메뉴 건너뛰기




Volumn 102, Issue 7, 2003, Pages 2615-2622

NVP-LAQ824 is a potent novel histone deacetylase inhibitor with significant activity against multiple myeloma

Author keywords

[No Author keywords available]

Indexed keywords

4 [N (2 HYDROXYETHYL) N [2 (3 INDOLYL)ETHYL]AMINOMETHYL]CINNAMOHYDROXAMIC ACID; ANNEXIN; CASPASE; CHYMOTRYPSIN; HISTONE DEACETYLASE INHIBITOR; HYDROXAMIC ACID DERIVATIVE; POLY(ADENOSINE DIPHOSPHATE RIBOSE); POLYUBIQUITIN; PROPIDIUM IODIDE; PROTEASOME INHIBITOR; PROTEIN P21; UNCLASSIFIED DRUG;

EID: 0141593496     PISSN: 00064971     EISSN: None     Source Type: Journal    
DOI: 10.1182/blood-2003-01-0233     Document Type: Article
Times cited : (212)

References (53)
  • 1
    • 0034254668 scopus 로고    scopus 로고
    • Targeting of N-CoR and histone deacetylase 3 by the oncoprotein v-erbA yields a chromatin infrastructure-dependent transcriptional repression pathway
    • Urnov FD, Yee J, Sachs L, et al. Targeting of N-CoR and histone deacetylase 3 by the oncoprotein v-erbA yields a chromatin infrastructure-dependent transcriptional repression pathway. Embo J. 2000;19:4074-4090.
    • (2000) Embo J , vol.19 , pp. 4074-4090
    • Urnov, F.D.1    Yee, J.2    Sachs, L.3
  • 2
    • 0034045040 scopus 로고    scopus 로고
    • Histone deacetylases, transcriptional control, and cancer
    • Cress WD, Seto E. Histone deacetylases, transcriptional control, and cancer. J Cell Physiol. 2000;184:1-16.
    • (2000) J Cell Physiol , vol.184 , pp. 1-16
    • Cress, W.D.1    Seto, E.2
  • 3
    • 0034252183 scopus 로고    scopus 로고
    • Histone acetylation modifiers in the pathogenesis of malignant disease
    • Mahlknecht U, Hoelzer D. Histone acetylation modifiers in the pathogenesis of malignant disease. Mol Med. 2000;6:623-644.
    • (2000) Mol Med , vol.6 , pp. 623-644
    • Mahlknecht, U.1    Hoelzer, D.2
  • 5
    • 0035328528 scopus 로고    scopus 로고
    • Inhibition of transformed cell growth and induction of cellular differentiation by pyroxamide, an inhibitor of histone deacetylase
    • Kutko MC, Glick RD, Butler LM, et al. Inhibition of transformed cell growth and induction of cellular differentiation by pyroxamide, an inhibitor of histone deacetylase. Cancer Res. 2001;61:3591-3594.
    • (2001) Cancer Res , vol.61 , pp. 3591-3594
    • Kutko, M.C.1    Glick, R.D.2    Butler, L.M.3
  • 6
    • 0034908978 scopus 로고    scopus 로고
    • Inhibitors of histone deacetylase are potentially effective anticancer agents
    • Marks PA, Rifkind RA, Richon VM, Breslow R. Inhibitors of histone deacetylase are potentially effective anticancer agents. Clin Cancer Res. 2001;7:759-760.
    • (2001) Clin Cancer Res , vol.7 , pp. 759-760
    • Marks, P.A.1    Rifkind, R.A.2    Richon, V.M.3    Breslow, R.4
  • 7
    • 0017886958 scopus 로고
    • Sodium butyrate inhibits histone deacetylation in cultured cells
    • Candido EP, Reeves R, Davie JR. Sodium butyrate inhibits histone deacetylation in cultured cells. Cell. 1978;14:105-113.
    • (1978) Cell , vol.14 , pp. 105-113
    • Candido, E.P.1    Reeves, R.2    Davie, J.R.3
  • 8
    • 0017809719 scopus 로고
    • Tumover of histone acetyl groups in cultured cells is inhibited by sodium butyrate
    • Reeves R, Candido EP. Tumover of histone acetyl groups in cultured cells is inhibited by sodium butyrate. FEBS Lett. 1978;91:117-120.
    • (1978) FEBS Lett , vol.91 , pp. 117-120
    • Reeves, R.1    Candido, E.P.2
  • 9
    • 0024996768 scopus 로고
    • Potent and specific inhibition of mammalian histone deacetylase both in vivo and in vitro by trichostatin A
    • Yoshida M, Kijima M, Akita M, Beppu T. Potent and specific inhibition of mammalian histone deacetylase both in vivo and in vitro by trichostatin A. J Biol Chem. 1990;265:17174-17179.
    • (1990) J Biol Chem , vol.265 , pp. 17174-17179
    • Yoshida, M.1    Kijima, M.2    Akita, M.3    Beppu, T.4
  • 10
    • 0031892734 scopus 로고    scopus 로고
    • Hexamethylene bisacetamide induces programmed cell death (apoptosis) and down-regulates BCL-2 expression in human myeloma cells
    • Siegel DS, Zhang X, Feinman R, et al. Hexamethylene bisacetamide induces programmed cell death (apoptosis) and down-regulates BCL-2 expression in human myeloma cells. Proc Natl Acad Sci U S A. 1998;95:162-166.
    • (1998) Proc Natl Acad Sci U S A , vol.95 , pp. 162-166
    • Siegel, D.S.1    Zhang, X.2    Feinman, R.3
  • 11
    • 1542588471 scopus 로고    scopus 로고
    • Second generation hybrid polar compounds are potent inducers of transformed cell differentiation
    • Richon VM, Webb Y, Merger R, et al. Second generation hybrid polar compounds are potent inducers of transformed cell differentiation. Proc Natl Acad Sci U S A. 1996;93:5705-5708.
    • (1996) Proc Natl Acad Sci U S A , vol.93 , pp. 5705-5708
    • Richon, V.M.1    Webb, Y.2    Merger, R.3
  • 12
    • 0033539092 scopus 로고    scopus 로고
    • Structures of a histone deacetylase homologue bound to the TSA and SAHA inhibitors
    • Finnin MS, Donigian JR, Cohen A, et al. Structures of a histone deacetylase homologue bound to the TSA and SAHA inhibitors. Nature. 1999;401:188-193.
    • (1999) Nature , vol.401 , pp. 188-193
    • Finnin, M.S.1    Donigian, J.R.2    Cohen, A.3
  • 13
    • 0036681989 scopus 로고    scopus 로고
    • Sulfonamide anilides, a novel class of histone deacetylase inhibitors, are antiproliferative against human tumors
    • Fournel M, Trachy-Bourget MC, Yan PT, et al. Sulfonamide anilides, a novel class of histone deacetylase inhibitors, are antiproliferative against human tumors. Cancer Res. 2002;62:4325-4330.
    • (2002) Cancer Res , vol.62 , pp. 4325-4330
    • Fournel, M.1    Trachy-Bourget, M.C.2    Yan, P.T.3
  • 15
    • 0034905872 scopus 로고    scopus 로고
    • Inhibition of transformed cell growth and induction of cellular differentiation by pyroxamide, an inhibitor of histone deacetylase
    • Butler LM, Webb Y, Agus DB, et al. Inhibition of transformed cell growth and induction of cellular differentiation by pyroxamide, an inhibitor of histone deacetylase. Clin Cancer Res. 2001;7:962-970.
    • (2001) Clin Cancer Res , vol.7 , pp. 962-970
    • Butler, L.M.1    Webb, Y.2    Agus, D.B.3
  • 16
    • 0344431240 scopus 로고    scopus 로고
    • FR901228, a potent antitumor antibiotic, is a novel histone deacetylase inhibitor
    • Nakajima H, Kim YB, Terano H, Yoshida M, Horinouchi S. FR901228, a potent antitumor antibiotic, is a novel histone deacetylase inhibitor. Exp Cell Res. 1998;241:126-133.
    • (1998) Exp Cell Res , vol.241 , pp. 126-133
    • Nakajima, H.1    Kim, Y.B.2    Terano, H.3    Yoshida, M.4    Horinouchi, S.5
  • 18
    • 0035525781 scopus 로고    scopus 로고
    • Inhibitor of h[stone deacetylation, depsipeptide (FR901228), in the treatment of peripheral and cutaneous T-cell lymphoma: A case report
    • Piekarz RL, Robey R, Sandor V, et al. Inhibitor of h[stone deacetylation, depsipeptide (FR901228), in the treatment of peripheral and cutaneous T-cell lymphoma: a case report. Blood. 2001;98:2865-2868.
    • (2001) Blood , vol.98 , pp. 2865-2868
    • Piekarz, R.L.1    Robey, R.2    Sandor, V.3
  • 19
    • 3643104150 scopus 로고    scopus 로고
    • Therapeutic targeting of transcription in acute promyelocytic leukemia by use of an inhibitor of histone deacetylase
    • Warrell RP Jr, He LZ, Richon V, Calleja E, Pandolfi PP. Therapeutic targeting of transcription in acute promyelocytic leukemia by use of an inhibitor of histone deacetylase. J Natl Cancer Inst. 1998:90:1621-1625.
    • (1998) J Natl Cancer Inst , vol.90 , pp. 1621-1625
    • Warrell R.P., Jr.1    He, L.Z.2    Richon, V.3    Calleja, E.4    Pandolfi, P.P.5
  • 20
    • 9144225360 scopus 로고    scopus 로고
    • Selective growth inhibition of tumor cells by a novel histone deacetylase inhibitor NVP-LAQ824
    • In press
    • Atadja P, Gao L, Kwon P, et al. Selective growth inhibition of tumor cells by a novel histone deacetylase inhibitor NVP-LAQ824. Cancer Res. In press.
    • Cancer Res
    • Atadja, P.1    Gao, L.2    Kwon, P.3
  • 21
    • 0141532453 scopus 로고    scopus 로고
    • Histone deacetylase inhibitor LAQ824 down regulates Her-2, induces growth arrest and apoptosis and sensitizes human breast cancer cells to Herceptin
    • Abstract R798
    • Donapaty S, Fuino L, Wittmann S. et al. Histone deacetylase inhibitor LAQ824 down regulates Her-2, induces growth arrest and apoptosis and sensitizes human breast cancer cells to Herceptin [abstract]. Proc AACR. 2003;44:156. Abstract R798.
    • (2003) Proc AACR , vol.44 , pp. 156
    • Donapaty, S.1    Fuino, L.2    Wittmann, S.3
  • 22
    • 0034730127 scopus 로고    scopus 로고
    • Histone deacetylase inhibitor selectively induces p21WAF1 expression and gene-associated histone acetylation
    • Richon VM, Sandhoff TW, Rifkind RA, Marks PA. Histone deacetylase inhibitor selectively induces p21WAF1 expression and gene-associated histone acetylation. Proc Natl Acad Sci U S A. 2000;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
  • 23
    • 0036731055 scopus 로고    scopus 로고
    • Histone deacetylase inhibitors all induce p21 but differentially cause tubulin acetylation, mitotic arrest, and cytotoxicity
    • Blagosklonny MV, Robey R, Sackett D, et al. Histone deacetylase inhibitors all induce p21 but differentially cause tubulin acetylation, mitotic arrest, and cytotoxicity. Mol Cancer Ther. 2002;1:937-941.
    • (2002) Mol Cancer Ther , vol.1 , pp. 937-941
    • Blagosklonny, M.V.1    Robey, R.2    Sackett, D.3
  • 24
    • 0033963601 scopus 로고    scopus 로고
    • Involvement of p21(Waf1/Cip1) and its cleavage by DEVD-caspase during apoptosis of colorectal cancer cells induced by butyrate
    • Chai F, Evdokiou A, Young GP, Zalewski PD. Involvement of p21(Waf1/Cip1) and its cleavage by DEVD-caspase during apoptosis of colorectal cancer cells induced by butyrate. Carcinogenesis. 2000;21:7-14.
    • (2000) Carcinogenesis , vol.21 , pp. 7-14
    • Chai, F.1    Evdokiou, A.2    Young, G.P.3    Zalewski, P.D.4
  • 25
    • 17744416444 scopus 로고    scopus 로고
    • Histone deacetylase inhibitor activates the WAF1/Cip1 gene promoter through the Sp1 sites
    • Sowa Y, Orita T, Minamikawa S, et al. Histone deacetylase inhibitor activates the WAF1/Cip1 gene promoter through the Sp1 sites. Biochem Biophys Res Commun. 1997;241:142-150.
    • (1997) Biochem Biophys Res Commun , vol.241 , pp. 142-150
    • Sowa, Y.1    Orita, T.2    Minamikawa, S.3
  • 26
    • 0030772026 scopus 로고    scopus 로고
    • Butyrate activates the WAF1/Cip1 gene promoter through Sp1 sites in a p53-negative human colon cancer cell line
    • Nakano K, Mizuno T, Sowa Y, et al. Butyrate activates the WAF1/Cip1 gene promoter through Sp1 sites in a p53-negative human colon cancer cell line. J Biol Chem. 1997;272:22199-22206.
    • (1997) J Biol Chem , vol.272 , pp. 22199-22206
    • Nakano, K.1    Mizuno, T.2    Sowa, Y.3
  • 27
    • 0032802314 scopus 로고    scopus 로고
    • Histone deacetylase 1 can repress transcription by binding to Sp1
    • Doetzlhofer A, Rotheneder H, Lagger G, et al. Histone deacetylase 1 can repress transcription by binding to Sp1. Mol Cell Biol. 1999;19:5504-5511.
    • (1999) Mol Cell Biol , vol.19 , pp. 5504-5511
    • Doetzlhofer, A.1    Rotheneder, H.2    Lagger, G.3
  • 28
    • 0035977063 scopus 로고    scopus 로고
    • Butyrate suppression of colonocyte NF-kappa B activation and cellular proteasome activity
    • Yin L, Laevsky G, Giardina C. Butyrate suppression of colonocyte NF-kappa B activation and cellular proteasome activity. J Biol Chem. 2001;276:44641-44646.
    • (2001) J Biol Chem , vol.276 , pp. 44641-44646
    • Yin, L.1    Laevsky, G.2    Giardina, C.3
  • 29
    • 0034770423 scopus 로고    scopus 로고
    • Histone deacetylase inhibitors increase p21(WAF1) and induce apoptosis of human myeloma cell lines independent of decreased IL-6 receptor expression
    • Lavelle D, Chen YH, Hankewych M, DeSimone J, Lee VS. Histone deacetylase inhibitors increase p21(WAF1) and induce apoptosis of human myeloma cell lines independent of decreased IL-6 receptor expression. Amer J Hematol. 2001;68:170-178.
    • (2001) Amer J Hematol , vol.68 , pp. 170-178
    • Lavelle, D.1    Chen, Y.H.2    Hankewych, M.3    DeSimone, J.4    Lee, V.S.5
  • 30
    • 0037589018 scopus 로고    scopus 로고
    • Molecular sequelae of histone deacetylase inhibition in human malignant B cells
    • Mitsiades N, Mitsiades CS, Richardson PG, et al. Molecular sequelae of histone deacetylase inhibition in human malignant B cells. Blood. 2003;101:4055-4062.
    • (2003) Blood , vol.101 , pp. 4055-4062
    • Mitsiades, N.1    Mitsiades, C.S.2    Richardson, P.G.3
  • 31
    • 0033822112 scopus 로고    scopus 로고
    • P21-dependent g(1)arrest with downregulation of cyclin D1 and upregulation of cyclin E by the histone deacetylase inhibitor FR901228
    • Sandor V, Senderowicz A, Mertiris S, et al. P21-dependent g(1)arrest with downregulation of cyclin D1 and upregulation of cyclin E by the histone deacetylase inhibitor FR901228. Br J Cancer. 2000;83:817-825.
    • (2000) Br J Cancer , vol.83 , pp. 817-825
    • Sandor, V.1    Senderowicz, A.2    Mertiris, S.3
  • 32
    • 0035406174 scopus 로고    scopus 로고
    • Evidence of a functional role for the cyclin-dependent kinase-inhibitor p21WAF1/CIP1/MDA6 in promoting differentiation and preventing mitochondrial dysfunction and apoptosis induced by sodium butyrate in human myelomonocytic leukemia cells (U937)
    • Rosato RR, Wang Z, Gopalkrishnan RV, Fisher PB, Grant S. Evidence of a functional role for the cyclin-dependent kinase-inhibitor p21WAF1/CIP1/MDA6 in promoting differentiation and preventing mitochondrial dysfunction and apoptosis induced by sodium butyrate in human myelomonocytic leukemia cells (U937). Int J Oncol. 2001;19:181-191.
    • (2001) Int J Oncol , vol.19 , pp. 181-191
    • Rosato, R.R.1    Wang, Z.2    Gopalkrishnan, R.V.3    Fisher, P.B.4    Grant, S.5
  • 33
    • 0032729215 scopus 로고    scopus 로고
    • Apoptosis induced by the histone deacetylase inhibitor sodium butyrate in human leukemic lymphoblasts
    • Bernhard D, Ausserlechner MJ, Tonko M, et al. Apoptosis induced by the histone deacetylase inhibitor sodium butyrate in human leukemic lymphoblasts. FASEB J. 1999;13:1991-2001.
    • (1999) FASEB J , vol.13 , pp. 1991-2001
    • Bernhard, D.1    Ausserlechner, M.J.2    Tonko, M.3
  • 34
    • 0033199896 scopus 로고    scopus 로고
    • Hybrid polar histone deacetylase inhibitor induces apoptosis and CD95/CD95 ligand expression in human neuroblastoma
    • Glick RD, Swendeman SL, Coffey DC, et al. Hybrid polar histone deacetylase inhibitor induces apoptosis and CD95/CD95 ligand expression in human neuroblastoma. Cancer Res. 1999;59:4392-4399.
    • (1999) Cancer Res , vol.59 , pp. 4392-4399
    • Glick, R.D.1    Swendeman, S.L.2    Coffey, D.C.3
  • 35
    • 0035724488 scopus 로고    scopus 로고
    • Histone deacetylase inhibitors induce caspase-dependent apoptosis and downregulation of daxx in acute promyelocytic leukaemia with t(15;17)
    • Amin HM, Saeed S, Alkan S. Histone deacetylase inhibitors induce caspase-dependent apoptosis and downregulation of daxx in acute promyelocytic leukaemia with t(15;17). Br J Haematol. 2001;115:287-297.
    • (2001) Br J Haematol , vol.115 , pp. 287-297
    • Amin, H.M.1    Saeed, S.2    Alkan, S.3
  • 36
    • 0035845541 scopus 로고    scopus 로고
    • The histone deacetylase inhibitor and chemotherapeutic agent suberoylanilide hydroxamic acid (SAHA) induces a cell-death pathway characterized by cleavage of Bid and production of reactive oxygen species
    • Ruefli AA, Ausserlechner MJ, Bernhard D, et al. The histone deacetylase inhibitor and chemotherapeutic agent suberoylanilide hydroxamic acid (SAHA) induces a cell-death pathway characterized by cleavage of Bid and production of reactive oxygen species. Proc Natl Acad Sci U S A. 2001;98:10833-10838.
    • (2001) Proc Natl Acad Sci U S A , vol.98 , pp. 10833-10838
    • Ruefli, A.A.1    Ausserlechner, M.J.2    Bernhard, D.3
  • 37
    • 0030796349 scopus 로고    scopus 로고
    • Induction of caspase-3 protease activity and apoptosis by butyrate and trichostatin A (inhibitors of histone deacetylase): Dependence on protein synthesis and synergy with a mitochondrial/cytochrome c-dependent pathway
    • Medina V, Edmonds B, Young GP, James R, Appleton S, Zalewski PD. Induction of caspase-3 protease activity and apoptosis by butyrate and trichostatin A (inhibitors of histone deacetylase): dependence on protein synthesis and synergy with a mitochondrial/cytochrome c-dependent pathway. Cancer Res. 1997;57:3697-3707.
    • (1997) Cancer Res , vol.57 , pp. 3697-3707
    • Medina, V.1    Edmonds, B.2    Young, G.P.3    James, R.4    Appleton, S.5    Zalewski, P.D.6
  • 38
    • 0033581897 scopus 로고    scopus 로고
    • RAFTK/PYK2-dependent and -independent apoptosis in multiple myeloma cells
    • Chauhan D, Hideshima T, Pandey P, et al. RAFTK/PYK2-dependent and -independent apoptosis in multiple myeloma cells. Oncogene. 1999;18:6733-6740.
    • (1999) Oncogene , vol.18 , pp. 6733-6740
    • Chauhan, D.1    Hideshima, T.2    Pandey, P.3
  • 39
    • 0035816553 scopus 로고    scopus 로고
    • Apaf-1/cytochrome c-independent and Smac-dependent induction of apoptosis in multiple myeloma (MM) cells
    • Chauhan D, Hideshima T, Rosen S, Reed JC, Kharbanda S, Anderson KC. Apaf-1/cytochrome c-independent and Smac-dependent induction of apoptosis in multiple myeloma (MM) cells. J Biol Chem. 2001;276:24453-24456.
    • (2001) J Biol Chem , vol.276 , pp. 24453-24456
    • Chauhan, D.1    Hideshima, T.2    Rosen, S.3    Reed, J.C.4    Kharbanda, S.5    Anderson, K.C.6
  • 40
    • 0034824495 scopus 로고    scopus 로고
    • p300/CBP/p53 interaction and regulation of the p53 response
    • Grossman SR. p300/CBP/p53 interaction and regulation of the p53 response. Eur J Biochem. 2001;268:2773-2778.
    • (2001) Eur J Biochem , vol.268 , pp. 2773-2778
    • Grossman, S.R.1
  • 41
    • 0026437723 scopus 로고
    • p53 and RAS gene mutations in multiple myeloma
    • Portier M, Moles JP, Mazars GR, et al. p53 and RAS gene mutations in multiple myeloma. Oncogene. 1992;7:2539-2543.
    • (1992) Oncogene , vol.7 , pp. 2539-2543
    • Portier, M.1    Moles, J.P.2    Mazars, G.R.3
  • 42
    • 0026508061 scopus 로고
    • Mutations of the p53 gene in human myeloma cell lines
    • Mazars GR, Portier M, Zhang XG, et al. Mutations of the p53 gene in human myeloma cell lines. Oncogene. 1992;7:1015-1018.
    • (1992) Oncogene , vol.7 , pp. 1015-1018
    • Mazars, G.R.1    Portier, M.2    Zhang, X.G.3
  • 43
    • 0030921866 scopus 로고    scopus 로고
    • MDM2 protein overexpression promotes proliferation and survival of multiple myeloma cells
    • Teoh G, Urashima M, Ogata A, et al. MDM2 protein overexpression promotes proliferation and survival of multiple myeloma cells. Blood. 1997;90:1982-1992.
    • (1997) Blood , vol.90 , pp. 1982-1992
    • Teoh, G.1    Urashima, M.2    Ogata, A.3
  • 44
    • 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, 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
  • 45
    • 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, 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
  • 46
    • 0036411742 scopus 로고    scopus 로고
    • Clinical trial design for target-based therapy
    • Fox E, Curt GA, Balis FM. Clinical trial design for target-based therapy. Oncologist. 2002;7:401-409.
    • (2002) Oncologist , vol.7 , pp. 401-409
    • Fox, E.1    Curt, G.A.2    Balis, F.M.3
  • 47
    • 0035113602 scopus 로고    scopus 로고
    • Histone deacetylase-targeted treatment restores retinoic acid signaling and differentiation in acute myeloid leukemia
    • Park SH, Kim JW, Sausville EA, et al. Histone deacetylase-targeted treatment restores retinoic acid signaling and differentiation in acute myeloid leukemia. Cancer Res. 2001;61:931-934.
    • (2001) Cancer Res , vol.61 , pp. 931-934
    • Park, S.H.1    Kim, J.W.2    Sausville, E.A.3
  • 48
    • 0032522962 scopus 로고    scopus 로고
    • Reduced retinoic acid-sensitivities of nuclear receptor corepressor binding to PML- and PLZF-RARalpha underlie molecular pathogenesis and treatment of acute promyelocytic leukemia
    • Guidez F, Ivins S, Zhu J, Soderstrom M, Waxman S, Zelent A. Reduced retinoic acid-sensitivities of nuclear receptor corepressor binding to PML- and PLZF-RARalpha underlie molecular pathogenesis and treatment of acute promyelocytic leukemia. Blood. 1998;91:2634-2642.
    • (1998) Blood , vol.91 , pp. 2634-2642
    • Guidez, F.1    Ivins, S.2    Zhu, J.3    Soderstrom, M.4    Waxman, S.5    Zelent, A.6
  • 49
    • 0033564130 scopus 로고    scopus 로고
    • Inhibitors of histone deacetylase relieve ETO-mediated repression and induce differentiation of AML1-ETO leukemia cells
    • Wang J, Saunthararajah Y, Redner RL, Liu JM. Inhibitors of histone deacetylase relieve ETO-mediated repression and induce differentiation of AML1-ETO leukemia cells. Cancer Res. 1999;59:2766-2769.
    • (1999) Cancer Res , vol.59 , pp. 2766-2769
    • Wang, J.1    Saunthararajah, Y.2    Redner, R.L.3    Liu, J.M.4
  • 50
    • 0035892119 scopus 로고    scopus 로고
    • Rearrangements of the c-myc oncogene are present in 15% of primary human multiple myeloma tumors
    • Avet-Loiseau H, Gerson F, Magrangeas F, Minvielle S, Harousseau JL, Bataille R. Rearrangements of the c-myc oncogene are present in 15% of primary human multiple myeloma tumors. Blood. 2001;98:3082-3086.
    • (2001) Blood , vol.98 , pp. 3082-3086
    • Avet-Loiseau, H.1    Gerson, F.2    Magrangeas, F.3    Minvielle, S.4    Harousseau, J.L.5    Bataille, R.6
  • 51
    • 0034602691 scopus 로고    scopus 로고
    • Diverse karyotypic abnormalities of the c-myc locus associated with c- myc dysregulation and tumor progression in multiple myeloma
    • Shou Y, Martelli ML, Gabrea A, et al. Diverse karyotypic abnormalities of the c-myc locus associated with c- myc dysregulation and tumor progression in multiple myeloma. Proc Natl Acad Sci U S A. 2000;97:228-233.
    • (2000) Proc Natl Acad Sci U S A , vol.97 , pp. 228-233
    • Shou, Y.1    Martelli, M.L.2    Gabrea, A.3
  • 52
    • 0033566302 scopus 로고    scopus 로고
    • Chromatin remodeling and leukemia: New therapeutic paradigms
    • Redner RL, Wang J, Liu JM. Chromatin remodeling and leukemia: new therapeutic paradigms. Blood. 1999;94:417-428.
    • (1999) Blood , vol.94 , pp. 417-428
    • Redner, R.L.1    Wang, J.2    Liu, J.M.3
  • 53
    • 0030271391 scopus 로고    scopus 로고
    • Histone acetylation and chromatin assembly: A single escort, multiple dances?
    • Roth SY, Allis CD. Histone acetylation and chromatin assembly: a single escort, multiple dances? Cell. 1996;87:5-8.
    • (1996) Cell , vol.87 , pp. 5-8
    • Roth, S.Y.1    Allis, C.D.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.