메뉴 건너뛰기




Volumn 123, Issue 12, 2014, Pages 1883-1886

Tracing the development of acute myeloid leukemia in CBL syndrome

Author keywords

[No Author keywords available]

Indexed keywords

CYTARABINE; DASATINIB;

EID: 84897535246     PISSN: 00064971     EISSN: 15280020     Source Type: Journal    
DOI: 10.1182/blood-2013-10-533844     Document Type: Article
Times cited : (23)

References (25)
  • 1
    • 66149148673 scopus 로고    scopus 로고
    • Age and acute myeloid leukemia: Real world data on decision to treat and outcomes from the Swedish Acute Leukemia Registry
    • Juliusson G, Antunovic P, Derolf A, et al. Age and acute myeloid leukemia: real world data on decision to treat and outcomes from the Swedish Acute Leukemia Registry. Blood. 2009;113(18):4179-4187.
    • (2009) Blood , vol.113 , Issue.18 , pp. 4179-4187
    • Juliusson, G.1    Antunovic, P.2    Derolf, A.3
  • 2
    • 68949124841 scopus 로고    scopus 로고
    • Gain-offunction of mutated C-CBL tumour suppressor in myeloid neoplasms
    • Sanada M, Suzuki T, Shih LY, et al. Gain-offunction of mutated C-CBL tumour suppressor in myeloid neoplasms. Nature. 2009;460(7257):904-908.
    • (2009) Nature , vol.460 , Issue.7257 , pp. 904-908
    • Sanada, M.1    Suzuki, T.2    Shih, L.Y.3
  • 3
    • 70349249988 scopus 로고    scopus 로고
    • Mutations in CBL occur frequently in juvenile myelomonocytic leukemia
    • Loh ML, Sakai DS, Flotho C, et al. Mutations in CBL occur frequently in juvenile myelomonocytic leukemia. Blood. 2009;114(9):1859-1863.
    • (2009) Blood , vol.114 , Issue.9 , pp. 1859-1863
    • Loh, M.L.1    Sakai, D.S.2    Flotho, C.3
  • 4
    • 74949108515 scopus 로고    scopus 로고
    • Mutations of e3 ubiquitin ligase cbl family members constitute a novel common pathogenic lesion in myeloid malignancies
    • Makishima H, Cazzolli H, Szpurka H, et al. Mutations of e3 ubiquitin ligase cbl family members constitute a novel common pathogenic lesion in myeloid malignancies. J Clin Oncol. 2009;27(36):6109-6116.
    • (2009) J Clin Oncol , vol.27 , Issue.36 , pp. 6109-6116
    • Makishima, H.1    Cazzolli, H.2    Szpurka, H.3
  • 5
    • 78349249756 scopus 로고    scopus 로고
    • Genetic typing of CBL, ASXL1, RUNX1, TET2 and JAK2 in juvenile myelomonocytic leukaemia reveals a genetic profile distinct from chronic myelomonocytic leukaemia
    • Pérez B, Kosmider O, Cassinat B, et al. Genetic typing of CBL, ASXL1, RUNX1, TET2 and JAK2 in juvenile myelomonocytic leukaemia reveals a genetic profile distinct from chronic myelomonocytic leukaemia. Br J Haematol. 2010;151(5):460-468.
    • (2010) Br J Haematol , vol.151 , Issue.5 , pp. 460-468
    • Pérez, B.1    Kosmider, O.2    Cassinat, B.3
  • 6
    • 77956237515 scopus 로고    scopus 로고
    • Next-generation sequencing technology reveals a characteristic pattern of molecular mutations in 72.8% of chronic myelomonocytic leukemia by detecting frequent alterations in TET2, CBL, RAS, and RUNX1
    • Kohlmann A, Grossmann V, Klein HU, et al. Next-generation sequencing technology reveals a characteristic pattern of molecular mutations in 72.8% of chronic myelomonocytic leukemia by detecting frequent alterations in TET2, CBL, RAS, and RUNX1. J Clin Oncol. 2010;28(24):3858-3865.
    • (2010) J Clin Oncol , vol.28 , Issue.24 , pp. 3858-3865
    • Kohlmann, A.1    Grossmann, V.2    Klein, H.U.3
  • 7
    • 84922336738 scopus 로고    scopus 로고
    • Prognostic score including gene mutations in chronic myelomonocytic leukemia
    • Itzykson R, Kosmider O, Renneville A, et al. Prognostic score including gene mutations in chronic myelomonocytic leukemia. J Clin Oncol. 2013;31(19):2428-2436.
    • (2013) J Clin Oncol , vol.31 , Issue.19 , pp. 2428-2436
    • Itzykson, R.1    Kosmider, O.2    Renneville, A.3
  • 8
    • 84984935016 scopus 로고    scopus 로고
    • Germline CBL mutations cause developmental abnormalities and predispose to juvenile myelomonocytic leukemia
    • Niemeyer CM, Kang MW, Shin DH, et al. Germline CBL mutations cause developmental abnormalities and predispose to juvenile myelomonocytic leukemia. Nat Genet. 2010;42(9):794-800.
    • (2010) Nat Genet , vol.42 , Issue.9 , pp. 794-800
    • Niemeyer, C.M.1    Kang, M.W.2    Shin, D.H.3
  • 9
    • 77955583599 scopus 로고    scopus 로고
    • Heterozygous germline mutations in the CBL tumor-suppressor gene cause a Noonan syndrome-like phenotype
    • Martinelli S, De Luca A, Stellacci E, et al. Heterozygous germline mutations in the CBL tumor-suppressor gene cause a Noonan syndrome-like phenotype. Am J Hum Genet. 2010;87(2):250-257.
    • (2010) Am J Hum Genet , vol.87 , Issue.2 , pp. 250-257
    • Martinelli, S.1    De Luca, A.2    Stellacci, E.3
  • 10
    • 77957809576 scopus 로고    scopus 로고
    • Germline mutations of the CBL gene define a new genetic syndrome with predisposition to juvenile myelomonocytic leukaemia
    • Pérez B, Mechinaud F, Galambrun C, et al. Germline mutations of the CBL gene define a new genetic syndrome with predisposition to juvenile myelomonocytic leukaemia. J Med Genet. 2010;47(10):686-691.
    • (2010) J Med Genet , vol.47 , Issue.10 , pp. 686-691
    • Pérez, B.1    Mechinaud, F.2    Galambrun, C.3
  • 11
    • 84860703461 scopus 로고    scopus 로고
    • Landscape of TET2 mutations in acute myeloid leukemia
    • Weissmann S, Alpermann T, Grossmann V, et al. Landscape of TET2 mutations in acute myeloid leukemia. Leukemia. 2012;26(5):934-942.
    • (2012) Leukemia , vol.26 , Issue.5 , pp. 934-942
    • Weissmann, S.1    Alpermann, T.2    Grossmann, V.3
  • 12
    • 54349105660 scopus 로고    scopus 로고
    • Exon 8 splice site mutations in the gene encoding the E3-ligase CBL are associated with core binding factor acute myeloid leukemias
    • Abbas S, Rotmans G, Löwenberg B, Valk PJ. Exon 8 splice site mutations in the gene encoding the E3-ligase CBL are associated with core binding factor acute myeloid leukemias. Haematologica. 2008;93(10):1595-1597.
    • (2008) Haematologica , vol.93 , Issue.10 , pp. 1595-1597
    • Abbas, S.1    Rotmans, G.2    Löwenberg, B.3    Valk, P.J.4
  • 13
    • 65249132999 scopus 로고    scopus 로고
    • CBL exon 8/9 mutants activate the FLT3 pathway and cluster in core binding factor/11q deletion acute myeloid leukemia/myelodysplastic syndrome subtypes
    • Reindl C, Quentmeier H, Petropoulos K, et al. CBL exon 8/9 mutants activate the FLT3 pathway and cluster in core binding factor/11q deletion acute myeloid leukemia/myelodysplastic syndrome subtypes. Clin Cancer Res. 2009;15(7):2238-2247.
    • (2009) Clin Cancer Res , vol.15 , Issue.7 , pp. 2238-2247
    • Reindl, C.1    Quentmeier, H.2    Petropoulos, K.3
  • 14
    • 77952420655 scopus 로고    scopus 로고
    • AML with CBFB-MYH11 rearrangement demonstrate RAS pathway alterations in 92% of all cases including a high frequency of NF1 deletions
    • Haferlach C, Dicker F, Kohlmann A, et al. AML with CBFB-MYH11 rearrangement demonstrate RAS pathway alterations in 92% of all cases including a high frequency of NF1 deletions. Leukemia. 2010;24(5):1065-1069.
    • (2010) Leukemia , vol.24 , Issue.5 , pp. 1065-1069
    • Haferlach, C.1    Dicker, F.2    Kohlmann, A.3
  • 15
    • 0037093105 scopus 로고    scopus 로고
    • Comparison of cytogenetic and molecular cytogenetic detection of chromosome abnormalities in 240 consecutive adult patients with acute myeloid leukemia
    • DOI 10.1200/JCO.2002.08.155
    • Fröhling S, Skelin S, Liebisch C, et al. Comparison of cytogenetic and molecular cytogenetic detection of chromosome abnormalities in 240 consecutive adult patients with acute myeloid leukemia. J Clin Oncol. 2002;20(10):2480-2485. (Pubitemid 34525733)
    • (2002) Journal of Clinical Oncology , vol.20 , Issue.10 , pp. 2480-2485
    • Frohling, S.1    Skelin, S.2    Liebisch, C.3    Scholl, C.4    Schlenk, R.F.5    Dohner, H.6    Dohner, K.7
  • 16
    • 0141923916 scopus 로고    scopus 로고
    • + acute myeloid leukemia based on quantification of fusion transcripts
    • DOI 10.1182/blood-2003-03-0880
    • Schnittger S, Weisser M, Schoch C, Hiddemann W, Haferlach T, Kern W. New score predicting for prognosis in PML-RARA+, AML1-ETO+, or CBFBMYH11+ acute myeloid leukemia based on quantification of fusion transcripts. Blood. 2003;102(8):2746-2755. (Pubitemid 37248843)
    • (2003) Blood , vol.102 , Issue.8 , pp. 2746-2755
    • Schnittger, S.1    Weisser, M.2    Schoch, C.3    Hiddemann, W.4    Haferlach, T.5    Kern, W.6
  • 17
    • 28444473100 scopus 로고    scopus 로고
    • Mutant nucleophosmin (NPM1) predicts favorable prognosis in younger adults with acute myeloid leukemia and normal cytogenetics: Interaction with other gene mutations
    • DOI 10.1182/blood-2005-05-2164
    • Döhner K, Schlenk RF, Habdank M, et al. Mutant nucleophosmin (NPM1) predicts favorable prognosis in younger adults with acute myeloid leukemia and normal cytogenetics: interaction with other gene mutations. Blood. 2005;106(12):3740-3746. (Pubitemid 41739007)
    • (2005) Blood , vol.106 , Issue.12 , pp. 3740-3746
    • Dohner, K.1    Schlenk, R.F.2    Habdank, M.3    Scholl, C.4    Rucker, F.G.5    Corbacioglu, A.6    Bullinger, L.7    Frohling, S.8    Dohner, H.9
  • 18
    • 84870406696 scopus 로고    scopus 로고
    • Use of CBL exon 8 and 9 mutations in diagnosis of myeloproliferative neoplasms and myelodysplastic/myeloproliferative disorders: An analysis of 636 cases
    • Schnittger S, Bacher U, Alpermann T, et al. Use of CBL exon 8 and 9 mutations in diagnosis of myeloproliferative neoplasms and myelodysplastic/ myeloproliferative disorders: an analysis of 636 cases. Haematologica. 2012;97(12):1890-1894.
    • (2012) Haematologica , vol.97 , Issue.12 , pp. 1890-1894
    • Schnittger, S.1    Bacher, U.2    Alpermann, T.3
  • 19
    • 80053900941 scopus 로고    scopus 로고
    • Frequent pathway mutations of splicing machinery in myelodysplasia
    • Yoshida K, Sanada M, Shiraishi Y, et al. Frequent pathway mutations of splicing machinery in myelodysplasia. Nature. 2011;478(7367):64-69.
    • (2011) Nature , vol.478 , Issue.7367 , pp. 64-69
    • Yoshida, K.1    Sanada, M.2    Shiraishi, Y.3
  • 20
    • 78651330430 scopus 로고    scopus 로고
    • COSMIC: Mining complete cancer genomes in the Catalogue of Somatic Mutations in Cancer
    • Accessed September 24, 2013
    • Forbes SA, Bindal N, Bamford S, et al. COSMIC: mining complete cancer genomes in the Catalogue of Somatic Mutations in Cancer. Nucleic Acids Res. 2011;39(Database issue): D945-D950. http://www.sanger.ac.uk/cosmic. Accessed September 24, 2013.
    • (2011) Nucleic Acids Res , vol.39 , Issue.DATABASE ISSUE
    • Forbes, S.A.1    Bindal, N.2    Bamford, S.3
  • 21
    • 84862776906 scopus 로고    scopus 로고
    • Clonal evolution in relapsed acute myeloid leukaemia revealed by whole-genome sequencing
    • Ding L, Ley TJ, Larson DE, et al. Clonal evolution in relapsed acute myeloid leukaemia revealed by whole-genome sequencing. Nature. 2012;481(7382):506-510.
    • (2012) Nature , vol.481 , Issue.7382 , pp. 506-510
    • Ding, L.1    Ley, T.J.2    Larson, D.E.3
  • 22
    • 84878372012 scopus 로고    scopus 로고
    • Genomic and epigenomic landscapes of adult de novo acute myeloid leukemia
    • Cancer Genome Atlas Research Network
    • Cancer Genome Atlas Research Network. Genomic and epigenomic landscapes of adult de novo acute myeloid leukemia. N Engl J Med. 2013;368(22):2059-2074.
    • (2013) N Engl J Med , vol.368 , Issue.22 , pp. 2059-2074
  • 23
    • 0026063878 scopus 로고
    • Selective hypersensitivity to granulocyte-macrophage colony-stimulating factor by juvenile chronic myeloid leukemia hematopoietic progenitors
    • Emanuel PD, Bates LJ, Castleberry RP, Gualtieri RJ, Zuckerman KS. Selective hypersensitivity to granulocyte-macrophage colony-stimulating factor by juvenile chronic myeloid leukemia hematopoietic progenitors. Blood. 1991;77(5):925-929.
    • (1991) Blood , vol.77 , Issue.5 , pp. 925-929
    • Emanuel, P.D.1    Bates, L.J.2    Castleberry, R.P.3    Gualtieri, R.J.4    Zuckerman, K.S.5
  • 24
    • 84890439281 scopus 로고    scopus 로고
    • In hematopoietic cells with a germline mutation of CBL, loss of heterozygosity is not a signature of juvenile myelo-monocytic leukemia
    • Strullu M, Caye A, Cassinat B, et al. In hematopoietic cells with a germline mutation of CBL, loss of heterozygosity is not a signature of juvenile myelo-monocytic leukemia. Leukemia. 2013;27(12):2404-2407.
    • (2013) Leukemia , vol.27 , Issue.12 , pp. 2404-2407
    • Strullu, M.1    Caye, A.2    Cassinat, B.3
  • 25
    • 37249015529 scopus 로고    scopus 로고
    • Familial myelodysplasia and acute myeloid leukaemia - A review
    • DOI 10.1111/j.1365-2141.2007.06909.x
    • Owen C, Barnett M, Fitzgibbon J. Familial myelodysplasia and acute myeloid leukaemia - a review. Br J Haematol. 2008;140(2):123-132. (Pubitemid 350265048)
    • (2008) British Journal of Haematology , vol.140 , Issue.2 , pp. 123-132
    • Owen, C.1    Barnett, M.2    Fitzgibbon, J.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.