메뉴 건너뛰기




Volumn 5, Issue , 2014, Pages

Ezh2 loss promotes development of myelodysplastic syndrome but attenuates its predisposition to leukaemic transformation

Author keywords

[No Author keywords available]

Indexed keywords

INTERLEUKIN 6; TRANSCRIPTION FACTOR EZH2; TRANSCRIPTION FACTOR HOXA9; EZH2 PROTEIN, HUMAN; EZH2 PROTEIN, MOUSE; HOMEODOMAIN PROTEIN; POLYCOMB REPRESSIVE COMPLEX 2; RUNX1 PROTEIN, MOUSE; TRANSCRIPTION FACTOR RUNX1;

EID: 84903178102     PISSN: None     EISSN: 20411723     Source Type: Journal    
DOI: 10.1038/ncomms5177     Document Type: Article
Times cited : (143)

References (54)
  • 1
    • 79959794787 scopus 로고    scopus 로고
    • Clinical effect of point mutations in myelodysplastic syndromes
    • Bejar, R. et al. Clinical effect of point mutations in myelodysplastic syndromes. N. Engl. J. Med. 364, 2496-2506 (2011).
    • (2011) N. Engl. J. Med. , vol.364 , pp. 2496-2506
    • Bejar, R.1
  • 2
    • 84866378702 scopus 로고    scopus 로고
    • The role of mutations in epigenetic regulators in myeloid malignancies
    • Shih, A. H., Abdel-Wahab, O., Patel, J. P. & Levine, R. L. The role of mutations in epigenetic regulators in myeloid malignancies. Nat. Rev. Cancer 12, 599-612 (2012).
    • (2012) Nat. Rev. Cancer , vol.12 , pp. 599-612
    • Shih, A.H.1    Abdel-Wahab, O.2    Patel, J.P.3    Levine, R.L.4
  • 3
    • 84868157863 scopus 로고    scopus 로고
    • Epigenetic alterations in hematopoietic malignancies
    • Chung, Y. R., Schatoff, E. & Abdel-Wahab, O. Epigenetic alterations in hematopoietic malignancies. Int. J. Hematol. 96, 413-427 (2012).
    • (2012) Int. J. Hematol. , vol.96 , pp. 413-427
    • Chung, Y.R.1    Schatoff, E.2    Abdel-Wahab, O.3
  • 4
    • 84868150262 scopus 로고    scopus 로고
    • Epigenetic regulation of hematopoiesis
    • Sashida, G. & Iwama, A. Epigenetic regulation of hematopoiesis. Int. J. Hematol. 96, 405-412 (2012).
    • (2012) Int. J. Hematol. , vol.96 , pp. 405-412
    • Sashida, G.1    Iwama, A.2
  • 5
    • 77956222562 scopus 로고    scopus 로고
    • Polycomb group proteins: Multi-faceted regulators of somatic stem cells and cancer
    • Sauvageau, M. & Sauvageau, G. Polycomb group proteins: multi-faceted regulators of somatic stem cells and cancer. Cell Stem Cell 7, 299-313 (2010).
    • (2010) Cell Stem Cell , vol.7 , pp. 299-313
    • Sauvageau, M.1    Sauvageau, G.2
  • 8
    • 33646882068 scopus 로고    scopus 로고
    • Polycomb complexes repress developmental regulators in murine embryonic stem cells
    • Boyer, L. a. et al. Polycomb complexes repress developmental regulators in murine embryonic stem cells. Nature 441, 349-353 (2006).
    • (2006) Nature , vol.441 , pp. 349-353
    • Boyer, L.A.1
  • 9
    • 9444244427 scopus 로고    scopus 로고
    • Chromatin compaction by a polycomb group protein complex
    • DOI 10.1126/science.1100576
    • Francis, N. J., Kingston, R. E. & Woodcock, C. L. Chromatin compaction by a polycomb group protein complex. Science 306, 1574-1577 (2004). (Pubitemid 39564957)
    • (2004) Science , vol.306 , Issue.5701 , pp. 1574-1577
    • Francis, N.J.1    Kingston, R.E.2    Woodcock, C.L.3
  • 10
    • 84857367297 scopus 로고    scopus 로고
    • RYBP-PRC1 complexes mediate H2A ubiquitylation at polycomb target sites independently of PRC2 and H3K27me3
    • Tavares, L. et al. RYBP-PRC1 complexes mediate H2A ubiquitylation at polycomb target sites independently of PRC2 and H3K27me3. Cell 148, 664-678 (2012).
    • (2012) Cell , vol.148 , pp. 664-678
    • Tavares, L.1
  • 11
    • 84876871047 scopus 로고    scopus 로고
    • Occupying chromatin: Polycomb mechanisms for getting to genomic targets, stopping transcriptional traffic, and staying put
    • Simon, J. a. & Kingston, R. E. Occupying chromatin: polycomb mechanisms for getting to genomic targets, stopping transcriptional traffic, and staying put. Mol. Cell 49, 808-824 (2013).
    • (2013) Mol. Cell , vol.49 , pp. 808-824
    • Simon, J.A.1    Kingston, R.E.2
  • 12
    • 84863012512 scopus 로고    scopus 로고
    • Direct recruitment of Polycomb repressive complex 1 to chromatin by core binding transcription factors
    • Yu, M. et al. Direct recruitment of Polycomb repressive complex 1 to chromatin by core binding transcription factors. Mol. Cell 45, 330-343 (2012).
    • (2012) Mol. Cell , vol.45 , pp. 330-343
    • Yu, M.1
  • 13
    • 75749124332 scopus 로고    scopus 로고
    • Somatic mutations altering EZH2 (Tyr641) in follicular and diffuse large B-cell lymphomas of germinal-center origin
    • Morin, R. D. et al. Somatic mutations altering EZH2 (Tyr641) in follicular and diffuse large B-cell lymphomas of germinal-center origin. Nat. Genet. 42, 181-185 (2010).
    • (2010) Nat. Genet. , vol.42 , pp. 181-185
    • Morin, R.D.1
  • 14
    • 84856746717 scopus 로고    scopus 로고
    • Ectopic expression of the histone methyltransferase Ezh2 in haematopoietic stem cells causes myeloproliferative disease
    • Herrera-Merchan, A. et al. Ectopic expression of the histone methyltransferase Ezh2 in haematopoietic stem cells causes myeloproliferative disease. Nat. Commun. 3, 623 (2012).
    • (2012) Nat. Commun. , vol.3 , pp. 623
    • Herrera-Merchan, A.1
  • 15
    • 84864567410 scopus 로고    scopus 로고
    • Ezh2 augments leukemogenicity by reinforcing differentiation blockage in acute myeloid leukemia
    • Tanaka, S. et al. Ezh2 augments leukemogenicity by reinforcing differentiation blockage in acute myeloid leukemia. Blood 120, 1107-1117 (2012).
    • (2012) Blood , vol.120 , pp. 1107-1117
    • Tanaka, S.1
  • 16
    • 77955085750 scopus 로고    scopus 로고
    • Inactivating mutations of the histone methyltransferase gene EZH2 in myeloid disorders
    • Ernst, T. et al. Inactivating mutations of the histone methyltransferase gene EZH2 in myeloid disorders. Nat. Genet. 42, 722-726 (2010).
    • (2010) Nat. Genet. , vol.42 , pp. 722-726
    • Ernst, T.1
  • 17
    • 77955087290 scopus 로고    scopus 로고
    • Somatic mutations of the histone methyltransferase gene EZH2 in myelodysplastic syndromes
    • Nikoloski, G. et al. Somatic mutations of the histone methyltransferase gene EZH2 in myelodysplastic syndromes. Nat. Genet. 42, 665-667 (2010).
    • (2010) Nat. Genet. , vol.42 , pp. 665-667
    • Nikoloski, G.1
  • 18
    • 84866749552 scopus 로고    scopus 로고
    • Validation of a prognostic model and the impact of mutations in patients with lower-risk myelodysplastic syndromes
    • Bejar, R. et al. Validation of a prognostic model and the impact of mutations in patients with lower-risk myelodysplastic syndromes. J. Clin. Oncol. 30, 3376-3382 (2012).
    • (2012) J. Clin. Oncol. , vol.30 , pp. 3376-3382
    • Bejar, R.1
  • 19
    • 84862731816 scopus 로고    scopus 로고
    • Loss of heterozygosity in 7q myeloid disorders: Clinical associations and genomic pathogenesis
    • Jerez, A. et al. Loss of heterozygosity in 7q myeloid disorders: clinical associations and genomic pathogenesis. Blood 119, 6109-6117 (2012).
    • (2012) Blood , vol.119 , pp. 6109-6117
    • Jerez, A.1
  • 20
    • 84888083126 scopus 로고    scopus 로고
    • Concurrent loss of Ezh2 and Tet2 cooperates in the pathogenesis of myelodysplastic disorders
    • Muto, T. et al. Concurrent loss of Ezh2 and Tet2 cooperates in the pathogenesis of myelodysplastic disorders. J. Exp. Med. 210, 2627-2639 (2013).
    • (2013) J. Exp. Med. , vol.210 , pp. 2627-2639
    • Muto, T.1
  • 21
    • 33646475438 scopus 로고    scopus 로고
    • Hyperactivation of the RAS signaling pathway in myelodysplastic syndrome with AML1/RUNX1 point mutations
    • Niimi, H. et al. Hyperactivation of the RAS signaling pathway in myelodysplastic syndrome with AML1/RUNX1 point mutations. Leukemia. 20, 635-644 (2006).
    • (2006) Leukemia. , vol.20 , pp. 635-644
    • Niimi, H.1
  • 22
    • 1542373639 scopus 로고    scopus 로고
    • High incidence of somatic mutations in the AML1/RUNX1 gene in myelodysplastic syndrome and low blast percentage myeloid leukemia with myelodysplasia
    • DOI 10.1182/blood-2003-09-3074
    • Harada, H. et al. High incidence of somatic mutations in the AML1/RUNX1 gene in myelodysplastic syndrome and low blast percentage myeloid leukemia with myelodysplasia. Blood 103, 2316-2324 (2004). (Pubitemid 38326252)
    • (2004) Blood , vol.103 , Issue.6 , pp. 2316-2324
    • Harada, H.1    Harada, Y.2    Niimi, H.3    Kyo, T.4    Kimura, A.5    Inaba, T.6
  • 23
    • 84888219405 scopus 로고    scopus 로고
    • Clinical and biological implications of driver mutations in myelodysplastic syndromes
    • Papaemmanuil, E. et al. Clinical and biological implications of driver mutations in myelodysplastic syndromes. Blood 122, 3616-3627 (2013).
    • (2013) Blood , vol.122 , pp. 3616-3627
    • Papaemmanuil, E.1
  • 24
    • 43249103972 scopus 로고    scopus 로고
    • AML1 mutations induced MDS and MDS/AML in a mouse BMT model
    • Watanabe-Okochi, N. et al. AML1 mutations induced MDS and MDS/AML in a mouse BMT model. Blood 111, 4297-4308 (2008).
    • (2008) Blood , vol.111 , pp. 4297-4308
    • Watanabe-Okochi, N.1
  • 25
    • 0028873731 scopus 로고
    • Proliferation and differentiation of myelodysplastic CD34 cells: Phenotypic subpopulations of marrow CD34 cells
    • Sawada, K. et al. Proliferation and differentiation of myelodysplastic CD34 cells: phenotypic subpopulations of marrow CD34 cells. Blood 85, 194-202 (1995).
    • (1995) Blood , vol.85 , pp. 194-202
    • Sawada, K.1
  • 28
    • 77950862042 scopus 로고    scopus 로고
    • Bone progenitor dysfunction induces myelodysplasia and secondary leukaemia
    • Raaijmakers, M. H. G. P. et al. Bone progenitor dysfunction induces myelodysplasia and secondary leukaemia. Nature 464, 852-857 (2010).
    • (2010) Nature , vol.464 , pp. 852-857
    • Raaijmakers, M.H.G.P.1
  • 29
    • 84859832491 scopus 로고    scopus 로고
    • Altered microenvironmental regulation of leukemic and normal stem cells in chronic myelogenous leukemia
    • Zhang, B. et al. Altered microenvironmental regulation of leukemic and normal stem cells in chronic myelogenous leukemia. Cancer Cell 21, 577-592 (2012).
    • (2012) Cancer Cell , vol.21 , pp. 577-592
    • Zhang, B.1
  • 30
    • 84884164883 scopus 로고    scopus 로고
    • Myeloproliferative neoplasia remodels the endosteal bone marrow niche into a self-reinforcing leukemic niche
    • Schepers, K. et al. Myeloproliferative neoplasia remodels the endosteal bone marrow niche into a self-reinforcing leukemic niche. Cell Stem Cell 13, 285-299 (2013).
    • (2013) Cell Stem Cell , vol.13 , pp. 285-299
    • Schepers, K.1
  • 32
    • 84055218931 scopus 로고    scopus 로고
    • Dependency on the polycomb gene Ezh2 distinguishes fetal from adult hematopoietic stem cells
    • Mochizuki-Kashio, M. et al. Dependency on the polycomb gene Ezh2 distinguishes fetal from adult hematopoietic stem cells. Blood 118, 6553-6561 (2011).
    • (2011) Blood , vol.118 , pp. 6553-6561
    • Mochizuki-Kashio, M.1
  • 34
    • 67651171730 scopus 로고    scopus 로고
    • MDS: A stem cell disorder-but what exactly is wrong with the primitive hematopoietic cells in this disease?
    • Nimer, S. D. MDS: a stem cell disorder-but what exactly is wrong with the primitive hematopoietic cells in this disease? Hematology. 2008, 43-51 (2008).
    • (2008) Hematology. , vol.2008 , pp. 43-51
    • Nimer, S.D.1
  • 35
    • 84870221419 scopus 로고    scopus 로고
    • The genetic basis of phenotypic heterogeneity in myelodysplastic syndromes
    • Raza, A. & Galili, N. The genetic basis of phenotypic heterogeneity in myelodysplastic syndromes. Nat. Rev. Cancer 12, 849-859 (2012).
    • (2012) Nat. Rev. Cancer , vol.12 , pp. 849-859
    • Raza, A.1    Galili, N.2
  • 36
    • 84888116023 scopus 로고    scopus 로고
    • Deletion of Asxl1 results in myelodysplasia and severe developmental defects in vivo
    • Abdel-Wahab, O. et al. Deletion of Asxl1 results in myelodysplasia and severe developmental defects in vivo. J. Exp. Med. 210, 2641-2659 (2013).
    • (2013) J. Exp. Med. , vol.210 , pp. 2641-2659
    • Abdel-Wahab, O.1
  • 37
    • 55949124844 scopus 로고    scopus 로고
    • EZH1 mediates methylation on histone H3 lysine 27 and complements EZH2 in maintaining stem cell identity and executing pluripotency
    • Shen, X. et al. EZH1 mediates methylation on histone H3 lysine 27 and complements EZH2 in maintaining stem cell identity and executing pluripotency. Mol. Cell 32, 491-502 (2008).
    • (2008) Mol. Cell , vol.32 , pp. 491-502
    • Shen, X.1
  • 39
    • 77954533006 scopus 로고    scopus 로고
    • Evi-1 as a critical regulator of leukemic cells
    • Goyama, S. & Kurokawa, M. Evi-1 as a critical regulator of leukemic cells. Int. J. Hematol. 91, 753-757 (2010).
    • (2010) Int. J. Hematol. , vol.91 , pp. 753-757
    • Goyama, S.1    Kurokawa, M.2
  • 40
    • 0345357773 scopus 로고    scopus 로고
    • Gene silencing in cancer in association with promoter hypermethylation
    • DOI 10.1056/NEJMra023075
    • Herman, J. G. & Baylin, S. B. Gene silencing in cancer in association with promoter hypermethylation. N. Engl. J. Med. 349, 2042-2054 (2003). (Pubitemid 37448928)
    • (2003) New England Journal of Medicine , vol.349 , Issue.21 , pp. 2042-2054
    • Herman, J.G.1    Baylin, S.B.2
  • 41
    • 66149115277 scopus 로고    scopus 로고
    • IFNalpha activates dormant haematopoietic stem cells in vivo
    • Essers, M. a. G. et al. IFNalpha activates dormant haematopoietic stem cells in vivo. Nature 458, 904-908 (2009).
    • (2009) Nature , vol.458 , pp. 904-908
    • Essers A. M, G.1
  • 42
    • 80053133049 scopus 로고    scopus 로고
    • Inflammatory modulation of HSCs: Viewing the HSC as a foundation for the immune response
    • King, K. Y. & Goodell, M. a. Inflammatory modulation of HSCs: viewing the HSC as a foundation for the immune response. Nat. Rev. Immunol. 11, 685-692 (2011).
    • (2011) Nat. Rev. Immunol. , vol.11 , pp. 685-692
    • King, K.Y.1    Goodell, M.A.2
  • 43
    • 78049434915 scopus 로고    scopus 로고
    • Mammalian target of rapamycin activation underlies HSC defects in autoimmune disease and inflammation in mice
    • Chen, C., Liu, Y., Liu, Y. & Zheng, P. Mammalian target of rapamycin activation underlies HSC defects in autoimmune disease and inflammation in mice. J. Clin. Invest. 120, 4091-4101 (2010).
    • (2010) J. Clin. Invest. , vol.120 , pp. 4091-4101
    • Chen, C.1    Liu, Y.2    Liu, Y.3    Zheng, P.4
  • 45
    • 33746167484 scopus 로고    scopus 로고
    • + hematopoietic cells
    • DOI 10.1158/0008-5472.CAN-06-0458
    • Takeda, A., Goolsby, C. & Yaseen, N. R. NUP98-HOXA9 induces long-term proliferation and blocks differentiation of primary human CD34 hematopoietic cells. Cancer Res. 66, 6628-6637 (2006). (Pubitemid 44085619)
    • (2006) Cancer Research , vol.66 , Issue.13 , pp. 6628-6637
    • Takeda, A.1    Goolsby, C.2    Yaseen, N.R.3
  • 46
    • 28444455240 scopus 로고    scopus 로고
    • Loss of expression of the Hoxa-9 homeobox gene impairs the proliferation and repopulating ability of hematopoietic stem cells
    • DOI 10.1182/blood-2005-05-2003
    • Lawrence, H. J. et al. Loss of expression of the Hoxa-9 homeobox gene impairs the proliferation and repopulating ability of hematopoietic stem cells. Blood 106, 3988-3994 (2005). (Pubitemid 41739043)
    • (2005) Blood , vol.106 , Issue.12 , pp. 3988-3994
    • Lawrence, H.J.1    Christensen, J.2    Fong, S.3    Hu, Y.-L.4    Weissman, I.5    Sauvageau, G.6    Humphries, R.K.7    Largman, C.8
  • 47
    • 84879350954 scopus 로고    scopus 로고
    • RUNX1/AML1 mutant collaborates with BMI1 overexpression in the development of human and murine myelodysplastic syndromes
    • Harada, Y. et al. RUNX1/AML1 mutant collaborates with BMI1 overexpression in the development of human and murine myelodysplastic syndromes. Blood 121, 3434-3446 (2013).
    • (2013) Blood , vol.121 , pp. 3434-3446
    • Harada, Y.1
  • 48
    • 0036090290 scopus 로고    scopus 로고
    • Overexpression of the myeloid leukemia-associated Hoxa9 gene in bone marrow cells induces stem cell expansion
    • Thorsteinsdottir, U. et al. Overexpression of the myeloid leukemia-associated Hoxa9 gene in bone marrow cells induces stem cell expansion. Blood 99, 121-129 (2002).
    • (2002) Blood , vol.99 , pp. 121-129
    • Thorsteinsdottir, U.1
  • 49
    • 73849121794 scopus 로고    scopus 로고
    • Identification of miR-145 and miR-146a as mediators of the 5q-syndrome phenotype
    • Starczynowski, D. T. et al. Identification of miR-145 and miR-146a as mediators of the 5q-syndrome phenotype. Nat. Med. 16, 49-58 (2010).
    • (2010) Nat. Med. , vol.16 , pp. 49-58
    • Starczynowski, D.T.1
  • 51
    • 79956268072 scopus 로고    scopus 로고
    • Forced expression of the histone demethylase Fbxl10 maintains self-renewing hematopoietic stem cells
    • Konuma, T. et al. Forced expression of the histone demethylase Fbxl10 maintains self-renewing hematopoietic stem cells. Exp. Hematol. 39, 697-709 (2011).
    • (2011) Exp. Hematol. , vol.39 , pp. 697-709
    • Konuma, T.1
  • 52
    • 79957868920 scopus 로고    scopus 로고
    • Bismark: A flexible aligner and methylation caller for Bisulfite-Seq applications
    • Krueger, F. & Andrews, S. R. Bismark: a flexible aligner and methylation caller for Bisulfite-Seq applications. Bioinformatics. 27, 1571-1572 (2011).
    • (2011) Bioinformatics. , vol.27 , pp. 1571-1572
    • Krueger, F.1    Andrews, S.R.2
  • 53
    • 84866860221 scopus 로고    scopus 로고
    • MethylKit: A comprehensive R package for the analysis of genome-wide DNA methylation profiles
    • Akalin, A. et al. methylKit: a comprehensive R package for the analysis of genome-wide DNA methylation profiles. Genome Biol. 13, R87 (2012).
    • (2012) Genome Biol. , vol.13
    • Akalin, A.1
  • 54
    • 1842583836 scopus 로고    scopus 로고
    • Gene expression profiles from hypertrophic scar fibroblasts before and after IL-6 stimulation
    • DOI 10.1002/path.1539
    • Dasu, M. R. K., Hawkins, H. K., Barrow, R. E., Xue, H. & Herndon, D. N. Gene expression profiles from hypertrophic scar fibroblasts before and after IL-6 stimulation. J. Pathol. 202, 476-485 (2004). (Pubitemid 38456166)
    • (2004) Journal of Pathology , vol.202 , Issue.4 , pp. 476-485
    • Dasu, M.R.K.1    Hawkins, H.K.2    Barrow, R.E.3    Xue, H.4    Herndon, D.N.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.