메뉴 건너뛰기




Volumn 34, Issue 5, 2013, Pages 1134-1143

CinQ-03, a novel allosteric MEK inhibitor, suppresses cancer growth in vitro and in vivo

Author keywords

[No Author keywords available]

Indexed keywords

ANTINEOPLASTIC AGENT; CINQ 01; CINQ 03; CINQ 06; MITOGEN ACTIVATED PROTEIN KINASE INHIBITOR; MITOGEN ACTIVATED PROTEIN KINASE KINASE 1; MITOGEN ACTIVATED PROTEIN KINASE KINASE 2; S6 KINASE; UNCLASSIFIED DRUG;

EID: 84877151489     PISSN: 01433334     EISSN: 14602180     Source Type: Journal    
DOI: 10.1093/carcin/bgt015     Document Type: Article
Times cited : (7)

References (38)
  • 1
    • 33947594129 scopus 로고    scopus 로고
    • Hyperactive Ras in developmental disorders and cancer
    • Schubbert,S. et al. (2007) Hyperactive Ras in developmental disorders and cancer. Nat. Rev. Cancer, 7, 295-308.
    • (2007) Nat. Rev. Cancer , vol.7 , pp. 295-308
    • Schubbert, S.1
  • 2
    • 33749993417 scopus 로고    scopus 로고
    • The consensus coding sequences of human breast and colorectal cancers
    • Sjöblom,T. et al. (2006) The consensus coding sequences of human breast and colorectal cancers. Science, 314, 268-274.
    • (2006) Science , vol.314 , pp. 268-274
    • Sjöblom, T.1
  • 3
    • 0034997845 scopus 로고    scopus 로고
    • Mitogen-activated protein (MAP) kinase pathways: regulation and physiological functions
    • Pearson,G. et al. (2001) Mitogen-activated protein (MAP) kinase pathways: regulation and physiological functions. Endocr. Rev., 22, 153-183.
    • (2001) Endocr. Rev. , vol.22 , pp. 153-183
    • Pearson, G.1
  • 4
    • 52449095361 scopus 로고    scopus 로고
    • The RSK family of kinases: emerging roles in cellular signalling
    • Anjum,R. et al. (2008) The RSK family of kinases: emerging roles in cellular signalling. Nat. Rev. Mol. Cell Biol., 9, 747-758.
    • (2008) Nat. Rev. Mol. Cell Biol. , vol.9 , pp. 747-758
    • Anjum, R.1
  • 5
    • 76349124051 scopus 로고    scopus 로고
    • RSK in tumorigenesis: connections to steroid signaling
    • Eisinger-Mathason,T.S. et al. (2010) RSK in tumorigenesis: connections to steroid signaling. Steroids, 75, 191-202.
    • (2010) Steroids , vol.75 , pp. 191-202
    • Eisinger-Mathason, T.S.1
  • 6
    • 0028228616 scopus 로고
    • Activation of MAP kinase kinase is necessary and sufficient for PC12 differentiation and for transformation of NIH 3T3 cells
    • Cowley,S. et al. (1994) Activation of MAP kinase kinase is necessary and sufficient for PC12 differentiation and for transformation of NIH 3T3 cells. Cell, 77, 841-852.
    • (1994) Cell , vol.77 , pp. 841-852
    • Cowley, S.1
  • 7
    • 0028141496 scopus 로고
    • Transformation of mammalian cells by constitutively active MAP kinase kinase
    • Mansour,S.J. et al. (1994) Transformation of mammalian cells by constitutively active MAP kinase kinase. Science, 265, 966-970.
    • (1994) Science , vol.265 , pp. 966-970
    • Mansour, S.J.1
  • 8
    • 0034175984 scopus 로고    scopus 로고
    • Understanding Ras: 'it ain't over 'til it's over'
    • Shields,J.M. et al. (2000) Understanding Ras: 'it ain't over 'til it's over'. Trends Cell Biol., 10, 147-154.
    • (2000) Trends Cell Biol , vol.10 , pp. 147-154
    • Shields, J.M.1
  • 9
    • 44249112553 scopus 로고    scopus 로고
    • Mutation analysis of BRAF, MEK1 and MEK2 in 15 ovarian cancer cell lines: implications for therapy.
    • Estep,A.L. et al. (2007) Mutation analysis of BRAF, MEK1 and MEK2 in 15 ovarian cancer cell lines: implications for therapy. PLoS ONE, 2, e1279.
    • (2007) PLoS ONE , vol.2
    • Estep, A.L.1
  • 10
    • 84862537371 scopus 로고    scopus 로고
    • Novel TOPK inhibitor HI-TOPK-032 effectively suppresses colon cancer growth
    • Kim,D.J. et al. (2012) Novel TOPK inhibitor HI-TOPK-032 effectively suppresses colon cancer growth. Cancer Res., 72, 3060-3068.
    • (2012) Cancer Res , vol.72 , pp. 3060-3068
    • Kim, D.J.1
  • 11
    • 34447102966 scopus 로고    scopus 로고
    • Bidirectional signals transduced by TOPK-ERK interaction increase tumorigenesis of HCT116 colorectal cancer cells
    • Zhu,F. et al. (2007) Bidirectional signals transduced by TOPK-ERK interaction increase tumorigenesis of HCT116 colorectal cancer cells. Gastroenterology, 133, 219-231.
    • (2007) Gastroenterology , vol.133 , pp. 219-231
    • Zhu, F.1
  • 12
  • 13
    • 1242272924 scopus 로고    scopus 로고
    • The MAP kinase pathway is required for entry into mitosis and cell survival
    • Liu,X. et al. (2004) The MAP kinase pathway is required for entry into mitosis and cell survival. Oncogene, 23, 763-776.
    • (2004) Oncogene , vol.23 , pp. 763-776
    • Liu, X.1
  • 14
    • 0027217533 scopus 로고
    • Cloning and characterization of two distinct human extracellular signal-regulated kinase activator kinases, MEK1 and MEK2.
    • Zheng,C.F. et al. (1993) Cloning and characterization of two distinct human extracellular signal-regulated kinase activator kinases, MEK1 and MEK2. J. Biol. Chem., 268, 11435-11439.
    • (1993) J. Biol. Chem. , vol.268 , pp. 11435-11439
    • Zheng, C.F.1
  • 15
    • 1242290740 scopus 로고    scopus 로고
    • Mek2 is dispensable for mouse growth and development
    • Bélanger,L.F. et al. (2003) Mek2 is dispensable for mouse growth and development. Mol. Cell. Biol., 23, 4778-4787.
    • (2003) Mol. Cell. Biol. , vol.23 , pp. 4778-4787
    • Bélanger, L.F.1
  • 16
    • 0033535584 scopus 로고    scopus 로고
    • Embryonic death of Mek1-deficient mice reveals a role for this kinase in angiogenesis in the labyrinthine region of the placenta
    • Giroux,S. et al. (1999) Embryonic death of Mek1-deficient mice reveals a role for this kinase in angiogenesis in the labyrinthine region of the placenta. Curr. Biol., 9, 369-372.
    • (1999) Curr. Biol. , vol.9 , pp. 369-372
    • Giroux, S.1
  • 17
    • 34548097240 scopus 로고    scopus 로고
    • AZD6244 (ARRY-142886), a potent inhibitor of mitogen-activated protein kinase/extracellular signal-regulated kinase kinase 1/2 kinases: mechanism of action in vivo, pharmacokinetic/pharmacodynamic relationship, and potential for combination in preclinical models
    • Davies,B.R. et al. (2007) AZD6244 (ARRY-142886), a potent inhibitor of mitogen-activated protein kinase/extracellular signal-regulated kinase kinase 1/2 kinases: mechanism of action in vivo, pharmacokinetic/pharmacodynamic relationship, and potential for combination in preclinical models. Mol. Cancer Ther., 6, 2209-2219.
    • (2007) Mol. Cancer Ther. , vol.6 , pp. 2209-2219
    • Davies, B.R.1
  • 18
    • 23944439944 scopus 로고    scopus 로고
    • Phase I and pharmacodynamic study of the oral MEK inhibitor CI-1040 in patients with advanced malignancies
    • Lorusso,P.M. et al. (2005) Phase I and pharmacodynamic study of the oral MEK inhibitor CI-1040 in patients with advanced malignancies. J. Clin. Oncol., 23, 5281-5293.
    • (2005) J. Clin. Oncol. , vol.23 , pp. 5281-5293
    • Lorusso, P.M.1
  • 19
    • 32944462043 scopus 로고    scopus 로고
    • Prospective study using the risk of ovarian cancer algorithm to screen for ovarian cancer
    • Menon,U. et al. (2005) Prospective study using the risk of ovarian cancer algorithm to screen for ovarian cancer. J. Clin. Oncol., 23, 7919-7926.
    • (2005) J. Clin. Oncol. , vol.23 , pp. 7919-7926
    • Menon, U.1
  • 20
    • 0029166667 scopus 로고
    • A synthetic inhibitor of the mitogen-activated protein kinase cascade
    • Dudley,D.T. et al. (1995) A synthetic inhibitor of the mitogen-activated protein kinase cascade. Proc. Natl. Acad. Sci. U.S.A., 92, 7686-7689.
    • (1995) Proc. Natl. Acad. Sci. U.S.A. , vol.92 , pp. 7686-7689
    • Dudley, D.T.1
  • 21
    • 14444279192 scopus 로고    scopus 로고
    • Identification of a novel inhibitor of mitogenactivated protein kinase kinase
    • Favata,M.F. et al. (1998) Identification of a novel inhibitor of mitogenactivated protein kinase kinase. J. Biol. Chem., 273, 18623-18632.
    • (1998) J. Biol. Chem. , vol.273 , pp. 18623-18632
    • Favata, M.F.1
  • 22
    • 0032984348 scopus 로고    scopus 로고
    • Blockade of the MAP kinase pathway suppresses growth of colon tumors in vivo
    • Sebolt-Leopold,J.S. et al. (1999) Blockade of the MAP kinase pathway suppresses growth of colon tumors in vivo. Nat. Med., 5, 810-816.
    • (1999) Nat. Med. , vol.5 , pp. 810-816
    • Sebolt-Leopold, J.S.1
  • 23
    • 31144453233 scopus 로고    scopus 로고
    • BRAF mutation predicts sensitivity to MEK inhibition
    • Solit,D.B. et al. (2006) BRAF mutation predicts sensitivity to MEK inhibition. Nature, 439, 358-362.
    • (2006) Nature , vol.439 , pp. 358-362
    • Solit, D.B.1
  • 24
    • 43749103335 scopus 로고    scopus 로고
    • Phase I pharmacokinetic and pharmacodynamic study of the oral, small-molecule mitogen-activated protein kinase kinase 1/2 inhibitor AZD6244 (ARRY-142886) in patients with advanced cancers
    • Adjei,A.A. et al. (2008) Phase I pharmacokinetic and pharmacodynamic study of the oral, small-molecule mitogen-activated protein kinase kinase 1/2 inhibitor AZD6244 (ARRY-142886) in patients with advanced cancers. J. Clin. Oncol., 26, 2139-2146.
    • (2008) J. Clin. Oncol. , vol.26 , pp. 2139-2146
    • Adjei, A.A.1
  • 25
    • 33846781365 scopus 로고    scopus 로고
    • Targeted inhibition of the extracellular signal-regulated kinase kinase pathway with AZD6244 (ARRY-142886) in the treatment of hepatocellular carcinoma
    • Huynh,H. et al. (2007) Targeted inhibition of the extracellular signal-regulated kinase kinase pathway with AZD6244 (ARRY-142886) in the treatment of hepatocellular carcinoma. Mol. Cancer Ther., 6, 138-146.
    • (2007) Mol. Cancer Ther. , vol.6 , pp. 138-146
    • Huynh, H.1
  • 26
    • 33947401129 scopus 로고    scopus 로고
    • Biological characterization of ARRY-142886 (AZD6244), a potent, highly selective mitogen-activated protein kinase kinase 1/2 inhibitor
    • Yeh,T.C. et al. (2007) Biological characterization of ARRY-142886 (AZD6244), a potent, highly selective mitogen-activated protein kinase kinase 1/2 inhibitor. Clin. Cancer Res., 13, 1576-1583.
    • (2007) Clin. Cancer Res. , vol.13 , pp. 1576-1583
    • Yeh, T.C.1
  • 27
    • 33845353775 scopus 로고    scopus 로고
    • Novel targets in solid tumors: MEK inhibitors
    • Messersmith,W.A. et al. (2006) Novel targets in solid tumors: MEK inhibitors. Clin. Adv. Hematol. Oncol., 4, 831-836.
    • (2006) Clin. Adv. Hematol. Oncol. , vol.4 , pp. 831-836
    • Messersmith, W.A.1
  • 28
    • 76049113589 scopus 로고    scopus 로고
    • Mitogen-activated protein/extracellular signal-regulated kinase kinase inhibition results in biphasic alteration of epidermal homeostasis with keratinocytic apoptosis and pigmentation disorders
    • Schad,K. et al. (2010) Mitogen-activated protein/extracellular signal-regulated kinase kinase inhibition results in biphasic alteration of epidermal homeostasis with keratinocytic apoptosis and pigmentation disorders. Clin. Cancer Res., 16, 1058-1064.
    • (2010) Clin. Cancer Res. , vol.16 , pp. 1058-1064
    • Schad, K.1
  • 29
    • 80755177739 scopus 로고    scopus 로고
    • Dermatologic side effects associated with the MEK 1/2 inhibitor selumetinib (AZD6244 ARRY-142886).
    • Balagula,Y. et al. (2011) Dermatologic side effects associated with the MEK 1/2 inhibitor selumetinib (AZD6244, ARRY-142886). Invest. New Drugs, 29, 1114-1121.
    • (2011) Invest. New Drugs , vol.29 , pp. 1114-1121
    • Balagula, Y.1
  • 30
    • 15744380263 scopus 로고    scopus 로고
    • Structures of human MAP kinase kinase 1 (MEK1) and MEK2 describe novel noncompetitive kinase inhibition
    • Ohren,J.F. et al. (2004) Structures of human MAP kinase kinase 1 (MEK1) and MEK2 describe novel noncompetitive kinase inhibition. Nat. Struct. Mol. Biol., 11, 1192-1197.
    • (2004) Nat. Struct. Mol. Biol. , vol.11 , pp. 1192-1197
    • Ohren, J.F.1
  • 31
    • 33750124980 scopus 로고    scopus 로고
    • Extra precision glide: docking and scoring incorporating a model of hydrophobic enclosure for protein-ligand complexes
    • Friesner,R.A. et al. (2006) Extra precision glide: docking and scoring incorporating a model of hydrophobic enclosure for protein-ligand complexes. J. Med. Chem., 49, 6177-6196.
    • (2006) J. Med. Chem. , vol.49 , pp. 6177-6196
    • Friesner, R.A.1
  • 32
    • 62449319246 scopus 로고    scopus 로고
    • Characterization of a novel mitogen-activated protein kinase kinase 1/2 inhibitor with a unique mechanism of action for cancer therapy
    • Daouti,S. et al. (2009) Characterization of a novel mitogen-activated protein kinase kinase 1/2 inhibitor with a unique mechanism of action for cancer therapy. Cancer Res., 69, 1924-1932.
    • (2009) Cancer Res , vol.69 , pp. 1924-1932
    • Daouti, S.1
  • 33
    • 70149119899 scopus 로고    scopus 로고
    • a potent, selective, allosteric inhibitor of MEK1/2 for the treatment of cancer
    • Iverson,C. et al. (2009) RDEA119/BAY 869766: a potent, selective, allosteric inhibitor of MEK1/2 for the treatment of cancer. Cancer Res., 69, 6839-6847.
    • (2009) Cancer Res , vol.69 , pp. 6839-6847
    • Iverson, C.1
  • 34
    • 77953161581 scopus 로고    scopus 로고
    • Activation of FOXO3a is sufficient to reverse mitogen-activated protein/extracellular signal-regulated kinase kinase inhibitor chemoresistance in human cancer
    • Yang,J.Y. et al. (2010) Activation of FOXO3a is sufficient to reverse mitogen-activated protein/extracellular signal-regulated kinase kinase inhibitor chemoresistance in human cancer. Cancer Res., 70, 4709-4718.
    • (2010) Cancer Res , vol.70 , pp. 4709-4718
    • Yang, J.Y.1
  • 35
    • 34547482919 scopus 로고    scopus 로고
    • Clinical experience of MEK inhibitors in cancer therapy
    • Wang,D. et al. (2007) Clinical experience of MEK inhibitors in cancer therapy. Biochim. Biophys. Acta, 1773, 1248-1255.
    • (2007) Biochim. Biophys. Acta , vol.1773 , pp. 1248-1255
    • Wang, D.1
  • 36
    • 34548822459 scopus 로고    scopus 로고
    • Recent advances of MEK inhibitors and their clinical progress
    • Wang,J.Y. et al. (2007) Recent advances of MEK inhibitors and their clinical progress. Curr. Top. Med. Chem., 7, 1364-1378.
    • (2007) Curr. Top. Med. Chem. , vol.7 , pp. 1364-1378
    • Wang, J.Y.1
  • 37
    • 65649099808 scopus 로고    scopus 로고
    • Erk1/2 MAP kinases are required for epidermal G2/M progression
    • Dumesic,P.A. et al. (2009) Erk1/2 MAP kinases are required for epidermal G2/M progression. J. Cell Biol., 185, 409-422.
    • (2009) J. Cell Biol. , vol.185 , pp. 409-422
    • Dumesic, P.A.1
  • 38
    • 63449113353 scopus 로고    scopus 로고
    • Mek1/2 gene dosage determines tissue response to oncogenic Ras signaling in the skin
    • Scholl,F.A. et al. (2009) Mek1/2 gene dosage determines tissue response to oncogenic Ras signaling in the skin. Oncogene, 28, 1485-1495.
    • (2009) Oncogene , vol.28 , pp. 1485-1495
    • Scholl, F.A.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.