메뉴 건너뛰기




Volumn 4, Issue 3, 2012, Pages 153-163

The crossregulation between ERK and PI3K signaling pathways determines the tumoricidal efficacy of MEK inhibitor

Author keywords

biochemical control analysis; ERK pathway; mathematical model; MEK inhibitor; PI3K pathway; resistance; robustness; systems biology

Indexed keywords

2 MORPHOLINO 8 PHENYLCHROMONE; B RAF KINASE; BINDING PROTEIN; GRB2 ASSOCIATED BINDING PROTEIN 1; MITOGEN ACTIVATED PROTEIN KINASE INHIBITOR; MITOGEN ACTIVATED PROTEIN KINASE KINASE; N (2,3 DIHYDROXYPROPOXY) 3,4 DIFLUORO 2 (2 FLUORO 4 IODOANILINO)BENZAMIDE; PHOSPHATIDYLINOSITOL 3 KINASE; PROTEIN KINASE B; RAF PROTEIN; RAS PROTEIN; SOS PROTEIN; UNCLASSIFIED DRUG;

EID: 84861871300     PISSN: 16742788     EISSN: 17594685     Source Type: Journal    
DOI: 10.1093/jmcb/mjs021     Document Type: Article
Times cited : (63)

References (36)
  • 1
    • 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., Cohen, R.B., Franklin, W., 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    Cohen, R.B.2    Franklin, W.3
  • 2
    • 64349110975 scopus 로고    scopus 로고
    • Systems-level interactions between insulin-EGF networks amplify mitogenic signaling
    • Borisov, N., Aksamitiene, E., Kiyatkin, A., et al. (2009). Systems-level interactions between insulin-EGF networks amplify mitogenic signaling. Mol. Syst. Biol. 5, 256.
    • (2009) Mol. Syst. Biol. , vol.5 , pp. 256
    • Borisov, N.1    Aksamitiene, E.2    Kiyatkin, A.3
  • 3
    • 33847095086 scopus 로고    scopus 로고
    • Pharmacodynamic and toxicokinetic evaluation of the novel MEK inhibitor, PD0325901, in the rat following oral and intravenous administration
    • Brown, A.P., Carlson, T.C., Loi, C.M., et al. (2007). Pharmacodynamic and toxicokinetic evaluation of the novel MEK inhibitor, PD0325901, in the rat following oral and intravenous administration. Cancer Chemother. Pharmacol. 59, 671-679.
    • (2007) Cancer Chemother. Pharmacol. , vol.59 , pp. 671-679
    • Brown, A.P.1    Carlson, T.C.2    Loi, C.M.3
  • 4
    • 78649436372 scopus 로고    scopus 로고
    • BRAF gene amplification can promote acquired resistance to MEK inhibitors in cancer cells harboring the BRAF V600E mutation
    • Corcoran, R.B., Dias-Santagata, D., Bergethon, K., et al. (2010). BRAF gene amplification can promote acquired resistance to MEK inhibitors in cancer cells harboring the BRAF V600E mutation. Sci. Signal. 3, ra84.
    • (2010) Sci. Signal. , vol.3
    • Corcoran, R.B.1    Dias-Santagata, D.2    Bergethon, K.3
  • 5
    • 73949083834 scopus 로고    scopus 로고
    • MEK1 mutations confer resistance to MEK and B-RAF inhibition
    • Emery, C.M., Vijayendran, K.G., Zipser, M.C., et al. (2009). MEK1 mutations confer resistance to MEK and B-RAF inhibition. Proc. Natl Acad. Sci. USA 106, 20411-20416.
    • (2009) Proc. Natl Acad. Sci. USA , vol.106 , pp. 20411-20416
    • Emery, C.M.1    Vijayendran, K.G.2    Zipser, M.C.3
  • 6
    • 57349194139 scopus 로고    scopus 로고
    • Effective use of PI3K and MEK inhibitors to treat mutant Kras G12D and PIK3CA H1047R murine lung cancers
    • Engelman, J.A., Chen, L., Tan, X., et al. (2008). Effective use of PI3K and MEK inhibitors to treat mutant Kras G12D and PIK3CA H1047R murine lung cancers. Nat. Med. 14, 1351-1356.
    • (2008) Nat. Med. , vol.14 , pp. 1351-1356
    • Engelman, J.A.1    Chen, L.2    Tan, X.3
  • 7
    • 78449275389 scopus 로고    scopus 로고
    • Basal and treatment-induced activation of AKT mediates resistance to cell death by AZD6244 (ARRY-142886) in Braf-mutant human cutaneous melanoma cells
    • Gopal, Y.N., Deng, W., Woodman, S.E., et al. (2010). Basal and treatment-induced activation of AKT mediates resistance to cell death by AZD6244 (ARRY-142886) in Braf-mutant human cutaneous melanoma cells. Cancer Res. 70, 8736-8747.
    • (2010) Cancer Res. , vol.70 , pp. 8736-8747
    • Gopal, Y.N.1    Deng, W.2    Woodman, S.E.3
  • 8
    • 77951016969 scopus 로고    scopus 로고
    • A phase II study of PD-0325901, an oral MEK inhibitor, in previously treated patients with advanced non-small cell lung cancer
    • Haura, E.B., Ricart, A.D., Larson, T.G., et al. (2010). A phase II study of PD-0325901, an oral MEK inhibitor, in previously treated patients with advanced non-small cell lung cancer. Clin. Cancer Res. 16, 2450-2457.
    • (2010) Clin. Cancer Res. , vol.16 , pp. 2450-2457
    • Haura, E.B.1    Ricart, A.D.2    Larson, T.G.3
  • 9
    • 77956274693 scopus 로고    scopus 로고
    • Identification of optimal drug combinations targeting cellular networks: Integrating phospho-proteomics and computational network analysis
    • Iadevaia, S., Lu, Y., Morales, F.C., et al. (2010). Identification of optimal drug combinations targeting cellular networks: integrating phospho-proteomics and computational network analysis. Cancer Res. 70, 6704-6714.
    • (2010) Cancer Res. , vol.70 , pp. 6704-6714
    • Iadevaia, S.1    Lu, Y.2    Morales, F.C.3
  • 10
    • 70149119899 scopus 로고    scopus 로고
    • RDEA119/BAY 869766: A potent, selective, allosteric inhibitor of MEK1/2 for the treatment of cancer
    • Iverson, C., Larson, G., Lai, 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    Larson, G.2    Lai, C.3
  • 11
    • 69949151386 scopus 로고    scopus 로고
    • Factors underlying sensitivity of cancers to small-molecule kinase inhibitors
    • Janne, P.A., Gray, N., and Settleman, J. (2009). Factors underlying sensitivity of cancers to small-molecule kinase inhibitors. Nat. Rev. DrugDiscov. 8, 709-723.
    • (2009) Nat. Rev. DrugDiscov. , vol.8 , pp. 709-723
    • Janne, P.A.1    Gray, N.2    Settleman, J.3
  • 12
    • 33847377573 scopus 로고    scopus 로고
    • A robustness-based approach to systems-oriented drug design
    • Kitano, H. (2007). A robustness-based approach to systems-oriented drug design. Nat. Rev. Drug Discov. 6, 202-210.
    • (2007) Nat. Rev. Drug Discov. , vol.6 , pp. 202-210
    • Kitano, H.1
  • 13
    • 75149130051 scopus 로고    scopus 로고
    • Targeting the cancer kinome through polypharmacology
    • Knight, Z.A., Lin, H., and Shokat, K.M. (2010). Targeting the cancer kinome through polypharmacology. Nat. Rev. Cancer 10, 130-137.
    • (2010) Nat. Rev. Cancer , vol.10 , pp. 130-137
    • Knight, Z.A.1    Lin, H.2    Shokat, K.M.3
  • 14
    • 49449101097 scopus 로고    scopus 로고
    • High-order combination effects and biological robustness
    • Lehar, J., Krueger, A., Zimmermann, G., et al. (2008). High-order combination effects and biological robustness. Mol. Syst. Biol. 4, 215.
    • (2008) Mol. Syst. Biol. , vol.4 , pp. 215
    • Lehar, J.1    Krueger, A.2    Zimmermann, G.3
  • 15
    • 77953896432 scopus 로고    scopus 로고
    • Cell signaling by receptor tyrosine kinases
    • Lemmon, M.A., and Schlessinger, J. (2010). Cell signaling by receptor tyrosine kinases. Cell 141, 1117-1134.
    • (2010) Cell , vol.141 , pp. 1117-1134
    • Lemmon, M.A.1    Schlessinger, J.2
  • 16
    • 77949766280 scopus 로고    scopus 로고
    • Phase i pharmacokinetic and pharmacodynamic study of the oral MAPK/ERK kinase inhibitor PD-0325901 in patients with advanced cancers
    • LoRusso, P.M., Krishnamurthi, S.S., Rinehart, J.J., et al. (2010). Phase I pharmacokinetic and pharmacodynamic study of the oral MAPK/ERK kinase inhibitor PD-0325901 in patients with advanced cancers. Clin. Cancer Res. 16, 1924-1937.
    • (2010) Clin. Cancer Res. , vol.16 , pp. 1924-1937
    • Lorusso, P.M.1    Krishnamurthi, S.S.2    Rinehart, J.J.3
  • 17
    • 13844256522 scopus 로고    scopus 로고
    • The docking protein Gab1 is the primary mediator of EGF-stimulated activation of the PI-3K/Akt cell survival pathway
    • Mattoon, D.R., Lamothe, B., Lax, I., et al. (2004). The docking protein Gab1 is the primary mediator of EGF-stimulated activation of the PI-3K/Akt cell survival pathway. BMC Biol. 2, 2-4.
    • (2004) BMC Biol. , vol.2 , pp. 2-4
    • Mattoon, D.R.1    Lamothe, B.2    Lax, I.3
  • 18
    • 69249087671 scopus 로고    scopus 로고
    • Environment-mediated drug resistance: A major contributor to minimal residual disease
    • Meads, M.B., Gatenby, R.A., and Dalton, W.S. (2009). Environment-mediated drug resistance: a major contributor to minimal residual disease. Nat. Rev. Cancer 9, 665-674.
    • (2009) Nat. Rev. Cancer , vol.9 , pp. 665-674
    • Meads, M.B.1    Gatenby, R.A.2    Dalton, W.S.3
  • 19
    • 79958026380 scopus 로고    scopus 로고
    • The Ras-ERK and PI3K-mTOR pathways: Cross-talk and compensation
    • Mendoza, M.C., Er, E.E., and Blenis, J. (2011). The Ras-ERK and PI3K-mTOR pathways: cross-talk and compensation. Trends Biochem. Sci. 36, 320-328.
    • (2011) Trends Biochem. Sci. , vol.36 , pp. 320-328
    • Mendoza, M.C.1    Er, E.E.2    Blenis, J.3
  • 20
    • 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, O.K., Das, D., Heiser, L.M., et al. (2009). 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) Cancer Res. , vol.69 , pp. 565-572
    • Mirzoeva, O.K.1    Das, D.2    Heiser, L.M.3
  • 21
    • 49649118852 scopus 로고    scopus 로고
    • Elevated CRAF as a potential mechanism of acquired resistance to BRAF inhibition in melanoma
    • Montagut, C., Sharma, S.V., Shioda, T., et al. (2008). Elevated CRAF as a potential mechanism of acquired resistance to BRAF inhibition in melanoma. Cancer Res. 68, 4853-4861.
    • (2008) Cancer Res. , vol.68 , pp. 4853-4861
    • Montagut, C.1    Sharma, S.V.2    Shioda, T.3
  • 22
    • 78650303507 scopus 로고    scopus 로고
    • Melanomas acquire resistance to B-RAF(V600E) inhibition by RTK or N-RAS upregulation
    • Nazarian, R., Shi, H., Wang, Q., et al. (2010). Melanomas acquire resistance to B-RAF(V600E) inhibition by RTK or N-RAS upregulation. Nature 468, 973-977.
    • (2010) Nature , vol.468 , pp. 973-977
    • Nazarian, R.1    Shi, H.2    Wang, Q.3
  • 23
    • 0033635157 scopus 로고    scopus 로고
    • Crystal structure and functional analysis of Ras binding to its effector phosphoinositide 3-kinase gamma
    • Pacold, M.E., Suire, S., Perisic, O., et al. (2000). Crystal structure and functional analysis of Ras binding to its effector phosphoinositide 3-kinase gamma. Cell 103, 931-943.
    • (2000) Cell , vol.103 , pp. 931-943
    • Pacold, M.E.1    Suire, S.2    Perisic, O.3
  • 24
    • 80052031934 scopus 로고    scopus 로고
    • Systems-biology approaches for predicting genomic evolution
    • Papp, B., Notebaart, R.A., and Pal, C. (2011). Systems-biology approaches for predicting genomic evolution. Nat. Rev. Genet. 12, 591-602.
    • (2011) Nat. Rev. Genet. , vol.12 , pp. 591-602
    • Papp, B.1    Notebaart, R.A.2    Pal, C.3
  • 25
    • 84863230465 scopus 로고    scopus 로고
    • Unresponsiveness of colon cancer to BRAF(V600E) inhibition through feedback activation of EGFR
    • Prahallad, A., Sun, C., Huang, S., et al. (2012). Unresponsiveness of colon cancer to BRAF(V600E) inhibition through feedback activation of EGFR. Nature 483, 100-103.
    • (2012) Nature , vol.483 , pp. 100-103
    • Prahallad, A.1    Sun, C.2    Huang, S.3
  • 26
    • 14844285975 scopus 로고    scopus 로고
    • Multicenter phase II study of the oral MEK inhibitor, CI-1040, in patients with advanced non-smallcell lung, breast, colon, and pancreatic cancer
    • Rinehart, J., Adjei, A.A., Lorusso, P.M., et al. (2004). Multicenter phase II study of the oral MEK inhibitor, CI-1040, in patients with advanced non-smallcell lung, breast, colon, and pancreatic cancer. J. Clin. Oncol. 22, 4456-4462.
    • (2004) J. Clin. Oncol. , vol.22 , pp. 4456-4462
    • Rinehart, J.1    Adjei, A.A.2    Lorusso, P.M.3
  • 27
    • 0028074316 scopus 로고
    • Phosphatidylinositol-3-OH kinase as a direct target of Ras
    • Rodriguez-Viciana, P., Warne, P.H., Dhand, R., et al. (1994). Phosphatidylinositol-3-OH kinase as a direct target of Ras. Nature 370, 527-532.
    • (1994) Nature , vol.370 , pp. 527-532
    • Rodriguez-Viciana, P.1    Warne, P.H.2    Dhand, R.3
  • 28
    • 78651092705 scopus 로고    scopus 로고
    • A hidden incoherent switch regulates RCAN1 in the calcineurin-NFAT signaling network
    • Shin, S.Y., Yang, H.W., Kim, J.R., et al. (2011). A hidden incoherent switch regulates RCAN1 in the calcineurin-NFAT signaling network. J. Cell Sci. 124, 82-90.
    • (2011) J. Cell Sci. , vol.124 , pp. 82-90
    • Shin, S.Y.1    Yang, H.W.2    Kim, J.R.3
  • 29
    • 31144453233 scopus 로고    scopus 로고
    • BRAF mutation predicts sensitivity to MEK inhibition
    • Solit, D.B., Garraway, L.A., Pratilas, C.A., 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    Garraway, L.A.2    Pratilas, C.A.3
  • 30
    • 4143066760 scopus 로고    scopus 로고
    • Gefitinib-sensitizing EGFR mutations in lung cancer activate anti-apoptotic pathways
    • Sordella, R., Bell, D.W., Haber, D.A., et al. (2004). Gefitinib-sensitizing EGFR mutations in lung cancer activate anti-apoptotic pathways. Science 305, 1163-1167.
    • (2004) Science , vol.305 , pp. 1163-1167
    • Sordella, R.1    Bell, D.W.2    Haber, D.A.3
  • 31
    • 0037046799 scopus 로고    scopus 로고
    • Activation of phosphoinositide 3-kinase gamma by Ras
    • Suire, S., Hawkins, P., and Stephens, L. (2002). Activation of phosphoinositide 3-kinase gamma by Ras. Curr. Biol. 12, 1068-1075.
    • (2002) Curr. Biol. , vol.12 , pp. 1068-1075
    • Suire, S.1    Hawkins, P.2    Stephens, L.3
  • 32
    • 0034029892 scopus 로고    scopus 로고
    • Robustness against mutations in genetic networks of yeast
    • Wagner, A. (2000). Robustness against mutations in genetic networks of yeast. Nat. Genet. 24, 355-361.
    • (2000) Nat. Genet. , vol.24 , pp. 355-361
    • Wagner, A.1
  • 33
    • 66249116702 scopus 로고    scopus 로고
    • PI3K pathway activation mediates resistance to MEK inhibitors in KRAS mutant cancers
    • Wee, S., Jagani, Z., Xiang, K.X., et al. (2009). PI3K pathway activation mediates resistance to MEK inhibitors in KRAS mutant cancers. Cancer Res. 69, 4286-4293.
    • (2009) Cancer Res. , vol.69 , pp. 4286-4293
    • Wee, S.1    Jagani, Z.2    Xiang, K.X.3
  • 34
    • 57349130526 scopus 로고    scopus 로고
    • Colorectal cancer cells with the BRAF(V600E) mutation are addicted to the ERK1/2 pathway for growth factor-independent survival and repression of BIM
    • Wickenden, J.A., Jin, H., Johnson, M., et al. (2008). Colorectal cancer cells with the BRAF(V600E) mutation are addicted to the ERK1/2 pathway for growth factor-independent survival and repression of BIM. Oncogene 27, 7150-7161.
    • (2008) Oncogene , vol.27 , pp. 7150-7161
    • Wickenden, J.A.1    Jin, H.2    Johnson, M.3
  • 35
    • 0034577530 scopus 로고    scopus 로고
    • Metabolic control analysis: Biological applications and insights
    • Wildermuth, M.C. (2000). Metabolic control analysis: biological applications and insights. Genome Biol. 1, REVIEWS1031.
    • (2000) Genome Biol. , vol.1
    • Wildermuth M., .C.1
  • 36
    • 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., Marsh, V., Bernat, B.A., 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    Marsh, V.2    Bernat, B.A.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.