메뉴 건너뛰기




Volumn 30, Issue 2, 2012, Pages 435-442

Novel histone deacetylase inhibitor CG200745 induces clonogenic cell death by modulating acetylation of p53 in cancer cells

Author keywords

Acetylation; CG200745; Histone deacetylase inhibitor; p53

Indexed keywords

CG 200745; CYCLIN DEPENDENT KINASE INHIBITOR 1; HISTONE DEACETYLASE INHIBITOR; HISTONE H3; N1 [3 (DIMETHYLAMINO)PROPYL] N8 HYDROXY 2 [(NAPHTHALENE 1 LOXY)METHYL]OCT 2 ENEDIAMIDE; PROTEIN MDM2; PROTEIN P53; UNCLASSIFIED DRUG; VORINOSTAT; ANTINEOPLASTIC AGENT; CDKN1A PROTEIN, HUMAN; CYCLIN DEPENDENT KINASE INHIBITOR 1A; HISTONE; HISTONE DEACETYLASE; HYDROXAMIC ACID; LYSINE; MDM2 PROTEIN, HUMAN; N1 (3 (DIMETHYLAMINO)PROPYL) N8 HYDROXY 2 ((NAPHTHALENE 1 LOXY)METHYL)OCT 2 ENEDIAMIDE; N1-(3-(DIMETHYLAMINO)PROPYL)-N8-HYDROXY-2-((NAPHTHALENE-1-LOXY)METHYL)OCT-2-ENEDIAMIDE; NAPHTHALENE DERIVATIVE; TP53 PROTEIN, HUMAN;

EID: 84862265924     PISSN: 01676997     EISSN: 15730646     Source Type: Journal    
DOI: 10.1007/s10637-010-9568-2     Document Type: Article
Times cited : (28)

References (33)
  • 1
    • 30344477367 scopus 로고    scopus 로고
    • Histone deacetylase inhibitors and the promise of epigenetic (and more) treatments for cancer
    • Minucci S, Pelicci PG (2006) Histone deacetylase inhibitors and the promise of epigenetic (and more) treatments for cancer. Nat Rev Cancer 6:38-51
    • (2006) Nat Rev Cancer , vol.6 , pp. 38-51
    • Minucci, S.1    Pelicci, P.G.2
  • 2
    • 29244469466 scopus 로고    scopus 로고
    • The epigenetic progenitor origin of human cancer
    • Feinberg AP, Ohlsson R, Henikoff S (2006) The epigenetic progenitor origin of human cancer. Nat Rev Genet 7:21-33
    • (2006) Nat Rev Genet , vol.7 , pp. 21-33
    • Feinberg, A.P.1    Ohlsson, R.2    Henikoff, S.3
  • 3
    • 20144388146 scopus 로고    scopus 로고
    • Loss of acetylation at Lys16 and trimethylation at Lys20 of histone H4 is a common hallmark of human cancer
    • Fraga MF, Ballestar E, Villar-Garea A (2005) Loss of acetylation at Lys16 and trimethylation at Lys20 of histone H4 is a common hallmark of human cancer. Nat Genet 37:391-400
    • (2005) Nat Genet , vol.37 , pp. 391-400
    • Fraga, M.F.1    Ballestar, E.2    Villar-Garea, A.3
  • 4
    • 0035063182 scopus 로고    scopus 로고
    • Transcriptional control at regulatory checkpoint by histone deacetylase: Molecular connections between cancer and chromatin
    • Wade PA (2001) Transcriptional control at regulatory checkpoint by histone deacetylase: molecular connections between cancer and chromatin. Hum Mol Genet 10:693-698
    • (2001) Hum Mol Genet , vol.10 , pp. 693-698
    • Wade, P.A.1
  • 5
    • 12444321545 scopus 로고    scopus 로고
    • Phase i clinical trial of histone deacetylase inhibitor: Suberoylanilide hydroxamic acid administered intravenously
    • Kelly WK, Richon VM, O'Connor O et al (2003) Phase I clinical trial of histone deacetylase inhibitor: suberoylanilide hydroxamic acid administered intravenously. Clin Cancer Res 9:3578-3588
    • (2003) Clin Cancer Res , vol.9 , pp. 3578-3588
    • Kelly, W.K.1    Richon, V.M.2    O'Connor, O.3
  • 6
    • 0036906832 scopus 로고    scopus 로고
    • Histone deacetylase inhibitors: From target to clinical trials
    • Kelly WK, O'Connor OA, Marks PA (2002) Histone deacetylase inhibitors: from target to clinical trials. Expert Opin Inv Drug 12:1695-1713
    • (2002) Expert Opin Inv Drug , vol.12 , pp. 1695-1713
    • Kelly, W.K.1    O'Connor, O.A.2    Marks, P.A.3
  • 7
    • 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 et al (1990) Potent and specific inhibition of mammalian histone deacetylase both in vivo and in vitro by trichostatin A. J Biol Chem 265:17174-17179
    • (1990) J Biol Chem , vol.265 , pp. 17174-17179
    • Yoshida, M.1    Kijima, M.2    Akita, M.3
  • 8
    • 0027378351 scopus 로고
    • Trapoxin, an antitumor cyclic tetrapeptide, is an irreversible inhibitor of mammalian histone deacetylase
    • Kijima M, Yoshida M, Sugita K et al (1993) Trapoxin, an antitumor cyclic tetrapeptide, is an irreversible inhibitor of mammalian histone deacetylase. J Biol Chem 268:22429-22435
    • (1993) J Biol Chem , vol.268 , pp. 22429-22435
    • Kijima, M.1    Yoshida, M.2    Sugita, K.3
  • 9
    • 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 (2001) 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 USA 98:10833-10838
    • (2001) Proc Natl Acad Sci USA , vol.98 , pp. 10833-10838
    • Ruefli, A.A.1    Ausserlechner, M.J.2    Bernhard, D.3
  • 10
    • 0033230594 scopus 로고    scopus 로고
    • The apoptotic effects and synergistic interaction of sodium butyrate and MG132 in human retinoblastoma Y79 cells
    • 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
  • 11
    • 0035184066 scopus 로고    scopus 로고
    • Histone deacetylase inhibitor down-regulation of bcl-xl gene expression leads to apoptotic cell death in mesothelioma
    • Cao XX, Mohuiddin I, Ece F et al (2001) Histone deacetylase inhibitor down-regulation of bcl-xl gene expression leads to apoptotic cell death in mesothelioma. Am J Respir Cell Mol Biol 25:562-568
    • (2001) Am J Respir Cell Mol Biol , vol.25 , pp. 562-568
    • Cao, X.X.1    Mohuiddin, I.2    Ece, F.3
  • 12
    • 0034871794 scopus 로고    scopus 로고
    • Phenylbutyrate attenuates the expression of Bcl-X(L), DNA-PK, caveolin-1, and VEGF in prostate cancer cells
    • Goh M, Chen F, Paulsen MT et al (2001) Phenylbutyrate attenuates the expression of Bcl-X(L), DNA-PK, caveolin-1, and VEGF in prostate cancer cells. Neoplasia 3:331-338
    • (2001) Neoplasia , vol.3 , pp. 331-338
    • Goh, M.1    Chen, F.2    Paulsen, M.T.3
  • 13
    • 0035839136 scopus 로고    scopus 로고
    • Translating the histone code
    • Jenuwein T, Allis CD (2001) Translating the histone code. Science 293:1074-1080
    • (2001) Science , vol.293 , pp. 1074-1080
    • Jenuwein, T.1    Allis, C.D.2
  • 14
    • 19644392125 scopus 로고    scopus 로고
    • Inhibitory effects of cancer cell proliferation by novel histone deacetylase inhibitors involves p21/WAF1 induction and G2/M arrest
    • Maeda T, Nagaoka Y, Kawai Y et al (2005) Inhibitory effects of cancer cell proliferation by novel histone deacetylase inhibitors involves p21/WAF1 induction and G2/M arrest. Biol Pharm Bull 28:849-853
    • (2005) Biol Pharm Bull , vol.28 , pp. 849-853
    • Maeda, T.1    Nagaoka, Y.2    Kawai, Y.3
  • 15
    • 18644365597 scopus 로고    scopus 로고
    • Histone deacetylase inhibitors differentially stabilize acetylated p53 and induces cell cycle arrest or apoptosis in prostate cancer cells
    • Laurenzi VD, Roy S, Packman K et al (2005) Histone deacetylase inhibitors differentially stabilize acetylated p53 and induces cell cycle arrest or apoptosis in prostate cancer cells. Cell Death Differ 12:482-491
    • (2005) Cell Death Differ , vol.12 , pp. 482-491
    • Laurenzi, V.D.1    Roy, S.2    Packman, K.3
  • 16
    • 33748360764 scopus 로고    scopus 로고
    • Vorinostat, a histone deacetylase inhibitor, enhances the response of human tumor cells to ionizing radiation through prolongation of gamma-H2AX foci
    • Munshi A, Tanaka T, Hobbs ML et al (2006) Vorinostat, a histone deacetylase inhibitor, enhances the response of human tumor cells to ionizing radiation through prolongation of gamma-H2AX foci. Mol Cancer Ther 5:1967-1974
    • (2006) Mol Cancer Ther , vol.5 , pp. 1967-1974
    • Munshi, A.1    Tanaka, T.2    Hobbs, M.L.3
  • 17
    • 27944501617 scopus 로고    scopus 로고
    • Histone modifying enzymes and cancer: Going beyond histones
    • Zhang K, Dent SY (2005) Histone modifying enzymes and cancer: going beyond histones. J Cell Biochem 96:1137-1148
    • (2005) J Cell Biochem , vol.96 , pp. 1137-1148
    • Zhang, K.1    Dent, S.Y.2
  • 18
    • 32944465688 scopus 로고    scopus 로고
    • Histone deacetylase inhibitor-mediated radiosensitization of human cancer cells: Class differences and the potential influence of p53
    • Kim IA, Shin JH, Kim IH et al (2006) Histone deacetylase inhibitor-mediated radiosensitization of human cancer cells: class differences and the potential influence of p53. Clin Cancer Res 12:940-949
    • (2006) Clin Cancer Res , vol.12 , pp. 940-949
    • Kim, I.A.1    Shin, J.H.2    Kim, I.H.3
  • 19
    • 0035694469 scopus 로고    scopus 로고
    • Acetylation of p53 activates transcription through recruitment of coactivators/histone acetyltransferases
    • Barlev NA, Liu L, Chehab NH et al (2001) Acetylation of p53 activates transcription through recruitment of coactivators/histone acetyltransferases. Mol Cell 8:1243-1254
    • (2001) Mol Cell , vol.8 , pp. 1243-1254
    • Barlev, N.A.1    Liu, L.2    Chehab, N.H.3
  • 21
    • 0033552595 scopus 로고    scopus 로고
    • Regulation of p53 in response to DNA damage
    • Lakin ND, Jackson SP (1999) Regulation of p53 in response to DNA damage. Oncogene 18:7644-7655
    • (1999) Oncogene , vol.18 , pp. 7644-7655
    • Lakin, N.D.1    Jackson, S.P.2
  • 22
    • 33645230001 scopus 로고    scopus 로고
    • Acetylation of p53 at lysine 373/382 by the histone deacetylase inhibitor depsipeptide induces expression of p21(Waf1/Cip1)
    • Zhao Y, Lu S, Wu L et al (2006) Acetylation of p53 at lysine 373/382 by the histone deacetylase inhibitor depsipeptide induces expression of p21(Waf1/Cip1). Mol Cell Biol 26:2782-2790
    • (2006) Mol Cell Biol , vol.26 , pp. 2782-2790
    • Zhao, Y.1    Lu, S.2    Wu, L.3
  • 23
    • 0035868964 scopus 로고    scopus 로고
    • P300/CBP-mediated p53 acetylation is commonly induced by p53-activating agents and inhibited by MDM2
    • Ito A, Lai CH, Zhao X et al (2001) P300/CBP-mediated p53 acetylation is commonly induced by p53-activating agents and inhibited by MDM2. EMBO J 20:1331-1340
    • (2001) EMBO J , vol.20 , pp. 1331-1340
    • Ito, A.1    Lai, C.H.2    Zhao, X.3
  • 24
    • 0032530486 scopus 로고    scopus 로고
    • DNA damage activates p53 through a phosphorylation-acetylation cascade
    • Sakaguchi K, Herrera JE, Saito S et al (1998) DNA damage activates p53 through a phosphorylation-acetylation cascade. Genes Dev 12:2831-2841
    • (1998) Genes Dev , vol.12 , pp. 2831-2841
    • Sakaguchi, K.1    Herrera, J.E.2    Saito, S.3
  • 25
    • 0032906633 scopus 로고    scopus 로고
    • P53 sites acetylated in vitro by PCAF and p300 are acetylated in vivo in response to DNA damage
    • Liu L, Scolnick DM, Trievel RC et al (1999) p53 sites acetylated in vitro by PCAF and p300 are acetylated in vivo in response to DNA damage. Mol Cell Biol 19:1202-1209
    • (1999) Mol Cell Biol , vol.19 , pp. 1202-1209
    • Liu, L.1    Scolnick, D.M.2    Trievel, R.C.3
  • 26
    • 0035966316 scopus 로고    scopus 로고
    • Why is p53 acetylated?
    • Prives C, Manley JL (2001) Why is p53 acetylated? Cell 107:815-818
    • (2001) Cell , vol.107 , pp. 815-818
    • Prives, C.1    Manley, J.L.2
  • 27
    • 9144266953 scopus 로고    scopus 로고
    • Induction of PIG3 and NOXA through acetylation of p53 at 320 and 373 lysine residues as a mechanism for apoptotic cell death by histone deacetylase
    • Terui T, Murakami K, Takimoto R et al (2003) Induction of PIG3 and NOXA through acetylation of p53 at 320 and 373 lysine residues as a mechanism for apoptotic cell death by histone deacetylase. Inhibitors Cancer Res 63:8948-8954
    • (2003) Inhibitors Cancer Res , vol.63 , pp. 8948-8954
    • Terui, T.1    Murakami, K.2    Takimoto, R.3
  • 28
    • 36048958965 scopus 로고    scopus 로고
    • Histone deacetylase inhibitors: Overview and perspectives
    • Dokmanovic M, Clarke C, Marks PA (2007) Histone deacetylase inhibitors: overview and perspectives. Mol Cancer Res 5:981-989
    • (2007) Mol Cancer Res , vol.5 , pp. 981-989
    • Dokmanovic, M.1    Clarke, C.2    Marks, P.A.3
  • 29
    • 0034676439 scopus 로고    scopus 로고
    • Deacetylation of p53 modulates its effect on cell growth and apoptosis
    • Luo J, Su F, Chen D, Shiloh A et al (2000) Deacetylation of p53 modulates its effect on cell growth and apoptosis. Nature 408:377-381
    • (2000) Nature , vol.408 , pp. 377-381
    • Luo, J.1    Su, F.2    Chen, D.3    Shiloh, A.4
  • 30
    • 33847779059 scopus 로고    scopus 로고
    • Site-specific acetylation of p53 directs selective transcription complex assembly
    • Roy S, Tenniswood M (2007) Site-specific acetylation of p53 directs selective transcription complex assembly. J Biol Chem 282:4765-4771
    • (2007) J Biol Chem , vol.282 , pp. 4765-4771
    • Roy, S.1    Tenniswood, M.2
  • 31
    • 0035028599 scopus 로고    scopus 로고
    • Kinetics of p53 binding to promoter sites in vivo
    • Szak ST, Mays D, Pietenpol JA (2001) Kinetics of p53 binding to promoter sites in vivo. Mol Cell Biol 21:3375-3386
    • (2001) Mol Cell Biol , vol.21 , pp. 3375-3386
    • Szak, S.T.1    Mays, D.2    Pietenpol, J.A.3
  • 33
    • 77956192675 scopus 로고    scopus 로고
    • Aurora-A contributes to radioresistance by increasing NF-κB DNA binding
    • Oh ET, Byun MS, Lee HM et al (2010) Aurora-A contributes to radioresistance by increasing NF-κB DNA binding. Radiat Res 174:265-273
    • (2010) Radiat Res , vol.174 , pp. 265-273
    • Oh, E.T.1    Byun, M.S.2    Lee, H.M.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.