메뉴 건너뛰기




Volumn 7, Issue 12, 2012, Pages

Class I and Class II Histone Deacetylases Are Potential Therapeutic Targets for Treating Pancreatic Cancer

Author keywords

[No Author keywords available]

Indexed keywords

3 [4 [3 (3 FLUOROPHENYL) 3 OXO 1 PROPENYL] 1 METHYL 1H PYRROL 2 YL]ACRYLOHYDROXAMIC ACID; ALPHA TUBULIN; DOUBLE STRANDED DNA; HISTONE DEACETYLASE 1; HISTONE DEACETYLASE 2; HISTONE DEACETYLASE INHIBITOR; HISTONE H2AX; HISTONE H4; MOCETINOSTAT; PROTEIN P21; TUBASTATIN A; UNCLASSIFIED DRUG;

EID: 84871273907     PISSN: None     EISSN: 19326203     Source Type: Journal    
DOI: 10.1371/journal.pone.0052095     Document Type: Article
Times cited : (45)

References (50)
  • 1
    • 80051580618 scopus 로고    scopus 로고
    • Cancer statistics, 2011: the impact of eliminating socioeconomic and racial disparities on premature cancer deaths
    • Siegel R, Ward E, Brawley O, Jemal A, (2011) Cancer statistics, 2011: the impact of eliminating socioeconomic and racial disparities on premature cancer deaths. CA Cancer J Clin 61: 212-236.
    • (2011) CA Cancer J Clin , vol.61 , pp. 212-236
    • Siegel, R.1    Ward, E.2    Brawley, O.3    Jemal, A.4
  • 3
    • 47949117602 scopus 로고    scopus 로고
    • Pancreatic cancer: from molecular pathogenesis to targeted therapy
    • Strimpakos A, Saif MW, Syrigos KN, (2008) Pancreatic cancer: from molecular pathogenesis to targeted therapy. Cancer Metastasis Rev 27: 495-522.
    • (2008) Cancer Metastasis Rev , vol.27 , pp. 495-522
    • Strimpakos, A.1    Saif, M.W.2    Syrigos, K.N.3
  • 4
    • 8244254377 scopus 로고    scopus 로고
    • Improvements in survival and clinical benefit with gemcitabine as first-line therapy for patients with advanced pancreas cancer: a randomized trial
    • Burris HA 3rd, Moore MJ, Andersen J, Green MR, Rothenberg ML, et al (1997) Improvements in survival and clinical benefit with gemcitabine as first-line therapy for patients with advanced pancreas cancer: a randomized trial. J Clin Oncol 15: 2403-2413.
    • (1997) J Clin Oncol , vol.15 , pp. 2403-2413
    • Burris 3rd, H.A.1    Moore, M.J.2    Andersen, J.3    Green, M.R.4    Rothenberg, M.L.5
  • 5
    • 63949086163 scopus 로고    scopus 로고
    • Cetuximab plus gemcitabine/oxaliplatin (GEMOXCET) in first-line metastatic pancreatic cancer: a multicentre phase II study
    • Kullmann F, Hollerbach S, Dollinger MM, Harder J, Fuchs M, et al. (2009) Cetuximab plus gemcitabine/oxaliplatin (GEMOXCET) in first-line metastatic pancreatic cancer: a multicentre phase II study. Br J Cancer 100: 1032-1036.
    • (2009) Br J Cancer , vol.100 , pp. 1032-1036
    • Kullmann, F.1    Hollerbach, S.2    Dollinger, M.M.3    Harder, J.4    Fuchs, M.5
  • 6
    • 66149153449 scopus 로고    scopus 로고
    • Advancements in the management of pancreatic cancer
    • Li J, Saif MW, (2009) Advancements in the management of pancreatic cancer. JOP 10: 109-117.
    • (2009) JOP , vol.10 , pp. 109-117
    • Li, J.1    Saif, M.W.2
  • 7
    • 49349098483 scopus 로고    scopus 로고
    • Histone deacetylase inhibitors: mechanisms of cell death and promise in combination cancer therapy
    • Carew JS, Giles FJ, Nawrocki ST, (2008) Histone deacetylase inhibitors: mechanisms of cell death and promise in combination cancer therapy. Cancer Lett 269: 7-17.
    • (2008) Cancer Lett , vol.269 , pp. 7-17
    • Carew, J.S.1    Giles, F.J.2    Nawrocki, S.T.3
  • 8
    • 61849144810 scopus 로고    scopus 로고
    • HDAC family: What are the cancer relevant targets?
    • Witt O, Deubzer HE, Milde T, Oehme I, (2009) HDAC family: What are the cancer relevant targets? Cancer Lett 277: 8-21.
    • (2009) Cancer Lett , vol.277 , pp. 8-21
    • Witt, O.1    Deubzer, H.E.2    Milde, T.3    Oehme, I.4
  • 10
    • 1842578986 scopus 로고    scopus 로고
    • Molecular evolution of the histone deacetylase family: functional implications of phylogenetic analysis
    • Gregoretti IV, Lee YM, Goodson HV, (2004) Molecular evolution of the histone deacetylase family: functional implications of phylogenetic analysis. J Mol Biol 338: 17-31.
    • (2004) J Mol Biol , vol.338 , pp. 17-31
    • Gregoretti, I.V.1    Lee, Y.M.2    Goodson, H.V.3
  • 11
    • 0037406061 scopus 로고    scopus 로고
    • Class II histone deacetylases: versatile regulators
    • Verdin E, Dequiedt F, Kasler HG, (2003) Class II histone deacetylases: versatile regulators. Trends Genet 19: 286-293.
    • (2003) Trends Genet , vol.19 , pp. 286-293
    • Verdin, E.1    Dequiedt, F.2    Kasler, H.G.3
  • 12
    • 0036479127 scopus 로고    scopus 로고
    • Molecular cloning and characterization of a novel histone deacetylase HDAC10
    • Guardiola AR, Yao TP, (2002) Molecular cloning and characterization of a novel histone deacetylase HDAC10. J Biol Chem 277: 3350-3356.
    • (2002) J Biol Chem , vol.277 , pp. 3350-3356
    • Guardiola, A.R.1    Yao, T.P.2
  • 13
    • 3943054839 scopus 로고    scopus 로고
    • The Sir2 family of protein deacetylases
    • Blander G, Guarente L, (2004) The Sir2 family of protein deacetylases. Annu Rev Biochem 73: 417-435.
    • (2004) Annu Rev Biochem , vol.73 , pp. 417-435
    • Blander, G.1    Guarente, L.2
  • 14
    • 33748163463 scopus 로고    scopus 로고
    • Comparative genomics of the class 4 histone deacetylase family indicates a complex evolutionary history
    • Ledent V, Vervoort M, (2006) Comparative genomics of the class 4 histone deacetylase family indicates a complex evolutionary history. BMC Biol 4: 24.
    • (2006) BMC Biol , vol.4 , pp. 24
    • Ledent, V.1    Vervoort, M.2
  • 15
    • 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
  • 16
    • 79956198574 scopus 로고    scopus 로고
    • Histone deacetylase inhibitor MGCD0103 synergizes with gemcitabine in human pancreatic cells
    • Sung V, Richard N, Brady H, Maier A, Kelter G, et al. (2011) Histone deacetylase inhibitor MGCD0103 synergizes with gemcitabine in human pancreatic cells. Cancer Sci 102: 1201-1207.
    • (2011) Cancer Sci , vol.102 , pp. 1201-1207
    • Sung, V.1    Richard, N.2    Brady, H.3    Maier, A.4    Kelter, G.5
  • 18
    • 41149162821 scopus 로고    scopus 로고
    • Expression of hypoxia-inducible factor-1alpha, histone deacetylase 1, and metastasis-associated protein 1 in pancreatic carcinoma: correlation with poor prognosis with possible regulation
    • Miyake K, Yoshizumi T, Imura S, Sugimoto K, Batmunkh E, et al. (2008) Expression of hypoxia-inducible factor-1alpha, histone deacetylase 1, and metastasis-associated protein 1 in pancreatic carcinoma: correlation with poor prognosis with possible regulation. Pancreas 36: e1-9.
    • (2008) Pancreas , vol.36
    • Miyake, K.1    Yoshizumi, T.2    Imura, S.3    Sugimoto, K.4    Batmunkh, E.5
  • 19
    • 77955643796 scopus 로고    scopus 로고
    • The clinical development of histone deacetylase inhibitors as targeted anticancer drugs
    • Marks PA, (2010) The clinical development of histone deacetylase inhibitors as targeted anticancer drugs. Expert Opin Investig Drugs 19: 1049-1066.
    • (2010) Expert Opin Investig Drugs , vol.19 , pp. 1049-1066
    • Marks, P.A.1
  • 20
  • 21
    • 76249090605 scopus 로고    scopus 로고
    • Combined targeting of histone deacetylases and hedgehog signaling enhances cytoxicity in pancreatic cancer
    • Chun SG, Zhou W, Yee NS, (2009) Combined targeting of histone deacetylases and hedgehog signaling enhances cytoxicity in pancreatic cancer. Cancer Biol Ther 8: 1328-1339.
    • (2009) Cancer Biol Ther , vol.8 , pp. 1328-1339
    • Chun, S.G.1    Zhou, W.2    Yee, N.S.3
  • 22
    • 34250810709 scopus 로고    scopus 로고
    • Histone deacetylase inhibitor, suberoylanilide hydroxamic acid (Vorinostat, SAHA) profoundly inhibits the growth of human pancreatic cancer cells
    • Kumagai T, Wakimoto N, Yin D, Gery S, Kawamata N, et al. (2007) Histone deacetylase inhibitor, suberoylanilide hydroxamic acid (Vorinostat, SAHA) profoundly inhibits the growth of human pancreatic cancer cells. Int J Cancer 121: 656-665.
    • (2007) Int J Cancer , vol.121 , pp. 656-665
    • Kumagai, T.1    Wakimoto, N.2    Yin, D.3    Gery, S.4    Kawamata, N.5
  • 23
    • 33846327942 scopus 로고    scopus 로고
    • The histone deacetylase inhibitor suberoylanilide hydroxamic acid induces growth inhibition and enhances gemcitabine-induced cell death in pancreatic cancer
    • Arnold NB, Arkus N, Gunn J, Korc M, (2007) The histone deacetylase inhibitor suberoylanilide hydroxamic acid induces growth inhibition and enhances gemcitabine-induced cell death in pancreatic cancer. Clin Cancer Res 13: 18-26.
    • (2007) Clin Cancer Res , vol.13 , pp. 18-26
    • Arnold, N.B.1    Arkus, N.2    Gunn, J.3    Korc, M.4
  • 24
    • 77955584671 scopus 로고    scopus 로고
    • c-FLIP degradation mediates sensitization of pancreatic cancer cells to TRAIL-induced apoptosis by the histone deacetylase inhibitor LBH589
    • Kauh J, Fan S, Xia M, Yue P, Yang L, et al. (2010) c-FLIP degradation mediates sensitization of pancreatic cancer cells to TRAIL-induced apoptosis by the histone deacetylase inhibitor LBH589. PLoS One 5: e10376.
    • (2010) PLoS One , vol.5
    • Kauh, J.1    Fan, S.2    Xia, M.3    Yue, P.4    Yang, L.5
  • 25
    • 0141570564 scopus 로고    scopus 로고
    • Role of class I and class II histone deacetylases in carcinoma cells using siRNA
    • Glaser KB, Li J, Staver MJ, Wei RQ, Albert DH, et al. (2003) Role of class I and class II histone deacetylases in carcinoma cells using siRNA. Biochem Biophys Res Commun 310: 529-536.
    • (2003) Biochem Biophys Res Commun , vol.310 , pp. 529-536
    • Glaser, K.B.1    Li, J.2    Staver, M.J.3    Wei, R.Q.4    Albert, D.H.5
  • 26
    • 18444414332 scopus 로고    scopus 로고
    • Essential function of histone deacetylase 1 in proliferation control and CDK inhibitor repression
    • Lagger G, O'Carroll D, Rembold M, Khier H, Tischler J, et al. (2002) Essential function of histone deacetylase 1 in proliferation control and CDK inhibitor repression. EMBO J 21: 2672-2681.
    • (2002) EMBO J , vol.21 , pp. 2672-2681
    • Lagger, G.1    O'Carroll, D.2    Rembold, M.3    Khier, H.4    Tischler, J.5
  • 27
    • 22844432021 scopus 로고    scopus 로고
    • Inhibition of histone deacetylase 6 acetylates and disrupts the chaperone function of heat shock protein 90: a novel basis for antileukemia activity of histone deacetylase inhibitors
    • Bali P, Pranpat M, Bradner J, Balasis M, Fiskus W, et al. (2005) Inhibition of histone deacetylase 6 acetylates and disrupts the chaperone function of heat shock protein 90: a novel basis for antileukemia activity of histone deacetylase inhibitors. J Biol Chem 280: 26729-26734.
    • (2005) J Biol Chem , vol.280 , pp. 26729-26734
    • Bali, P.1    Pranpat, M.2    Bradner, J.3    Balasis, M.4    Fiskus, W.5
  • 29
    • 37849019672 scopus 로고    scopus 로고
    • Determination of the class and isoform selectivity of small-molecule histone deacetylase inhibitors
    • Khan N, Jeffers M, Kumar S, Hackett C, Boldog F, et al. (2008) Determination of the class and isoform selectivity of small-molecule histone deacetylase inhibitors. Biochem J 409: 581-589.
    • (2008) Biochem J , vol.409 , pp. 581-589
    • Khan, N.1    Jeffers, M.2    Kumar, S.3    Hackett, C.4    Boldog, F.5
  • 30
    • 57749101152 scopus 로고    scopus 로고
    • Specific activity of class II histone deacetylases in human breast cancer cells
    • Duong V, Bret C, Altucci L, Mai A, Duraffourd C, et al. (2008) Specific activity of class II histone deacetylases in human breast cancer cells. Mol Cancer Res 6: 1908-1919.
    • (2008) Mol Cancer Res , vol.6 , pp. 1908-1919
    • Duong, V.1    Bret, C.2    Altucci, L.3    Mai, A.4    Duraffourd, C.5
  • 31
    • 0242362600 scopus 로고    scopus 로고
    • Discovery of (aryloxopropenyl)pyrrolyl hydroxyamides as selective inhibitors of class IIa histone deacetylase homologue HD1-A
    • Mai A, Massa S, Pezzi R, Rotili D, Loidl P, et al. (2003) Discovery of (aryloxopropenyl)pyrrolyl hydroxyamides as selective inhibitors of class IIa histone deacetylase homologue HD1-A. J Med Chem 46: 4826-4829.
    • (2003) J Med Chem , vol.46 , pp. 4826-4829
    • Mai, A.1    Massa, S.2    Pezzi, R.3    Rotili, D.4    Loidl, P.5
  • 32
    • 20944435415 scopus 로고    scopus 로고
    • Class II (IIa)-selective histone deacetylase inhibitors. 1. Synthesis and biological evaluation of novel (aryloxopropenyl)pyrrolyl hydroxyamides
    • Mai A, Massa S, Pezzi R, Simeoni S, Rotili D, et al. (2005) Class II (IIa)-selective histone deacetylase inhibitors. 1. Synthesis and biological evaluation of novel (aryloxopropenyl)pyrrolyl hydroxyamides. J Med Chem 48: 3344-3353.
    • (2005) J Med Chem , vol.48 , pp. 3344-3353
    • Mai, A.1    Massa, S.2    Pezzi, R.3    Simeoni, S.4    Rotili, D.5
  • 33
    • 77955355838 scopus 로고    scopus 로고
    • Rational design and simple chemistry yield a superior, neuroprotective HDAC6 inhibitor, tubastatin A
    • Butler KV, Kalin J, Brochier C, Vistoli G, Langley B, et al. (2010) Rational design and simple chemistry yield a superior, neuroprotective HDAC6 inhibitor, tubastatin A. J Am Chem Soc. 132: 10842-10846.
    • (2010) J Am Chem Soc , vol.132 , pp. 10842-10846
    • Butler, K.V.1    Kalin, J.2    Brochier, C.3    Vistoli, G.4    Langley, B.5
  • 35
    • 78349242181 scopus 로고    scopus 로고
    • Mechanisms of synergistic antileukemic interactions between valproic acid and cytarabine in pediatric acute myeloid leukemia
    • Xie C, Edwards H, Xu X, Zhou H, Buck SA, et al. (2010) Mechanisms of synergistic antileukemic interactions between valproic acid and cytarabine in pediatric acute myeloid leukemia. Clin Cancer Res 16: 5499-5510.
    • (2010) Clin Cancer Res , vol.16 , pp. 5499-5510
    • Xie, C.1    Edwards, H.2    Xu, X.3    Zhou, H.4    Buck, S.A.5
  • 36
    • 79951864878 scopus 로고    scopus 로고
    • Inhibition of histone deacetylases 1 and 6 enhances cytarabine-induced apoptosis in pediatric acute myeloid leukemia cells
    • Xu X, Xie C, Edwards H, Zhou H, Buck SA, et al. (2011) Inhibition of histone deacetylases 1 and 6 enhances cytarabine-induced apoptosis in pediatric acute myeloid leukemia cells. PLoS One 6: e17138.
    • (2011) PLoS One , vol.6
    • Xu, X.1    Xie, C.2    Edwards, H.3    Zhou, H.4    Buck, S.A.5
  • 37
    • 33748794547 scopus 로고    scopus 로고
    • Theoretical basis, experimental design, and computerized simulation of synergism and antagonism in drug combination studies
    • Chou TC, (2006) Theoretical basis, experimental design, and computerized simulation of synergism and antagonism in drug combination studies. Pharmacol Rev 58: 621-681.
    • (2006) Pharmacol Rev , vol.58 , pp. 621-681
    • Chou, T.C.1
  • 38
    • 0034889197 scopus 로고    scopus 로고
    • Drug synergism: its detection and applications
    • Tallarida RJ, (2001) Drug synergism: its detection and applications. J Pharmacol Exp Ther 298: 865-872.
    • (2001) J Pharmacol Exp Ther , vol.298 , pp. 865-872
    • Tallarida, R.J.1
  • 39
    • 70350506780 scopus 로고    scopus 로고
    • RUNX1 regulates phosphoinositide 3-kinase/AKT pathway: role in chemotherapy sensitivity in acute megakaryocytic leukemia
    • Edwards H, Xie C, LaFiura KM, Dombkowski AA, Buck SA, et al. (2009) RUNX1 regulates phosphoinositide 3-kinase/AKT pathway: role in chemotherapy sensitivity in acute megakaryocytic leukemia. Blood 114: 2744-2752.
    • (2009) Blood , vol.114 , pp. 2744-2752
    • Edwards, H.1    Xie, C.2    LaFiura, K.M.3    Dombkowski, A.A.4    Buck, S.A.5
  • 40
    • 13744252262 scopus 로고    scopus 로고
    • GATA1, cytidine deaminase, and the high cure rate of Down syndrome children with acute megakaryocytic leukemia
    • Ge Y, Stout ML, Tatman DA, Jensen TL, Buck S, et al. (2005) GATA1, cytidine deaminase, and the high cure rate of Down syndrome children with acute megakaryocytic leukemia. J Natl Cancer Inst 97: 226-231.
    • (2005) J Natl Cancer Inst , vol.97 , pp. 226-231
    • Ge, Y.1    Stout, M.L.2    Tatman, D.A.3    Jensen, T.L.4    Buck, S.5
  • 41
    • 84867371231 scopus 로고    scopus 로고
    • Valproic acid synergistically enhances the cytotoxicity of clofarabine in pediatric acute myeloid leukemia cells
    • Xie C, Edwards H, Lograsso SB, Buck SA, Matherly LH, et al. (2012) Valproic acid synergistically enhances the cytotoxicity of clofarabine in pediatric acute myeloid leukemia cells. Pediatr Blood Cancer 59: 1245-1251.
    • (2012) Pediatr Blood Cancer , vol.59 , pp. 1245-1251
    • Xie, C.1    Edwards, H.2    Lograsso, S.B.3    Buck, S.A.4    Matherly, L.H.5
  • 42
    • 77953170728 scopus 로고    scopus 로고
    • Inhibition of histone deacetylase in cancer cells slows down replication forks, activates dormant origins, and induces DNA damage
    • Conti C, Leo E, Eichler GS, Sordet O, Martin MM, et al. (2010) Inhibition of histone deacetylase in cancer cells slows down replication forks, activates dormant origins, and induces DNA damage. Cancer Res 70: 4470-4480.
    • (2010) Cancer Res , vol.70 , pp. 4470-4480
    • Conti, C.1    Leo, E.2    Eichler, G.S.3    Sordet, O.4    Martin, M.M.5
  • 43
    • 33748427812 scopus 로고    scopus 로고
    • Histone deacetylase inhibitors (HDI) cause DNA damage in leukemia cells: a mechanism for leukemia-specific HDI-dependent apoptosis?
    • Gaymes TJ, Padua RA, Pla M, Orr S, Omidvar N, et al. (2006) Histone deacetylase inhibitors (HDI) cause DNA damage in leukemia cells: a mechanism for leukemia-specific HDI-dependent apoptosis? Mol Cancer Res 4: 563-573.
    • (2006) Mol Cancer Res , vol.4 , pp. 563-573
    • Gaymes, T.J.1    Padua, R.A.2    Pla, M.3    Orr, S.4    Omidvar, N.5
  • 44
    • 74549189337 scopus 로고    scopus 로고
    • New insights into checkpoint kinase 1 in the DNA damage response signaling network
    • Dai Y, Grant S, (2010) New insights into checkpoint kinase 1 in the DNA damage response signaling network. Clin Cancer Res 16: 376-383.
    • (2010) Clin Cancer Res , vol.16 , pp. 376-383
    • Dai, Y.1    Grant, S.2
  • 45
    • 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
  • 46
    • 77956686608 scopus 로고    scopus 로고
    • Histone gammaH2AX and poly(ADP-ribose) as clinical pharmacodynamic biomarkers
    • Redon CE, Nakamura AJ, Zhang YW, Ji JJ, Bonner WM, et al. (2010) Histone gammaH2AX and poly(ADP-ribose) as clinical pharmacodynamic biomarkers. Clin Cancer Res 16: 4532-4542.
    • (2010) Clin Cancer Res , vol.16 , pp. 4532-4542
    • Redon, C.E.1    Nakamura, A.J.2    Zhang, Y.W.3    Ji, J.J.4    Bonner, W.M.5
  • 47
    • 67449127082 scopus 로고    scopus 로고
    • Clinical studies of histone deacetylase inhibitors
    • Prince HM, Bishton MJ, Harrison SJ, (2009) Clinical studies of histone deacetylase inhibitors. Clin Cancer Res 15: 3958-3969.
    • (2009) Clin Cancer Res , vol.15 , pp. 3958-3969
    • Prince, H.M.1    Bishton, M.J.2    Harrison, S.J.3
  • 48
    • 17144378591 scopus 로고    scopus 로고
    • Inhibition of histone deacetylase 2 increases apoptosis and p21Cip1/WAF1 expression, independent of histone deacetylase 1
    • Huang BH, Laban M, Leung CH, Lee L, Lee CK, et al. (2005) Inhibition of histone deacetylase 2 increases apoptosis and p21Cip1/WAF1 expression, independent of histone deacetylase 1. Cell Death Differ 12: 395-404.
    • (2005) Cell Death Differ , vol.12 , pp. 395-404
    • Huang, B.H.1    Laban, M.2    Leung, C.H.3    Lee, L.4    Lee, C.K.5
  • 49
    • 33845514708 scopus 로고    scopus 로고
    • Will broad-spectrum histone deacetylase inhibitors be superseded by more specific compounds?
    • Karagiannis TC, El-Osta A, (2007) Will broad-spectrum histone deacetylase inhibitors be superseded by more specific compounds? Leukemia 21: 61-65.
    • (2007) Leukemia , vol.21 , pp. 61-65
    • Karagiannis, T.C.1    El-Osta, A.2
  • 50
    • 78650575875 scopus 로고    scopus 로고
    • Selective inhibition of histone deacetylase 6 (HDAC6) induces DNA damage and sensitizes transformed cells to anticancer agents
    • Namdar M, Perez G, Ngo L, Marks PA, (2010) Selective inhibition of histone deacetylase 6 (HDAC6) induces DNA damage and sensitizes transformed cells to anticancer agents. Proc Natl Acad Sci U S A 107: 20003-20008.
    • (2010) Proc Natl Acad Sci U S A , vol.107 , pp. 20003-20008
    • Namdar, M.1    Perez, G.2    Ngo, L.3    Marks, P.A.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.