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Volumn 13, Issue 1, 2007, Pages 331-340

The combi-targeting concept: In vitro and in vivo fragmentation of a stable combi-nitrosourea engineered to interact with the epidermal growth factor receptor while remaining DNA reactive

Author keywords

[No Author keywords available]

Indexed keywords

AMINE; ANTINEOPLASTIC AGENT; CARMUSTINE; DRUG METABOLITE; EPIDERMAL GROWTH FACTOR RECEPTOR; EPIDERMAL GROWTH FACTOR RECEPTOR KINASE; JDA 35; JDA 41; JDA 58; NITROSOUREA DERIVATIVE; UNCLASSIFIED DRUG;

EID: 33846302437     PISSN: 10780432     EISSN: None     Source Type: Journal    
DOI: 10.1158/1078-0432.CCR-06-0812     Document Type: Article
Times cited : (25)

References (41)
  • 1
    • 0033505039 scopus 로고    scopus 로고
    • Structure-based design of potent inhibitors of EGF-receptor tyrosine kinase as anti-cancer agents
    • Ghosh S, Narla RK, Zheng Y, et al. Structure-based design of potent inhibitors of EGF-receptor tyrosine kinase as anti-cancer agents. Anticancer Drug Des 1999;14:403-10.
    • (1999) Anticancer Drug Des , vol.14 , pp. 403-410
    • Ghosh, S.1    Narla, R.K.2    Zheng, Y.3
  • 2
    • 0034068319 scopus 로고    scopus 로고
    • Antitumor effect and potentiation of cytotoxic drugs activity in human cancer cells by ZD-1839 (Iressa), an epidermal growth factor receptor-sensitive tyrosine kinase inhibitor
    • Ciardiello F, Caputo R, Bianco R, et al. Antitumor effect and potentiation of cytotoxic drugs activity in human cancer cells by ZD-1839 (Iressa), an epidermal growth factor receptor-sensitive tyrosine kinase inhibitor. Clin Cancer Res 2001;6:2053-63.
    • (2001) Clin Cancer Res , vol.6 , pp. 2053-2063
    • Ciardiello, F.1    Caputo, R.2    Bianco, R.3
  • 3
    • 0033025369 scopus 로고    scopus 로고
    • Inhibition of the epidermal growth factor receptor family of tyrosine kinase as an approach to cancer chemotherapy: Progression from reversible to irreversible inhibitors
    • Fry DW. Inhibition of the epidermal growth factor receptor family of tyrosine kinase as an approach to cancer chemotherapy: progression from reversible to irreversible inhibitors. Pharmacol Ther 1999;82: 207-18.
    • (1999) Pharmacol Ther , vol.82 , pp. 207-218
    • Fry, D.W.1
  • 4
    • 0030044628 scopus 로고    scopus 로고
    • Enhancement of chemosensitivity by tyrphostin AG825 in high-p185(neu) expressing non-small cell lung cancer cells
    • Tsai CM, Levitzki A, Wu LH, et al. Enhancement of chemosensitivity by tyrphostin AG825 in high-p185(neu) expressing non-small cell lung cancer cells. Cancer Res 1996;56:1068-74.
    • (1996) Cancer Res , vol.56 , pp. 1068-1074
    • Tsai, C.M.1    Levitzki, A.2    Wu, L.H.3
  • 5
    • 0033369229 scopus 로고    scopus 로고
    • High-dose ifosfamide for patients with stage IV non-small cell lung cancer: Phase II trial from the Groupe francais de pneumo-cancerologie (GFPC) [in French]
    • Vergnene A, Thomas P, Robinet G, et al. High-dose ifosfamide for patients with stage IV non-small cell lung cancer: phase II trial from the Groupe francais de pneumo-cancerologie (GFPC) [in French]. Bull Cancer 2003;86:1017-21.
    • (2003) Bull Cancer , vol.86 , pp. 1017-1021
    • Vergnene, A.1    Thomas, P.2    Robinet, G.3
  • 8
    • 0037217857 scopus 로고    scopus 로고
    • The combi-targeting concept: A novel 3,3-disubstituted nitrosourea with EGFR tyrosine kinase inhibitory properties
    • Qiu Q, Dudouit F, Matheson SL, et al. The combi-targeting concept: a novel 3,3-disubstituted nitrosourea with EGFR tyrosine kinase inhibitory properties. Cancer Chemother Pharmacol 2003;51:1-10.
    • (2003) Cancer Chemother Pharmacol , vol.51 , pp. 1-10
    • Qiu, Q.1    Dudouit, F.2    Matheson, S.L.3
  • 9
    • 1642402869 scopus 로고    scopus 로고
    • Inhibition of cell signaling by the combi-nitrosourea FD137 in the androgen independent DU145 prostate cancer cell line
    • Qiu Q, Dudouit F, Banerjee R, McNamee JP, Jean-Claude BJ. Inhibition of cell signaling by the combi-nitrosourea FD137 in the androgen independent DU145 prostate cancer cell line. Prostate 2004;59: 13-21.
    • (2004) Prostate , vol.59 , pp. 13-21
    • Qiu, Q.1    Dudouit, F.2    Banerjee, R.3    McNamee, J.P.4    Jean-Claude, B.J.5
  • 10
    • 33745123646 scopus 로고    scopus 로고
    • The combi-targeting concept: Synthesis of stable nitrosoureas designed to inhibit the epidermal growth factor receptor (EGFR)
    • Domarkas J, Dudouit F, Williams C, et al. The combi-targeting concept: synthesis of stable nitrosoureas designed to inhibit the epidermal growth factor receptor (EGFR). J Med Chem 2006;49:3544-52.
    • (2006) J Med Chem , vol.49 , pp. 3544-3552
    • Domarkas, J.1    Dudouit, F.2    Williams, C.3
  • 11
    • 0037220070 scopus 로고    scopus 로고
    • Differential responses of EGFR/AGT-expressing cells to the "combi-triazene" SMA41
    • Matheson SL, McNamee J, Jean-Claude BJ. Differential responses of EGFR/AGT-expressing cells to the "combi-triazene" SMA41. Cancer Chemother Pharmacol 2003;51:11-20.
    • (2003) Cancer Chemother Pharmacol , vol.51 , pp. 11-20
    • Matheson, S.L.1    McNamee, J.2    Jean-Claude, B.J.3
  • 12
    • 0345412531 scopus 로고    scopus 로고
    • Synthesis of a prodrug designed to release multiple inhibitors of the epidermal growth factor receptor (EGFR) tyrosine kinase and an alkylating agent: A novel tumour targeting concept
    • Banerjee R, Rachid Z, McNamee JP, Jean-Claude BJ. Synthesis of a prodrug designed to release multiple inhibitors of the epidermal growth factor receptor (EGFR) tyrosine kinase and an alkylating agent: a novel tumour targeting concept. J Med Chem 2003;46: 5546-51.
    • (2003) J Med Chem , vol.46 , pp. 5546-5551
    • Banerjee, R.1    Rachid, Z.2    McNamee, J.P.3    Jean-Claude, B.J.4
  • 14
    • 0036145181 scopus 로고    scopus 로고
    • EGFR family expression in breast carcinomas. c-erbB-2 and c-erbB-4 receptors have different effects on survival
    • Suo Z, Risberg B, Kalsson MG, et al. EGFR family expression in breast carcinomas. c-erbB-2 and c-erbB-4 receptors have different effects on survival. J Pathol 2002;196:17-25.
    • (2002) J Pathol , vol.196 , pp. 17-25
    • Suo, Z.1    Risberg, B.2    Kalsson, M.G.3
  • 15
    • 0030774045 scopus 로고    scopus 로고
    • Induction of apoptosis and cell cycle arrest by CP-358, 774, an inhibitor of epidermal growth factor receptor tyrosine kinase
    • Moyer JD, Barbacci EG, Iwata K, et al. Induction of apoptosis and cell cycle arrest by CP-358, 774, an inhibitor of epidermal growth factor receptor tyrosine kinase. Cancer Res 1997;57:4838-48.
    • (1997) Cancer Res , vol.57 , pp. 4838-4848
    • Moyer, J.D.1    Barbacci, E.G.2    Iwata, K.3
  • 16
    • 0033968986 scopus 로고    scopus 로고
    • Anticancer efficacy of the irreversible EGFR tyrosine kinase inhibitor PD 0169414 against human tumor xenografts
    • Vincent PW, Bridges AJ, Dykes DJ, et al. Anticancer efficacy of the irreversible EGFR tyrosine kinase inhibitor PD 0169414 against human tumor xenografts. Cancer Chemother Pharmacol 2000;45:231-8.
    • (2000) Cancer Chemother Pharmacol , vol.45 , pp. 231-238
    • Vincent, P.W.1    Bridges, A.J.2    Dykes, D.J.3
  • 17
    • 0033587022 scopus 로고    scopus 로고
    • Tyrosine kinase inhibitors. 15. 4-(phenylamino)quinazoline and 4-(phenylamino)pyrido[d]pyrimidine acrylamides as irreversible inhibitors of the ATP binding site of the epidermal growth factor receptor
    • Smaill JB, Palmer BD, Rewcastle Gw, et al. Tyrosine kinase inhibitors. 15. 4-(phenylamino)quinazoline and 4-(phenylamino)pyrido[d]pyrimidine acrylamides as irreversible inhibitors of the ATP binding site of the epidermal growth factor receptor. J Med Chem 1999; 42:1803-15.
    • (1999) J Med Chem , vol.42 , pp. 1803-1815
    • Smaill, J.B.1    Palmer, B.D.2    Rewcastle, G.3
  • 18
    • 0025341331 scopus 로고
    • New colorimetric cytotoxicity assay for anti-cancer drug screening
    • Skehan P, Storeng R, Scudiero D, et al. New colorimetric cytotoxicity assay for anti-cancer drug screening. J Natl Cancer Inst 1990;82:1107-12.
    • (1990) J Natl Cancer Inst , vol.82 , pp. 1107-1112
    • Skehan, P.1    Storeng, R.2    Scudiero, D.3
  • 19
    • 0030514288 scopus 로고    scopus 로고
    • Comparison of two colorimetric assays as cytotoxicity endpoints for an in vitro screen for antitumour agents
    • Fricker SP, Buckley RG. Comparison of two colorimetric assays as cytotoxicity endpoints for an in vitro screen for antitumour agents. Anticancer Res 1996;16: 3755-60.
    • (1996) Anticancer Res , vol.16 , pp. 3755-3760
    • Fricker, S.P.1    Buckley, R.G.2
  • 20
    • 0025367455 scopus 로고
    • Comparison of in vitro anticancer-drug-screening data generated with a tetrazolium assay versus a protein assay against a diverse panel of human tumor cell lines
    • Rubinstein LV, Shoemaker RH, Paull KD, et al. Comparison of in vitro anticancer-drug-screening data generated with a tetrazolium assay versus a protein assay against a diverse panel of human tumor cell lines. J Natl Cancer Inst 1990;82:1113-8.
    • (1990) J Natl Cancer Inst , vol.82 , pp. 1113-1118
    • Rubinstein, L.V.1    Shoemaker, R.H.2    Paull, K.D.3
  • 21
    • 0034029237 scopus 로고    scopus 로고
    • Serum predominantly activates MAPK and AKT kinases in EGFR- and ErbB2-overexpressing cells, respectively
    • Tari A, Lopez-Berestein G. Serum predominantly activates MAPK and AKT kinases in EGFR- and ErbB2-overexpressing cells, respectively. Int J Cancer 2000;86:295-7.
    • (2000) Int J Cancer , vol.86 , pp. 295-297
    • Tari, A.1    Lopez-Berestein, G.2
  • 22
    • 0036785528 scopus 로고    scopus 로고
    • Inhibition of epidermal growth factor receptor-mediated signaling by "combi-triazene" BJ2000, a new probe for combi-targeting postulates
    • Brahimi F, Matheson SL, Dudouit F, McNamee JP, Tari AM, Jean-Claude BJ. Inhibition of epidermal growth factor receptor-mediated signaling by "combi-triazene" BJ2000, a new probe for combi-targeting postulates. J Pharmacol Exp Ther 2002; 303:238-46.
    • (2002) J Pharmacol Exp Ther , vol.303 , pp. 238-246
    • Brahimi, F.1    Matheson, S.L.2    Dudouit, F.3    McNamee, J.P.4    Tari, A.M.5    Jean-Claude, B.J.6
  • 23
    • 1542270647 scopus 로고    scopus 로고
    • The combi-targeting concept: Intracellular fragmentation of the binary epidermal growth factor (EGFR)/DNA targeting "combi-triazene" SMA41
    • Matheson SL, Brahimi F, Jean-Claude BJ. The combi-targeting concept: intracellular fragmentation of the binary epidermal growth factor (EGFR)/DNA targeting "combi-triazene" SMA41. Biochem Pharmacol 2004;67:1131-8.
    • (2004) Biochem Pharmacol , vol.67 , pp. 1131-1138
    • Matheson, S.L.1    Brahimi, F.2    Jean-Claude, B.J.3
  • 24
    • 6344231968 scopus 로고    scopus 로고
    • Multiple mechanisms of action of ZR2002 in human breast cancer cells: A novel combi-molecule designed to block signaling mediated by the erbB family of oncogenes and to damage genomic DNA
    • Brahimi F, Rachid Z, McNamee JP, Li Y, Tari AM, Jean-Claude BJ. Multiple mechanisms of action of ZR2002 in human breast cancer cells: a novel combi-molecule designed to block signaling mediated by the erbB family of oncogenes and to damage genomic DNA. Int J Cancer 2004;112:484-91.
    • (2004) Int J Cancer , vol.112 , pp. 484-491
    • Brahimi, F.1    Rachid, Z.2    McNamee, J.P.3    Li, Y.4    Tari, A.M.5    Jean-Claude, B.J.6
  • 26
    • 0036899978 scopus 로고    scopus 로고
    • Studies with CWR22 xenografts in nude mice suggest that ZD1839 may have a role in the treatment of both androgen-dependent and androgen-independent human prostate cancer
    • Sirotnak FM, She Y, Lee F, Chen J, Scher HI. Studies with CWR22 xenografts in nude mice suggest that ZD1839 may have a role in the treatment of both androgen-dependent and androgen-independent human prostate cancer. Clin Cancer Res 2002; 8:3870-6.
    • (2002) Clin Cancer Res , vol.8 , pp. 3870-3876
    • Sirotnak, F.M.1    She, Y.2    Lee, F.3    Chen, J.4    Scher, H.I.5
  • 27
    • 0034666255 scopus 로고    scopus 로고
    • Novel strategies and therapeutics for the treatment of prostate carcinoma
    • Morris MJ, Scher HI. Novel strategies and therapeutics for the treatment of prostate carcinoma. Cancer 2000;89:1329-48.
    • (2000) Cancer , vol.89 , pp. 1329-1348
    • Morris, M.J.1    Scher, H.I.2
  • 30
    • 0024403939 scopus 로고
    • Denitrosation of 1,3-bis(2-chloroethyl)-1-nitrosourea by class μ glutathione transferases and its role in cellular resistance in rat brain tumor cells
    • Smith MT, Evans CG, Doane-Setzer P, Mannervik B. Denitrosation of 1,3-bis(2-chloroethyl)-1-nitrosourea by class μ glutathione transferases and its role in cellular resistance in rat brain tumor cells. Cancer Res 1989; 49:2621-5.
    • (1989) Cancer Res , vol.49 , pp. 2621-2625
    • Smith, M.T.1    Evans, C.G.2    Doane-Setzer, P.3    Mannervik, B.4
  • 31
    • 0020684046 scopus 로고
    • Effect of plasma and carboxylesterase on the stability, mutagenicity, and DNA cross-linking activity of some direct acting N-nitroso compounds
    • Aukerman SL, Brundrett RB, Hilton J, Hartman PE. Effect of plasma and carboxylesterase on the stability, mutagenicity, and DNA cross-linking activity of some direct acting N-nitroso compounds. Cancer Res 1983; 43:175-81.
    • (1983) Cancer Res , vol.43 , pp. 175-181
    • Aukerman, S.L.1    Brundrett, R.B.2    Hilton, J.3    Hartman, P.E.4
  • 32
    • 0022260386 scopus 로고
    • Detection of a deuterium isotope effect in di- and trisubstituted alkylphenylnitrosoureas. An SCE study in Chinese hamster V79-E cells
    • Thust R, Mendel J, Bach B, Schwarz H. Detection of a deuterium isotope effect in di- and trisubstituted alkylphenylnitrosoureas. An SCE study in Chinese hamster V79-E cells. Carcinogenesis 1985; 6:873-6.
    • (1985) Carcinogenesis , vol.6 , pp. 873-876
    • Thust, R.1    Mendel, J.2    Bach, B.3    Schwarz, H.4
  • 33
    • 0024376523 scopus 로고
    • Serine hydrolases activate/ inactivate trisubstituted nitrosoureas in dependence on intra- and extracellular enzyme location: An SCE study in Chinese hamster V79-E cells
    • Thust R, Schneider M. Serine hydrolases activate/ inactivate trisubstituted nitrosoureas in dependence on intra- and extracellular enzyme location: an SCE study in Chinese hamster V79-E cells. Carcinogenesis 1989;10:1787-91.
    • (1989) Carcinogenesis , vol.10 , pp. 1787-1791
    • Thust, R.1    Schneider, M.2
  • 34
    • 10044268467 scopus 로고    scopus 로고
    • The combi-targeting concept: Dissection of the binary mechanism of action of the combi-triazene SMA41 in vitro and antiproliferative effects in vivo
    • Matheson SL, McNamee JP, WangT, Alaoui-Jamali MA, Tari A, Jean-Claude BJ. The combi-targeting concept: dissection of the binary mechanism of action of the combi-triazene SMA41 in vitro and antiproliferative effects in vivo. J Pharmacol Exp Ther 2004;311: 1163-70.
    • (2004) J Pharmacol Exp Ther , vol.311 , pp. 1163-1170
    • Matheson, S.L.1    McNamee, J.P.2    WangT3    Alaoui-Jamali, M.A.4    Tari, A.5    Jean-Claude, B.J.6
  • 35
    • 0344158314 scopus 로고
    • Chemical decomposition of chloroethylnitrosoureas
    • London, New York: Academic Press;
    • Colvin M, Brundett R. Chemical decomposition of chloroethylnitrosoureas. In: Nitrosoureas, current status and development. London, New York: Academic Press; 1980. 43-9.
    • (1980) Nitrosoureas, current status and development , pp. 43-49
    • Colvin, M.1    Brundett, R.2
  • 36
    • 0027141005 scopus 로고
    • Denitrosation of the anticancer drug 1,3-bis(2-chloroethyl)-1-nitrosourea catalyzed by microsomal glutathione S-transferase and cytochrome P450 monooxygenases
    • Weber GF, Waxman DJ. Denitrosation of the anticancer drug 1,3-bis(2-chloroethyl)-1-nitrosourea catalyzed by microsomal glutathione S-transferase and cytochrome P450 monooxygenases. Arch Biochem Biophys 1993;307:369-78.
    • (1993) Arch Biochem Biophys , vol.307 , pp. 369-378
    • Weber, G.F.1    Waxman, D.J.2
  • 37
    • 11144292081 scopus 로고    scopus 로고
    • Phosphorylation of both EGFR and ErbB2 is a reliable predictor of prostate cancer cell proliferation in response to EGF
    • El Sheikh SS, Domin J, Abel P, Stamp G, Lalani el-N. Phosphorylation of both EGFR and ErbB2 is a reliable predictor of prostate cancer cell proliferation in response to EGF. Neoplasia 2004;6:846-53.
    • (2004) Neoplasia , vol.6 , pp. 846-853
    • El Sheikh, S.S.1    Domin, J.2    Abel, P.3    Stamp, G.4    el-N, L.5
  • 38
    • 0037382902 scopus 로고    scopus 로고
    • Epidermal growth factor and ionizing radiation up-regulate the DNA repair genes XRCC1 and ERCC1 in DU145 and LNCaP prostate carcinoma through MAPK signaling
    • Yacoub A, McKinstry R, Hinman D, Chung T, Dent P, Hagan MP. Epidermal growth factor and ionizing radiation up-regulate the DNA repair genes XRCC1 and ERCC1 in DU145 and LNCaP prostate carcinoma through MAPK signaling. Radiat Res 2003;159: 439-52.
    • (2003) Radiat Res , vol.159 , pp. 439-452
    • Yacoub, A.1    McKinstry, R.2    Hinman, D.3    Chung, T.4    Dent, P.5    Hagan, M.P.6
  • 39
    • 4444230648 scopus 로고    scopus 로고
    • Ionizing radiation causes a dose-dependent release of transforming growth factor α in vitro from irradiated xenografts and during palliative treatment of hormone-refractory prostate carcinoma
    • Hagan M, Yacoub A, Dent P. Ionizing radiation causes a dose-dependent release of transforming growth factor α in vitro from irradiated xenografts and during palliative treatment of hormone-refractory prostate carcinoma. Clin Cancer Res 2004;10: 5724-31.
    • (2004) Clin Cancer Res , vol.10 , pp. 5724-5731
    • Hagan, M.1    Yacoub, A.2    Dent, P.3
  • 40
    • 10744219536 scopus 로고    scopus 로고
    • Yang A, Bagheri-yarmand, Wang R-A, Asam L, Papdimitrakopoulou V, Kumar R. The epidermal growth factor receptor tyrosine kinase inhibitor ZD1839 (Iressa) suppresses s-Src and Park1 pathways and invasiveness of human cancer cells. Clin Cancer Res 2004;10:658-67.
    • Yang A, Bagheri-yarmand, Wang R-A, Asam L, Papdimitrakopoulou V, Kumar R. The epidermal growth factor receptor tyrosine kinase inhibitor ZD1839 (Iressa) suppresses s-Src and Park1 pathways and invasiveness of human cancer cells. Clin Cancer Res 2004;10:658-67.
  • 41
    • 0022515076 scopus 로고
    • Perinuclear location and recycling of epidermal growth factor receptor kinase: Immunofluorescent visualization using antibodies directed to kinase and extracellular domains
    • Murthy U, Basu M, Sen-Majumdar A, Das M. Perinuclear location and recycling of epidermal growth factor receptor kinase: immunofluorescent visualization using antibodies directed to kinase and extracellular domains. J Cell Biol 1986;103:333-42.
    • (1986) J Cell Biol , vol.103 , pp. 333-342
    • Murthy, U.1    Basu, M.2    Sen-Majumdar, A.3    Das, M.4


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