메뉴 건너뛰기




Volumn 16, Issue 5, 2005, Pages 475-481

Proteasome: An emerging target for cancer therapy

Author keywords

Bortezomib; Cancer; Multiple myeloma; Proteasome; PS 341

Indexed keywords

26S PROTEASOME; ANTINEOPLASTIC AGENT; BORTEZOMIB; CYCLIN DEPENDENT KINASE INHIBITOR; CYCLINE; IMMUNOGLOBULIN ENHANCER BINDING PROTEIN; PROTEASOME; PROTEASOME INHIBITOR; THREONINE PROTEINASE; TRANSCRIPTION FACTOR; TUMOR SUPPRESSOR PROTEIN; UBIQUITIN; UNCLASSIFIED DRUG;

EID: 18844381179     PISSN: 09594973     EISSN: None     Source Type: Journal    
DOI: 10.1097/00001813-200506000-00002     Document Type: Review
Times cited : (64)

References (74)
  • 1
    • 0023701618 scopus 로고
    • Proteasomes (multi-protease complexes) as 20 S ring-shaped particles in a variety of eukaryotic cells
    • Tanaka K, Yoshimura T, Kumatori A, Ichihara A, Ikai A, Nishigai M, et al. Proteasomes (multi-protease complexes) as 20 S ring-shaped particles in a variety of eukaryotic cells. J Biol Chem 1988; 263:16209-16217.
    • (1988) J Biol Chem , vol.263 , pp. 16209-16217
    • Tanaka, K.1    Yoshimura, T.2    Kumatori, A.3    Ichihara, A.4    Ikai, A.5    Nishigai, M.6
  • 2
    • 0029934284 scopus 로고    scopus 로고
    • Functional analysis of eukaryotic 20S proteasome nuclear localization signal
    • Knuehl C, Seelig A, Brecht B, Henklein P, Kloetzel PM. Functional analysis of eukaryotic 20S proteasome nuclear localization signal. Exp Cell Res 1996; 225:67-74.
    • (1996) Exp Cell Res , vol.225 , pp. 67-74
    • Knuehl, C.1    Seelig, A.2    Brecht, B.3    Henklein, P.4    Kloetzel, P.M.5
  • 4
    • 0023655017 scopus 로고
    • Purification of two high molecular weight proteases from rabbit reticulocyte lysate
    • Hough R, Pratt G, Rechsteiner M. Purification of two high molecular weight proteases from rabbit reticulocyte lysate. J Biol Chem 1987; 262: 8303-8313.
    • (1987) J Biol Chem , vol.262 , pp. 8303-8313
    • Hough, R.1    Pratt, G.2    Rechsteiner, M.3
  • 6
    • 0035902778 scopus 로고    scopus 로고
    • Crystal structure of the 20 S proteasome: TMC-95A complex: A non-covalent proteasome inhibitor
    • Groll M, Koguchi Y, Huber R, Kohno J. Crystal structure of the 20 S proteasome: TMC-95A complex: a non-covalent proteasome inhibitor. J Mol Biol 2001; 311:543-548.
    • (2001) J Mol Biol , vol.311 , pp. 543-548
    • Groll, M.1    Koguchi, Y.2    Huber, R.3    Kohno, J.4
  • 7
    • 0028365076 scopus 로고
    • Activation of the multicatalytic protease. The 11 S regulator and 20 S ATPase complexes contain distinct 30-kilodalton submits
    • Hoffman L, Rechsteiner M. Activation of the multicatalytic protease. The 11 S regulator and 20 S ATPase complexes contain distinct 30-kilodalton submits. J Biol Chem 1994; 269:16890-16895.
    • (1994) J Biol Chem , vol.269 , pp. 16890-16895
    • Hoffman, L.1    Rechsteiner, M.2
  • 8
    • 0029886022 scopus 로고    scopus 로고
    • Kinetic characterization of the chymotryptic activity of the 20S proteasome
    • Stein RL, Melandri F, Dick L. Kinetic characterization of the chymotryptic activity of the 20S proteasome. Biochemistry 1996; 35:3899-3908.
    • (1996) Biochemistry , vol.35 , pp. 3899-3908
    • Stein, R.L.1    Melandri, F.2    Dick, L.3
  • 9
    • 0031105057 scopus 로고    scopus 로고
    • The 26S proteasome: A dynamic structure
    • Seeger M, Ferrell K, Dubiel W. The 26S proteasome: a dynamic structure. Mol Biol Rep 1997; 24:83-88.
    • (1997) Mol Biol Rep , vol.24 , pp. 83-88
    • Seeger, M.1    Ferrell, K.2    Dubiel, W.3
  • 11
    • 0029025606 scopus 로고
    • The cyclosome, a large complex containing cyclin-selective ubiquitin ligase activity, targets cyclins for destruction at the end of mitosis
    • Sudakin V, Ganoth D, Dahan A, Heller H, Hershko J, Luca FC, et al. The cyclosome, a large complex containing cyclin-selective ubiquitin ligase activity, targets cyclins for destruction at the end of mitosis. Mol Biol Cell 1995; 6:185-197.
    • (1995) Mol Biol Cell , vol.6 , pp. 185-197
    • Sudakin, V.1    Ganoth, D.2    Dahan, A.3    Heller, H.4    Hershko, J.5    Luca, F.C.6
  • 12
    • 0031914641 scopus 로고    scopus 로고
    • Ubiquitin-dependent degradation of cyclin B is accelerated in polyploid megakaryocytes
    • Zhang Y, Wang Z, Liu DX, Pagano M, Ravid K. Ubiquitin-dependent degradation of cyclin B is accelerated in polyploid megakaryocytes. J Biol Chem 1998; 273:1387-1392.
    • (1998) J Biol Chem , vol.273 , pp. 1387-1392
    • Zhang, Y.1    Wang, Z.2    Liu, D.X.3    Pagano, M.4    Ravid, K.5
  • 13
    • 0032961411 scopus 로고    scopus 로고
    • Oxidative stress-induced destruction of the yeast C-type cyclin Ume3p requires phosphatidylinositol-specific phospholipase C and the 26S proteasome
    • Cooper KF, Mallory MJ, Strich R. Oxidative stress-induced destruction of the yeast C-type cyclin Ume3p requires phosphatidylinositol-specific phospholipase C and the 26S proteasome. Mol Cell Biol 1999; 19: 3338-3348.
    • (1999) Mol Cell Biol , vol.19 , pp. 3338-3348
    • Cooper, K.F.1    Mallory, M.J.2    Strich, R.3
  • 14
    • 0030916209 scopus 로고    scopus 로고
    • Inhibition of cyclin D1 phosphorylation on threonine-286 prevents its rapid degradation via the ubiquitin-proteasome pathway
    • Diehl JA, Zindy F, Sherr CJ. Inhibition of cyclin D1 phosphorylation on threonine-286 prevents its rapid degradation via the ubiquitin-proteasome pathway. Genes Dev 1997; 11:957-972.
    • (1997) Genes Dev , vol.11 , pp. 957-972
    • Diehl, J.A.1    Zindy, F.2    Sherr, C.J.3
  • 15
    • 0029957947 scopus 로고    scopus 로고
    • Turnover of cyclin E by the ubiquitin-proteasome pathway is regulated by cdk2 binding and cyclin phosphorylation
    • Clurman BE, Sheaff RJ, Thress K, Groudine M, Roberts JM. Turnover of cyclin E by the ubiquitin-proteasome pathway is regulated by cdk2 binding and cyclin phosphorylation. Genes Dev 1996; 10:1979-1990.
    • (1996) Genes Dev , vol.10 , pp. 1979-1990
    • Clurman, B.E.1    Sheaff, R.J.2    Thress, K.3    Groudine, M.4    Roberts, J.M.5
  • 16
    • 0034213405 scopus 로고    scopus 로고
    • Ubiquitin/proteasome-mediated degradation of p19INK4d determines its periodic expression during the cell cycle
    • Thullberg M, Bartek J, Lukas J. Ubiquitin/proteasome-mediated degradation of p19INK4d determines its periodic expression during the cell cycle. Oncogene 2000; 19:2870-2876.
    • (2000) Oncogene , vol.19 , pp. 2870-2876
    • Thullberg, M.1    Bartek, J.2    Lukas, J.3
  • 18
    • 0029024015 scopus 로고
    • Role of the ubiquitin-proteasome pathway in regulating abundance of the cyclin-dependent kinase inhibitor p27
    • Pagano M, Tam SW, Theodoras AM, Beer-Romero P, Del Sal G, Chau V, et al. Role of the ubiquitin-proteasome pathway in regulating abundance of the cyclin-dependent kinase inhibitor p27. Science 1995; 269:682-685.
    • (1995) Science , vol.269 , pp. 682-685
    • Pagano, M.1    Tam, S.W.2    Theodoras, A.M.3    Beer-Romero, P.4    Del Sal, G.5    Chau, V.6
  • 19
    • 0033617188 scopus 로고    scopus 로고
    • p57(Kip2) is degraded through the proteasome in osteoblasts stimulated to proliferation by transforming growth factor beta1
    • Urano T, Yashiroda H, Muraoka M, Tanaka K, Hosoi T, Inoue S, et al. p57(Kip2) is degraded through the proteasome in osteoblasts stimulated to proliferation by transforming growth factor beta1. J Biol Chem 1999; 274:12197-12200.
    • (1999) J Biol Chem , vol.274 , pp. 12197-12200
    • Urano, T.1    Yashiroda, H.2    Muraoka, M.3    Tanaka, K.4    Hosoi, T.5    Inoue, S.6
  • 20
    • 0029952441 scopus 로고    scopus 로고
    • In vivo ubiquitination and proteasome-mediated degradation of p53(1)
    • Maki CG, Huibregtse JM, Howley PM. In vivo ubiquitination and proteasome-mediated degradation of p53(1). Cancer Res 1996; 56: 2649-2654.
    • (1996) Cancer Res , vol.56 , pp. 2649-2654
    • Maki, C.G.1    Huibregtse, J.M.2    Howley, P.M.3
  • 21
    • 0029834371 scopus 로고    scopus 로고
    • E7 protein of human papilloma virus-16 induces degradation of retinoblastoma protein through the ubiquitin-proteasome pathway
    • Boyer SN, Wazer DE, Band V. E7 protein of human papilloma virus-16 induces degradation of retinoblastoma protein through the ubiquitin-proteasome pathway. Cancer Res 1996; 56:4620-4624.
    • (1996) Cancer Res , vol.56 , pp. 4620-4624
    • Boyer, S.N.1    Wazer, D.E.2    Band, V.3
  • 23
    • 0028834782 scopus 로고
    • Degradation of the proto-oncogene product c-Fos by the ubiquitin proteolytic system in vivo and in vitro: Identification and characterization of the conjugating enzymes
    • Stancovski I, Gonen H, Orian A, Schwartz AL, Ciechanover A. Degradation of the proto-oncogene product c-Fos by the ubiquitin proteolytic system in vivo and in vitro: identification and characterization of the conjugating enzymes. Mol Cell Biol 1995; 15:7106-7116.
    • (1995) Mol Cell Biol , vol.15 , pp. 7106-7116
    • Stancovski, I.1    Gonen, H.2    Orian, A.3    Schwartz, A.L.4    Ciechanover, A.5
  • 24
    • 0029661437 scopus 로고    scopus 로고
    • Degradation of topoisomerase IIalpha during adenovirus E1A-induced apoptosis is mediated by the activation of the ubiquitin proteolysis system
    • Nakajima T, Morita K, Ohi N, Arai T, Nozaki N, Kikuchi A, et al. Degradation of topoisomerase IIalpha during adenovirus E1A-induced apoptosis is mediated by the activation of the ubiquitin proteolysis system. J Biol Chem 1996; 271:24842-24849.
    • (1996) J Biol Chem , vol.271 , pp. 24842-24849
    • Nakajima, T.1    Morita, K.2    Ohi, N.3    Arai, T.4    Nozaki, N.5    Kikuchi, A.6
  • 25
    • 0031985007 scopus 로고    scopus 로고
    • mdm2 and bax, downstream mediators of the p53 response, are degraded by the ubiquitin-proteasome pathway
    • Chang YC, Lee YS, Tejima T, Tanaka K, Omura S, Heintz NH, et al. mdm2 and bax, downstream mediators of the p53 response, are degraded by the ubiquitin-proteasome pathway. Cell Growth Differ 1998; 9:79-84.
    • (1998) Cell Growth Differ , vol.9 , pp. 79-84
    • Chang, Y.C.1    Lee, Y.S.2    Tejima, T.3    Tanaka, K.4    Omura, S.5    Heintz, N.H.6
  • 26
    • 0034607655 scopus 로고    scopus 로고
    • Ubiquitin protein ligase activity of IAPs and their degradation in proteasomes in response to apoptotic stimuli
    • Yang Y, Fang S, Jensen JP, Weissman AM, Ashwell JD. Ubiquitin protein ligase activity of IAPs and their degradation in proteasomes in response to apoptotic stimuli. Science 2000; 288:874-877.
    • (2000) Science , vol.288 , pp. 874-877
    • Yang, Y.1    Fang, S.2    Jensen, J.P.3    Weissman, A.M.4    Ashwell, J.D.5
  • 28
    • 0030903750 scopus 로고    scopus 로고
    • Regulation of E2F through ubiquitin-proteasome-dependent degradation: Stabilization by the pRB tumor suppressor protein
    • Campanero MR, Flemington EK. Regulation of E2F through ubiquitin-proteasome-dependent degradation: stabilization by the pRB tumor suppressor protein. Proc Natl Acad Sci USA 1997; 94:2221-2226.
    • (1997) Proc Natl Acad Sci USA , vol.94 , pp. 2221-2226
    • Campanero, M.R.1    Flemington, E.K.2
  • 29
    • 0000413462 scopus 로고    scopus 로고
    • Regulation of interferon-gamma-activated STAT1 by the ubiquitin-proteasome pathway
    • Kim TK, Maniatis T. Regulation of interferon-gamma-activated STAT1 by the ubiquitin-proteasome pathway. Science 1996; 273:1717-1719.
    • (1996) Science , vol.273 , pp. 1717-1719
    • Kim, T.K.1    Maniatis, T.2
  • 30
    • 0027980321 scopus 로고
    • The ubiquitin-proteasome pathway is required for processing the NF-kappa B1 precursor protein and the activation of NF-kappa B
    • Palombella VJ, Rando OJ, Goldberg AL, Maniatis T. The ubiquitin-proteasome pathway is required for processing the NF-kappa B1 precursor protein and the activation of NF-kappa B. Cell 1994; 78:773-785.
    • (1994) Cell , vol.78 , pp. 773-785
    • Palombella, V.J.1    Rando, O.J.2    Goldberg, A.L.3    Maniatis, T.4
  • 31
    • 0028148227 scopus 로고
    • A proteasome inhibitor prevents activation of NF-kappa B and stabilizes a newly phosphorylated form of I kappa B-alpha that is still bound to NF-kappa B
    • Traenckner EB, Wilk S, Baeuerle PA. A proteasome inhibitor prevents activation of NF-kappa B and stabilizes a newly phosphorylated form of I kappa B-alpha that is still bound to NF-kappa B. EMBO J 1994; 13: 5433-5441.
    • (1994) EMBO J , vol.13 , pp. 5433-5441
    • Traenckner, E.B.1    Wilk, S.2    Baeuerle, P.A.3
  • 32
    • 0035725855 scopus 로고    scopus 로고
    • Analysis of expression of nuclear factor kappa B (NF-kappa B) in multiple myeloma: Downregulation of NF-kappa B induces apoptosis
    • Ni H, Ergin M, Huang Q, Qin JZ, Amin HM, Martinez RL, et al. Analysis of expression of nuclear factor kappa B (NF-kappa B) in multiple myeloma: downregulation of NF-kappa B induces apoptosis. Br J Haematol 2001; 115:279-286.
    • (2001) Br J Haematol , vol.115 , pp. 279-286
    • Ni, H.1    Ergin, M.2    Huang, Q.3    Qin, J.Z.4    Amin, H.M.5    Martinez, R.L.6
  • 33
    • 18844465632 scopus 로고    scopus 로고
    • Constitutive nuclear factor-kappaB-RelA activation is required for proliferation and survival of Hodgkin's disease tumor cells
    • Bargou RC, Emmerich F, Krappmann D, Bommert K, Mapara MY, Arnold W, et al. Constitutive nuclear factor-kappaB-RelA activation is required for proliferation and survival of Hodgkin's disease tumor cells. J Clin Invest 1997; 100:2961-2969.
    • (1997) J Clin Invest , vol.100 , pp. 2961-2969
    • Bargou, R.C.1    Emmerich, F.2    Krappmann, D.3    Bommert, K.4    Mapara, M.Y.5    Arnold, W.6
  • 34
    • 0031810458 scopus 로고    scopus 로고
    • Inhibition of nuclear factor kappaB activation attenuates apoptosis resistance in lymphoid cells
    • Jeremias I, Kupatt C, Baumann B, Herr I, Wirth T, Debatin KM. Inhibition of nuclear factor kappaB activation attenuates apoptosis resistance in lymphoid cells. Blood 1998; 91:4624-4631.
    • (1998) Blood , vol.91 , pp. 4624-4631
    • Jeremias, I.1    Kupatt, C.2    Baumann, B.3    Herr, I.4    Wirth, T.5    Debatin, K.M.6
  • 35
    • 0029858387 scopus 로고    scopus 로고
    • TNF- and cancer therapy-induced apoptosis: Potentiation by inhibition of NF-kappaB
    • Wang CY, Mayo MW, Baldwin Jr AS. TNF- and cancer therapy-induced apoptosis: potentiation by inhibition of NF-kappaB. Science 1996; 274:784-787.
    • (1996) Science , vol.274 , pp. 784-787
    • Wang, C.Y.1    Mayo, M.W.2    Baldwin Jr., A.S.3
  • 36
    • 0035137882 scopus 로고    scopus 로고
    • Control of oncogenesis and cancer therapy resistance by the transcription factor NF-kappaB
    • Baldwin AS. Control of oncogenesis and cancer therapy resistance by the transcription factor NF-kappaB. J Clin Invest 2001; 107:241-246.
    • (2001) J Clin Invest , vol.107 , pp. 241-246
    • Baldwin, A.S.1
  • 37
    • 0037443551 scopus 로고    scopus 로고
    • The proteasome inhibitor PS-341 potentiates sensitivity of multiple myeloma cells to conventional chemotherapeutic agents: Therapeutic applications
    • Mitsiades N, Mitsiades CS, Richardson PG, Poulaki V, Tai YT, Chauhan D, et al. The proteasome inhibitor PS-341 potentiates sensitivity of multiple myeloma cells to conventional chemotherapeutic agents: therapeutic applications. Blood 2003; 101:2377-2380.
    • (2003) Blood , vol.101 , pp. 2377-2380
    • Mitsiades, N.1    Mitsiades, C.S.2    Richardson, P.G.3    Poulaki, V.4    Tai, Y.T.5    Chauhan, D.6
  • 39
    • 0029033981 scopus 로고
    • Inhibition of proteasome activities and subunit-specific amino-terminal threonine modification by lactacystin
    • Fenteany G, Standaert RF, Lane WS, Choi S, Corey EJ, Schreiber SL. Inhibition of proteasome activities and subunit-specific amino-terminal threonine modification by lactacystin. Science 1995; 268:726-731.
    • (1995) Science , vol.268 , pp. 726-731
    • Fenteany, G.1    Standaert, R.F.2    Lane, W.S.3    Choi, S.4    Corey, E.J.5    Schreiber, S.L.6
  • 44
    • 0033621851 scopus 로고    scopus 로고
    • p27Kip1 accumulation by inhibition of proteasome function induces apoptosis in oral squamous cell carcinoma cells
    • Kudo Y, Takata T, Ogawa I, Kaneda T, Sato S, Takekoshi T. et al. p27Kip1 accumulation by inhibition of proteasome function induces apoptosis in oral squamous cell carcinoma cells. Clin Cancer Res 2000; 6:916-923.
    • (2000) Clin Cancer Res , vol.6 , pp. 916-923
    • Kudo, Y.1    Takata, T.2    Ogawa, I.3    Kaneda, T.4    Sato, S.5    Takekoshi, T.6
  • 45
    • 0034902354 scopus 로고    scopus 로고
    • Novel proteasome inhibitor PS-341 inhibits activation of nuclear factor-kappa B, cell survival, tumor growth, and angiogenesis in squamous cell carcinoma
    • Sunwoo JB, Chen Z, Dong G, Yeh N, Crowl Bancroft C, et al. Novel proteasome inhibitor PS-341 inhibits activation of nuclear factor-kappa B, cell survival, tumor growth, and angiogenesis in squamous cell carcinoma. Clin Cancer Res 2001; 7:1419-1428.
    • (2001) Clin Cancer Res , vol.7 , pp. 1419-1428
    • Sunwoo, J.B.1    Chen, Z.2    Dong, G.3    Yeh, N.4    Crowl Bancroft, C.5
  • 46
    • 0042235056 scopus 로고    scopus 로고
    • Schedule-dependent molecular effects of the proteasome inhibitor bortezomib and gemcitabine in pancreatic cancer
    • Fahy BN, Schlieman MG, Virudachalam S, Bold RJ. Schedule-dependent molecular effects of the proteasome inhibitor bortezomib and gemcitabine in pancreatic cancer. J Surg Res 2003; 113:88-95.
    • (2003) J Surg Res , vol.113 , pp. 88-95
    • Fahy, B.N.1    Schlieman, M.G.2    Virudachalam, S.3    Bold, R.J.4
  • 47
    • 0033817518 scopus 로고    scopus 로고
    • Lack of multicellular drug resistance observed in human ovarian and prostate carcinoma treated with the proteasome inhibitor PS-341
    • Frankel A, Man S, Elliott P, Adams J, Kerbel RS. Lack of multicellular drug resistance observed in human ovarian and prostate carcinoma treated with the proteasome inhibitor PS-341. Clin Cancer Res 2000; 6:3719-3728.
    • (2000) Clin Cancer Res , vol.6 , pp. 3719-3728
    • Frankel, A.1    Man, S.2    Elliott, P.3    Adams, J.4    Kerbel, R.S.5
  • 48
    • 0033038942 scopus 로고    scopus 로고
    • Proteasome inhibitors induce mitochondria-independent apoptosis in human glioma cells
    • Kitagawa H, Tani E, Ikemoto H, Ozaki I, Nakano A, Omura S. Proteasome inhibitors induce mitochondria-independent apoptosis in human glioma cells. FEBS Lett 1999; 443:181-186.
    • (1999) FEBS Lett , vol.443 , pp. 181-186
    • Kitagawa, H.1    Tani, E.2    Ikemoto, H.3    Ozaki, I.4    Nakano, A.5    Omura, S.6
  • 49
    • 0035000515 scopus 로고    scopus 로고
    • The apoptogenic response of human myeloid leukaemia cell lines and of normal and malignant haematopoietic progenitor cells to the proteasome inhibitor PSI
    • Soligo D, Servida F, Delia D, Fontanella E, Lamorte G, Caneva L, et al. The apoptogenic response of human myeloid leukaemia cell lines and of normal and malignant haematopoietic progenitor cells to the proteasome inhibitor PSI. Br J Haematol 2001; 113:126-135.
    • (2001) Br J Haematol , vol.113 , pp. 126-135
    • Soligo, D.1    Servida, F.2    Delia, D.3    Fontanella, E.4    Lamorte, G.5    Caneva, L.6
  • 50
    • 0033623487 scopus 로고    scopus 로고
    • Proteasome inhibitors induced caspase-dependent apoptosis and accumulation of p21WAF1/Cip1 in human immature leukemic cells
    • Naujokat C, Sezer O, Zinke H, Ledere A, Hauptmann S, Possinger K. Proteasome inhibitors induced caspase-dependent apoptosis and accumulation of p21WAF1/Cip1 in human immature leukemic cells. Eur J Haematol 2000; 65:221-236.
    • (2000) Eur J Haematol , vol.65 , pp. 221-236
    • Naujokat, C.1    Sezer, O.2    Zinke, H.3    Ledere, A.4    Hauptmann, S.5    Possinger, K.6
  • 51
    • 0034066860 scopus 로고    scopus 로고
    • Lactacystin activates FLICE (caspase 8) protease and induces apoptosis in Fas-resistant adult T-cell leukemia cell lines
    • Yamada Y, Sugahara K, Tsuruda K, Nohda K, Mori N, Hata T, et al. Lactacystin activates FLICE (caspase 8) protease and induces apoptosis in Fas-resistant adult T-cell leukemia cell lines. Eur J Haematol 2000; 64: 315-322.
    • (2000) Eur J Haematol , vol.64 , pp. 315-322
    • Yamada, Y.1    Sugahara, K.2    Tsuruda, K.3    Nohda, K.4    Mori, N.5    Hata, T.6
  • 52
    • 0035300479 scopus 로고    scopus 로고
    • The proteasome inhibitor PS-341 inhibits growth, induces apoptosis, and overcomes drug resistance in human multiple myeloma cells
    • Hideshima T, Richardson P, Chauhan D, Palombella VJ, Elliott PJ, Adams J, et al. The proteasome inhibitor PS-341 inhibits growth, induces apoptosis, and overcomes drug resistance in human multiple myeloma cells. Cancer Res 2001; 61:3071-3076.
    • (2001) Cancer Res , vol.61 , pp. 3071-3076
    • Hideshima, T.1    Richardson, P.2    Chauhan, D.3    Palombella, V.J.4    Elliott, P.J.5    Adams, J.6
  • 53
    • 0037342894 scopus 로고    scopus 로고
    • The proteasome inhibitor PS-341 markedly enhances sensitivity of multiple myeloma tumor cells to chemotherapeutic agents
    • Ma MH, Yang HH, Parker K, Manyak S, Friedman JM, Altamirano C, et al. The proteasome inhibitor PS-341 markedly enhances sensitivity of multiple myeloma tumor cells to chemotherapeutic agents. Clin Cancer Res 2003; 9:1136-1144.
    • (2003) Clin Cancer Res , vol.9 , pp. 1136-1144
    • Ma, M.H.1    Yang, H.H.2    Parker, K.3    Manyak, S.4    Friedman, J.M.5    Altamirano, C.6
  • 54
    • 0043164960 scopus 로고    scopus 로고
    • Proteasome inhibitors induce growth inhibition and apoptosis in myeloma cell lines and in human bone marrow myeloma cells irrespective of chromosome 13 deletion
    • Zavrski I, Naujokat C, Niemoller K, Jakob C, Heider U, Langelotz C, et al. Proteasome inhibitors induce growth inhibition and apoptosis in myeloma cell lines and in human bone marrow myeloma cells irrespective of chromosome 13 deletion. J Cancer Res Clin Oncol 2003; 129:383-391.
    • (2003) J Cancer Res Clin Oncol , vol.129 , pp. 383-391
    • Zavrski, I.1    Naujokat, C.2    Niemoller, K.3    Jakob, C.4    Heider, U.5    Langelotz, C.6
  • 55
    • 0030854371 scopus 로고    scopus 로고
    • Ubiquitin-dependent destruction of topoisomerase I is stimulated by the antitumor drug camptothecin
    • Desai SD, Liu LF, Vazquez-Abad D, D'Arpa P. Ubiquitin-dependent destruction of topoisomerase I is stimulated by the antitumor drug camptothecin. J Biol Chem 1997; 272:24159-24164.
    • (1997) J Biol Chem , vol.272 , pp. 24159-24164
    • Desai, S.D.1    Liu, L.F.2    Vazquez-Abad, D.3    D'Arpa, P.4
  • 56
    • 0035328584 scopus 로고    scopus 로고
    • Enhanced chemosensitivity to CPT-11 with proteasome inhibitor PS-341: Implications for systemic nuclear factor-kappaB inhibition
    • Cusack JC Jr, Liu R, Houston M, Abendroth K, Elliott PJ, Adams J, et al. Enhanced chemosensitivity to CPT-11 with proteasome inhibitor PS-341: implications for systemic nuclear factor-kappaB inhibition. Cancer Res 2001; 61:3535-3540.
    • (2001) Cancer Res , vol.61 , pp. 3535-3540
    • Cusack Jr., J.C.1    Liu, R.2    Houston, M.3    Abendroth, K.4    Elliott, P.J.5    Adams, J.6
  • 57
    • 0037111832 scopus 로고    scopus 로고
    • Phase I trial of the proteasome inhibitor PS-341 in patients with refractory hematologic malignancies
    • Orlowski RZ, Stinchcombe TE, Mitchell BS, Shea TC, Baldwin AS, Stahl S, et al. Phase I trial of the proteasome inhibitor PS-341 in patients with refractory hematologic malignancies. J Clin Oncol 2002; 20:4420-4427
    • (2002) J Clin Oncol , vol.20 , pp. 4420-4427
    • Orlowski, R.Z.1    Stinchcombe, T.E.2    Mitchell, B.S.3    Shea, T.C.4    Baldwin, A.S.5    Stahl, S.6
  • 58
  • 59
    • 2942692143 scopus 로고    scopus 로고
    • Phase I trial of the proteasome inhibitor bortezomib in patients with advanced solid tumors with observations in androgen-independent prostate cancer
    • Papandreou CN, Daliani DD, Nix D, Yang H, Madden T, Wang X, et al. Phase I trial of the proteasome inhibitor bortezomib in patients with advanced solid tumors with observations in androgen-independent prostate cancer. J Clin Oncol 2004; 22:2108-2121.
    • (2004) J Clin Oncol , vol.22 , pp. 2108-2121
    • Papandreou, C.N.1    Daliani, D.D.2    Nix, D.3    Yang, H.4    Madden, T.5    Wang, X.6
  • 60
    • 0036023407 scopus 로고    scopus 로고
    • A phase I trial of the novel proteasome inhibitor PS341 in advanced solid tumor malignancies
    • Aghajanian C, Soignet S, Dizon DS, Pien CS, Adams J, Elliott PJ, et al. A phase I trial of the novel proteasome inhibitor PS341 in advanced solid tumor malignancies. Clin Cancer Res 2002; 8:2505-2511.
    • (2002) Clin Cancer Res , vol.8 , pp. 2505-2511
    • Aghajanian, C.1    Soignet, S.2    Dizon, D.S.3    Pien, C.S.4    Adams, J.5    Elliott, P.J.6
  • 61
    • 11344263355 scopus 로고    scopus 로고
    • The proteasome inhibitor, bortezomib, in combination with gemcitabine (Gem) and carboplatin (Carbo) in advanced non-small cell lung cancer (NSCLC): Final results of a phase I California Cancer Consortium study
    • abstr 7106
    • Davies M, Lara PN, Lau DH, Mack PC, Gumerlock PH, Gandara DR, et al. The proteasome inhibitor, bortezomib, in combination with gemcitabine (Gem) and carboplatin (Carbo) in advanced non-small cell lung cancer (NSCLC): final results of a phase I California Cancer Consortium study. Proc Am Soc Clin Oncol 2004; 23:639 (abstr 7106).
    • (2004) Proc Am Soc Clin Oncol , vol.23 , pp. 639
    • Davies, M.1    Lara, P.N.2    Lau, D.H.3    Mack, P.C.4    Gumerlock, P.H.5    Gandara, D.R.6
  • 65
    • 29344470572 scopus 로고    scopus 로고
    • PAD therapy (bortezomib, doxorubicin and dexamethasone) for untreated multiple myeloma (MM)
    • abstr 6550
    • Cavenagh JD, Curry N, Stec J, Drake M, Morris TCM, Agrawal S, et al. PAD therapy (bortezomib, doxorubicin and dexamethasone) for untreated multiple myeloma (MM). Proc Am Soc Clin Oncol 2004; 23:568 (abstr 6550).
    • (2004) Proc Am Soc Clin Oncol , vol.23 , pp. 568
    • Cavenagh, J.D.1    Curry, N.2    Stec, J.3    Drake, M.4    Morris, T.C.M.5    Agrawal, S.6
  • 66
    • 6344246477 scopus 로고    scopus 로고
    • First-line therapy with bortezomib (formerly PS-341) in patients with multiple myeloma (MM)
    • abstr 6551
    • Jagannath S, Durie B, Wolf J, Camacho E, Irwin D, Lutzky J, et al. First-line therapy with bortezomib (formerly PS-341) in patients with multiple myeloma (MM). Proc Am Soc Clin Oncol 2004; 23:568 (abstr 6551).
    • (2004) Proc Am Soc Clin Oncol , vol.23 , pp. 568
    • Jagannath, S.1    Durie, B.2    Wolf, J.3    Camacho, E.4    Irwin, D.5    Lutzky, J.6
  • 68
    • 4644248931 scopus 로고    scopus 로고
    • Phase II study of the proteasome inhibitor bortezomib (PS-341) in patients with metastatic neuroendocrine tumors
    • Shah MH, Young D, Kindler HL, Webb I, Kleiber B, Wright J, et al. Phase II study of the proteasome inhibitor bortezomib (PS-341) in patients with metastatic neuroendocrine tumors. Clin Cancer Res 2004; 10: 6111-6118.
    • (2004) Clin Cancer Res , vol.10 , pp. 6111-6118
    • Shah, M.H.1    Young, D.2    Kindler, H.L.3    Webb, I.4    Kleiber, B.5    Wright, J.6
  • 69
    • 2442510143 scopus 로고    scopus 로고
    • Phase Ii trial of PS-341 in patients with renal cell cancer: A University of Chicago phase II consortium study
    • Davis NB, Taber DA, Ansari RH, Ryan CW, George C, Vokes EE, et al. Phase Ii trial of PS-341 in patients with renal cell cancer: a University of Chicago phase II consortium study. J Clin Oncol 2004; 22:115-119.
    • (2004) J Clin Oncol , vol.22 , pp. 115-119
    • Davis, N.B.1    Taber, D.A.2    Ansari, R.H.3    Ryan, C.W.4    George, C.5    Vokes, E.E.6
  • 71
    • 18844421493 scopus 로고    scopus 로고
    • Bortezomib ± irinotecan in relapsed/refractory colorectal cancer: Interim analysis results from phase 2b study
    • abstr 3591
    • Dragovich T, Lenz HJ, Rocha Lima CMS, Kozuch P, Hochster H, et al. Bortezomib ± irinotecan in relapsed/refractory colorectal cancer: interim analysis results from phase 2b study. Proc Am Soc Clin Oncol 2004; 23:268 (abstr 3591).
    • (2004) Proc Am Soc Clin Oncol , vol.23 , pp. 268
    • Dragovich, T.1    Lenz, H.J.2    Rocha Lima, C.M.S.3    Kozuch, P.4    Hochster, H.5
  • 72
    • 18844461545 scopus 로고    scopus 로고
    • A phase II study of the proteasome inhibitor PS-341 in patients with metastatic breast cancer
    • abstr 546
    • Brown J, Von Roenn J, O'Regan R, Bergan R, Badve S, Rademaker A, et al. A phase II study of the proteasome inhibitor PS-341 in patients with metastatic breast cancer. Proc Am Soc Clin Oncol 2004; 23:13 (abstr 546).
    • (2004) Proc Am Soc Clin Oncol , vol.23 , pp. 13
    • Brown, J.1    Von Roenn, J.2    O'Regan, R.3    Bergan, R.4    Badve, S.5    Rademaker, A.6
  • 73
    • 10044292218 scopus 로고    scopus 로고
    • Phase 2 study of bortezomib ± docetaxel in previously treated patients with advanced non-small cell lung cancer (NSCLC): Preliminary results
    • abstr 7107
    • Fanucchi MP, Belt RJ, Fossella FV, Natale RB, Robert F, Fidias P, et al. Phase 2 study of bortezomib ± docetaxel in previously treated patients with advanced non-small cell lung cancer (NSCLC): preliminary results. Proc Am Soc Clin Oncol 2004; 23:640 (abstr 7107).
    • (2004) Proc Am Soc Clin Oncol , vol.23 , pp. 640
    • Fanucchi, M.P.1    Belt, R.J.2    Fossella, F.V.3    Natale, R.B.4    Robert, F.5    Fidias, P.6
  • 74
    • 5744224934 scopus 로고    scopus 로고
    • Update on a phase 2 study of bortezomib in patients with relapsed or refractory indolent or aggressive non-Hodgkin's lymphomas (NHL)
    • abstr 6581
    • Goy A, Younes A, McLaughlin P, Pro B, Romaguera J, Hagemeister F, et al. Update on a phase 2 study of bortezomib in patients with relapsed or refractory indolent or aggressive non-Hodgkin's lymphomas (NHL). Proc Am Soc Clin Oncol 2004; 23:575 (abstr 6581).
    • (2004) Proc Am Soc Clin Oncol , vol.23 , pp. 575
    • Goy, A.1    Younes, A.2    McLaughlin, P.3    Pro, B.4    Romaguera, J.5    Hagemeister, F.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.