Combined HAT/EZH2 modulation leads to cancer-selective cell death
Epigenetic alterations have been associated with both pathogenesis and progression of cancer. By screening of library compounds, we identified a novel hybrid epi-drug MC2884, a HAT/EZH2 inhibitor, able to induce cancer-selective cell death in both solid and hematological cancers , and xenograft mode...
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Published in | Oncotarget Vol. 9; no. 39; pp. 25630 - 25646 |
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Main Authors | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
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United States
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22.05.2018
Impact Journals LLC |
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Online Access | Get full text |
ISSN | 1949-2553 1949-2553 |
DOI | 10.18632/oncotarget.25428 |
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Abstract | Epigenetic alterations have been associated with both pathogenesis and progression of cancer. By screening of library compounds, we identified a novel hybrid epi-drug MC2884, a HAT/EZH2 inhibitor, able to induce
cancer-selective cell death in both solid and hematological cancers
,
and
xenograft models. Anticancer action was due to an epigenome modulation by H3K27me3, H3K27ac, H3K9/14ac decrease, and to caspase-dependent apoptosis induction. MC2884 triggered mitochondrial pathway apoptosis by up-regulation of cleaved-BID, and strong down-regulation of BCL2. Even aggressive models of cancer, such as p53
or TET2
cells, responded to MC2884, suggesting MC2884 therapeutic potential also for the therapy of TP53 or TET2-deficient human cancers. MC2884 induced massive apoptosis in
human primary leukemia blasts with poor prognosis
, by targeting BCL2 expression. MC2884-treatment reduced acetylation of the BCL2 promoter at higher level than combined p300 and EZH2 inhibition. This suggests a key role for BCL-2 reduction in potentiating responsiveness, also in combination therapy with BCL2 inhibitors. Finally, we identified both the mechanism of MC2884 action as well as a potential therapeutic scheme of its use. Altogether, this provides proof of concept for the use of epi-drugs coupled with epigenome analyses to 'personalize' precision medicine. |
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AbstractList | Epigenetic alterations have been associated with both pathogenesis and progression of cancer. By screening of library compounds, we identified a novel hybrid epi-drug MC2884, a HAT/EZH2 inhibitor, able to induce
bona fide
cancer-selective cell death in both solid and hematological cancers
in vitro
,
ex vivo
and
in vivo
xenograft models. Anticancer action was due to an epigenome modulation by H3K27me3, H3K27ac, H3K9/14ac decrease, and to caspase-dependent apoptosis induction. MC2884 triggered mitochondrial pathway apoptosis by up-regulation of cleaved-BID, and strong down-regulation of BCL2. Even aggressive models of cancer, such as p53
–/–
or TET2
–/–
cells, responded to MC2884, suggesting MC2884 therapeutic potential also for the therapy of TP53 or TET2-deficient human cancers. MC2884 induced massive apoptosis in
ex vivo
human primary leukemia blasts with poor prognosis
in vivo
, by targeting BCL2 expression. MC2884-treatment reduced acetylation of the BCL2 promoter at higher level than combined p300 and EZH2 inhibition. This suggests a key role for BCL-2 reduction in potentiating responsiveness, also in combination therapy with BCL2 inhibitors.
Finally, we identified both the mechanism of MC2884 action as well as a potential therapeutic scheme of its use. Altogether, this provides proof of concept for the use of epi-drugs coupled with epigenome analyses to ‘personalize’ precision medicine. Epigenetic alterations have been associated with both pathogenesis and progression of cancer. By screening of library compounds, we identified a novel hybrid epi-drug MC2884, a HAT/EZH2 inhibitor, able to induce bona fide cancer-selective cell death in both solid and hematological cancers in vitro, ex vivo and in vivo xenograft models. Anticancer action was due to an epigenome modulation by H3K27me3, H3K27ac, H3K9/14ac decrease, and to caspase-dependent apoptosis induction. MC2884 triggered mitochondrial pathway apoptosis by up-regulation of cleaved-BID, and strong down-regulation of BCL2. Even aggressive models of cancer, such as p53-/- or TET2-/- cells, responded to MC2884, suggesting MC2884 therapeutic potential also for the therapy of TP53 or TET2-deficient human cancers. MC2884 induced massive apoptosis in ex vivo human primary leukemia blasts with poor prognosis in vivo, by targeting BCL2 expression. MC2884-treatment reduced acetylation of the BCL2 promoter at higher level than combined p300 and EZH2 inhibition. This suggests a key role for BCL-2 reduction in potentiating responsiveness, also in combination therapy with BCL2 inhibitors. Finally, we identified both the mechanism of MC2884 action as well as a potential therapeutic scheme of its use. Altogether, this provides proof of concept for the use of epi-drugs coupled with epigenome analyses to 'personalize' precision medicine. Epigenetic alterations have been associated with both pathogenesis and progression of cancer. By screening of library compounds, we identified a novel hybrid epi-drug MC2884, a HAT/EZH2 inhibitor, able to induce bona fide cancer-selective cell death in both solid and hematological cancers in vitro, ex vivo and in vivo xenograft models. Anticancer action was due to an epigenome modulation by H3K27me3, H3K27ac, H3K9/14ac decrease, and to caspase-dependent apoptosis induction. MC2884 triggered mitochondrial pathway apoptosis by up-regulation of cleaved-BID, and strong down-regulation of BCL2. Even aggressive models of cancer, such as p53-/- or TET2-/- cells, responded to MC2884, suggesting MC2884 therapeutic potential also for the therapy of TP53 or TET2-deficient human cancers. MC2884 induced massive apoptosis in ex vivo human primary leukemia blasts with poor prognosis in vivo, by targeting BCL2 expression. MC2884-treatment reduced acetylation of the BCL2 promoter at higher level than combined p300 and EZH2 inhibition. This suggests a key role for BCL-2 reduction in potentiating responsiveness, also in combination therapy with BCL2 inhibitors. Finally, we identified both the mechanism of MC2884 action as well as a potential therapeutic scheme of its use. Altogether, this provides proof of concept for the use of epi-drugs coupled with epigenome analyses to 'personalize' precision medicine.Epigenetic alterations have been associated with both pathogenesis and progression of cancer. By screening of library compounds, we identified a novel hybrid epi-drug MC2884, a HAT/EZH2 inhibitor, able to induce bona fide cancer-selective cell death in both solid and hematological cancers in vitro, ex vivo and in vivo xenograft models. Anticancer action was due to an epigenome modulation by H3K27me3, H3K27ac, H3K9/14ac decrease, and to caspase-dependent apoptosis induction. MC2884 triggered mitochondrial pathway apoptosis by up-regulation of cleaved-BID, and strong down-regulation of BCL2. Even aggressive models of cancer, such as p53-/- or TET2-/- cells, responded to MC2884, suggesting MC2884 therapeutic potential also for the therapy of TP53 or TET2-deficient human cancers. MC2884 induced massive apoptosis in ex vivo human primary leukemia blasts with poor prognosis in vivo, by targeting BCL2 expression. MC2884-treatment reduced acetylation of the BCL2 promoter at higher level than combined p300 and EZH2 inhibition. This suggests a key role for BCL-2 reduction in potentiating responsiveness, also in combination therapy with BCL2 inhibitors. Finally, we identified both the mechanism of MC2884 action as well as a potential therapeutic scheme of its use. Altogether, this provides proof of concept for the use of epi-drugs coupled with epigenome analyses to 'personalize' precision medicine. Epigenetic alterations have been associated with both pathogenesis and progression of cancer. By screening of library compounds, we identified a novel hybrid epi-drug MC2884, a HAT/EZH2 inhibitor, able to induce cancer-selective cell death in both solid and hematological cancers , and xenograft models. Anticancer action was due to an epigenome modulation by H3K27me3, H3K27ac, H3K9/14ac decrease, and to caspase-dependent apoptosis induction. MC2884 triggered mitochondrial pathway apoptosis by up-regulation of cleaved-BID, and strong down-regulation of BCL2. Even aggressive models of cancer, such as p53 or TET2 cells, responded to MC2884, suggesting MC2884 therapeutic potential also for the therapy of TP53 or TET2-deficient human cancers. MC2884 induced massive apoptosis in human primary leukemia blasts with poor prognosis , by targeting BCL2 expression. MC2884-treatment reduced acetylation of the BCL2 promoter at higher level than combined p300 and EZH2 inhibition. This suggests a key role for BCL-2 reduction in potentiating responsiveness, also in combination therapy with BCL2 inhibitors. Finally, we identified both the mechanism of MC2884 action as well as a potential therapeutic scheme of its use. Altogether, this provides proof of concept for the use of epi-drugs coupled with epigenome analyses to 'personalize' precision medicine. |
Author | Carafa, Vincenzo Altucci, Lucia Cicatiello, Valeria Nebbioso, Angela Petrizzi, Valeria Belsito Scisciola, Lucia De Falco, Sandro Yaspo, Marie Laure Feoli, Alessandra Mandoli, Amit Valente, Sergio Mai, Antonello Yi, Guoqiang Singh, Abhishek A. Janssen-Megens, Eva M. Baldi, Alfonso Wierenga, Albertus T.J. Tomassi, Stefano Ruvo, Menotti Conte, Mariarosaria Apicella, Ivana Gut, Ivo Stunnenberg, Hendrik G. Petraglia, Francesca Flicek, Paul Della Valle, Veronique Bernard, Olivier Ingenito, Concetta Martens, Joost H.A. Heath, Simon Novellino, Ettore Vellenga, Edo Logie, Colin Sbardella, Gianluca Kim, Bowon |
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CitedBy_id | crossref_primary_10_1016_j_semcancer_2020_12_004 crossref_primary_10_3390_molecules25143122 crossref_primary_10_1016_j_celrep_2018_12_098 |
Cites_doi | 10.1038/sj.onc.1210608 10.1016/j.febslet.2010.04.002 10.1182/blood-2008-01-136366 10.1016/j.celrep.2016.08.082 10.1182/blood.V88.7.2671.bloodjournal8872671 10.1021/acs.jmedchem.5b01117 10.1038/leu.2011.271 10.1056/NEJMoa1301689 10.1158/1078-0432.CCR-15-0530 10.1016/j.celrep.2015.07.024 10.1182/blood-2011-10-386086 10.1016/j.molonc.2012.09.004 10.1038/nrc3130 10.1002/jcb.24000 10.1056/NEJMoa1516192 10.1021/jm4012802 10.1158/0008-5472.CAN-13-2568 10.1056/NEJMoa0810069 10.1016/j.bbadis.2010.10.005 10.1038/nrd4360 10.1186/1471-2407-10-524 10.1158/1078-0432.CCR-12-2037 10.1124/mi.9.6.7 10.1016/j.ccr.2011.06.003 10.1016/j.ccr.2012.06.008 10.1038/nature09504 10.1177/1947601911418499 10.1038/ng.2764 10.1038/nm1161 10.1038/embor.2009.88 10.1089/ars.2013.5776 10.1186/gb-2005-6-8-227 10.1038/nrg3173 10.3892/ijo.2014.2766 10.1038/leu.2017.64 10.1158/1535-7163.MCT-15-0429 10.1038/416552a 10.1158/0008-5472.CAN-13-3056 10.1517/14728222.2015.1051728 10.1016/j.ccell.2016.09.014 10.1016/j.biochi.2012.06.003 10.1186/s13148-016-0223-4 10.1371/journal.pone.0083737 10.18632/oncotarget.2816 10.1158/1078-0432.CCR-15-2388 10.1089/scd.2012.0498 10.1016/j.biocel.2015.10.016 10.1002/pmic.201500223 10.1080/15592294.2016.1249089 10.1371/journal.pone.0084147 10.1016/j.cell.2013.03.008 10.1038/cddis.2012.109 10.3389/fonc.2015.00108 10.1017/S1462399411001992 |
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Keywords | acetylation apoptosis cancer methylation epigenetics |
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References | Altucci (30) 2015; 69 Mandoli (47) 2014; 74 Schapira (24) 2013; 8 Johnstone (6) 2014; 13 McKeown (9) 2010; 468 Vogelstein (51) 2002; 416 Gronemeyer (44) 2005; 11 Vainchenker (42) 2008; 112 Richardson (23) 2015; 21 Shi (5) 2012; 13 Lania (21) 2016 Altucci (28) 2016 Altucci (20) 2012; 6 1 Jung (29) 2016; 8 Miller (37) 1996; 88 Jones (22) 2011; 11 Martincorena (17) 2016; 374 Tumber (35) 2014; 57 Collette (49) 2012; 26 Galinsky (50) 2015; 14 Brodeur (10) 2014; 74 Cencioni (46) 2016 Cheng (27) 2005; 6 Signorile (32) 2012; 113 Altucci (13) 2012; 18 Matarese (16) 2016; 17 Clarke (7) 2011; 2 Sarkar (11) 2015; 46 Cote (4) 2007; 26 Laird (15) 2013; 153 Jones (14) 2012; 22 Altucci (48) 2015; 6 Hohenfellner (25) 2010; 10 Tilly (41) 2011; 20 Altucci (33) 2013; 22 Mai (31) 2012; 94 Wang (3) 2015; 5 Knapp (8) 2011; 13 Carissimo (39) 2017 Altucci (45) 2009; 10 Stunnenberg (53) 2012; 120 Altucci (19) 2015; 19 Verdaguer-Dot (18) 2016; 30 Chambery (34) 2015 Altucci (38) 2015; 23 Stunnenberg (52) 2011; 1812 Borst (43) 2012; 3 Kutateladze (12) 2009; 9 Stunnenberg (54) 2010; 584 Dreyfus (40) 2009; 360 Stuart (2) 2013; 45 Gately Luz (26) 2013; 8 Stamatoyannopoulos (36) 2015; 12 21933453 - Expert Rev Mol Med. 2011 Sep 13;13:e29 27846393 - Cancer Cell. 2016 Nov 14;30(5):806-821 25131830 - Nat Rev Drug Discov. 2014 Sep;13(9):673-91 27276561 - N Engl J Med. 2016 Jun 9;374(23 ):2209-2221 22109698 - J Cell Biochem. 2012 Apr;113(4):1292-301 26206331 - Mol Cancer Ther. 2015 Oct;14 (10 ):2249-59 22923494 - Blood. 2012 Oct 11;120(15):3058-68 15619633 - Nat Med. 2005 Jan;11(1):77-84 24071849 - Nat Genet. 2013 Oct;45(10):1113-20 21941284 - Nat Rev Cancer. 2011 Sep 23;11(10):726-34 22789535 - Cancer Cell. 2012 Jul 10;22(1):9-20 19474426 - N Engl J Med. 2009 May 28;360(22):2289-301 24419087 - Cancer Res. 2014 Feb 1;74(3):652-8 20048137 - Mol Interv. 2009 Dec;9(6):314-23 26689352 - J Med Chem. 2016 Feb 25;59(4):1471-91 22904103 - Clin Cancer Res. 2012 Oct 15;18(20):5526-34 24382114 - Antioxid Redox Signal. 2015 Jul 1;23(1):99-126 23597129 - Stem Cells Dev. 2013 Sep 1;22(17 ):2368-83 21723201 - Cancer Cell. 2011 Jul 12;20(1):25-38 16086857 - Genome Biol. 2005;6(8):227 18755984 - Blood. 2008 Nov 15;112(10):4220-6 21979880 - Leukemia. 2012 Apr;26(4):662-74 17694081 - Oncogene. 2007 Aug 13;26(37):5395-407 27851970 - Cell Rep. 2016 Nov 15;17 (8):2087-2100 26494003 - Int J Biochem Cell Biol. 2015 Dec;69:121-31 23540689 - Cell. 2013 Mar 28;153(1):38-55 11932749 - Nature. 2002 Apr 4;416(6880):552-6 23103179 - Mol Oncol. 2012 Dec;6(6):657-82 27767379 - Epigenetics. 2017 Mar 4;12 (3):198-205 23634996 - N Engl J Med. 2013 May 30;368(22):2059-74 27222667 - Clin Epigenetics. 2016 May 24;8:57 24566867 - Cancer Res. 2014 Apr 15;74(8):2328-39 22875003 - Cell Death Dis. 2012 Aug 09;3:e366 20388510 - FEBS Lett. 2010 Jun 18;584(12):2662-9 25405367 - Int J Oncol. 2015 Feb;46(2):465-73 20871596 - Nature. 2010 Dec 23;468(7327):1067-73 26257180 - Cell Rep. 2015 Aug 18;12(7):1184-95 22473383 - Nat Rev Genet. 2012 Apr 03;13(5):343-57 8839862 - Blood. 1996 Oct 1;88(7):2671-82 26028314 - Expert Opin Ther Targets. 2015;19(9):1187-202 20970499 - Biochim Biophys Acta. 2011 Aug;1812(8):818-23 27358484 - Clin Cancer Res. 2017 May 15;23 (10 ):2542-2555 22709867 - Biochimie. 2012 Nov;94(11):2308-13 19498465 - EMBO Rep. 2009 Jul;10(7):776-82 25473896 - Oncotarget. 2015 Jan 20;6(2):886-901 24367637 - PLoS One. 2013 Dec 19;8(12 ):e84147 21941618 - Genes Cancer. 2011 Jun;2(6):618-30 24325601 - J Med Chem. 2014 Jan 9;57(1):42-55 28216661 - Leukemia. 2017 Nov;31(11):2315-2325 26604074 - Proteomics. 2016 Feb;16(4):674-88 20920340 - BMC Cancer. 2010 Oct 04;10:524 24367611 - PLoS One. 2013 Dec 19;8(12 ):e83737 26362997 - Clin Cancer Res. 2015 Nov 1;21(21):4767-73 26075180 - Front Oncol. 2015 May 26;5:108 |
References_xml | – volume: 26 start-page: 5395 year: 2007 ident: 4 article-title: The MYST family of histone acetyltransferases and their intimate links to cancer publication-title: Oncogene doi: 10.1038/sj.onc.1210608 – volume: 584 start-page: 2662 year: 2010 ident: 54 article-title: The molecular signature of oncofusion proteins in acute myeloid leukemia publication-title: FEBS Lett doi: 10.1016/j.febslet.2010.04.002 – volume: 112 start-page: 4220 year: 2008 ident: 42 article-title: Activating mutations in human acute megakaryoblastic leukemia publication-title: Blood doi: 10.1182/blood-2008-01-136366 – volume: 17 start-page: 2087 year: 2016 ident: 16 article-title: The Hematopoietic Transcription Factors RUNX1 and ERG Prevent AML1-ETO Oncogene Overexpression and Onset of the Apoptosis Program in t(8;21) AMLs publication-title: Cell Rep doi: 10.1016/j.celrep.2016.08.082 – volume: 88 start-page: 2671 year: 1996 ident: 37 article-title: Alterations in expression, binding to ligand and DNA, and transcriptional activity of rearranged and wild-type retinoid receptors in retinoid-resistant acute promyelocytic leukemia cell lines publication-title: Blood doi: 10.1182/blood.V88.7.2671.bloodjournal8872671 – year: 2016 ident: 46 article-title: 1,4-Dihydropyridines Active on the SIRT1/AMPK Pathway Ameliorate Skin Repair and Mitochondrial Function and Exhibit Inhibition of Proliferation in Cancer Cells publication-title: J Med Chem doi: 10.1021/acs.jmedchem.5b01117 – volume: 26 start-page: 662 year: 2012 ident: 49 article-title: Anti-leukemia activity of chaetocin via death receptor-dependent apoptosis and dual modulation of the histone methyl-transferase SUV39H1 publication-title: Leukemia doi: 10.1038/leu.2011.271 – ident: 1 doi: 10.1056/NEJMoa1301689 – volume: 21 start-page: 4767 year: 2015 ident: 23 article-title: Panobinostat for the Treatment of Multiple Myeloma publication-title: Clin Cancer Res doi: 10.1158/1078-0432.CCR-15-0530 – volume: 12 start-page: 1184 year: 2015 ident: 36 article-title: Role of DNA Methylation in Modulating Transcription Factor Occupancy publication-title: Cell Rep doi: 10.1016/j.celrep.2015.07.024 – volume: 120 start-page: 3058 year: 2012 ident: 53 article-title: Chromatin accessibility, p300, and histone acetylation define PML-RARalpha and AML1-ETO binding sites in acute myeloid leukemia publication-title: Blood doi: 10.1182/blood-2011-10-386086 – volume: 6 start-page: 657 year: 2012 ident: 20 article-title: Trials with ‘epigenetic’ drugs: an update publication-title: Mol Oncol doi: 10.1016/j.molonc.2012.09.004 – volume: 11 start-page: 726 year: 2011 ident: 22 article-title: A decade of exploring the cancer epigenome - biological and translational implications publication-title: Nat Rev Cancer doi: 10.1038/nrc3130 – volume: 113 start-page: 1292 year: 2012 ident: 32 article-title: model of stromal and epithelial immortalized endometriotic cells publication-title: J Cell Biochem doi: 10.1002/jcb.24000 – volume: 374 start-page: 2209 year: 2016 ident: 17 article-title: Genomic Classification and Prognosis in Acute Myeloid Leukemia publication-title: N Engl J Med doi: 10.1056/NEJMoa1516192 – volume: 57 start-page: 42 year: 2014 ident: 35 article-title: Pan-histone demethylase inhibitors simultaneously targeting Jumonji C and lysine-specific demethylases display high anticancer activities publication-title: J Med Chem doi: 10.1021/jm4012802 – volume: 74 start-page: 2328 year: 2014 ident: 47 article-title: Context-selective death of acute myeloid leukemia cells triggered by the novel hybrid retinoid-HDAC inhibitor MC2392 publication-title: Cancer Res doi: 10.1158/0008-5472.CAN-13-2568 – volume: 360 start-page: 2289 year: 2009 ident: 40 article-title: Mutation in TET2 in myeloid cancers publication-title: N Engl J Med doi: 10.1056/NEJMoa0810069 – volume: 1812 start-page: 818 year: 2011 ident: 52 article-title: Genome-wide interplay of nuclear receptors with the epigenome publication-title: Biochim Biophys Acta doi: 10.1016/j.bbadis.2010.10.005 – volume: 13 start-page: 673 year: 2014 ident: 6 article-title: Histone deacetylases and their inhibitors in cancer, neurological diseases and immune disorders publication-title: Nat Rev Drug Discov doi: 10.1038/nrd4360 – volume: 10 start-page: 524 year: 2010 ident: 25 article-title: Enhancer of zeste homolog 2 (EZH2) expression is an independent prognostic factor in renal cell carcinoma publication-title: BMC Cancer doi: 10.1186/1471-2407-10-524 – volume: 18 start-page: 5526 year: 2012 ident: 13 article-title: Molecular pathways: the complexity of the epigenome in cancer and recent clinical advances publication-title: Clin Cancer Res doi: 10.1158/1078-0432.CCR-12-2037 – volume: 9 start-page: 314 year: 2009 ident: 12 article-title: PHD fingers: epigenetic effectors and potential drug targets publication-title: Mol Interv doi: 10.1124/mi.9.6.7 – volume: 20 start-page: 25 year: 2011 ident: 41 article-title: TET2 inactivation results in pleiotropic hematopoietic abnormalities in mouse and is a recurrent event during human lymphomagenesis publication-title: Cancer Cell doi: 10.1016/j.ccr.2011.06.003 – volume: 22 start-page: 9 year: 2012 ident: 14 article-title: Cancer genetics and epigenetics: two sides of the same coin? publication-title: Cancer Cell doi: 10.1016/j.ccr.2012.06.008 – volume: 468 start-page: 1067 year: 2010 ident: 9 article-title: Selective inhibition of BET bromodomains publication-title: Nature doi: 10.1038/nature09504 – volume: 2 start-page: 618 year: 2011 ident: 7 article-title: The Roles of the Methyl-CpG Binding Proteins in Cancer publication-title: Genes Cancer doi: 10.1177/1947601911418499 – volume: 45 start-page: 1113 year: 2013 ident: 2 article-title: The Cancer Genome Atlas Pan-Cancer analysis project publication-title: Nat Genet doi: 10.1038/ng.2764 – volume: 11 start-page: 77 year: 2005 ident: 44 article-title: Tumor-selective action of HDAC inhibitors involves TRAIL induction in acute myeloid leukemia cells publication-title: Nat Med doi: 10.1038/nm1161 – volume: 10 start-page: 776 year: 2009 ident: 45 article-title: Selective class II HDAC inhibitors impair myogenesis by modulating the stability and activity of HDAC-MEF2 complexes publication-title: EMBO Rep doi: 10.1038/embor.2009.88 – volume: 23 start-page: 99 year: 2015 ident: 38 article-title: Targeting Histone Deacetylases in Diseases: Where Are We? publication-title: Antioxid Redox Signal doi: 10.1089/ars.2013.5776 – volume: 6 start-page: 227 year: 2005 ident: 27 article-title: The SET-domain protein superfamily: protein lysine methyltransferases publication-title: Genome Biol doi: 10.1186/gb-2005-6-8-227 – volume: 13 start-page: 343 year: 2012 ident: 5 article-title: Histone methylation: a dynamic mark in health, disease and inheritance publication-title: Nat Rev Genet doi: 10.1038/nrg3173 – volume: 46 start-page: 465 year: 2015 ident: 11 article-title: Role of the staphylococcal nuclease and tudor domain containing 1 in oncogenesis (review) publication-title: Int J Oncol doi: 10.3892/ijo.2014.2766 – year: 2017 ident: 39 article-title: miR-194-5p/BCLAF1 deregulation in AML tumorigenesis publication-title: Leukemia doi: 10.1038/leu.2017.64 – volume: 14 start-page: 2249 year: 2015 ident: 50 article-title: Inhibition of Wild-Type p53-Expressing AML by the Novel Small Molecule HDM2 Inhibitor CGM097 publication-title: Mol Cancer Ther doi: 10.1158/1535-7163.MCT-15-0429 – volume: 416 start-page: 552 year: 2002 ident: 51 article-title: DNMT1 and DNMT3b cooperate to silence genes in human cancer cells publication-title: Nature doi: 10.1038/416552a – volume: 74 start-page: 652 year: 2014 ident: 10 article-title: Role of CHD5 in human cancers: 10 years later publication-title: Cancer Res doi: 10.1158/0008-5472.CAN-13-3056 – volume: 19 start-page: 1187 year: 2015 ident: 19 article-title: Genetic mutations in epigenetic modifiers as therapeutic targets in acute myeloid leukemia publication-title: Expert Opin Ther Targets doi: 10.1517/14728222.2015.1051728 – volume: 30 start-page: 806 year: 2016 ident: 18 article-title: Decoding the DNA Methylome of Mantle Cell Lymphoma in the Light of the Entire B Cell Lineage publication-title: Cancer Cell doi: 10.1016/j.ccell.2016.09.014 – volume: 94 start-page: 2308 year: 2012 ident: 31 article-title: Identification of PR-SET7 and EZH2 selective inhibitors inducing cell death in human leukemia U937 cells publication-title: Biochimie doi: 10.1016/j.biochi.2012.06.003 – volume: 8 start-page: 57 year: 2016 ident: 29 article-title: Targeting histone methyltransferases and demethylases in clinical trials for cancer therapy publication-title: Clin Epigenetics doi: 10.1186/s13148-016-0223-4 – volume: 8 start-page: e83737 year: 2013 ident: 24 article-title: Structure of the catalytic domain of EZH2 reveals conformational plasticity in cofactor and substrate binding sites and explains oncogenic mutations publication-title: PLoS One doi: 10.1371/journal.pone.0083737 – volume: 6 start-page: 886 year: 2015 ident: 48 article-title: HDAC2 deregulation in tumorigenesis is causally connected to repression of immune modulation and defense escape publication-title: Oncotarget doi: 10.18632/oncotarget.2816 – year: 2016 ident: 21 article-title: c-Myc modulation & acetylation is a key HDAC inhibitor target in cancer publication-title: Clin Cancer Res doi: 10.1158/1078-0432.CCR-15-2388 – volume: 22 start-page: 2368 year: 2013 ident: 33 article-title: MePR: a novel human mesenchymal progenitor model with characteristics of pluripotency publication-title: Stem Cells Dev doi: 10.1089/scd.2012.0498 – volume: 69 start-page: 121 year: 2015 ident: 30 article-title: Epigenetic-based therapy: From single- to multi-target approaches publication-title: Int J Biochem Cell Biol doi: 10.1016/j.biocel.2015.10.016 – year: 2015 ident: 34 article-title: Secretome profiling of cytokines and growth factors reveals that neuro-glial differentiation is associated with the down-regulation of Chemokine Ligand 2 (MCP-1/CCL2) in amniotic fluid derived-mesenchymal progenitor cells publication-title: Proteomics doi: 10.1002/pmic.201500223 – start-page: 0 year: 2016 ident: 28 article-title: Identification and characterization of PKF118-310 as a KDM4A inhibitor publication-title: Epigenetics doi: 10.1080/15592294.2016.1249089 – volume: 8 start-page: e84147 year: 2013 ident: 26 article-title: Structural context of disease-associated mutations and putative mechanism of autoinhibition revealed by X-ray crystallographic analysis of the EZH2-SET domain publication-title: PLoS One doi: 10.1371/journal.pone.0084147 – volume: 153 start-page: 38 year: 2013 ident: 15 article-title: Interplay between the cancer genome and epigenome publication-title: Cell doi: 10.1016/j.cell.2013.03.008 – volume: 3 start-page: e366 year: 2012 ident: 43 article-title: Bcl-2 is a better ABT-737 target than Bcl-xL or Bcl-w and only Noxa overcomes resistance mediated by Mcl-1, Bfl-1, or Bcl-B publication-title: Cell Death Dis doi: 10.1038/cddis.2012.109 – volume: 5 start-page: 108 year: 2015 ident: 3 article-title: The Role of Histone Acetyltransferases in Normal and Malignant Hematopoiesis publication-title: Front Oncol doi: 10.3389/fonc.2015.00108 – volume: 13 start-page: e29 year: 2011 ident: 8 article-title: Bromodomains as therapeutic targets publication-title: Expert Rev Mol Med doi: 10.1017/S1462399411001992 – reference: 25405367 - Int J Oncol. 2015 Feb;46(2):465-73 – reference: 22109698 - J Cell Biochem. 2012 Apr;113(4):1292-301 – reference: 24367611 - PLoS One. 2013 Dec 19;8(12 ):e83737 – reference: 23103179 - Mol Oncol. 2012 Dec;6(6):657-82 – reference: 20388510 - FEBS Lett. 2010 Jun 18;584(12):2662-9 – reference: 27276561 - N Engl J Med. 2016 Jun 9;374(23 ):2209-2221 – reference: 19498465 - EMBO Rep. 2009 Jul;10(7):776-82 – reference: 27767379 - Epigenetics. 2017 Mar 4;12 (3):198-205 – reference: 24419087 - Cancer Res. 2014 Feb 1;74(3):652-8 – reference: 17694081 - Oncogene. 2007 Aug 13;26(37):5395-407 – reference: 22923494 - Blood. 2012 Oct 11;120(15):3058-68 – reference: 20871596 - Nature. 2010 Dec 23;468(7327):1067-73 – reference: 26362997 - Clin Cancer Res. 2015 Nov 1;21(21):4767-73 – reference: 27222667 - Clin Epigenetics. 2016 May 24;8:57 – reference: 19474426 - N Engl J Med. 2009 May 28;360(22):2289-301 – reference: 27846393 - Cancer Cell. 2016 Nov 14;30(5):806-821 – reference: 22473383 - Nat Rev Genet. 2012 Apr 03;13(5):343-57 – reference: 26257180 - Cell Rep. 2015 Aug 18;12(7):1184-95 – reference: 15619633 - Nat Med. 2005 Jan;11(1):77-84 – reference: 27851970 - Cell Rep. 2016 Nov 15;17 (8):2087-2100 – reference: 22709867 - Biochimie. 2012 Nov;94(11):2308-13 – reference: 21941284 - Nat Rev Cancer. 2011 Sep 23;11(10):726-34 – reference: 24367637 - PLoS One. 2013 Dec 19;8(12 ):e84147 – reference: 26075180 - Front Oncol. 2015 May 26;5:108 – reference: 26206331 - Mol Cancer Ther. 2015 Oct;14 (10 ):2249-59 – reference: 21933453 - Expert Rev Mol Med. 2011 Sep 13;13:e29 – reference: 23540689 - Cell. 2013 Mar 28;153(1):38-55 – reference: 27358484 - Clin Cancer Res. 2017 May 15;23 (10 ):2542-2555 – reference: 20920340 - BMC Cancer. 2010 Oct 04;10:524 – reference: 21723201 - Cancer Cell. 2011 Jul 12;20(1):25-38 – reference: 26028314 - Expert Opin Ther Targets. 2015;19(9):1187-202 – reference: 24382114 - Antioxid Redox Signal. 2015 Jul 1;23(1):99-126 – reference: 26689352 - J Med Chem. 2016 Feb 25;59(4):1471-91 – reference: 21941618 - Genes Cancer. 2011 Jun;2(6):618-30 – reference: 24566867 - Cancer Res. 2014 Apr 15;74(8):2328-39 – reference: 20048137 - Mol Interv. 2009 Dec;9(6):314-23 – reference: 22904103 - Clin Cancer Res. 2012 Oct 15;18(20):5526-34 – reference: 21979880 - Leukemia. 2012 Apr;26(4):662-74 – reference: 8839862 - Blood. 1996 Oct 1;88(7):2671-82 – reference: 11932749 - Nature. 2002 Apr 4;416(6880):552-6 – reference: 16086857 - Genome Biol. 2005;6(8):227 – reference: 24325601 - J Med Chem. 2014 Jan 9;57(1):42-55 – reference: 22789535 - Cancer Cell. 2012 Jul 10;22(1):9-20 – reference: 25131830 - Nat Rev Drug Discov. 2014 Sep;13(9):673-91 – reference: 28216661 - Leukemia. 2017 Nov;31(11):2315-2325 – reference: 20970499 - Biochim Biophys Acta. 2011 Aug;1812(8):818-23 – reference: 26494003 - Int J Biochem Cell Biol. 2015 Dec;69:121-31 – reference: 22875003 - Cell Death Dis. 2012 Aug 09;3:e366 – reference: 25473896 - Oncotarget. 2015 Jan 20;6(2):886-901 – reference: 23597129 - Stem Cells Dev. 2013 Sep 1;22(17 ):2368-83 – reference: 26604074 - Proteomics. 2016 Feb;16(4):674-88 – reference: 24071849 - Nat Genet. 2013 Oct;45(10):1113-20 – reference: 18755984 - Blood. 2008 Nov 15;112(10):4220-6 – reference: 23634996 - N Engl J Med. 2013 May 30;368(22):2059-74 |
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Title | Combined HAT/EZH2 modulation leads to cancer-selective cell death |
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