메뉴 건너뛰기




Volumn 18, Issue 15, 2012, Pages 4104-4113

Cancer network disruption by a single molecule inhibitor targeting both histone deacetylase activity and phosphatidylinositol 3-kinase signaling

Author keywords

[No Author keywords available]

Indexed keywords

ANTINEOPLASTIC AGENT; CUDC 907; HISTONE DEACETYLASE; MAMMALIAN TARGET OF RAPAMYCIN; MITOGEN ACTIVATED PROTEIN KINASE; MITOGEN ACTIVATED PROTEIN KINASE KINASE; PANOBINOSTAT; PHOSPHATIDYLINOSITOL 3 KINASE; PICTRELISIB; PROTEIN KINASE B; PROTEIN TYROSINE KINASE; RAF PROTEIN; STAT3 PROTEIN; UNCLASSIFIED DRUG; VORINOSTAT;

EID: 84864484251     PISSN: 10780432     EISSN: 15573265     Source Type: Journal    
DOI: 10.1158/1078-0432.CCR-12-0055     Document Type: Article
Times cited : (201)

References (36)
  • 1
  • 2
    • 67749122122 scopus 로고    scopus 로고
    • Targeting PI3K signaling in cancer: Opportunities, challenges and limitations
    • Engelman JA. Targeting PI3K signaling in cancer: opportunities, challenges and limitations. Nat Rev Cancer 2009;9:550-62.
    • (2009) Nat Rev Cancer , vol.9 , pp. 550-562
    • Engelman, J.A.1
  • 3
    • 51849111524 scopus 로고    scopus 로고
    • NVP-BEZ235, a dual PI3K/mTOR inhibitor, prevents PI3K signaling and inhibits the growth of cancer cells with activating PI3K mutations
    • Serra V, Markman B, Scaltriti M, Eichhorn PJ, Valero V, Guzman M, et al. NVP-BEZ235, a dual PI3K/mTOR inhibitor, prevents PI3K signaling and inhibits the growth of cancer cells with activating PI3K mutations. Cancer Res 2008;68:8022-30.
    • (2008) Cancer Res , vol.68 , pp. 8022-8030
    • Serra, V.1    Markman, B.2    Scaltriti, M.3    Eichhorn, P.J.4    Valero, V.5    Guzman, M.6
  • 4
    • 67651155960 scopus 로고    scopus 로고
    • Biological properties of potent inhibitors of class I phosphatidylinositide 3-kinases: From PI-103 through PI-540, PI-620 to the oral agent GDC-0941
    • Raynaud FI, Eccles SA, Patel S, Alix S, Box G, Chuckowree I, et al. Biological properties of potent inhibitors of class I phosphatidylinositide 3-kinases: from PI-103 through PI-540, PI-620 to the oral agent GDC-0941. Mol Cancer Ther 2009;8:1725-38.
    • (2009) Mol Cancer Ther , vol.8 , pp. 1725-1738
    • Raynaud, F.I.1    Eccles, S.A.2    Patel, S.3    Alix, S.4    Box, G.5    Chuckowree, I.6
  • 5
    • 34548596728 scopus 로고    scopus 로고
    • A dual phosphoinositide-3-kinase alpha/mTOR inhibitor cooperates with blockade of epidermal growth factor receptor in PTEN-mutant glioma
    • DOI 10.1158/0008-5472.CAN-07-2154
    • Fan QW, Cheng CK, Nicolaides TP, Hackett CS, Knight ZA, Shokat KM, et al. A dual phosphoinositide-3-kinase alpha/mTOR inhibitor cooperates with blockade of epidermal growth factor receptor in PTEN-mutant glioma. Cancer Res 2007;67:7960-65. (Pubitemid 47395125)
    • (2007) Cancer Research , vol.67 , Issue.17 , pp. 7960-7965
    • Fan, Q.-W.1    Cheng, C.K.2    Nicolaides, T.P.3    Hackett, C.S.4    Knight, Z.A.5    Shokat, K.M.6    Weiss, W.A.7
  • 6
    • 51849098272 scopus 로고    scopus 로고
    • Drug discovery approaches targeting the PI3K/Akt pathway in cancer
    • Garcia-Echeverria C, Sellers WR. Drug discovery approaches targeting the PI3K/Akt pathway in cancer. Oncogene 2008;27:5511-26.
    • (2008) Oncogene , vol.27 , pp. 5511-5526
    • Garcia-Echeverria, C.1    Sellers, W.R.2
  • 8
    • 70449995469 scopus 로고    scopus 로고
    • Identifying genotype-dependent efficacy of single and combined PI3K- And MAPK-pathway inhibition in cancer
    • Sos ML, Fischer S, Ullrich R, Peifer M, Heuckmann JM, Koker M, et al. Identifying genotype-dependent efficacy of single and combined PI3K- and MAPK-pathway inhibition in cancer. Proc Natl Acad Sci U S A 2009;106:18351-56.
    • (2009) Proc Natl Acad Sci U S A , vol.106 , pp. 18351-18356
    • Sos, M.L.1    Fischer, S.2    Ullrich, R.3    Peifer, M.4    Heuckmann, J.M.5    Koker, M.6
  • 9
    • 66249116702 scopus 로고    scopus 로고
    • PI3K pathway activation mediates resistance to MEK inhibitors in KRAS mutant cancers
    • Wee S, Jagani Z, Xiang KX, Loo A, Dorsch M, Yao YM, et al. PI3K pathway activation mediates resistance to MEK inhibitors in KRAS mutant cancers. Cancer Res 2009;69:4286-93.
    • (2009) Cancer Res , vol.69 , pp. 4286-4293
    • Wee, S.1    Jagani, Z.2    Xiang, K.X.3    Loo, A.4    Dorsch, M.5    Yao, Y.M.6
  • 10
    • 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, Cavet G, Guerrero S, Jung K, et al. In vivo antitumor activity of MEK and phosphatidylinositol 3-kinase inhibitors in basal-like breast cancer models. Clin Cancer Res 2009;15:4649-64.
    • (2009) Clin Cancer Res , vol.15 , pp. 4649-4664
    • Hoeflich, K.P.1    O'Brien, C.2    Boyd, Z.3    Cavet, G.4    Guerrero, S.5    Jung, K.6
  • 11
    • 79959712087 scopus 로고    scopus 로고
    • Ras/RAF/MEK/MAPK and PI3K/PTEN/Akt/mTOR inhibitors: Rationale and importance to inhibiting these pathways in human health
    • Chappell WH, Steelman LS, Long JM, Kempf RC, Abrams SL, Franklin RA, et al. Ras/RAF/MEK/MAPK and PI3K/PTEN/Akt/mTOR inhibitors: rationale and importance to inhibiting these pathways in human health. Oncotarget 2011;2:135-64.
    • (2011) Oncotarget , vol.2 , pp. 135-164
    • Chappell, W.H.1    Steelman, L.S.2    Long, J.M.3    Kempf, R.C.4    Abrams, S.L.5    Franklin, R.A.6
  • 12
    • 57349194139 scopus 로고    scopus 로고
    • Effective use of PI3K and MEK inhibitors to treat mutant Kras G12D and PIK3CA H1047R murine lung cancers
    • Engelman JA, Chen L, Tan X, Crosby K, Guimaraes AR, Upadhyay R, et al. Effective use of PI3K and MEK inhibitors to treat mutant Kras G12D and PIK3CA H1047R murine lung cancers. Nat Med 2008;14:1351-6.
    • (2008) Nat Med , vol.14 , pp. 1351-1356
    • Engelman, J.A.1    Chen, L.2    Tan, X.3    Crosby, K.4    Guimaraes, A.R.5    Upadhyay, R.6
  • 14
    • 79952932076 scopus 로고    scopus 로고
    • Histone deacetylase inhibitors: Molecular mechanisms of action and clinical trials as anti-cancer drugs
    • Kim H-J, Bae S-C. Histone deacetylase inhibitors: molecular mechanisms of action and clinical trials as anti-cancer drugs. Am J Transl Res 2011;3:166-79.
    • (2011) Am J Transl Res , vol.3 , pp. 166-179
    • Kim, H.-J.1    Bae, S.-C.2
  • 15
    • 78650848615 scopus 로고    scopus 로고
    • Histone deacetylase inhibitors in the treatment of lymphoma
    • Lemoine M, Younes A. Histone deacetylase inhibitors in the treatment of lymphoma. Discov Med 2010;10:462-70.
    • (2010) Discov Med , vol.10 , pp. 462-470
    • Lemoine, M.1    Younes, A.2
  • 16
    • 77950644059 scopus 로고    scopus 로고
    • Vorinostat interferes with the signaling transduction pathway of T-cell receptor and synergizes with phosphoinositide-3 kinase inhibitors in cutaneous T-cell lymphoma
    • Wozniak MB, Villuendas R, Bischoff JR, Aparicio CB, Martínez Leal JF, de La Cueva P, et al. Vorinostat interferes with the signaling transduction pathway of T-cell receptor and synergizes with phosphoinositide-3 kinase inhibitors in cutaneous T-cell lymphoma. Haematologica 2010;95:613-21.
    • (2010) Haematologica , vol.95 , pp. 613-621
    • Wozniak, M.B.1    Villuendas, R.2    Bischoff, J.R.3    Aparicio, C.B.4    Martínez Leal, J.F.5    De La Cueva, P.6
  • 17
    • 74449089863 scopus 로고    scopus 로고
    • Blockade of the MAPK or PI3K-Akt signaling pathway enhances the cytotoxicity of histone deacetylase inhibitors in tumor cells resistant to gefitinib or imatinib
    • Ozaki K, Kosugi M, Baba N, Fujio K, Sakamoto T, Kimura S, et al. Blockade of the MAPK or PI3K-Akt signaling pathway enhances the cytotoxicity of histone deacetylase inhibitors in tumor cells resistant to gefitinib or imatinib. Biochem BiophysResCommun2009;391:1610-5.
    • (2009) Biochem BiophysResCommun , vol.391 , pp. 1610-1615
    • Ozaki, K.1    Kosugi, M.2    Baba, N.3    Fujio, K.4    Sakamoto, T.5    Kimura, S.6
  • 18
    • 0021118703 scopus 로고
    • Quantitative analysis of dose-effect relationships: The combined effects of multiple drugs or enzyme inhibitors
    • Chou TC, Talalay P. Quantitative analysis of dose-effect relationships: the combined effects of multiple drugs or enzyme inhibitors. Adv Enzyme Regul 1984;22:27-55.
    • (1984) Adv Enzyme Regul , vol.22 , pp. 27-55
    • Chou, T.C.1    Talalay, P.2
  • 20
    • 39449138853 scopus 로고    scopus 로고
    • Inhibitors of histone deacetylase (HDAC) restore the p53 pathway in neuroblastoma cells
    • DOI 10.1038/sj.bjp.0707608, PII 0707608
    • Condorelli F, Gnemmi I, Vallario A, Genazzani AA, Canonico PL. Inhibitors of histone deacetylase (HDAC) restore the p53 pathway in neuroblastoma cells. Br J Pharmacol 2008;153:657-68. (Pubitemid 351271755)
    • (2008) British Journal of Pharmacology , vol.153 , Issue.4 , pp. 657-668
    • Condorelli, F.1    Gnemmi, I.2    Vallario, A.3    Genazzani, A.A.4    Canonico, P.L.5
  • 21
    • 67349201377 scopus 로고    scopus 로고
    • Targeting tumor angiogenesis with histone deacetylase inhibitors
    • Ellis L, Hammers H, Pili R. Targeting tumor angiogenesis with histone deacetylase inhibitors. Cancer Lett 2009;280:145-53.
    • (2009) Cancer Lett , vol.280 , pp. 145-153
    • Ellis, L.1    Hammers, H.2    Pili, R.3
  • 24
    • 49649108912 scopus 로고    scopus 로고
    • Role of acetylation and extracellular location of heat shock protein 90alpha in tumor cell invasion
    • Yang Y, Rao R, Shen J, Tang Y, Fiskus W, Nechtman J, et al. Role of acetylation and extracellular location of heat shock protein 90alpha in tumor cell invasion. Cancer Res 2008;68:4833-42.
    • (2008) Cancer Res , vol.68 , pp. 4833-4842
    • Yang, Y.1    Rao, R.2    Shen, J.3    Tang, Y.4    Fiskus, W.5    Nechtman, J.6
  • 27
    • 70449494636 scopus 로고    scopus 로고
    • Inhibition of histone deacetylase overcomes rapamycin-mediated resistance in diffuse large B-cell lymphoma by inhibiting Akt signaling through mTORC2
    • Gupta M, Ansell SM, Novak AJ, Kumar S, Kaufmann SH, Witzig TE. Inhibition of histone deacetylase overcomes rapamycin-mediated resistance in diffuse large B-cell lymphoma by inhibiting Akt signaling through mTORC2. Blood 2009;114:2926-35.
    • (2009) Blood , vol.114 , pp. 2926-2935
    • Gupta, M.1    Ansell, S.M.2    Novak, A.J.3    Kumar, S.4    Kaufmann, S.H.5    Witzig, T.E.6
  • 28
    • 50349091316 scopus 로고    scopus 로고
    • Combination strategy targeting the hypoxia inducible factor-1 alpha with mammalian target of rapamycin and histone deacetylase inhibitors
    • Verheul HM, Salumbides B, Van Erp K, Hammers H, Qian DZ, Sanni T, et al. Combination strategy targeting the hypoxia inducible factor-1 alpha with mammalian target of rapamycin and histone deacetylase inhibitors. Clin Cancer Res 2008;14:3589-97.
    • (2008) Clin Cancer Res , vol.14 , pp. 3589-3597
    • Verheul, H.M.1    Salumbides, B.2    Van Erp, K.3    Hammers, H.4    Qian, D.Z.5    Sanni, T.6
  • 29
    • 48449091227 scopus 로고    scopus 로고
    • Discovery of drug-resistant and drug-sensitizing mutations in the oncogenic PI3K isoform p110 alpha
    • Zuner ER, Knight ZA, Houseman BT, Apsel B, Shokat KM. Discovery of drug-resistant and drug-sensitizing mutations in the oncogenic PI3K isoform p110 alpha. Cancer Cell 2008;14:180-92.
    • (2008) Cancer Cell , vol.14 , pp. 180-192
    • Zuner, E.R.1    Knight, Z.A.2    Houseman, B.T.3    Apsel, B.4    Shokat, K.M.5
  • 30
    • 33847043595 scopus 로고    scopus 로고
    • Development and validation of high-performance liquid chromatography-tandem mass spectrometry assay for 6-(3-benzoyl-ureido)-hexanoic acid hydroxyamide, a novel HDAC inhibitor, in mouse plasma for pharmacokinetic studies
    • Yeo P, Xin L, Goh E, New LS, Zeng P, Wu X, et al. Development and validation of high-performance liquid chromatography-tandem mass spectrometry assay for 6-(3-benzoyl-ureido)-hexanoic acid hydroxyamide, a novel HDAC inhibitor, in mouse plasma for pharmacokinetic studies. Biomed Chromatogr 2007;21:184-9.
    • (2007) Biomed Chromatogr , vol.21 , pp. 184-189
    • Yeo, P.1    Xin, L.2    Goh, E.3    New, L.S.4    Zeng, P.5    Wu, X.6
  • 32
    • 84872607289 scopus 로고    scopus 로고
    • Development and validation of an LC-MS/MS method for determination of vorinostat in beagle dog plasma and its application to a pharmacokinetic study
    • Liu L, Ju HL, Zhang J, Liang Y, Liu X-D, Xie L, et al. Development and validation of an LC-MS/MS method for determination of vorinostat in beagle dog plasma and its application to a pharmacokinetic study. Asian J Pharmacodyn Pharmacokinet 2010;10:209-19.
    • (2010) Asian J Pharmacodyn Pharmacokinet , vol.10 , pp. 209-219
    • Liu, L.1    Ju, H.L.2    Zhang, J.3    Liang, Y.4    Liu, X.-D.5    Xie, L.6
  • 34
    • 77949353758 scopus 로고    scopus 로고
    • Discovery of 7-(4-(3-ethynylphenylamino)-7-methoxyquinazolin-6-yloxy)-N- hydroxyheptanamide (CUDc-101) as a potent multi-acting HDAC, EGFR, and HER2 inhibitor for the treatment of cancer
    • Cai X, Zhai HX, Wang J, Forrester J, Qu H, Yin L, et al. Discovery of 7-(4-(3-ethynylphenylamino)-7-methoxyquinazolin-6-yloxy)-N-hydroxyheptanamide (CUDc-101) as a potent multi-acting HDAC, EGFR, and HER2 inhibitor for the treatment of cancer. J Med Chem 2010;53:2000-9.
    • (2010) J Med Chem , vol.53 , pp. 2000-2009
    • Cai, X.1    Zhai, H.X.2    Wang, J.3    Forrester, J.4    Qu, H.5    Yin, L.6
  • 35
    • 77951708371 scopus 로고    scopus 로고
    • CUDC-101, a multitargeted inhibitor of histone deacetylase, epidermal growth factor receptor, and human epidermal growth factor receptor 2, exerts potent anticancer activity
    • Lai CJ, Bao R, Tao X, Wang J, Atoyan R, Qu H, et al. CUDC-101, a multitargeted inhibitor of histone deacetylase, epidermal growth factor receptor, and human epidermal growth factor receptor 2, exerts potent anticancer activity. Cancer Res 2010;70:3647-56.
    • (2010) Cancer Res , vol.70 , pp. 3647-3656
    • Lai, C.J.1    Bao, R.2    Tao, X.3    Wang, J.4    Atoyan, R.5    Qu, H.6
  • 36
    • 84872606776 scopus 로고    scopus 로고
    • The first-in-human, first-in-class study of CUDC-101, a multi-targeted inhibitor of HDAC,EGFRand HER2: A phase I study in patients with advanced cancer
    • [abstract]. Philadelphia (PA): AACR; Abstract nr 364
    • Shimizu T, Tolcher AW, Papadopoulos K, Patnaik A, LoRusso P, Smith LS, et al. The first-in-human, first-in-class study of CUDC-101, a multi-targeted inhibitor of HDAC,EGFRand HER2: a phase I study in patients with advanced cancer [abstract]. In: Proceedings of the 22nd EORTCNCI-AACR; 2010; Berlin, Germany. Philadelphia (PA): AACR; 2010. Abstract nr 364.
    • (2010) Proceedings of the 22nd EORTCNCI-AACR; 2010; Berlin, Germany
    • Shimizu, T.1    Tolcher, A.W.2    Papadopoulos, K.3    Patnaik, A.4    LoRusso, P.5    Smith, L.S.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.