Lancet Oncol 11:1029-1035
-
(2010)
Lancet Oncol
, vol.11
, pp. 1029-1035
-
-
Mahon, F.X.1
Réa, D.2
Guilhot, J.3
-
26
-
-
77958012952
-
Patients with chronic myeloid leukemia who maintain a complete molecular response after stopping imatinib treatment have evidence of persistent leukemia by DNA PCR
-
10.1038/leu.2010.185 1:CAS:528:DC%2BC3cXht1OmtbjN 20811403
-
Ross DM, Branford S, Seymour JF et al (2010) Patients with chronic myeloid leukemia who maintain a complete molecular response after stopping imatinib treatment have evidence of persistent leukemia by DNA PCR. Leukemia 24:1719-1724
-
(2010)
Leukemia
, vol.24
, pp. 1719-1724
-
-
Ross, D.M.1
Branford, S.2
Seymour, J.F.3
-
27
-
-
84855677061
-
Allogeneic stem cell transplant for chronic myeloid leukemia as a still promising option in the era of the new target therapy
-
10.2298/VSP1201037S 22397295
-
Stamatović D, Balint B, Tukić L et al (2012) Allogeneic stem cell transplant for chronic myeloid leukemia as a still promising option in the era of the new target therapy. Vojnosanit Pregl 69:37-42
-
(2012)
Vojnosanit Pregl
, vol.69
, pp. 37-42
-
-
Stamatović, D.1
Balint, B.2
Tukić, L.3
-
28
-
-
0035252894
-
Protein phosphatase 2A: A highly regulated family of serine/threonine phosphatases implicated in cell growth and signalling
-
10.1042/0264-6021:3530417 1:CAS:528:DC%2BD3MXhtlOrs70%3D 11171037
-
Janssens V, Goris J (2001) Protein phosphatase 2A: a highly regulated family of serine/threonine phosphatases implicated in cell growth and signalling. Biochem J 353:417-439
-
(2001)
Biochem J
, vol.353
, pp. 417-439
-
-
Janssens, V.1
Goris, J.2
-
29
-
-
12344308021
-
PP2A: The expected tumor suppressor
-
10.1016/j.gde.2004.12.004 1:CAS:528:DC%2BD2MXmvFekug%3D%3D 15661531
-
Janssens V, Goris J, Van Hoof C (2005) PP2A: the expected tumor suppressor. Curr Opin Genet Dev 15:34-41
-
(2005)
Curr Opin Genet Dev
, vol.15
, pp. 34-41
-
-
Janssens, V.1
Goris, J.2
Van Hoof, C.3
-
30
-
-
0036494268
-
Marked Prevention of Tumor Growth and Metastasis by a Novel Immunosuppressive Agent, FTY720, in Mouse Breast Cancer Models
-
1:CAS:528:DC%2BD38Xit1Khur4%3D 11888913
-
Azuma H, Takahara S, Ichimaru N et al (2002) Marked Prevention of Tumor Growth and Metastasis by a Novel Immunosuppressive Agent, FTY720, in Mouse Breast Cancer Models. Cancer Res 62:1410-1419
-
(2002)
Cancer Res
, vol.62
, pp. 1410-1419
-
-
Azuma, H.1
Takahara, S.2
Ichimaru, N.3
-
31
-
-
0034708257
-
Low frequency of alterations of the alpha (PPP2R1A) and beta (PPP2R1B) isoforms of the subunit A of the serine-threonine phosphatase 2A in human neoplasms
-
10.1038/sj.onc.1203389 1:CAS:528:DC%2BD3cXitFeqtLY%3D 10713707
-
Calin GA, di Iasio MG, Caprini E et al (2000) Low frequency of alterations of the alpha (PPP2R1A) and beta (PPP2R1B) isoforms of the subunit A of the serine-threonine phosphatase 2A in human neoplasms. Oncogene 19:1191-1195
-
(2000)
Oncogene
, vol.19
, pp. 1191-1195
-
-
Calin, G.A.1
Di Iasio, M.G.2
Caprini, E.3
-
32
-
-
3142688531
-
Reduced expression of the regulatory A subunit of serine/threonine protein phosphatase 2A in human breast cancer MCF-7 cells
-
1:CAS:528:DC%2BD3sXptFCktbY%3D 14532964
-
Suzuki K, Takahashi K (2003) Reduced expression of the regulatory A subunit of serine/threonine protein phosphatase 2A in human breast cancer MCF-7 cells. Int J Oncol 23:1263-1268
-
(2003)
Int J Oncol
, vol.23
, pp. 1263-1268
-
-
Suzuki, K.1
Takahashi, K.2
-
33
-
-
0033916381
-
Alterations of the PPP2R1B gene located at 11q23 in human colorectal cancers
-
10.1136/gut.47.2.268 1:CAS:528:DC%2BD3cXlvVygu7o%3D 10896920
-
Takagi Y, Futamura M, Yamaguchi K, Aoki S, Takahashi T, Saji S (2000) Alterations of the PPP2R1B gene located at 11q23 in human colorectal cancers. Gut 47:268-271
-
(2000)
Gut
, vol.47
, pp. 268-271
-
-
Takagi, Y.1
Futamura, M.2
Yamaguchi, K.3
Aoki, S.4
Takahashi, T.5
Saji, S.6
-
34
-
-
27644569730
-
The tumor suppressor PP2A is functionally inactivated in blast crisis CML through the inhibitory activity of the BCR/ABL-regulated SET protein
-
10.1016/j.ccr.2005.10.015 1:CAS:528:DC%2BD2MXht12gsbvJ 16286244
-
Neviani P, Santhanam R, Trotta R et al (2005) The tumor suppressor PP2A is functionally inactivated in blast crisis CML through the inhibitory activity of the BCR/ABL-regulated SET protein. Cancer Cell 8:355-368
-
(2005)
Cancer Cell
, vol.8
, pp. 355-368
-
-
Neviani, P.1
Santhanam, R.2
Trotta, R.3
-
35
-
-
77955799815
-
Oral fingolimod (FTY720) for relapsing multiple sclerosis
-
10.1056/NEJMoa052643 1:CAS:528:DC%2BD28XpsFKku78%3D 16971719
-
Kappos L, Antel J, Comi G et al (2006) Oral fingolimod (FTY720) for relapsing multiple sclerosis. N Engl J Med 355:1124-1140
-
(2006)
N Engl J Med
, vol.355
, pp. 1124-1140
-
-
Kappos, L.1
Antel, J.2
Comi, G.3
-
36
-
-
76149140914
-
Oral fingolimod or intramuscular interferon for relapsing multiple sclerosis
-
10.1056/NEJMoa0907839 1:CAS:528:DC%2BC3cXhvVWrsbk%3D 20089954
-
Cohen JA, Barkhof F, Comi G et al (2010) Oral fingolimod or intramuscular interferon for relapsing multiple sclerosis. N Engl J Med 362:402-415
-
(2010)
N Engl J Med
, vol.362
, pp. 402-415
-
-
Cohen, J.A.1
Barkhof, F.2
Comi, G.3
-
37
-
-
85027946124
-
Relapse and disability outcomes in patients with multiple sclerosis treated with fingolimod: Subgroup analyses of the double-blind, randomised, placebo-controlled FREEDOMS study
-
10.1016/S1474-4422(12)70056-X 1:CAS:528:DC%2BC38XlvFaktL4%3D 22494956
-
Devonshire V, Havrdova E, Radue EW et al (2012) Relapse and disability outcomes in patients with multiple sclerosis treated with fingolimod: subgroup analyses of the double-blind, randomised, placebo-controlled FREEDOMS study. Lancet Neurol 11:420-428
-
(2012)
Lancet Neurol
, vol.11
, pp. 420-428
-
-
Devonshire, V.1
Havrdova, E.2
Radue, E.W.3
-
38
-
-
0037077308
-
The immune modulator FTY720 targets sphingosine 1-phosphate receptors
-
10.1074/jbc.C200176200 1:CAS:528:DC%2BD38Xkslyqtb4%3D 11967257
-
Brinkmann V, Davis MD, Heise CE et al (2002) The immune modulator FTY720 targets sphingosine 1-phosphate receptors. J Biol Chem 277:21453-21457
-
(2002)
J Biol Chem
, vol.277
, pp. 21453-21457
-
-
Brinkmann, V.1
Davis, M.D.2
Heise, C.E.3
-
39
-
-
0037066466
-
Alteration of lymphocyte trafficking by sphingosine-1-phosphate receptor agonists
-
10.1126/science.1070238 1:CAS:528:DC%2BD38XjtVWhsrc%3D 11923495
-
Mandala S, Hajdu R, Bergstrom J et al (2002) Alteration of lymphocyte trafficking by sphingosine-1-phosphate receptor agonists. Science 296:346-349
-
(2002)
Science
, vol.296
, pp. 346-349
-
-
Mandala, S.1
Hajdu, R.2
Bergstrom, J.3
-
40
-
-
1642580757
-
Lymphocyte egress from thymus and peripheral lymphoid organs is dependent on S1P receptor 1
-
10.1038/nature02284 1:CAS:528:DC%2BD2cXltFCguw%3D%3D 14737169
-
Matloubian M, Lo CG, Cinamon G et al (2004) Lymphocyte egress from thymus and peripheral lymphoid organs is dependent on S1P receptor 1. Nature 427:355-360
-
(2004)
Nature
, vol.427
, pp. 355-360
-
-
Matloubian, M.1
Lo, C.G.2
Cinamon, G.3
-
41
-
-
34648832173
-
FTY720, a new alternative for treating blast crisis chronic myelogenous leukemia and Philadelphia chromosome-positive acute lymphocytic leukemia
-
10.1172/JCI31095 1:CAS:528:DC%2BD2sXhtVCms7vM 17717597
-
Neviani P, Santhanam R, Oaks JJ et al (2007) FTY720, a new alternative for treating blast crisis chronic myelogenous leukemia and Philadelphia chromosome-positive acute lymphocytic leukemia. J Clin Invest 117:2408-2421
-
(2007)
J Clin Invest
, vol.117
, pp. 2408-2421
-
-
Neviani, P.1
Santhanam, R.2
Oaks, J.J.3
-
42
-
-
80052653011
-
Therapeutic efficacy of FTY720 in a rat model of NK-cell leukemia
-
10.1182/blood-2011-01-331447 1:CAS:528:DC%2BC3MXht1ansLzK 21768294
-
Liao A, Broeg K, Fox T et al (2011) Therapeutic efficacy of FTY720 in a rat model of NK-cell leukemia. Blood 118:2793-2800
-
(2011)
Blood
, vol.118
, pp. 2793-2800
-
-
Liao, A.1
Broeg, K.2
Fox, T.3
-
43
-
-
38049166147
-
FTY720 demonstrates promising preclinical activity for chronic lymphocytic leukemia and lymphoblastic leukemia/lymphoma
-
10.1182/blood-2006-10-053884 1:CAS:528:DC%2BD1cXjtVKhug%3D%3D 17761520
-
Liu Q, Zhao X, Frissora F et al (2008) FTY720 demonstrates promising preclinical activity for chronic lymphocytic leukemia and lymphoblastic leukemia/lymphoma. Blood 111:275-284
-
(2008)
Blood
, vol.111
, pp. 275-284
-
-
Liu, Q.1
Zhao, X.2
Frissora, F.3
-
44
-
-
77953694847
-
FTY720 shows promising in vitro and in vivo preclinical activity by downmodulating Cyclin D1 and phospho-Akt in mantle cell lymphoma
-
10.1158/1078-0432.CCR-09-2484 1:CAS:528:DC%2BC3cXntlKru7k%3D 20460491
-
Liu Q, Alinari L, Chen CS et al (2010) FTY720 shows promising in vitro and in vivo preclinical activity by downmodulating Cyclin D1 and phospho-Akt in mantle cell lymphoma. Clin Cancer Res 16:3182-3192
-
(2010)
Clin Cancer Res
, vol.16
, pp. 3182-3192
-
-
Liu, Q.1
Alinari, L.2
Chen, C.S.3
-
45
-
-
77954376747
-
Essential requirement for PP2A inhibition by the oncogenic receptor c-KIT suggests PP2A reactivation as a strategy to treat c-KIT+ cancers
-
10.1158/0008-5472.CAN-09-2544 1:CAS:528:DC%2BC3cXot1Wks74%3D 20551067
-
Roberts KG, Smith AM, McDougall F et al (2010) Essential requirement for PP2A inhibition by the oncogenic receptor c-KIT suggests PP2A reactivation as a strategy to treat c-KIT+ cancers. Cancer Res 70:5438-5447
-
(2010)
Cancer Res
, vol.70
, pp. 5438-5447
-
-
Roberts, K.G.1
Smith, A.M.2
McDougall, F.3
-
46
-
-
0030794189
-
An immunosuppressive agent, FTY720, increases intracellular concentration of calcium ion and induces apoptosis in HL-60
-
10.1046/j.1365-2567.1997.d01-2281.x 1:CAS:528:DyaK2sXltFSmt7g%3D 9378500
-
Shinomiya T, Li XK, Amemiya H, Suzuki S (1997) An immunosuppressive agent, FTY720, increases intracellular concentration of calcium ion and induces apoptosis in HL-60. Immunology 91:594-600
-
(1997)
Immunology
, vol.91
, pp. 594-600
-
-
Shinomiya, T.1
Li, X.K.2
Amemiya, H.3
Suzuki, S.4
-
47
-
-
0037051102
-
Anticarcinogenic effect of FTY720 in human prostate carcinoma DU145 cells: Modulation of mitogenic signaling, FAK, cell-cycle entry and apoptosis
-
10.1002/ijc.10178 1:CAS:528:DC%2BD38XhsVSktb8%3D 11857403
-
Permpongkosol S, Wang JD, Takahara S et al (2002) Anticarcinogenic effect of FTY720 in human prostate carcinoma DU145 cells: modulation of mitogenic signaling, FAK, cell-cycle entry and apoptosis. Int J Cancer 98:167-172
-
(2002)
Int J Cancer
, vol.98
, pp. 167-172
-
-
Permpongkosol, S.1
Wang, J.D.2
Takahara, S.3
-
48
-
-
0035674643
-
FTY720: Dissection of membrane receptor-operated, stereospecific effects on cell migration from receptor-independent antiproliferative and apoptotic effects
-
10.1016/S0041-1345(01)02312-0 1:CAS:528:DC%2BD3MXpt1altbo%3D 11750323
-
Brinkmann V, Wilt C, Kristofic C et al (2001) FTY720: dissection of membrane receptor-operated, stereospecific effects on cell migration from receptor-independent antiproliferative and apoptotic effects. Transplant Proc 33:3078-3080
-
(2001)
Transplant Proc
, vol.33
, pp. 3078-3080
-
-
Brinkmann, V.1
Wilt, C.2
Kristofic, C.3
-
49
-
-
3543114272
-
Biologically active sphingolipids in cancer pathogenesis and treatment
-
10.1038/nrc1411 1:CAS:528:DC%2BD2cXmtVOhsb4%3D 15286740
-
Ogretmen B, Hannun YA (2004) Biologically active sphingolipids in cancer pathogenesis and treatment. Nat Rev Cancer 4:604-616
-
(2004)
Nat Rev Cancer
, vol.4
, pp. 604-616
-
-
Ogretmen, B.1
Hannun, Y.A.2
-
50
-
-
6944241423
-
Sphingosine-dependent apoptosis: A unified concept based on multiple mechanisms operating in concert
-
10.1073/pnas.0406536101 1:CAS:528:DC%2BD2cXovVyju7w%3D 15466700
-
Suzuki E, Handa K, Toledo MS, Hakomori S (2004) Sphingosine-dependent apoptosis: a unified concept based on multiple mechanisms operating in concert. Proc Natl Acad Sci USA 101:14788-14793
-
(2004)
Proc Natl Acad Sci USA
, vol.101
, pp. 14788-14793
-
-
Suzuki, E.1
Handa, K.2
Toledo, M.S.3
Hakomori, S.4
-
51
-
-
84871375573
-
RSK2Ser227 at N-terminal kinase domain is a potential therapeutic target for multiple myeloma
-
10.1158/1535-7163.MCT-12-0605 1:CAS:528:DC%2BC38XhvVSqt7nN 23012246
-
Shimura Y, Kuroda J, Ri M et al (2012) RSK2Ser227 at N-terminal kinase domain is a potential therapeutic target for multiple myeloma. Mol Cancer Ther 11:2600-2609
-
(2012)
Mol Cancer Ther
, vol.11
, pp. 2600-2609
-
-
Shimura, Y.1
Kuroda, J.2
Ri, M.3
-
52
-
-
0036827727
-
Mutation in the ATP-binding pocket of the ABL kinase domain in an STI571-resistant BCR/ABL-positive cell line
-
1:CAS:528:DC%2BD38XosF2nurc%3D 12414617
-
Ricci C, Scappini B, Divoky V et al (2002) Mutation in the ATP-binding pocket of the ABL kinase domain in an STI571-resistant BCR/ABL-positive cell line. Cancer Res 62:5995-5998
-
(2002)
Cancer Res
, vol.62
, pp. 5995-5998
-
-
Ricci, C.1
Scappini, B.2
Divoky, V.3
-
53
-
-
67649388154
-
Involvement of BH3-only proteins in hematologic malignancies
-
10.1016/j.critrevonc.2008.10.004 19022681
-
Kuroda J, Taniwaki M (2009) Involvement of BH3-only proteins in hematologic malignancies. Crit Rev Oncol Hematol 71:89-101
-
(2009)
Crit Rev Oncol Hematol
, vol.71
, pp. 89-101
-
-
Kuroda, J.1
Taniwaki, M.2
-
54
-
-
13944277343
-
BH3 domeins of BH3-only proteins differentially regulate Bax-mediated mitochondrial membrane permeabilization both directly and indirectly
-
10.1016/j.molcel.2005.02.003 1:CAS:528:DC%2BD2MXit12rt7c%3D 15721256
-
Kuwana T, Bouchier-Hayes L, Chipuk JE et al (2005) BH3 domeins of BH3-only proteins differentially regulate Bax-mediated mitochondrial membrane permeabilization both directly and indirectly. Mol Cell 17:525-535
-
(2005)
Mol Cell
, vol.17
, pp. 525-535
-
-
Kuwana, T.1
Bouchier-Hayes, L.2
Chipuk, J.E.3
-
55
-
-
33846964621
-
Apopotosis initiated when BH3 ligands engage multiple Bcl-2 homologys, not Bax or Bak
-
10.1126/science.1133289 1:CAS:528:DC%2BD2sXhsVShsL4%3D 17289999
-
Willis SN, Fletcher JI, Kaufmann T et al (2007) Apopotosis initiated when BH3 ligands engage multiple Bcl-2 homologys, not Bax or Bak. Science 315:856-859
-
(2007)
Science
, vol.315
, pp. 856-859
-
-
Willis, S.N.1
Fletcher, J.I.2
Kaufmann, T.3
-
56
-
-
37249013938
-
ABT-737 is a useful component of combinatory chemotherapies for chronic myeloid leukaemias with diverse drug-resistance mechanisms
-
1:CAS:528:DC%2BD1cXitVOntL8%3D 18028486
-
Kuroda J, Kimura S, Andreeff M et al (2008) ABT-737 is a useful component of combinatory chemotherapies for chronic myeloid leukaemias with diverse drug-resistance mechanisms. Br J Haematol 140:181-190
-
(2008)
Br J Haematol
, vol.140
, pp. 181-190
-
-
Kuroda, J.1
Kimura, S.2
Andreeff, M.3
-
57
-
-
77954594460
-
BCR-ABL: A multi-faceted promoter of DNA mutation in chronic myelogeneous leukemia
-
10.1038/leu.2010.67 1:CAS:528:DC%2BC3cXntFShs7w%3D 20445577
-
Burke BA, Carroll M (2010) BCR-ABL: a multi-faceted promoter of DNA mutation in chronic myelogeneous leukemia. Leukemia 24:1105-1112
-
(2010)
Leukemia
, vol.24
, pp. 1105-1112
-
-
Burke, B.A.1
Carroll, M.2
-
58
-
-
66949171787
-
Epigenetic down-regulation of BIM expression is associated with reduced optimal responses to imatinib treatment in chronic myeloid leukaemia
-
10.1016/j.ejca.2009.04.005 19403302
-
San José-Eneriz E, Agirre X, Jiménez-Velasco A et al (2009) Epigenetic down-regulation of BIM expression is associated with reduced optimal responses to imatinib treatment in chronic myeloid leukaemia. Eur J Cancer 45:1877-1889
-
(2009)
Eur J Cancer
, vol.45
, pp. 1877-1889
-
-
San José-Eneriz, E.1
Agirre, X.2
Jiménez-Velasco, A.3
-
59
-
-
77955461316
-
Targeting activating transcription factor 3 by Galectin-9 induces apoptosis and overcomes various types of treatment resistance in chronic myelogenous leukemia
-
10.1158/1541-7786.MCR-10-0040 1:CAS:528:DC%2BC3cXovVamsLs%3D 20571063
-
Kuroda J, Yamamoto M, Nagoshi H et al (2010) Targeting activating transcription factor 3 by Galectin-9 induces apoptosis and overcomes various types of treatment resistance in chronic myelogenous leukemia. Mol Cancer Res 8:994-1001
-
(2010)
Mol Cancer Res
, vol.8
, pp. 994-1001
-
-
Kuroda, J.1
Yamamoto, M.2
Nagoshi, H.3
-
60
-
-
84861671713
-
Lysosomal pathways to cell death and their therapeutic applications
-
10.1016/j.yexcr.2012.03.005 22465226
-
Česen MH, Pegan K, Spes A, Turk B (2012) Lysosomal pathways to cell death and their therapeutic applications. Exp Cell Res 318:1245-1251
-
(2012)
Exp Cell Res
, vol.318
, pp. 1245-1251
-
-
Česen, M.H.1
Pegan, K.2
Spes, A.3
Turk, B.4
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