메뉴 건너뛰기




Volumn 6, Issue , 2016, Pages

The use of cellular thermal shift assay (CETSA) to study Crizotinib resistance in ALK-expressing human cancers

Author keywords

[No Author keywords available]

Indexed keywords

ANAPLASTIC LYMPHOMA KINASE; ANTINEOPLASTIC AGENT; BETA CATENIN; CRIZOTINIB; PROTEIN BINDING; PROTEIN KINASE INHIBITOR; PROTEIN TYROSINE KINASE; PYRAZOLE DERIVATIVE; PYRIDINE DERIVATIVE; SMALL INTERFERING RNA;

EID: 84988492916     PISSN: None     EISSN: 20452322     Source Type: Journal    
DOI: 10.1038/srep33710     Document Type: Article
Times cited : (38)

References (63)
  • 1
    • 0028198206 scopus 로고
    • Fusion of a kinase gene, ALK, to a nucleolar protein gene, NPM, in non-hodgkin's lymphoma
    • Morris, S. W. et al. Fusion of a kinase gene, ALK, to a nucleolar protein gene, NPM, in non-Hodgkin's lymphoma. Science 263, 1281-1284 (1994).
    • (1994) Science , vol.263 , pp. 1281-1284
    • Morris, S.W.1
  • 2
    • 0028275645 scopus 로고
    • Hyperphosphorylation of a novel 80 kDa protein-tyrosine kinase similar to ltk in a human Ki-1 lymphoma cell line, AMS3
    • Shiota, M. et al. Hyperphosphorylation of a novel 80 kDa protein-tyrosine kinase similar to Ltk in a human Ki-1 lymphoma cell line, AMS3. Oncogene 9, 1567-1574 (1994).
    • (1994) Oncogene , vol.9 , pp. 1567-1574
    • Shiota, M.1
  • 3
    • 84884549747 scopus 로고    scopus 로고
    • Mechanistic insight into ALK receptor tyrosine kinase in human cancer biology
    • Hallberg, B. & Palmer, R. H. Mechanistic insight into ALK receptor tyrosine kinase in human cancer biology. Nat Rev Cancer 13, 685-700 (2013).
    • (2013) Nat Rev Cancer , vol.13 , pp. 685-700
    • Hallberg, B.1    Palmer, R.H.2
  • 4
    • 79955755025 scopus 로고    scopus 로고
    • Targeting oncogenic ALK: A promising strategy for cancer treatment
    • Grande, E., Bolos, M. V. & Arriola, E. Targeting oncogenic ALK: a promising strategy for cancer treatment. Mol Cancer Ther 10, 569-579 (2011).
    • (2011) Mol Cancer Ther , vol.10 , pp. 569-579
    • Grande, E.1    Bolos, M.V.2    Arriola, E.3
  • 5
    • 34547638047 scopus 로고    scopus 로고
    • Identification of the transforming EML4-ALK fusion gene in non-small-cell lung cancer
    • Soda, M. et al. Identification of the transforming EML4-ALK fusion gene in non-small-cell lung cancer. Nature 448, 561-566 (2007).
    • (2007) Nature , vol.448 , pp. 561-566
    • Soda, M.1
  • 6
    • 36849065315 scopus 로고    scopus 로고
    • Global survey of phosphotyrosine signaling identifies oncogenic kinases in lung cancer
    • Rikova, K. et al. Global survey of phosphotyrosine signaling identifies oncogenic kinases in lung cancer. Cell 131, 1190-1203 (2007).
    • (2007) Cell , vol.131 , pp. 1190-1203
    • Rikova, K.1
  • 7
    • 54049118823 scopus 로고    scopus 로고
    • Oncogenic mutations of ALK kinase in neuroblastoma
    • Chen, Y. et al. Oncogenic mutations of ALK kinase in neuroblastoma. Nature 455, 971-974 (2008).
    • (2008) Nature , vol.455 , pp. 971-974
    • Chen, Y.1
  • 8
    • 54049120220 scopus 로고    scopus 로고
    • Activating mutations in ALK provide a therapeutic target in neuroblastoma
    • George, R. E. et al. Activating mutations in ALK provide a therapeutic target in neuroblastoma. Nature 455, 975-978 (2008).
    • (2008) Nature , vol.455 , pp. 975-978
    • George, R.E.1
  • 9
    • 54049149961 scopus 로고    scopus 로고
    • Somatic and germline activating mutations of the ALK kinase receptor in neuroblastoma
    • Janoueix-Lerosey, I. et al. Somatic and germline activating mutations of the ALK kinase receptor in neuroblastoma. Nature 455, 967-970 (2008).
    • (2008) Nature , vol.455 , pp. 967-970
    • Janoueix-Lerosey, I.1
  • 10
    • 54049094708 scopus 로고    scopus 로고
    • Identification of ALK as a major familial neuroblastoma predisposition gene
    • Mosse, Y. P. et al. Identification of ALK as a major familial neuroblastoma predisposition gene. Nature 455, 930-935 (2008).
    • (2008) Nature , vol.455 , pp. 930-935
    • Mosse, Y.P.1
  • 11
    • 58149289668 scopus 로고    scopus 로고
    • High incidence of DNA mutations and gene amplifications of the ALK gene in advanced sporadic neuroblastoma tumours
    • Caren, H., Abel, F., Kogner, P. & Martinsson, T. High incidence of DNA mutations and gene amplifications of the ALK gene in advanced sporadic neuroblastoma tumours. The Biochemical journal 416, 153-159 (2008).
    • (2008) The Biochemical Journal , vol.416 , pp. 153-159
    • Caren, H.1    Abel, F.2    Kogner, P.3    Martinsson, T.4
  • 12
    • 84912059340 scopus 로고    scopus 로고
    • ALK mutations confer differential oncogenic activation and sensitivity to ALK inhibition therapy in neuroblastoma
    • Bresler, S. C. et al. ALK mutations confer differential oncogenic activation and sensitivity to ALK inhibition therapy in neuroblastoma. Cancer Cell 26, 682-694 (2014).
    • (2014) Cancer Cell , vol.26 , pp. 682-694
    • Bresler, S.C.1
  • 13
    • 79961088497 scopus 로고    scopus 로고
    • Anaplastic lymphoma kinase in human cancer
    • Barreca, A. et al. Anaplastic lymphoma kinase in human cancer. J Mol Endocrinol 47, R11-R23 (2011).
    • (2011) J Mol Endocrinol , vol.47 , pp. R11-R23
    • Barreca, A.1
  • 14
    • 84876966952 scopus 로고    scopus 로고
    • Safety and activity of crizotinib for paediatric patients with refractory solid tumours or anaplastic large-cell lymphoma: A Children's oncology group phase 1 consortium study
    • Mosse, Y. P. et al. Safety and activity of crizotinib for paediatric patients with refractory solid tumours or anaplastic large-cell lymphoma: a Children's Oncology Group phase 1 consortium study. The Lancet. Oncology 14, 472-480 (2013).
    • (2013) The Lancet. Oncology , vol.14 , pp. 472-480
    • Mosse, Y.P.1
  • 16
    • 84899488652 scopus 로고    scopus 로고
    • Overcoming the resistance to crizotinib in patients with non-small cell lung cancer harboring EML4/ALK translocation
    • Perez, C. A., Velez, M., Raez, L. E. & Santos, E. S. Overcoming the resistance to Crizotinib in patients with Non-Small Cell Lung Cancer harboring EML4/ALK translocation. Lung Cancer 84, 110-115 (2014).
    • (2014) Lung Cancer , vol.84 , pp. 110-115
    • Perez, C.A.1    Velez, M.2    Raez, L.E.3    Santos, E.S.4
  • 17
    • 84868679921 scopus 로고    scopus 로고
    • The battle against ALK resistance: Successes and setbacks
    • Voena, C. & Chiarle, R. The battle against ALK resistance: successes and setbacks. Expert opinion on investigational drugs 21, 1751-1754 (2012).
    • (2012) Expert Opinion on Investigational Drugs , vol.21 , pp. 1751-1754
    • Voena, C.1    Chiarle, R.2
  • 18
    • 84856999699 scopus 로고    scopus 로고
    • Mechanisms of acquired crizotinib resistance in ALK-rearranged lung cancers
    • Katayama, R. et al. Mechanisms of Acquired Crizotinib Resistance in ALK-Rearranged Lung Cancers. Science Translational Medicine 4, 120ra117-120ra117 (2012).
    • (2012) Science Translational Medicine , vol.4 , pp. 120ra117-120ra117
    • Katayama, R.1
  • 20
    • 84939645330 scopus 로고    scopus 로고
    • Clinical efficacy of crizotinib in Chinese patients with ALK-positive non-small-cell lung cancer with brain metastases
    • Lei, Y.-Y. et al. Clinical efficacy of crizotinib in Chinese patients with ALK-positive non-small-cell lung cancer with brain metastases. Journal of Thoracic Disease 7, 1181-1188 (2015).
    • (2015) Journal of Thoracic Disease , vol.7 , pp. 1181-1188
    • Lei, Y.-Y.1
  • 21
    • 84879748358 scopus 로고    scopus 로고
    • Monitoring drug target engagement in cells and tissues using the cellular thermal shift assay
    • Martinez Molina, D. et al. Monitoring drug target engagement in cells and tissues using the cellular thermal shift assay. Science 341, 84-87 (2013).
    • (2013) Science , vol.341 , pp. 84-87
    • Martinez Molina, D.1
  • 22
    • 84907020021 scopus 로고    scopus 로고
    • The cellular thermal shift assay for evaluating drug target interactions in cells
    • Jafari, R. et al. The cellular thermal shift assay for evaluating drug target interactions in cells. Nature protocols 9, 2100-2122 (2014).
    • (2014) Nature Protocols , vol.9 , pp. 2100-2122
    • Jafari, R.1
  • 23
    • 84931023975 scopus 로고    scopus 로고
    • CETSA: A target engagement assay with potential to transform drug discovery
    • Jensen, A. J., Martinez Molina, D. & Lundback, T. CETSA: a target engagement assay with potential to transform drug discovery. Future medicinal chemistry 7, 975-978 (2015).
    • (2015) Future Medicinal Chemistry , vol.7 , pp. 975-978
    • Jensen, A.J.1    Martinez Molina, D.2    Lundback, T.3
  • 24
    • 84876366299 scopus 로고    scopus 로고
    • Control of ALK (wild type and mutated forms) phosphorylation: Specific role of the phosphatase PTP1B
    • Boutterin, M. C. et al. Control of ALK (wild type and mutated forms) phosphorylation: Specific role of the phosphatase PTP1B. Cellular Signalling 25, 1505-1513 (2013).
    • (2013) Cellular Signalling , vol.25 , pp. 1505-1513
    • Boutterin, M.C.1
  • 25
    • 59649127007 scopus 로고    scopus 로고
    • EML4-ALK rearrangement in non-small cell lung cancer and non-tumor lung tissues
    • Martelli, M. P. et al. EML4-ALK Rearrangement in Non-Small Cell Lung Cancer and Non-Tumor Lung Tissues. The American Journal of Pathology 174, 661-670 (2009).
    • (2009) The American Journal of Pathology , vol.174 , pp. 661-670
    • Martelli, M.P.1
  • 27
    • 37549059613 scopus 로고    scopus 로고
    • Cytoreductive antitumor activity of PF-2341066, a novel inhibitor of anaplastic lymphoma kinase and c-met, in experimental models of anaplastic large-cell lymphoma
    • Christensen, J. G. et al. Cytoreductive antitumor activity of PF-2341066, a novel inhibitor of anaplastic lymphoma kinase and c-Met, in experimental models of anaplastic large-cell lymphoma. Mol Cancer Ther 6, 3314-3322 (2007).
    • (2007) Mol Cancer Ther , vol.6 , pp. 3314-3322
    • Christensen, J.G.1
  • 28
    • 84940048300 scopus 로고    scopus 로고
    • Understanding the interplay between expression, mutation and activity of ALK receptor in rhabdomyosarcoma cells for clinical application of small-molecule inhibitors
    • Peron, M., Lovisa, F., Poli, E., Basso, G. & Bonvini, P. Understanding the Interplay between Expression, Mutation and Activity of ALK Receptor in Rhabdomyosarcoma Cells for Clinical Application of Small-Molecule Inhibitors. PLoS One 10, e0132330 (2015).
    • (2015) PLoS One , vol.10 , pp. e0132330
    • Peron, M.1    Lovisa, F.2    Poli, E.3    Basso, G.4    Bonvini, P.5
  • 29
    • 84887265101 scopus 로고    scopus 로고
    • Presence of anaplastic lymphoma kinase in inflammatory breast cancer
    • Robertson, F. et al. Presence of anaplastic lymphoma kinase in inflammatory breast cancer. SpringerPlus 2, 497 (2013).
    • (2013) SpringerPlus , vol.2 , pp. 497
    • Robertson, F.1
  • 30
    • 84859169877 scopus 로고    scopus 로고
    • The cancer cell line encyclopedia enables predictive modelling of anticancer drug sensitivity
    • Barretina, J. et al. The Cancer Cell Line Encyclopedia enables predictive modelling of anticancer drug sensitivity. Nature 483, 603-307 (2012).
    • (2012) Nature , vol.483 , pp. 307-603
    • Barretina, J.1
  • 31
    • 84993728402 scopus 로고    scopus 로고
    • The pathobiology of the oncogenic tyrosine kinase NPM-ALK: A brief update
    • Lai, R. & Ingham, R. J. The pathobiology of the oncogenic tyrosine kinase NPM-ALK: a brief update. Ther Adv Hematol 4, 119-131 (2013).
    • (2013) Ther Adv Hematol , vol.4 , pp. 119-131
    • Lai, R.1    Ingham, R.J.2
  • 32
    • 79551623658 scopus 로고    scopus 로고
    • Beta-catenin is constitutively active and increases STAT3 expression/activation in anaplastic lymphoma kinase-positive anaplastic large cell lymphoma
    • Anand, M., Lai, R. & Gelebart, P. beta-catenin is constitutively active and increases STAT3 expression/activation in anaplastic lymphoma kinase-positive anaplastic large cell lymphoma. Haematologica 96, 253-261 (2011).
    • (2011) Haematologica , vol.96 , pp. 253-261
    • Anand, M.1    Lai, R.2    Gelebart, P.3
  • 33
    • 84868308598 scopus 로고    scopus 로고
    • Disheveled proteins promote cell growth and tumorigenicity in ALK-positive anaplastic large cell lymphoma
    • Hegazy, S. A. et al. Disheveled proteins promote cell growth and tumorigenicity in ALK-positive anaplastic large cell lymphoma. Cell Signal 25, 295-307 (2013).
    • (2013) Cell Signal , vol.25 , pp. 295-307
    • Hegazy, S.A.1
  • 34
    • 0036494113 scopus 로고    scopus 로고
    • + lymphoma cells by the hsp90 antagonist 17-allylamino,17-demethoxygeldanamycin
    • + Lymphoma Cells by the Hsp90 Antagonist 17-Allylamino,17-demethoxygeldanamycin. Cancer Research 62, 1559-1566 (2002).
    • (2002) Cancer Research , vol.62 , pp. 1559-1566
    • Bonvini, P.1    Gastaldi, T.2    Falini, B.3    Rosolen, A.4
  • 35
    • 84877679409 scopus 로고    scopus 로고
    • Targeted inhibition of the molecular chaperone hsp90 overcomes ALK inhibitor resistance in non-small cell lung cancer
    • Sang, J. et al. Targeted Inhibition of the Molecular Chaperone Hsp90 Overcomes ALK Inhibitor Resistance in Non-Small Cell Lung Cancer. Cancer Discovery 3, 430-443 (2013).
    • (2013) Cancer Discovery , vol.3 , pp. 430-443
    • Sang, J.1
  • 36
    • 79956318797 scopus 로고    scopus 로고
    • Therapeutic strategies to overcome crizotinib resistance in non-small cell lung cancers harboring the fusion oncogene EML4-ALK
    • Katayama, R. et al. Therapeutic strategies to overcome crizotinib resistance in non-small cell lung cancers harboring the fusion oncogene EML4-ALK. Proceedings of the National Academy of Sciences 108, 7535-7540 (2011).
    • (2011) Proceedings of the National Academy of Sciences , vol.108 , pp. 7535-7540
    • Katayama, R.1
  • 37
    • 80052806086 scopus 로고    scopus 로고
    • Structure based drug design of crizotinib (PF-02341066), a potent and selective dual inhibitor of mesenchymal-epithelial transition factor (c-MET) kinase and anaplastic lymphoma kinase (ALK)
    • Cui, J. J. et al. Structure based drug design of crizotinib (PF-02341066), a potent and selective dual inhibitor of mesenchymal-epithelial transition factor (c-MET) kinase and anaplastic lymphoma kinase (ALK). Journal of medicinal chemistry 54, 6342-6363 (2011).
    • (2011) Journal of Medicinal Chemistry , vol.54 , pp. 6342-6363
    • Cui, J.J.1
  • 38
    • 78049426513 scopus 로고    scopus 로고
    • EML4-ALK mutations in lung cancer that confer resistance to ALK inhibitors
    • Choi, Y. L. et al. EML4-ALK mutations in lung cancer that confer resistance to ALK inhibitors. The New England journal of medicine 363, 1734-1739 (2010).
    • (2010) The New England Journal of Medicine , vol.363 , pp. 1734-1739
    • Choi, Y.L.1
  • 39
    • 78651406003 scopus 로고    scopus 로고
    • Appearance of the novel activating F1174S ALK mutation in neuroblastoma correlates with aggressive tumor progression and unresponsiveness to therapy
    • Martinsson, T. et al. Appearance of the novel activating F1174S ALK mutation in neuroblastoma correlates with aggressive tumor progression and unresponsiveness to therapy. Cancer Res 71, 98-105 (2011).
    • (2011) Cancer Res , vol.71 , pp. 98-105
    • Martinsson, T.1
  • 40
    • 84856990335 scopus 로고    scopus 로고
    • Mechanisms of resistance to crizotinib in patients with ALK gene rearranged non-small cell lung cancer
    • Doebele, R. C. et al. Mechanisms of Resistance to Crizotinib in Patients with ALK Gene Rearranged Non-Small Cell Lung Cancer. Clinical Cancer Research 18, 1472-1482 (2012).
    • (2012) Clinical Cancer Research , vol.18 , pp. 1472-1482
    • Doebele, R.C.1
  • 42
    • 79955964568 scopus 로고    scopus 로고
    • CH5424802, a selective ALK inhibitor capable of blocking the resistant gatekeeper mutant
    • Sakamoto, H. et al. CH5424802, a selective ALK inhibitor capable of blocking the resistant gatekeeper mutant. Cancer Cell 19, 679-690 (2011).
    • (2011) Cancer Cell , vol.19 , pp. 679-690
    • Sakamoto, H.1
  • 43
    • 84904722206 scopus 로고    scopus 로고
    • Selective ALK inhibitor alectinib with potent antitumor activity in models of crizotinib resistance
    • Kodama, T., Tsukaguchi, T., Yoshida, M., Kondoh, O. & Sakamoto, H. Selective ALK inhibitor alectinib with potent antitumor activity in models of crizotinib resistance. Cancer letters 351, 215-221 (2014).
    • (2014) Cancer Letters , vol.351 , pp. 215-221
    • Kodama, T.1    Tsukaguchi, T.2    Yoshida, M.3    Kondoh, O.4    Sakamoto, H.5
  • 44
    • 81055126433 scopus 로고    scopus 로고
    • Differential inhibitor sensitivity of anaplastic lymphoma kinase variants found in neuroblastoma
    • Bresler, S. C. et al. Differential inhibitor sensitivity of anaplastic lymphoma kinase variants found in neuroblastoma. Science translational medicine 3, 108ra114 (2011).
    • (2011) Science Translational Medicine , vol.3 , pp. 108ra114
    • Bresler, S.C.1
  • 45
    • 84899474680 scopus 로고    scopus 로고
    • Activating mutations in ALK kinase domain confer resistance to structurally unrelated ALK inhibitors in NPMALK-positive anaplastic large-cell lymphoma
    • Zdzalik, D. et al. Activating mutations in ALK kinase domain confer resistance to structurally unrelated ALK inhibitors in NPMALK-positive anaplastic large-cell lymphoma. Journal of Cancer Research and Clinical Oncology 140, 589-598 (2014).
    • (2014) Journal of Cancer Research and Clinical Oncology , vol.140 , pp. 589-598
    • Zdzalik, D.1
  • 47
    • 84908011214 scopus 로고    scopus 로고
    • Molecular rationale for the use of PI3K/AKT/mTOR pathway inhibitors in combination with crizotinib in ALKmutated neuroblastoma
    • Moore, N. F. et al. Molecular rationale for the use of PI3K/AKT/mTOR pathway inhibitors in combination with crizotinib in ALKmutated neuroblastoma. Oncotarget 5, 8737-8749 (2014).
    • (2014) Oncotarget , vol.5 , pp. 8737-8749
    • Moore, N.F.1
  • 48
    • 33947123268 scopus 로고    scopus 로고
    • Bcr-abl stabilizes β -catenin in chronic myeloid leukemia through its tyrosine phosphorylation
    • Coluccia, A. M. L. et al. Bcr-Abl stabilizes β -catenin in chronic myeloid leukemia through its tyrosine phosphorylation. The EMBO Journal 26, 1456-1466 (2007).
    • (2007) The EMBO Journal , vol.26 , pp. 1456-1466
    • Coluccia, A.M.L.1
  • 49
    • 84859523707 scopus 로고    scopus 로고
    • Genetic and pharmacologic inhibition of β -catenin targets imatinib-resistant leukemia stem cells in CML
    • Heidel, F. H. et al. Genetic and Pharmacologic Inhibition of β -Catenin Targets Imatinib-Resistant Leukemia Stem Cells in CML. Cell Stem Cell 10, 412-424 (2012).
    • (2012) Cell Stem Cell , vol.10 , pp. 412-424
    • Heidel, F.H.1
  • 50
    • 0028170977 scopus 로고
    • Beta-catenin mediates the interaction of the cadherin-catenin complex with epidermal growth factor receptor
    • Hoschuetzky, H., Aberle, H. & Kemler, R. Beta-catenin mediates the interaction of the cadherin-catenin complex with epidermal growth factor receptor. The Journal of Cell Biology 127, 1375-1380 (1994).
    • (1994) The Journal of Cell Biology , vol.127 , pp. 1375-1380
    • Hoschuetzky, H.1    Aberle, H.2    Kemler, R.3
  • 51
    • 77952302757 scopus 로고    scopus 로고
    • Epidermal growth factor receptor regulates β -catenin location, stability, and transcriptional activity in oral cancer
    • Lee, C.-H., Hung, H.-W., Hung, P.-H. & Shieh, Y.-S. Epidermal growth factor receptor regulates β -catenin location, stability, and transcriptional activity in oral cancer. Molecular Cancer 9, 1-12 (2010).
    • (2010) Molecular Cancer , vol.9 , pp. 1-12
    • Lee, C.-H.1    Hung, H.-W.2    Hung, P.-H.3    Shieh, Y.-S.4
  • 53
    • 84899619048 scopus 로고    scopus 로고
    • Stereospecific targeting of MTH1 by (S)-crizotinib as an anticancer strategy
    • Huber, K. V. et al. Stereospecific targeting of MTH1 by (S)-crizotinib as an anticancer strategy. Nature 508, 222-227 (2014).
    • (2014) Nature , vol.508 , pp. 222-227
    • Huber, K.V.1
  • 54
    • 84937010431 scopus 로고    scopus 로고
    • Assessing the efficacy of Mdm2/Mdm4-inhibiting stapled peptides using cellular thermal shift assays
    • Tan, B. X. et al. Assessing the Efficacy of Mdm2/Mdm4-Inhibiting Stapled Peptides Using Cellular Thermal Shift Assays. Scientific reports 5, 12116 (2015).
    • (2015) Scientific Reports , vol.5 , pp. 12116
    • Tan, B.X.1
  • 55
    • 84922804264 scopus 로고    scopus 로고
    • A small-molecule protein-protein interaction inhibitor of PARP1 that targets its BRCT domain
    • Na, Z. et al. A small-molecule protein-protein interaction inhibitor of PARP1 that targets its BRCT domain. Angewandte Chemie (International ed. in English) 54, 2515-2519 (2015).
    • (2015) Angewandte Chemie (International Ed. in English) , vol.54 , pp. 2515-2519
    • Na, Z.1
  • 56
    • 84902477584 scopus 로고    scopus 로고
    • BM-1197: A novel and specific Bcl-2/Bcl-xL inhibitor inducing complete and long-lasting tumor regression in vivo
    • Bai, L. et al. BM-1197: a novel and specific Bcl-2/Bcl-xL inhibitor inducing complete and long-lasting tumor regression in vivo. PLoS One 9, e99404 (2014).
    • (2014) PLoS One , vol.9 , pp. e99404
    • Bai, L.1
  • 57
    • 84930619097 scopus 로고    scopus 로고
    • Discovery and characterization of novel small-molecule inhibitors targeting nicotinamide phosphoribosyltransferase
    • Xu, T. Y. et al. Discovery and characterization of novel small-molecule inhibitors targeting nicotinamide phosphoribosyltransferase. Scientific reports 5, 10043 (2015).
    • (2015) Scientific Reports , vol.5 , pp. 10043
    • Xu, T.Y.1
  • 58
    • 84937397052 scopus 로고    scopus 로고
    • A selective inhibitor of PRMT5 with in vivo and in vitro potency in MCL models
    • Chan-Penebre, E. et al. A selective inhibitor of PRMT5 with in vivo and in vitro potency in MCL models. Nature chemical biology 11, 432-437 (2015).
    • (2015) Nature Chemical Biology , vol.11 , pp. 432-437
    • Chan-Penebre, E.1
  • 59
    • 0033564831 scopus 로고    scopus 로고
    • Recurrent involvement of 2p23 in inflammatory myofibroblastic tumors
    • Griffin, C. A. et al. Recurrent involvement of 2p23 in inflammatory myofibroblastic tumors. Cancer Res 59, 2776-2780 (1999).
    • (1999) Cancer Res , vol.59 , pp. 2776-2780
    • Griffin, C.A.1
  • 60
    • 0037391344 scopus 로고    scopus 로고
    • Characterization of 4 mantle cell lymphoma cell lines
    • Amin, H. M. et al. Characterization of 4 mantle cell lymphoma cell lines. Archives of pathology & laboratory medicine 127, 424-431 (2003).
    • (2003) Archives of Pathology & Laboratory Medicine , vol.127 , pp. 424-431
    • Amin, H.M.1
  • 61
    • 54049118823 scopus 로고    scopus 로고
    • Oncogenic mutations of ALK kinase in neuroblastoma
    • Chen, Y. et al. Oncogenic mutations of ALK kinase in neuroblastoma. Nature 455, 971-974 (2008).
    • (2008) Nature , vol.455 , pp. 971-974
    • Chen, Y.1
  • 62
    • 84891317257 scopus 로고    scopus 로고
    • Discovery and preclinical characterization of novel small molecule TRK and ROS1 tyrosine kinase inhibitors for the treatment of cancer and inflammation
    • Narayanan, R. et al. Discovery and Preclinical Characterization of Novel Small Molecule TRK and ROS1 Tyrosine Kinase Inhibitors for the Treatment of Cancer and Inflammation. PLoS One 8, e83380 (2013).
    • (2013) PLoS One , vol.8 , pp. e83380
    • Narayanan, R.1
  • 63
    • 59649123222 scopus 로고    scopus 로고
    • Proteome-wide identification of novel binding partners to the oncogenic fusion gene protein, NPM-ALK, using tandem affinity purification and mass spectrometry
    • Wu, F., Wang, P., Young, L. C., Lai, R. & Li, L. Proteome-Wide Identification of Novel Binding Partners to the Oncogenic Fusion Gene Protein, NPM-ALK, using Tandem Affinity Purification and Mass Spectrometry. The American Journal of Pathology 174, 361-370 (2009).
    • (2009) The American Journal of Pathology , vol.174 , pp. 361-370
    • Wu, F.1    Wang, P.2    Young, L.C.3    Lai, R.4    Li, L.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.