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Volumn 30, Issue 2, 2012, Pages 518-523

Evaluation of a multi-kinase inhibitor KRC-108 as an anti-tumor agent in vitro and in vivo

Author keywords

Aminopyridine; c Met; Cancer; Flt3; Kinase inhibitor; Ron

Indexed keywords

CD135 ANTIGEN; CYTOCHROME P450; KRC 108; PROTEIN KINASE; PROTEIN KINASE INHIBITOR; PROTEIN TYROSINE KINASE A; RON KINASE; SCATTER FACTOR RECEPTOR; UNCLASSIFIED DRUG; AMINOPYRIDINE DERIVATIVE; ANTINEOPLASTIC AGENT; BENZOXAZOLE DERIVATIVE; KRC-108; PROTEIN TYROSINE KINASE; RON PROTEIN;

EID: 84861576695     PISSN: 01676997     EISSN: 15730646     Source Type: Journal    
DOI: 10.1007/s10637-010-9584-2     Document Type: Article
Times cited : (17)

References (26)
  • 1
    • 57749188299 scopus 로고    scopus 로고
    • Targeting cancer with small molecule kinase inhibitors
    • doi:10.1038/nrc2559
    • Zhang J, Yang PL, Gray NS (2009) Targeting cancer with small molecule kinase inhibitors. Nat Rev Cancer 9:28-39. doi:10.1038/nrc2559
    • (2009) Nat Rev Cancer , vol.9 , pp. 28-39
    • Zhang, J.1    Yang, P.L.2    Gray, N.S.3
  • 2
    • 75149130051 scopus 로고    scopus 로고
    • Targeting the cancer kinome through polypharmacology
    • doi:10.1038/nrc2787
    • Knight ZA, Lin H, Shokat KM (2010) Targeting the cancer kinome through polypharmacology. Nat Rev Cancer 10:130-137. doi:10.1038/nrc2787
    • (2010) Nat Rev Cancer , vol.10 , pp. 130-137
    • Knight, Z.A.1    Lin, H.2    Shokat, K.M.3
  • 3
    • 69949151386 scopus 로고    scopus 로고
    • Factors underlying sensitivity of cancers to small-molecule kinase inhibitors
    • doi:10.1038/nrd2871
    • Jänne PA, Gray N, Settleman J (2009) Factors underlying sensitivity of cancers to small-molecule kinase inhibitors. Nat Rev Drug Discov 8:709-723. doi:10.1038/nrd2871
    • (2009) Nat Rev Drug Discov , vol.8 , pp. 709-723
    • Jänne, P.A.1    Gray, N.2    Settleman, J.3
  • 5
    • 33646712747 scopus 로고    scopus 로고
    • Mechanisms of disease: Understanding resistance to HER2-targeted therapy in human breast cancer
    • doi:10.1038/ncponc0509
    • Nahta R, Yu D, Hung M-C, Hortobagyi GN, Esteva FJ (2006) Mechanisms of disease: understanding resistance to HER2-targeted therapy in human breast cancer. Nat Clin Pract Oncol 3:269-280. doi:10.1038/ncponc0509
    • (2006) Nat Clin Pract Oncol , vol.3 , pp. 269-280
    • Nahta, R.1    Yu, D.2    Hung, M.-C.3    Hortobagyi, G.N.4    Esteva, F.J.5
  • 6
    • 34548316976 scopus 로고    scopus 로고
    • Molecular basis for sunitinib efficacy and future clinical development
    • doi:10.1038/nrd2380
    • Faivre S, Demetri G, Sargent W, Raymond E (2007) Molecular basis for sunitinib efficacy and future clinical development. Nat Rev Drug Discov 6:734-745. doi:10.1038/nrd2380
    • (2007) Nat Rev Drug Discov , vol.6 , pp. 734-745
    • Faivre, S.1    Demetri, G.2    Sargent, W.3    Raymond, E.4
  • 8
    • 77953869562 scopus 로고    scopus 로고
    • Discovery of aminopyridines substituted with benzoxazole as orally active c-Met kinase inhibitors
    • doi:10.1016/j.bmcl.2010.05.031
    • Cho SY, Han S-Y, Ha JD, Ryu JW, Lee CO, Jung H, Kang NS, Kim HR, Koh JS, Lee J (2010) Discovery of aminopyridines substituted with benzoxazole as orally active c-Met kinase inhibitors. Bioorg Med Chem Lett 20:4223-4227. doi:10.1016/j.bmcl.2010.05.031
    • (2010) Bioorg Med Chem Lett , vol.20 , pp. 4223-4227
    • Cho, S.Y.1    Han, S.-Y.2    Ha, J.D.3    Ryu, J.W.4    Lee, C.O.5    Jung, H.6    Kang, N.S.7    Kim, H.R.8    Koh, J.S.9    Lee, J.10
  • 11
    • 67049134253 scopus 로고    scopus 로고
    • Enzymatic characterization of c-Met receptor tyrosine kinase oncogenic mutants and kinetic studies with aminopyridine and triazolopyrazine inhibitors
    • doi:10.1021/bi900438w
    • Timofeevski SL, McTigue MA, Ryan K, Cui J, Zou HY, Zhu JX, Chau F, Alton G, Karlicek S, Christensen JG, Murray BW (2009) Enzymatic characterization of c-Met receptor tyrosine kinase oncogenic mutants and kinetic studies with aminopyridine and triazolopyrazine inhibitors. Biochem 48:5339-5349. doi:10.1021/bi900438w
    • (2009) Biochem , vol.48 , pp. 5339-5349
    • Timofeevski, S.L.1    McTigue, M.A.2    Ryan, K.3    Cui, J.4    Zou, H.Y.5    Zhu, J.X.6    Chau, F.7    Alton, G.8    Karlicek, S.9    Christensen, J.G.10    Murray, B.W.11
  • 14
    • 0034715897 scopus 로고    scopus 로고
    • Overexpression and activation of the RON receptor tyrosine kinase in a panel of human colorectal carcinoma cell lines
    • doi:10.1006/excr.2000.5012
    • Chen Y-Q, Zhou Y-Q, Angeloni D, Kurtz AL, Qiang X-Z, Wang M-H (2000) Overexpression and activation of the RON receptor tyrosine kinase in a panel of human colorectal carcinoma cell lines. Exp Cell Res 261:229-238. doi:10.1006/excr.2000.5012
    • (2000) Exp Cell Res , vol.261 , pp. 229-238
    • Chen, Y.-Q.1    Zhou, Y.-Q.2    Angeloni, D.3    Kurtz, A.L.4    Qiang, X.-Z.5    Wang, M.-H.6
  • 15
    • 46749115181 scopus 로고    scopus 로고
    • Met-related receptor tyrosine kinase ron in tumor growth and metastasis
    • Wagh PK, Peace BE, Waltz SE (2008) Met-related receptor tyrosine kinase ron in tumor growth and metastasis. Adv Cancer Res 100:1-33
    • (2008) Adv Cancer Res , vol.100 , pp. 1-33
    • Wagh, P.K.1    Peace, B.E.2    Waltz, S.E.3
  • 16
    • 35148819860 scopus 로고    scopus 로고
    • Multiple variants of the RON receptor tyrosine kinase: Biochemical properties, tumorigenic activities, and potential drug targets
    • doi:10.1016/j.canlet.2007.08.007
    • Lu Y, Yao H-P, Wang M-H (2007) Multiple variants of the RON receptor tyrosine kinase: biochemical properties, tumorigenic activities, and potential drug targets. Cancer Lett 257:157-164. doi:10.1016/j.canlet.2007.08.007
    • (2007) Cancer Lett , vol.257 , pp. 157-164
    • Lu, Y.1    Yao, H.-P.2    Wang, M.-H.3
  • 17
    • 34548181032 scopus 로고    scopus 로고
    • FLT3 inhibition in acute myeloid leukemia
    • doi:10.1111/j.1365-2141.2007.06700.x
    • Knapper S (2007) FLT3 inhibition in acute myeloid leukemia. Br J Haematol 138:687-699. doi:10.1111/j.1365-2141.2007.06700.x
    • (2007) Br J Haematol , vol.138 , pp. 687-699
    • Knapper, S.1
  • 19
    • 10644289454 scopus 로고    scopus 로고
    • Hepatocyte growth factor, its receptor, and their potential value in cancer therapies
    • doi:10.1016/j.critrevonc.2004.09.004
    • Jiang WG, Martin TA, Parr C, Davies G, Matsumoto K, Nakamura T (2005) Hepatocyte growth factor, its receptor, and their potential value in cancer therapies. Crit Rev Oncol Hematol 53:35-69. doi:10.1016/j.critrevonc.2004.09.004
    • (2005) Crit Rev Oncol Hematol , vol.53 , pp. 35-69
    • Jiang, W.G.1    Martin, T.A.2    Parr, C.3    Davies, G.4    Matsumoto, K.5    Nakamura, T.6
  • 20
    • 44449151030 scopus 로고    scopus 로고
    • Drug development of MET inhibitors: Targeting oncogene addiction and expedience
    • doi:10.1038/nrd2530
    • Comoglio PM, Giordano S, Trusolino L (2008) Drug development of MET inhibitors: targeting oncogene addiction and expedience. Nat Rev Drug Discov 7:504-516. doi:10.1038/nrd2530
    • (2008) Nat Rev Drug Discov , vol.7 , pp. 504-516
    • Comoglio, P.M.1    Giordano, S.2    Trusolino, L.3
  • 21
    • 19544389146 scopus 로고    scopus 로고
    • C-Met as a target for human cancer and characterization of inhibitors for therapeutic intervention
    • doi:10.1016/j.canlet.2004.09.044
    • Christensen JG, Burrows J, Salgia R (2005) c-Met as a target for human cancer and characterization of inhibitors for therapeutic intervention. Cancer Lett 225:1-26. doi:10.1016/j.canlet.2004.09.044
    • (2005) Cancer Lett , vol.225 , pp. 1-26
    • Christensen, J.G.1    Burrows, J.2    Salgia, R.3
  • 23
    • 0141925960 scopus 로고    scopus 로고
    • FLT3 expressing leukemias are selectively sensitive to inhibitors of the molecular chaperone heat shock protein 90 through destabilization of signal transduction associated kinases
    • Yao Q, Nishiuchi R, Li Q, Kumar AR, Hudson WA, Kersey JH (2003) FLT3 expressing leukemias are selectively sensitive to inhibitors of the molecular chaperone heat shock protein 90 through destabilization of signal transduction associated kinases. Clin Cancer Res 9:4483-4493
    • (2003) Clin Cancer Res , vol.9 , pp. 4483-4493
    • Yao, Q.1    Nishiuchi, R.2    Li, Q.3    Kumar, A.R.4    Hudson, W.A.5    Kersey, J.H.6
  • 24
    • 0030041139 scopus 로고    scopus 로고
    • Molecular analysis of the NPM-ALK rearrangement in Hodgkin's disease
    • Xerri L, Parc P, Hassoun J, Birnbaum D (1996) Molecular analysis of the NPM-ALK rearrangement in Hodgkin's disease. J Pathol 178:128-132. doi:10.1002/(SICI)1096-9896(199602) 178:2<128::AID-PATH444>3.0.CO;2-H
    • (1996) J Pathol , vol.178 , pp. 128-132
    • Xerri, L.1    Parc, P.2    Hassoun, J.3    Birnbaum, D.4
  • 25
    • 45949086656 scopus 로고    scopus 로고
    • Drug-like properties: Concepts, structure design and methods from ADME to toxicity optimization
    • Academic Press, Oxford, and references cited
    • Kerns EH, Di L (2007) Drug-like properties: concepts, structure design and methods from ADME to toxicity optimization. In: Cytochrome P450 inhibition. Academic Press, Oxford, pp 197-208 and references cited
    • (2007) Cytochrome P450 Inhibition , pp. 197-208
    • Kerns, E.H.1    Di, L.2
  • 26
    • 70349448421 scopus 로고    scopus 로고
    • Understanding CYP2D6 interactions
    • doi:10.1016/j.drudis.2009.07.005
    • de Groot MJ, Wakenhut F, Whitlock G, Hyland R (2009) Understanding CYP2D6 interactions. Drug Discov Today 14:964-972. doi:10.1016/j.drudis.2009.07.005
    • (2009) Drug Discov Today , vol.14 , pp. 964-972
    • De Groot, M.J.1    Wakenhut, F.2    Whitlock, G.3    Hyland, R.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.