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Volumn 31, Issue 6, 2013, Pages 1539-1546

A phase i study of vorinostat in combination with bortezomib in patients with advanced malignancies

Author keywords

Bortezomib; Phase I; PS 341; SAHA; Vorinostat

Indexed keywords

4 ANILINO 4 OXOBUTANOIC ACID; BORTEZOMIB; DRUG METABOLITE; UNCLASSIFIED DRUG; VORINOSTAT; VORINOSTAT GLUCURONIDE;

EID: 84888607613     PISSN: 01676997     EISSN: 15730646     Source Type: Journal    
DOI: 10.1007/s10637-013-0029-6     Document Type: Article
Times cited : (26)

References (37)
  • 1
    • 0031707751 scopus 로고    scopus 로고
    • Alteration of nucleosome structure as a mechanism of transcriptional regulation
    • 9759497 10.1146/annurev.biochem.67.1.545 1:CAS:528:DyaK1cXlsFOmsbw%3D
    • Workman JL, Kingston RE (1998) Alteration of nucleosome structure as a mechanism of transcriptional regulation. Annu Rev Biochem 67:545-579
    • (1998) Annu Rev Biochem , vol.67 , pp. 545-579
    • Workman, J.L.1    Kingston, R.E.2
  • 2
    • 0141953936 scopus 로고    scopus 로고
    • Histone deacetylase inhibitors: From chromatin remodeling to experimental cancer therapeutics
    • 14529477 10.2174/0929867033456657 1:CAS:528:DC%2BD3sXotFKlsLY%3D
    • Arts J, de Schepper S, Van Emelen K (2003) Histone deacetylase inhibitors: from chromatin remodeling to experimental cancer therapeutics. Curr Med Chem 10:2343-2350
    • (2003) Curr Med Chem , vol.10 , pp. 2343-2350
    • Arts, J.1    De Schepper, S.2    Van Emelen, K.3
  • 3
    • 0036274359 scopus 로고    scopus 로고
    • The fundamental role of epigenetic events in cancer
    • 12042769 10.1038/nrg962 1:CAS:528:DC%2BD38XksFOmsrw%3D
    • Jones PA, Baylin SB (2002) The fundamental role of epigenetic events in cancer. Nat Rev Genet 3:415-428
    • (2002) Nat Rev Genet , vol.3 , pp. 415-428
    • Jones, P.A.1    Baylin, S.B.2
  • 4
    • 0035724488 scopus 로고    scopus 로고
    • Histone deacetylase inhibitors induce caspase-dependent apoptosis and downregulation of daxx in acute promyelocytic leukaemia with t(15;17)
    • 11703323 10.1046/j.1365-2141.2001.03123.x 1:CAS:528:DC%2BD3MXptVyqsrs%3D
    • Amin HM, Saeed S, Alkan S (2001) Histone deacetylase inhibitors induce caspase-dependent apoptosis and downregulation of daxx in acute promyelocytic leukaemia with t(15;17). Br J Haematol 115:287-297
    • (2001) Br J Haematol , vol.115 , pp. 287-297
    • Amin, H.M.1    Saeed, S.2    Alkan, S.3
  • 5
    • 0037589018 scopus 로고    scopus 로고
    • Molecular sequelae of histone deacetylase inhibition in human malignant B cells
    • 12531799 10.1182/blood-2002-11-3514 1:CAS:528:DC%2BD3sXktVGnu7w%3D
    • Mitsiades N, Mitsiades CS, Richardson PG et al (2003) Molecular sequelae of histone deacetylase inhibition in human malignant B cells. Blood 101:4055-4062
    • (2003) Blood , vol.101 , pp. 4055-4062
    • Mitsiades, N.1    Mitsiades, C.S.2    Richardson, P.G.3
  • 6
    • 9144220841 scopus 로고    scopus 로고
    • Transcriptional signature of histone deacetylase inhibition in multiple myeloma: Biological and clinical implications
    • 14695887 10.1073/pnas.2536759100 1:CAS:528:DC%2BD2cXmsFGnsA%3D%3D
    • Mitsiades CS, Mitsiades NS, McMullan CJ et al (2004) Transcriptional signature of histone deacetylase inhibition in multiple myeloma: biological and clinical implications. Proc Natl Acad Sci U S A 101:540-545
    • (2004) Proc Natl Acad Sci U S A , vol.101 , pp. 540-545
    • Mitsiades, C.S.1    Mitsiades, N.S.2    McMullan, C.J.3
  • 7
    • 0038620379 scopus 로고    scopus 로고
    • Cotreatment with the histone deacetylase inhibitor suberoylanilide hydroxamic acid (SAHA) enhances imatinib-induced apoptosis of Bcr-Abl-positive human acute leukemia cells
    • 12446442 10.1182/blood-2002-08-2675 1:CAS:528:DC%2BD3sXjtFCqtbg%3D
    • Nimmanapalli R, Fuino L, Stobaugh C, Richon V, Bhalla K (2003) Cotreatment with the histone deacetylase inhibitor suberoylanilide hydroxamic acid (SAHA) enhances imatinib-induced apoptosis of Bcr-Abl-positive human acute leukemia cells. Blood 101:3236-3239
    • (2003) Blood , vol.101 , pp. 3236-3239
    • Nimmanapalli, R.1    Fuino, L.2    Stobaugh, C.3    Richon, V.4    Bhalla, K.5
  • 8
    • 21644464967 scopus 로고    scopus 로고
    • The histone deacetylase inhibitor suberoylanilide hydroxamic acid down-regulates expression levels of Bcr-abl, c-Myc and HDAC3 in chronic myeloid leukemia cell lines
    • 15583844 1:CAS:528:DC%2BD2MXmsFeiug%3D%3D
    • Xu Y, Voelter-Mahlknecht S, Mahlknecht U (2005) The histone deacetylase inhibitor suberoylanilide hydroxamic acid down-regulates expression levels of Bcr-abl, c-Myc and HDAC3 in chronic myeloid leukemia cell lines. Int J Mol Med 15:169-172
    • (2005) Int J Mol Med , vol.15 , pp. 169-172
    • Xu, Y.1    Voelter-Mahlknecht, S.2    Mahlknecht, U.3
  • 9
    • 0038066488 scopus 로고    scopus 로고
    • Histone deacetylase inhibitors promote STI571-mediated apoptosis in STI571-sensitive and -resistant Bcr/Abl+ human myeloid leukemia cells
    • 12727828 1:CAS:528:DC%2BD3sXjtlGmsbc%3D
    • Yu C, Rahmani M, Almenara J et al (2003) Histone deacetylase inhibitors promote STI571-mediated apoptosis in STI571-sensitive and -resistant Bcr/Abl+ human myeloid leukemia cells. Cancer Res 63:2118-2126
    • (2003) Cancer Res , vol.63 , pp. 2118-2126
    • Yu, C.1    Rahmani, M.2    Almenara, J.3
  • 10
    • 0242670014 scopus 로고    scopus 로고
    • Novel biologically based therapies for Waldenstrom's macroglobulinemia
    • 12720159 10.1053/sonc.2003.50065 1:CAS:528:DC%2BD3sXjsl2msLc%3D
    • Mitsiades CS, Mitsiades N, Richardson PG, Treon SP, Anderson KC (2003) Novel biologically based therapies for Waldenstrom's macroglobulinemia. Semin Oncol 30:309-312
    • (2003) Semin Oncol , vol.30 , pp. 309-312
    • Mitsiades, C.S.1    Mitsiades, N.2    Richardson, P.G.3    Treon, S.P.4    Anderson, K.C.5
  • 11
    • 33644814867 scopus 로고    scopus 로고
    • Selective induction of apoptosis by histone deacetylase inhibitor SAHA in cutaneous T-cell lymphoma cells: Relevance to mechanism of therapeutic action
    • 16297208 10.1111/j.0022-202X.2005.23925.x 1:CAS:528:DC%2BD2MXht1GrtrvN
    • Zhang C, Richon V, Ni X, Talpur R, Duvic M (2005) Selective induction of apoptosis by histone deacetylase inhibitor SAHA in cutaneous T-cell lymphoma cells: relevance to mechanism of therapeutic action. J Invest Dermatol 125:1045-1052
    • (2005) J Invest Dermatol , vol.125 , pp. 1045-1052
    • Zhang, C.1    Richon, V.2    Ni, X.3    Talpur, R.4    Duvic, M.5
  • 12
    • 0034730127 scopus 로고    scopus 로고
    • Histone deacetylase inhibitor selectively induces p21WAF1 expression and gene-associated histone acetylation
    • 10954755 10.1073/pnas.180316197 1:CAS:528:DC%2BD3cXmtlehsL4%3D
    • Richon VM, Sandhoff TW, Rifkind RA, Marks PA (2000) Histone deacetylase inhibitor selectively induces p21WAF1 expression and gene-associated histone acetylation. Proc Natl Acad Sci U S A 97:10014-10019
    • (2000) Proc Natl Acad Sci U S A , vol.97 , pp. 10014-10019
    • Richon, V.M.1    Sandhoff, T.W.2    Rifkind, R.A.3    Marks, P.A.4
  • 13
    • 0034297220 scopus 로고    scopus 로고
    • Suberoylanilide hydroxamic acid as a potential therapeutic agent for human breast cancer treatment
    • 11126200 1:CAS:528:DC%2BD3cXot1WgtL4%3D
    • Huang L, Pardee AB (2000) Suberoylanilide hydroxamic acid as a potential therapeutic agent for human breast cancer treatment. Mol Med 6:849-866
    • (2000) Mol Med , vol.6 , pp. 849-866
    • Huang, L.1    Pardee, A.B.2
  • 14
    • 0035577768 scopus 로고    scopus 로고
    • The histone deacetylase inhibitor suberoylanilide hydroxamic acid induces differentiation of human breast cancer cells
    • 11731433 1:CAS:528:DC%2BD3MXptFCkur8%3D
    • Munster PN, Troso-Sandoval T, Rosen N, Rifkind R, Marks PA, Richon VM (2001) The histone deacetylase inhibitor suberoylanilide hydroxamic acid induces differentiation of human breast cancer cells. Cancer Res 61:8492-8497
    • (2001) Cancer Res , vol.61 , pp. 8492-8497
    • Munster, P.N.1    Troso-Sandoval, T.2    Rosen, N.3    Rifkind, R.4    Marks, P.A.5    Richon, V.M.6
  • 15
    • 0034665124 scopus 로고    scopus 로고
    • Suberoylanilide hydroxamic acid, an inhibitor of histone deacetylase, suppresses the growth of prostate cancer cells in vitro and in vivo
    • 11016644 1:CAS:528:DC%2BD3cXntVamur0%3D
    • Butler LM, Agus DB, Scher HI et al (2000) Suberoylanilide hydroxamic acid, an inhibitor of histone deacetylase, suppresses the growth of prostate cancer cells in vitro and in vivo. Cancer Res 60:5165-5170
    • (2000) Cancer Res , vol.60 , pp. 5165-5170
    • Butler, L.M.1    Agus, D.B.2    Scher, H.I.3
  • 16
    • 36749029400 scopus 로고    scopus 로고
    • Histone deacetylase inhibitor suberoylanilide hydroxamic acid induces apoptosis through both mitochondrial and Fas (Cd95) signaling in head and neck squamous carcinoma cells
    • 18025281 10.1158/1535-7163.MCT-04-0344 1:CAS:528:DC%2BD2sXhtlWkt7bL
    • Gillenwater AM, Zhong M, Lotan R (2007) Histone deacetylase inhibitor suberoylanilide hydroxamic acid induces apoptosis through both mitochondrial and Fas (Cd95) signaling in head and neck squamous carcinoma cells. Mol Cancer Ther 6:2967-2975
    • (2007) Mol Cancer Ther , vol.6 , pp. 2967-2975
    • Gillenwater, A.M.1    Zhong, M.2    Lotan, R.3
  • 17
    • 0042090495 scopus 로고    scopus 로고
    • Novel mechanisms of apoptosis induced by histone deacetylase inhibitors
    • 12907619 1:CAS:528:DC%2BD3sXmtFersrs%3D
    • Peart MJ, Tainton KM, Ruefli AA et al (2003) Novel mechanisms of apoptosis induced by histone deacetylase inhibitors. Cancer Res 63:4460-4471
    • (2003) Cancer Res , vol.63 , pp. 4460-4471
    • Peart, M.J.1    Tainton, K.M.2    Ruefli, A.A.3
  • 18
    • 67650090545 scopus 로고    scopus 로고
    • Histone deacetylase inhibitors: Potential in cancer therapy
    • 19459166 10.1002/jcb.22185 1:CAS:528:DC%2BD1MXosFOiurg%3D
    • Marks PA, Xu WS (2009) Histone deacetylase inhibitors: potential in cancer therapy. J Cell Biochem 107:600-608
    • (2009) J Cell Biochem , vol.107 , pp. 600-608
    • Marks, P.A.1    Xu, W.S.2
  • 19
    • 14544303662 scopus 로고    scopus 로고
    • Proteasome inhibition as a novel therapeutic target in human cancer
    • 15659509 10.1200/JCO.2005.11.030 1:CAS:528:DC%2BD2MXitVartb0%3D
    • Rajkumar SV, Richardson PG, Hideshima T, Anderson KC (2005) Proteasome inhibition as a novel therapeutic target in human cancer. J Clin Oncol 23:630-639
    • (2005) J Clin Oncol , vol.23 , pp. 630-639
    • Rajkumar, S.V.1    Richardson, P.G.2    Hideshima, T.3    Anderson, K.C.4
  • 20
    • 33645737411 scopus 로고    scopus 로고
    • Aggresome disruption: A novel strategy to enhance bortezomib-induced apoptosis in pancreatic cancer cells
    • 16585204 10.1158/0008-5472.CAN-05-2961 1:CAS:528:DC%2BD28XjtVOrtbw%3D
    • Nawrocki ST, Carew JS, Pino MS et al (2006) Aggresome disruption: a novel strategy to enhance bortezomib-induced apoptosis in pancreatic cancer cells. Cancer Res 66:3773-3781
    • (2006) Cancer Res , vol.66 , pp. 3773-3781
    • Nawrocki, S.T.1    Carew, J.S.2    Pino, M.S.3
  • 21
    • 0036303981 scopus 로고    scopus 로고
    • Hassles with taking out the garbage: Aggravating aggresomes
    • 12010457 10.1034/j.1600-0854.2002.30602.x 1:CAS:528:DC%2BD38XktlGhtLs%3D
    • Garcia-Mata R, Gao YS, Sztul E (2002) Hassles with taking out the garbage: aggravating aggresomes. Traffic 3:388-396
    • (2002) Traffic , vol.3 , pp. 388-396
    • Garcia-Mata, R.1    Gao, Y.S.2    Sztul, E.3
  • 22
    • 67650462779 scopus 로고    scopus 로고
    • Clinical development of novel proteasome inhibitors for cancer treatment
    • 19505187 10.1517/13543780903002074 1:CAS:528:DC%2BD1MXns1eru7s%3D
    • Yang H, Zonder JA, Dou QP (2009) Clinical development of novel proteasome inhibitors for cancer treatment. Expert Opin Investig Drugs 18:957-971
    • (2009) Expert Opin Investig Drugs , vol.18 , pp. 957-971
    • Yang, H.1    Zonder, J.A.2    Dou, Q.P.3
  • 23
    • 34547692973 scopus 로고    scopus 로고
    • Incorporating bortezomib into the treatment of lung cancer
    • 17671158 10.1158/1078-0432.CCR-07-0334
    • Davies AM, Lara PN Jr, Mack PC, Gandara DR (2007) Incorporating bortezomib into the treatment of lung cancer. Clin Cancer Res 13:s4647-s4651
    • (2007) Clin Cancer Res , vol.13
    • Davies, A.M.1    Lara, Jr.P.N.2    Mack, P.C.3    Gandara, D.R.4
  • 24
    • 4644304196 scopus 로고    scopus 로고
    • Phase II trial of bortezomib for patients with advanced renal cell carcinoma
    • 15365068 10.1200/JCO.2004.10.155 1:CAS:528:DC%2BD2cXhtVCitb7P
    • Kondagunta GV, Drucker B, Schwartz L et al (2004) Phase II trial of bortezomib for patients with advanced renal cell carcinoma. J Clin Oncol 22:3720-3725
    • (2004) J Clin Oncol , vol.22 , pp. 3720-3725
    • Kondagunta, G.V.1    Drucker, B.2    Schwartz, L.3
  • 25
    • 0033230594 scopus 로고    scopus 로고
    • The apoptotic effects and synergistic interaction of sodium butyrate and MG132 in human retinoblastoma Y79 cells
    • 10554039 1:CAS:528:DyaK1MXnt1Gisrc%3D
    • Giuliano M, Lauricella M, Calvaruso G et al (1999) The apoptotic effects and synergistic interaction of sodium butyrate and MG132 in human retinoblastoma Y79 cells. Cancer Res 59:5586-5595
    • (1999) Cancer Res , vol.59 , pp. 5586-5595
    • Giuliano, M.1    Lauricella, M.2    Calvaruso, G.3
  • 26
    • 0242493856 scopus 로고    scopus 로고
    • The proteasome inhibitor bortezomib interacts synergistically with histone deacetylase inhibitors to induce apoptosis in Bcr/Abl+ cells sensitive and resistant to STI571
    • 12893773 10.1182/blood-2003-03-0737 1:CAS:528:DC%2BD3sXptVymtb0%3D
    • Yu C, Rahmani M, Conrad D, Subler M, Dent P, Grant S (2003) The proteasome inhibitor bortezomib interacts synergistically with histone deacetylase inhibitors to induce apoptosis in Bcr/Abl+ cells sensitive and resistant to STI571. Blood 102:3765-3774
    • (2003) Blood , vol.102 , pp. 3765-3774
    • Yu, C.1    Rahmani, M.2    Conrad, D.3    Subler, M.4    Dent, P.5    Grant, S.6
  • 27
    • 70450227260 scopus 로고    scopus 로고
    • Proteasome inhibitors in the treatment of multiple myeloma
    • Shah JJ, Orlowski RZ (2009) Proteasome inhibitors in the treatment of multiple myeloma. Leukemia 23(11):1964-1979
    • (2009) Leukemia , vol.23 , Issue.11 , pp. 1964-1979
    • Shah, J.J.1    Orlowski, R.Z.2
  • 28
    • 27744490852 scopus 로고    scopus 로고
    • HDACs and the senescent phenotype of WI-38 cells
    • 16250917 10.1186/1471-2121-6-37
    • Place RF, Noonan EJ, Giardina C (2005) HDACs and the senescent phenotype of WI-38 cells. BMC Cell Biol 6:37
    • (2005) BMC Cell Biol , vol.6 , pp. 37
    • Place, R.F.1    Noonan, E.J.2    Giardina, C.3
  • 29
    • 34249993174 scopus 로고    scopus 로고
    • SAHA induces apoptosis in hepatoma cells and synergistically interacts with the proteasome inhibitor Bortezomib
    • 17351739 10.1007/s10495-007-0063-y 1:CAS:528:DC%2BD2sXmtlShtLk%3D
    • Emanuele S, Lauricella M, Carlisi D et al (2007) SAHA induces apoptosis in hepatoma cells and synergistically interacts with the proteasome inhibitor Bortezomib. Apoptosis 12:1327-1338
    • (2007) Apoptosis , vol.12 , pp. 1327-1338
    • Emanuele, S.1    Lauricella, M.2    Carlisi, D.3
  • 30
    • 77958575758 scopus 로고    scopus 로고
    • Autophagy inhibition enhances vorinostat-induced apoptosis via ubiquitinated protein accumulation
    • Carew JS, Medina EC, Esquivel JA 2nd et al (2010) Autophagy inhibition enhances vorinostat-induced apoptosis via ubiquitinated protein accumulation. J Cell Mol Med 14(10):2448-2459
    • (2010) J Cell Mol Med , vol.14 , Issue.10 , pp. 2448-2459
    • Carew, J.S.1    Medina, E.C.2    Esquivel, I.I.J.A.3
  • 31
    • 21344464730 scopus 로고    scopus 로고
    • HDAC inhibition prevents NF-kappa B activation by suppressing proteasome activity: Down-regulation of proteasome subunit expression stabilizes i kappa B alpha
    • 15950952 10.1016/j.bcp.2005.04.030 1:CAS:528:DC%2BD2MXlvVWms7w%3D
    • Place RF, Noonan EJ, Giardina C (2005) HDAC inhibition prevents NF-kappa B activation by suppressing proteasome activity: down-regulation of proteasome subunit expression stabilizes I kappa B alpha. Biochem Pharmacol 70:394-406
    • (2005) Biochem Pharmacol , vol.70 , pp. 394-406
    • Place, R.F.1    Noonan, E.J.2    Giardina, C.3
  • 32
    • 33746759383 scopus 로고    scopus 로고
    • A liquid chromatography-electrospray ionization tandem mass spectrometric assay for quantitation of the histone deacetylase inhibitor, vorinostat (suberoylanilide hydroxamicacid, SAHA) and its metabolites in human serum
    • 10.1016/j.jchromb.2006.04.044 1:CAS:528:DC%2BD28XotFyks74%3D
    • Parise RA, Holleran JL, Beumer JH, Ramalingam S, Egoran MJ (2006) A liquid chromatography-electrospray ionization tandem mass spectrometric assay for quantitation of the histone deacetylase inhibitor, vorinostat (suberoylanilide hydroxamicacid, SAHA) and its metabolites in human serum. J Chromatogr B Anal Technol Biomed Life Sci 840(2):108-115
    • (2006) J Chromatogr B Anal Technol Biomed Life Sci , vol.840 , Issue.2 , pp. 108-115
    • Parise, R.A.1    Holleran, J.L.2    Beumer, J.H.3    Ramalingam, S.4    Egoran, M.J.5
  • 33
    • 69249209745 scopus 로고    scopus 로고
    • Vorinostat in solid and hematologic malignancies
    • 19635146 10.1186/1756-8722-2-31
    • Siegel D, Hussein M, Belani C et al (2009) Vorinostat in solid and hematologic malignancies. J Hematol Oncol 2:31
    • (2009) J Hematol Oncol , vol.2 , pp. 31
    • Siegel, D.1    Hussein, M.2    Belani, C.3
  • 34
    • 67649604329 scopus 로고    scopus 로고
    • Targeting the proteasome pathway
    • 19397479 10.1517/14728220902866851 1:CAS:528:DC%2BD1MXltVOmur8%3D
    • Tsukamoto S, Yokosawa H (2009) Targeting the proteasome pathway. Expert Opin Ther Targets 13:605-621
    • (2009) Expert Opin Ther Targets , vol.13 , pp. 605-621
    • Tsukamoto, S.1    Yokosawa, H.2
  • 35
    • 15744364211 scopus 로고    scopus 로고
    • A multicenter Phase II study of bortezomib in recurrent or metastatic sarcomas
    • 15739208 10.1002/cncr.20968 1:CAS:528:DC%2BD2MXjtFamtr0%3D
    • Maki RG, Kraft AS, Scheu K et al (2005) A multicenter Phase II study of bortezomib in recurrent or metastatic sarcomas. Cancer 103:1431-1438
    • (2005) Cancer , vol.103 , pp. 1431-1438
    • Maki, R.G.1    Kraft, A.S.2    Scheu, K.3
  • 36
    • 67649399669 scopus 로고    scopus 로고
    • Vorinostat (NSC# 701852) in patients with relapsed non-small cell lung cancer: A Wisconsin Oncology Network phase II study
    • 19347984 10.1097/JTO.0b013e3181952478
    • Traynor AM, Dubey S, Eickhoff JC et al (2009) Vorinostat (NSC# 701852) in patients with relapsed non-small cell lung cancer: a Wisconsin Oncology Network phase II study. J Thorac Oncol 4:522-526
    • (2009) J Thorac Oncol , vol.4 , pp. 522-526
    • Traynor, A.M.1    Dubey, S.2    Eickhoff, J.C.3
  • 37
    • 34250696097 scopus 로고    scopus 로고
    • Phase i and pharmacokinetic study of vorinostat, a histone deacetylase inhibitor, in combination with carboplatin and paclitaxel for advanced solid malignancies
    • 17510206 10.1158/1078-0432.CCR-07-0162 1:CAS:528:DC%2BD2sXmsFCqur8%3D
    • Ramalingam SS, Parise RA, Ramanathan RK et al (2007) Phase I and pharmacokinetic study of vorinostat, a histone deacetylase inhibitor, in combination with carboplatin and paclitaxel for advanced solid malignancies. Clin Cancer Res 13:3605-3610
    • (2007) Clin Cancer Res , vol.13 , pp. 3605-3610
    • Ramalingam, S.S.1    Parise, R.A.2    Ramanathan, R.K.3


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