메뉴 건너뛰기




Volumn 23, Issue 8, 2009, Pages 1426-1431

RUNX1 mutations are frequent in chronic myelomonocytic leukemia and mutations at the C-terminal region might predict acute myeloid leukemia transformation

Author keywords

[No Author keywords available]

Indexed keywords

CD135 ANTIGEN; RAS PROTEIN; TRANSCRIPTION FACTOR RUNX1;

EID: 68749109365     PISSN: 08876924     EISSN: 14765551     Source Type: Journal    
DOI: 10.1038/leu.2009.48     Document Type: Article
Times cited : (130)

References (32)
  • 3
    • 17344371122 scopus 로고    scopus 로고
    • RAS, FMS and p53 mutations and poor clinical outcome in myelodysplasias: A 10-year follow-up
    • Padua RA, Guinn BA, Al-Sabah AI, Smith M, Taylor C, Pettersson T et al. RAS, FMS and p53 mutations and poor clinical outcome in myelodysplasias: A 10-year follow-up. Leukemia 1998; 12: 887-892.
    • (1998) Leukemia , vol.12 , pp. 887-892
    • Padua, R.A.1    Guinn, B.A.2    Al-Sabah, A.I.3    Smith, M.4    Taylor, C.5    Pettersson, T.6
  • 4
    • 0024998851 scopus 로고
    • RAS mutations are rare events in Philadelphia chromosome-negative/bcr gene rearrangement-negative chronic myelogenous leukemia, but are prevalent in chronic myelomonocytic leukemia
    • Hirsch-Ginsberg C, LeMaistre AC, Kantarjian H, Talpaz M, Cork A, Freireich EJ et al. RAS mutations are rare events in Philadelphia chromosome-negative/bcr gene rearrangement-negative chronic myelogenous leukemia, but are prevalent in chronic myelomonocytic leukemia. Blood 1990; 76: 1214-1219.
    • (1990) Blood , vol.76 , pp. 1214-1219
    • Hirsch-Ginsberg, C.1    LeMaistre, A.C.2    Kantarjian, H.3    Talpaz, M.4    Cork, A.5    Freireich, E.J.6
  • 5
    • 0036045381 scopus 로고    scopus 로고
    • Tyrosine kinase fusion genes in chronic myeloproliferative diseases
    • Cross NC, Reiter A. Tyrosine kinase fusion genes in chronic myeloproliferative diseases. Leukemia 2002; 16: 1207-1212.
    • (2002) Leukemia , vol.16 , pp. 1207-1212
    • Cross, N.C.1    Reiter, A.2
  • 6
    • 1542503817 scopus 로고    scopus 로고
    • Acquisition of FLT3 or N-ras mutations is frequently associated with progression of myelodysplastic syndrome to acute myeloid leukemia
    • Shih LY, Huang CF, Wang PN, Wu JH, Lin TL, Dunn P et al. Acquisition of FLT3 or N-ras mutations is frequently associated with progression of myelodysplastic syndrome to acute myeloid leukemia. Leukemia 2004; 18: 466-475.
    • (2004) Leukemia , vol.18 , pp. 466-475
    • Shih, L.Y.1    Huang, C.F.2    Wang, P.N.3    Wu, J.H.4    Lin, T.L.5    Dunn, P.6
  • 7
    • 4143053704 scopus 로고    scopus 로고
    • Internal tandem duplication of fms-like tyrosine kinase 3 is associated with poor outcome in patients with myelodysplastic syndrome
    • Shih LY, Lin TL, Wang PN, Wu JH, Dunn P, Kuo MC et al. Internal tandem duplication of fms-like tyrosine kinase 3 is associated with poor outcome in patients with myelodysplastic syndrome. Cancer 2004; 101: 989-998.
    • (2004) Cancer , vol.101 , pp. 989-998
    • Shih, L.Y.1    Lin, T.L.2    Wang, P.N.3    Wu, J.H.4    Dunn, P.5    Kuo, M.C.6
  • 8
    • 16344370044 scopus 로고    scopus 로고
    • Heterogeneous patterns of CEBPα mutation status in the progression of myelodysplastic syndrome and chronic myelomonocytic leukemia to acute myeloid leukemia
    • Shih LY, Huang CF, Lin TL, Wu JH, Wang PN, Dunn P et al. Heterogeneous patterns of CEBPα mutation status in the progression of myelodysplastic syndrome and chronic myelomonocytic leukemia to acute myeloid leukemia. Clin Cancer Res 2005; 11: 1821-1826.
    • (2005) Clin Cancer Res , vol.11 , pp. 1821-1826
    • Shih, L.Y.1    Huang, C.F.2    Lin, T.L.3    Wu, J.H.4    Wang, P.N.5    Dunn, P.6
  • 9
    • 0030061554 scopus 로고    scopus 로고
    • AML1, the target of multiple chromosomal translocations in human leukemia, is essential for normal fetal liver hematopoiesis
    • Okuda T, van Deursen J, Hiebert SW, Grosveld G, Downing JR. AML1, the target of multiple chromosomal translocations in human leukemia, is essential for normal fetal liver hematopoiesis. Cell 1996; 84 321-330.
    • (1996) Cell , vol.84 , pp. 321-330
    • Okuda, T.1    van Deursen, J.2    Hiebert, S.W.3    Grosveld, G.4    Downing, J.R.5
  • 10
    • 0029918597 scopus 로고    scopus 로고
    • Disruption of the Cbfa2 gene causes necrosis and hemorrhaging in the central nervous system and blocks definitive hematopoiesis
    • Wang Q, Stacy T, Binder M, Marin-Padilla M, Sharpe AH, Speck NA. Disruption of the Cbfa2 gene causes necrosis and hemorrhaging in the central nervous system and blocks definitive hematopoiesis. Proc Natl Acad Sci USA 1996; 93: 3444-3449.
    • (1996) Proc Natl Acad Sci USA , vol.93 , pp. 3444-3449
    • Wang, Q.1    Stacy, T.2    Binder, M.3    Marin-Padilla, M.4    Sharpe, A.H.5    Speck, N.A.6
  • 11
    • 0037321711 scopus 로고    scopus 로고
    • The role of a Runt domain transcription factor AML1/RUNX1 in leukemogenesis and its clinical implications
    • Asou N. The role of a Runt domain transcription factor AML1/RUNX1 in leukemogenesis and its clinical implications. Crit Rev Oncol Hematol 2003; 45: 129-150.
    • (2003) Crit Rev Oncol Hematol , vol.45 , pp. 129-150
    • Asou, N.1
  • 12
    • 0036636857 scopus 로고    scopus 로고
    • Core-binding factors in haematopoiesis and leukaemia
    • Speck NA, Gilliland DG. Core-binding factors in haematopoiesis and leukaemia. Nat Rev Cancer 2002; 2: 502-513.
    • (2002) Nat Rev Cancer , vol.2 , pp. 502-513
    • Speck, N.A.1    Gilliland, D.G.2
  • 13
    • 0033559746 scopus 로고    scopus 로고
    • Biallelic and heterozygous point mutations in the runt domain of the AML1/PEBP2alphaB gene associated with myeloblastic leukemias
    • Osato M, Asou N, Abdalla E, Hoshino K, Yamasaki H, Okubo T et al. Biallelic and heterozygous point mutations in the runt domain of the AML1/PEBP2alphaB gene associated with myeloblastic leukemias. Blood 1999; 93: 1817-1824.
    • (1999) Blood , vol.93 , pp. 1817-1824
    • Osato, M.1    Asou, N.2    Abdalla, E.3    Hoshino, K.4    Yamasaki, H.5    Okubo, T.6
  • 14
    • 0037441589 scopus 로고    scopus 로고
    • M0 AML, clinical and biologic features of the disease, including AML1 gene mutations: A report of 59 cases by the Groupe Francais d'Hematologie Cellulaire (GFHC) and the Groupe Francais de Cytogenetique Hematologique (GFCH)
    • Roumier C, Eclache V, Imbert M, Davi F, MacIntyre E, Garand R et al M0 AML, clinical and biologic features of the disease, including AML1 gene mutations: A report of 59 cases by the Groupe Francais d'Hematologie Cellulaire (GFHC) and the Groupe Francais de Cytogenetique Hematologique (GFCH). Blood 2003; 101: 1277-1283.
    • (2003) Blood , vol.101 , pp. 1277-1283
    • Roumier, C.1    Eclache, V.2    Imbert, M.3    Davi, F.4    MacIntyre, E.5    Garand, R.6
  • 15
    • 0037438508 scopus 로고    scopus 로고
    • Implications of somatic mutations in the AML1 gene in radiation-associated and therapy-related myelodysplastic syndrome/acute myeloid leukemia
    • Harada H, Harada Y, Tanaka H, Kimura A, Inaba T. Implications of somatic mutations in the AML1 gene in radiation-associated and therapy-related myelodysplastic syndrome/acute myeloid leukemia. Blood 2003; 101: 673-680.
    • (2003) Blood , vol.101 , pp. 673-680
    • Harada, H.1    Harada, Y.2    Tanaka, H.3    Kimura, A.4    Inaba, T.5
  • 16
    • 4444302228 scopus 로고    scopus 로고
    • Mutations of AML1 are common in therapy-related myelodysplasia following therapy with alkylating agents and are significantly associated with deletion or loss of chromosome arm 7q and with subsequent leukemic transformation
    • Christiansen DH, Andersen MK, Pedersen-Bjergaard J. Mutations of AML1 are common in therapy-related myelodysplasia following therapy with alkylating agents and are significantly associated with deletion or loss of chromosome arm 7q and with subsequent leukemic transformation. Blood 2004; 104: 1474-1481.
    • (2004) Blood , vol.104 , pp. 1474-1481
    • Christiansen, D.H.1    Andersen, M.K.2    Pedersen-Bjergaard, J.3
  • 17
    • 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
    • Harada H, Harada Y, Niimi H, Kyo T, Kimura A, Inaba T. High incidence of somatic mutations in the AML1/RUNX1 gene in myelodysplastic syndrome and low blast percentage myeloid leukemia with myelodysplasia. Blood 2004; 103: 2316-2324.
    • (2004) Blood , vol.103 , pp. 2316-2324
    • Harada, H.1    Harada, Y.2    Niimi, H.3    Kyo, T.4    Kimura, A.5    Inaba, T.6
  • 18
    • 12444314088 scopus 로고    scopus 로고
    • Somatic point mutations in RUNX1/CBFA2/AML1 are common in high-risk myelodysplastic syndrome, but not in myelofibrosis with myeloid metaplasia
    • Steensma DP, Gibbons RJ, Mesa RA, Tefferi A, Higgs DR. Somatic point mutations in RUNX1/CBFA2/AML1 are common in high-risk myelodysplastic syndrome, but not in myelofibrosis with myeloid metaplasia. Eur J Haematol 2005; 74: 47-53.
    • (2005) Eur J Haematol , vol.74 , pp. 47-53
    • Steensma, D.P.1    Gibbons, R.J.2    Mesa, R.A.3    Tefferi, A.4    Higgs, D.R.5
  • 19
    • 3042541853 scopus 로고    scopus 로고
    • Novel loss-of-function mutations of the haematopoiesis-related transcription factor, acute myeloid leukaemia 1/ runt-related transcription factor 1, detected in acute myeloblastic leukaemia and myelodysplastic syndrome
    • Nakao M, Horiike S, Fukushima-Nakase Y, Nishimura M, Fujita Y, Taniwaki M et al. Novel loss-of-function mutations of the haematopoiesis-related transcription factor, acute myeloid leukaemia 1/ runt-related transcription factor 1, detected in acute myeloblastic leukaemia and myelodysplastic syndrome. Br J Haematol 2004; 125 709-719.
    • (2004) Br J Haematol , vol.125 , pp. 709-719
    • Nakao, M.1    Horiike, S.2    Fukushima-Nakase, Y.3    Nishimura, M.4    Fujita, Y.5    Taniwaki, M.6
  • 20
    • 2942667930 scopus 로고    scopus 로고
    • Point mutations in the RUNX1/AML1 gene: Another actor in RUNX leukemia
    • Osato M. Point mutations in the RUNX1/AML1 gene: Another actor in RUNX leukemia. Oncogene 2004; 23: 4284-4296.
    • (2004) Oncogene , vol.23 , pp. 4284-4296
    • Osato, M.1
  • 21
    • 0030897009 scopus 로고    scopus 로고
    • International scoring system for evaluating prognosis in myelodysplastic syndromes
    • Greenberg P, Cox C, LeBeau MM, Fenaux P, Morel P, Sanz G et al. International scoring system for evaluating prognosis in myelodysplastic syndromes. Blood 1997; 89: 2079-2088.
    • (1997) Blood , vol.89 , pp. 2079-2088
    • Greenberg, P.1    Cox, C.2    LeBeau, M.M.3    Fenaux, P.4    Morel, P.5    Sanz, G.6
  • 22
    • 0036786289 scopus 로고    scopus 로고
    • Internal tandem duplication of FLT3 in relapsed acute myeloid leukemia: A comparative analysis of bone marrow samples from 108 adult patients at diagnosis and relapse
    • Shih LY, Huang CF, Wu JH, Lin TL, Dunn P, Wang PN et al. Internal tandem duplication of FLT3 in relapsed acute myeloid leukemia: A comparative analysis of bone marrow samples from 108 adult patients at diagnosis and relapse. Blood 2002; 100: 2387-2392.
    • (2002) Blood , vol.100 , pp. 2387-2392
    • Shih, L.Y.1    Huang, C.F.2    Wu, J.H.3    Lin, T.L.4    Dunn, P.5    Wang, P.N.6
  • 24
    • 0032830638 scopus 로고    scopus 로고
    • Haploinsufficiency of CBFA2 causes familial thrombocytopenia with propensity to develop acute myelogenous leukaemia
    • Song WJ, Sullivan MG, Legare RD, Hutchings S, Tan X, Kufrin D et al Haploinsufficiency of CBFA2 causes familial thrombocytopenia with propensity to develop acute myelogenous leukaemia. Nat Genet 1999; 23: 166-175.
    • (1999) Nat Genet , vol.23 , pp. 166-175
    • Song, W.J.1    Sullivan, M.G.2    Legare, R.D.3    Hutchings, S.4    Tan, X.5    Kufrin, D.6
  • 25
    • 0034332068 scopus 로고    scopus 로고
    • Mutations of the AML1 gene in myelodysplastic syndrome and their functional implications in leukemogenesis
    • Imai Y, Kurokawa M, Izutsu K, Hangaishi A, Takeuchi K, Maki K et al Mutations of the AML1 gene in myelodysplastic syndrome and their functional implications in leukemogenesis. Blood 2000; 96: 3154-3160.
    • (2000) Blood , vol.96 , pp. 3154-3160
    • Imai, Y.1    Kurokawa, M.2    Izutsu, K.3    Hangaishi, A.4    Takeuchi, K.5    Maki, K.6
  • 26
    • 34548044732 scopus 로고    scopus 로고
    • Trisomy 13 is strongly associated with AML1/RUNX1 mutations and increased FLT3 expression in acute myeloid leukemia
    • Dicker F, Haferlach C, Kern W, Haferlach T, Schnittger S. Trisomy 13 is strongly associated with AML1/RUNX1 mutations and increased FLT3 expression in acute myeloid leukemia. Blood 2007; 110: 1308-1316.
    • (2007) Blood , vol.110 , pp. 1308-1316
    • Dicker, F.1    Haferlach, C.2    Kern, W.3    Haferlach, T.4    Schnittger, S.5
  • 27
    • 0036124315 scopus 로고    scopus 로고
    • Mutational analyses of the AML1 gene in patients with myelodysplastic syndrome
    • Imai O, Kurokawa M, Izutsu K, Hangaishi A, Maki K, Ogawa S et al. Mutational analyses of the AML1 gene in patients with myelodysplastic syndrome. Leuk Lymphoma 2002; 43: 617-621.
    • (2002) Leuk Lymphoma , vol.43 , pp. 617-621
    • Imai, O.1    Kurokawa, M.2    Izutsu, K.3    Hangaishi, A.4    Maki, K.5    Ogawa, S.6
  • 28
    • 0037082499 scopus 로고    scopus 로고
    • In vitro analyses of known and novel RUNX1/AML1 mutations in dominant familial platelet disorder with predisposition to acute myelogenous leukemia: Implications for mechanisms of pathogenesis
    • Michaud J, Wu F, Osato M, Cottles GM, Yanagida M, Asou N et al. In vitro analyses of known and novel RUNX1/AML1 mutations in dominant familial platelet disorder with predisposition to acute myelogenous leukemia: Implications for mechanisms of pathogenesis. Blood 2002; 99: 1364-1372.
    • (2002) Blood , vol.99 , pp. 1364-1372
    • Michaud, J.1    Wu, F.2    Osato, M.3    Cottles, G.M.4    Yanagida, M.5    Asou, N.6
  • 29
    • 33644881695 scopus 로고    scopus 로고
    • Point mutations in the AML1/RUNX1 gene associated with myelodysplastic syndrome
    • Harada H, Harada Y. Point mutations in the AML1/RUNX1 gene associated with myelodysplastic syndrome. Crit Rev Eukartyot Gene Expr 2005; 15: 183-196.
    • (2005) Crit Rev Eukartyot Gene Expr , vol.15 , pp. 183-196
    • Harada, H.1    Harada, Y.2
  • 30
    • 0031940065 scopus 로고    scopus 로고
    • Intrinsic transcriptional activation-inhibition domains of the polyomavirus enhancer binding protein 2/core binding factor alpha subunit revealed in the presence of the beta subunit
    • Kanno T, Kanno Y, Chen LF, Ogawa E, Kim WY, Ito Y. Intrinsic transcriptional activation-inhibition domains of the polyomavirus enhancer binding protein 2/core binding factor alpha subunit revealed in the presence of the beta subunit. Mol Cell Biol 1998; 18: 2444-2454.
    • (1998) Mol Cell Biol , vol.18 , pp. 2444-2454
    • Kanno, T.1    Kanno, Y.2    Chen, L.F.3    Ogawa, E.4    Kim, W.Y.5    Ito, Y.6
  • 32
    • 0034667690 scopus 로고    scopus 로고
    • High incidence of biallelic point mutations in the Runt domain of the AML1/PEBP2 alpha B gene in Mo acute myeloid leukemia and in myeloid malignancies with acquired trisomy 21
    • Preudhomme C, Warot-Loze D, Roumier C, Grardel-Duflos N, Garand R, Lai JL et al. High incidence of biallelic point mutations in the Runt domain of the AML1/PEBP2 alpha B gene in Mo acute myeloid leukemia and in myeloid malignancies with acquired trisomy 21. Blood 2000; 96: 2862-2869.
    • (2000) Blood , vol.96 , pp. 2862-2869
    • Preudhomme, C.1    Warot-Loze, D.2    Roumier, C.3    Grardel-Duflos, N.4    Garand, R.5    Lai, J.L.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.