메뉴 건너뛰기




Volumn 39, Issue 1, 2011, Pages 23-31

Antitumor activities of JTP-74057 (GSK1120212), a novel MEK1/2 inhibitor, on colorectal cancer cell lines in vitro and in vivo

Author keywords

Antitumor activity; GSK1120212; JTP 74057; MEK; PI3K Akt

Indexed keywords

7 ETHYL 10 HYDROXYCAMPTOTHECIN; ANTINEOPLASTIC AGENT; FLUOROURACIL; JTP 74057; MITOGEN ACTIVATED PROTEIN KINASE KINASE 1; MITOGEN ACTIVATED PROTEIN KINASE KINASE 2; N [3 [3 CYCLOPROPYL 5 (2 FLUORO 4 IODOPHENYLAMINO) 6,8 DIMETHYL 2,4,7 TRIOXO 3,4,6,7 TETRAHYDRO 2H PYRIDO[4,3 D]PYRIMIDIN 1 YL]PHENYL]ACETAMIDE; OXALIPLATIN; PROTEIN KINASE B INHIBITOR; UNCLASSIFIED DRUG;

EID: 79956018943     PISSN: 10196439     EISSN: 17912423     Source Type: Journal    
DOI: 10.3892/ijo.2011.1015     Document Type: Article
Times cited : (201)

References (34)
  • 1
    • 10344258041 scopus 로고    scopus 로고
    • Targeting the mitogen-activated protein kinase cascade to treat cancer
    • DOI 10.1038/nrc1503
    • Sebolt-Leopold JS and Herrera R: Targeting the mitogen-activated protein kinase cascade to treat cancer. Nat Rev Cancer 4: 937-947, 2004 (Pubitemid 39626217)
    • (2004) Nature Reviews Cancer , vol.4 , Issue.12 , pp. 937-947
    • Sebolt-Leopold, J.S.1    Herrera, R.2
  • 2
    • 44649089666 scopus 로고    scopus 로고
    • Targeting the Raf/MEK/ERK pathway with small-molecule inhibitors
    • McCubrey JA, Milella M, Tafuri A, et al: Targeting the Raf/MEK/ERK pathway with small-molecule inhibitors. Curr Opin Investig Drugs 9: 614-630, 2008.
    • (2008) Curr Opin Investig Drugs , vol.9 , pp. 614-630
    • McCubrey, J.A.1    Milella, M.2    Tafuri, A.3
  • 3
    • 0024376173 scopus 로고
    • Ras oncogenes in human cancer: A review
    • Bos JL: Ras oncogenes in human cancer: a review. Cancer Res 49: 4682-4689, 1989
    • (1989) Cancer Res , vol.49 , pp. 4682-4689
    • Bos, J.L.1
  • 4
    • 0035908493 scopus 로고    scopus 로고
    • Blocking oncogenic Ras signaling for cancer therapy
    • Adjei AA: Blocking oncogenic Ras signaling for cancer therapy. J Natl Cancer Inst 93: 1062-1074, 2001.
    • (2001) J Natl Cancer Inst , vol.93 , pp. 1062-1074
    • Adjei, A.A.1
  • 5
    • 18444374405 scopus 로고    scopus 로고
    • Mutations of the BRAF gene in human cancer
    • Davies H, Bignell GR, Cox C, et al: Mutations of the BRAF gene in human cancer. Nature 417: 949-954, 2002.
    • (2002) Nature , vol.417 , pp. 949-954
    • Davies, H.1    Bignell, G.R.2    Cox, C.3
  • 6
    • 33745925864 scopus 로고    scopus 로고
    • BRAF somatic mutations in malignant melanoma and melanocytic naevi
    • Thomas NE: BRAF somatic mutations in malignant melanoma and melanocytic naevi. Melanoma Res 16: 97-103, 2006.
    • (2006) Melanoma Res , vol.16 , pp. 97-103
    • Thomas, N.E.1
  • 9
    • 0037379904 scopus 로고    scopus 로고
    • High prevalence of BRAF mutations in thyroid cancer: Genetic evidence for constitutive activation of the RET/PTC-RAS-BRAF signaling pathway in papillary thyroid carcinoma
    • Kimura ET, Nikiforova MN, Zhu Z, Knauf JA, Nikiforov YE and Fagin JA: High prevalence of BRAF mutations in thyroid cancer: genetic evidence for constitutive activation of the RET/PTC-RAS-BRAF signaling pathway in papillary thyroid carcinoma. Cancer Res 63: 1454-1457, 2003. (Pubitemid 36373628)
    • (2003) Cancer Research , vol.63 , Issue.7 , pp. 1454-1457
    • Kimura, E.T.1    Nikiforova, M.N.2    Zhu, Z.3    Knauf, J.A.4    Nikiforov, Y.E.5    Fagin, J.A.6
  • 10
    • 0035902180 scopus 로고    scopus 로고
    • Oncogenic kinase signaling
    • Blume-Jensen P and Hunter T: Oncogenic kinase signaling. Nature 411: 355-365, 2001.
    • (2001) Nature , vol.411 , pp. 355-365
    • Blume-Jensen, P.1    Hunter, T.2
  • 11
    • 0032541677 scopus 로고    scopus 로고
    • Tyrosine kinase receptor-activated signal transduction pathways which lead to oncogenesis
    • Porter AC and Vaillancourt RR: Tyrosine kinase receptor-activated signal transduction pathways which lead to oncogenesis. Oncogene 17: 1343-1352, 1998. (Pubitemid 28458404)
    • (1998) Oncogene , vol.17 , Issue.11 REV. ISS. 1 , pp. 1343-1352
    • Porter, A.C.1    Vaillancourt, R.R.2
  • 18
    • 0037663473 scopus 로고    scopus 로고
    • Suppression of ARG kinase activity by STI571 induces cell cycle arrest through up-regulation of CDK inhibitor p18/INK4c
    • DOI 10.1038/sj.onc.1206498
    • Nishimura N, Furukawa Y, Sutheesophon K, et al: Suppression of ARG kinase activity by STI571 induces cell cycle arrest through up-regulation of CDK inhibitor p18/INK4c. Oncogene 22: 4074-4082, 2003. (Pubitemid 36819647)
    • (2003) Oncogene , vol.22 , Issue.26 , pp. 4074-4082
    • Nishimura, N.1    Furukawa, Y.2    Sutheesophon, K.3    Nakamura, M.4    Kishi, K.5    Okuda, K.6    Sato, Y.7    Kano, Y.8
  • 21
    • 34748852495 scopus 로고    scopus 로고
    • INK4b-inductive compound, as a novel MEK1/2 inhibitor
    • INK4b-inductive compound, as a novel MEK1/2 inhibitor. Cancer Sci 98: 1809-1816, 2007
    • (2007) Cancer Sci , vol.98 , pp. 1809-1816
    • Yamaguchi, T.1    Yoshida, T.2    Kurachi, R.3
  • 22
    • 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
    • DOI 10.1158/1535-7163.MCT-07-0231
    • Davies BR, Logie A, McKay JS, et al: 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 (Pubitemid 47294749)
    • (2007) Molecular Cancer Therapeutics , vol.6 , Issue.8 , pp. 2209-2219
    • Davies, B.R.1    Logie, A.2    McKay, J.S.3    Martin, P.4    Steele, S.5    Jenkins, R.6    Cockerill, M.7    Cartlidge, S.8    Smith, P.D.9
  • 23
    • 58349091262 scopus 로고    scopus 로고
    • Basal subtype and MAPK/ERK kinase (MEK)-phosphoinositide 3-kinase feedback signaling determine susceptibility of breast cancer cells to MEK inhibition
    • Mirzoeva OK, Das D, Heiser LM, et al: Basal subtype and MAPK/ERK kinase (MEK)-phosphoinositide 3-kinase feedback signaling determine susceptibility of breast cancer cells to MEK inhibition. Cancer Res 69: 565-572, 2009
    • (2009) Cancer Res , vol.69 , pp. 565-572
    • Mirzoeva, O.K.1    Das, D.2    Heiser, L.M.3
  • 24
    • 68049085887 scopus 로고    scopus 로고
    • In vivo antitumor activity of MEK and phosphatidylinositol 3-kinase inhibitors in basal-like breast cancer models
    • Hoeflich KP, O'Brien C, Boyd Z, et al: In vivo antitumor activity of MEK and phosphatidylinositol 3-kinase inhibitors in basal-like breast cancer models. Clin Cancer Res 15: 4649-4664, 2009
    • (2009) Clin Cancer Res , vol.15 , pp. 4649-4664
    • Hoeflich, K.P.1    O'Brien, C.2    Boyd, Z.3
  • 25
    • 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 JY, Chang CJ, Xia W, et al: 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.
    • (2010) Cancer Res , vol.70 , pp. 4709-4718
    • Yang, J.Y.1    Chang, C.J.2    Xia, W.3
  • 26
    • 0032905667 scopus 로고    scopus 로고
    • Cellular pharmacology of the combination of the DNA topoisomerase I inhibitor SN-38 and the diaminocyclohexane platinum derivative oxaliplatin
    • Zeghari-Squalli N, Raymond E, Cvitkovic E and Goldwasser F: Cellular pharmacology of the combination of the DNA topoisomerase I inhibitor SN-38 and the diaminocyclohexane platinum derivative oxaliplatin. Clin Cancer Res 5: 1189-1196, 1999 (Pubitemid 29233237)
    • (1999) Clinical Cancer Research , vol.5 , Issue.5 , pp. 1189-1196
    • Zeghari-Squalli, N.1    Raymond, E.2    Cvitkovic, E.3    Goldwasser, F.4
  • 27
    • 0028145844 scopus 로고
    • Efficacy of combination therapy of irinotecan (CPT-11) and other anticancer drugs: Evaluation in B-lymphoid tumor cell lines
    • Akutsu M, Suzuki K, Tsunoda S, Kano Y and Miura Y: Efficacy of combination therapy of irinotecan (CPT-11) and other anticancer drugs: evaluation in B-lymphoid tumor cell lines. Jpn J Cancer Chemotherapy 21: 1607-1611, 1994
    • (1994) Jpn J Cancer Chemotherapy , vol.21 , pp. 1607-1611
    • Akutsu, M.1    Suzuki, K.2    Tsunoda, S.3    Kano, Y.4    Miura, Y.5
  • 28
    • 70349878470 scopus 로고    scopus 로고
    • Intrinsic resistance to the MEK1/2 inhibitor AZD6244 (ARRY-142886) is associated with weak ERK1/2 signalling and/or strong PI3K signalling in colorectal cancer cell lines
    • Balmanno K, Chell SD, Gillings AS, Hayat S and Cook SJ: Intrinsic resistance to the MEK1/2 inhibitor AZD6244 (ARRY-142886) is associated with weak ERK1/2 signalling and/or strong PI3K signalling in colorectal cancer cell lines. Int J Cancer 125: 2332-2341, 2009
    • (2009) Int J Cancer , vol.125 , pp. 2332-2341
    • Balmanno, K.1    Chell, S.D.2    Gillings, A.S.3    Hayat, S.4    Cook, S.J.5
  • 30
    • 0041327168 scopus 로고    scopus 로고
    • Proliferation of cancer cells despite CDK2 inhibition
    • DOI 10.1016/S1535-6108(03)00053-9
    • Tetsu O and McCormick F: Proliferation of cancer cells despite CDK2 inhibition. Cancer Cell 3: 233-245, 2003. (Pubitemid 37443879)
    • (2003) Cancer Cell , vol.3 , Issue.3 , pp. 233-245
    • Tetsu, O.1    McCormick, F.2
  • 31
    • 11144358645 scopus 로고    scopus 로고
    • High frequency of mutations of the PIK3CA gene in human cancers
    • Samuels Y, Wang Z and Bardelli A: High frequency of mutations of the PIK3CA gene in human cancers. Science 304: 554, 2004
    • (2004) Science , vol.304 , pp. 554
    • Samuels, Y.1    Wang, Z.2    Bardelli, A.3
  • 33
    • 79956035933 scopus 로고    scopus 로고
    • Models for response to the MEK inhibitor GSK1120212 confirm RAS and BRAF mutations as predictive biomarkers and suggest other, unexpected tumor types for clinical evaluation
    • Woosterl R, Cornwell W, Jing J, et al: Models for response to the MEK inhibitor GSK1120212 confirm RAS and BRAF mutations as predictive biomarkers and suggest other, unexpected tumor types for clinical evaluation. Eur J Cancer (Suppl) 6: S33-S34, 2008.
    • (2008) Eur J Cancer (Suppl) , vol.6
    • Woosterl, R.1    Cornwell, W.2    Jing, J.3
  • 34
    • 22844431902 scopus 로고    scopus 로고
    • Role of genomic markers in colorectal cancer treatment
    • DOI 10.1200/JCO.2005.19.752
    • Allen WL and Johnston PG. Role of genomic markers in colorectal cancer treatment. J Clin Oncol 23: 4545-4552, 2005. (Pubitemid 46196585)
    • (2005) Journal of Clinical Oncology , vol.23 , Issue.20 , pp. 4545-4552
    • Allen, W.L.1    Johnston, P.G.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.