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Volumn 151, Issue 5, 2010, Pages 460-468

Genetic typing of CBL, ASXL1, RUNX1, TET2 and JAK2 in juvenile myelomonocytic leukaemia reveals a genetic profile distinct from chronic myelomonocytic leukaemia

Author keywords

ASXL1; CBL; Chronic myelomonocytic leukaemia; JAK2; Juvenile myelomonocytic leukaemia; RUNX1; TET2

Indexed keywords

CBL PROTEIN; DNA BINDING PROTEIN; JANUS KINASE 2; PROTEIN ASXL1; PROTEIN TET2; REPRESSOR PROTEIN; TRANSCRIPTION FACTOR RUNX1; UNCLASSIFIED DRUG;

EID: 78349249756     PISSN: 00071048     EISSN: 13652141     Source Type: Journal    
DOI: 10.1111/j.1365-2141.2010.08393.x     Document Type: Article
Times cited : (57)

References (51)
  • 6
    • 0021233189 scopus 로고
    • Subacute and chronic myelomonocytic leukemia in children (juvenile CML). Clinical and hematologic observations, and identification of prognostic factors
    • Castro-Malaspina, H., Schaison, G., Passe, S., Pasquier, A., Berger, R., Bayle-Weisgerber, C., Miller, D., Seligmann, M. & Bernard, J. (1984) Subacute and chronic myelomonocytic leukemia in children (juvenile CML). Clinical and hematologic observations, and identification of prognostic factors. Cancer, 54, 675-686.
    • (1984) Cancer , vol.54 , pp. 675-686
    • Castro-Malaspina, H.1    Schaison, G.2    Passe, S.3    Pasquier, A.4    Berger, R.5    Bayle-Weisgerber, C.6    Miller, D.7    Seligmann, M.8    Bernard, J.9
  • 7
    • 58549090093 scopus 로고    scopus 로고
    • Juvenile myelomonocytic leukemia: a report from the 2nd International JMML Symposium
    • Chan, R.J., Cooper, T., Kratz, C.P., Weiss, B. & Loh, M.L. (2009) Juvenile myelomonocytic leukemia: a report from the 2nd International JMML Symposium. Leukemia Research, 33, 355-362.
    • (2009) Leukemia Research , vol.33 , pp. 355-362
    • Chan, R.J.1    Cooper, T.2    Kratz, C.P.3    Weiss, B.4    Loh, M.L.5
  • 9
    • 57749114621 scopus 로고    scopus 로고
    • 250K single nucleotide polymorphism array karyotyping identifies acquired uniparental disomy and homozygous mutations, including novel missense substitutions of c-Cbl, in myeloid malignancies
    • Dunbar, A.J., Gondek, L.P., O'Keefe, C.L., Makishima, H., Rataul, M.S., Szpurka, H., Sekeres, M.A., Wang, X.F., McDevitt, M.A. & Maciejewski, J.P. (2008) 250K single nucleotide polymorphism array karyotyping identifies acquired uniparental disomy and homozygous mutations, including novel missense substitutions of c-Cbl, in myeloid malignancies. Cancer Research, 68, 10349-10357.
    • (2008) Cancer Research , vol.68 , pp. 10349-10357
    • Dunbar, A.J.1    Gondek, L.P.2    O'Keefe, C.L.3    Makishima, H.4    Rataul, M.S.5    Szpurka, H.6    Sekeres, M.A.7    Wang, X.F.8    McDevitt, M.A.9    Maciejewski, J.P.10
  • 10
    • 47649104857 scopus 로고    scopus 로고
    • Juvenile myelomonocytic leukemia and chronic myelomonocytic leukemia
    • Emanuel, P.D. (2008) Juvenile myelomonocytic leukemia and chronic myelomonocytic leukemia. Leukemia, 22, 1335-1342.
    • (2008) Leukemia , vol.22 , pp. 1335-1342
    • Emanuel, P.D.1
  • 12
    • 74949143986 scopus 로고    scopus 로고
    • Loss-of-function Additional sex combs like 1 mutations disrupt hematopoiesis but do not cause severe myelodysplasia or leukemia
    • Fisher, C.L., Pineault, N., Brookes, C., Helgason, C.D., Ohta, H., Bodner, C., Hess, J.L., Humphries, R.K. & Brock, H.W. (2010) Loss-of-function Additional sex combs like 1 mutations disrupt hematopoiesis but do not cause severe myelodysplasia or leukemia. Blood, 115, 38-46.
    • (2010) Blood , vol.115 , pp. 38-46
    • Fisher, C.L.1    Pineault, N.2    Brookes, C.3    Helgason, C.D.4    Ohta, H.5    Bodner, C.6    Hess, J.L.7    Humphries, R.K.8    Brock, H.W.9
  • 14
    • 36348932201 scopus 로고    scopus 로고
    • How a rare pediatric neoplasia can give important insights into biological concepts: a perspective on juvenile myelomonocytic leukemia
    • Flotho, C., Kratz, C.P. & Niemeyer, C.M. (2007) How a rare pediatric neoplasia can give important insights into biological concepts: a perspective on juvenile myelomonocytic leukemia. Haematologica, 92, 1441-1446.
    • (2007) Haematologica , vol.92 , pp. 1441-1446
    • Flotho, C.1    Kratz, C.P.2    Niemeyer, C.M.3
  • 18
    • 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, A.C., Kantarjian, H., Talpaz, M., Cork, A., Freireich, E.J., Trujillo, J.M., Lee, M.S. & Stass, S.A. (1990) RAS mutations are rare events in Philadelphia chromosome-negative/bcr gene rearrangement-negative chronic myelogenous leukemia, but are prevalent in chronic myelomonocytic leukemia. Blood, 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    Trujillo, J.M.7    Lee, M.S.8    Stass, S.A.9
  • 20
    • 25844447519 scopus 로고    scopus 로고
    • JAK2 mutation 1849G>T is rare in acute leukemias but can be found in CMML, Philadelphia chromosome-negative CML, and megakaryocytic leukemia
    • Jelinek, J., Oki, Y., Gharibyan, V., Bueso-Ramos, C., Prchal, J.T., Verstovsek, S., Beran, M., Estey, E., Kantarjian, H.M. & Issa, J.P. (2005) JAK2 mutation 1849G>T is rare in acute leukemias but can be found in CMML, Philadelphia chromosome-negative CML, and megakaryocytic leukemia. Blood, 106, 3370-3373.
    • (2005) Blood , vol.106 , pp. 3370-3373
    • Jelinek, J.1    Oki, Y.2    Gharibyan, V.3    Bueso-Ramos, C.4    Prchal, J.T.5    Verstovsek, S.6    Beran, M.7    Estey, E.8    Kantarjian, H.M.9    Issa, J.P.10
  • 21
    • 77953768742 scopus 로고    scopus 로고
    • Cbl and human myeloid neoplasms: the Cbl oncogene comes of age
    • Kales, S.C., Ryan, P.E., Nau, M.M. & Lipkowitz, S. (2010) Cbl and human myeloid neoplasms: the Cbl oncogene comes of age. Cancer Research, 70, 4789-4794.
    • (2010) Cancer Research , vol.70 , pp. 4789-4794
    • Kales, S.C.1    Ryan, P.E.2    Nau, M.M.3    Lipkowitz, S.4
  • 23
    • 43449083229 scopus 로고    scopus 로고
    • Recent advances in the pathogenesis and management of juvenile myelomonocytic leukaemia
    • Koike, K. & Matsuda, K. (2008) Recent advances in the pathogenesis and management of juvenile myelomonocytic leukaemia. British Journal of Haematology, 141, 567-575.
    • (2008) British Journal of Haematology , vol.141 , pp. 567-575
    • Koike, K.1    Matsuda, K.2
  • 25
    • 68749109365 scopus 로고    scopus 로고
    • RUNX1 mutations are frequent in chronic myelomonocytic leukemia and mutations at the C-terminal region might predict acute myeloid leukemia transformation
    • Kuo, M.C., Liang, D.C., Huang, C.F., Shih, Y.S., Wu, J.H., Lin, T.L. & Shih, L.Y. (2009) RUNX1 mutations are frequent in chronic myelomonocytic leukemia and mutations at the C-terminal region might predict acute myeloid leukemia transformation. Leukemia, 23, 1426-1431.
    • (2009) Leukemia , vol.23 , pp. 1426-1431
    • Kuo, M.C.1    Liang, D.C.2    Huang, C.F.3    Shih, Y.S.4    Wu, J.H.5    Lin, T.L.6    Shih, L.Y.7
  • 26
    • 33645280589 scopus 로고    scopus 로고
    • Inherited predispositions and hyperactive Ras in myeloid leukemogenesis
    • Lauchle, J.O., Braun, B.S., Loh, M.L. & Shannon, K. (2006) Inherited predispositions and hyperactive Ras in myeloid leukemogenesis. Pediatric Blood & Cancer, 46, 579-585.
    • (2006) Pediatric Blood & Cancer , vol.46 , pp. 579-585
    • Lauchle, J.O.1    Braun, B.S.2    Loh, M.L.3    Shannon, K.4
  • 37
    • 0026502986 scopus 로고
    • Monosomy 7 myeloproliferative disease in children with neurofibromatosis, type 1: epidemiology and molecular analysis
    • Shannon, K.M., Watterson, J., Johnson, P., O'Connell, P., Lange, B., Shah, N., Steinherz, P., Kan, Y.W. & Priest, J.R. (1992) Monosomy 7 myeloproliferative disease in children with neurofibromatosis, type 1: epidemiology and molecular analysis. Blood, 79, 1311-1318.
    • (1992) Blood , vol.79 , pp. 1311-1318
    • Shannon, K.M.1    Watterson, J.2    Johnson, P.3    O'Connell, P.4    Lange, B.5    Shah, N.6    Steinherz, P.7    Kan, Y.W.8    Priest, J.R.9
  • 40
    • 21344440357 scopus 로고    scopus 로고
    • The JAK2 V617F activating tyrosine kinase mutation is an infrequent event in both "atypical" myeloproliferative disorders and myelodysplastic syndromes
    • Steensma, D.P., Dewald, G.W., Lasho, T.L., Powell, H.L., McClure, R.F., Levine, R.L., Gilliland, D.G. & Tefferi, A. (2005) The JAK2 V617F activating tyrosine kinase mutation is an infrequent event in both "atypical" myeloproliferative disorders and myelodysplastic syndromes. Blood, 106, 1207-1209.
    • (2005) Blood , vol.106 , pp. 1207-1209
    • Steensma, D.P.1    Dewald, G.W.2    Lasho, T.L.3    Powell, H.L.4    McClure, R.F.5    Levine, R.L.6    Gilliland, D.G.7    Tefferi, A.8
  • 42
    • 33749325187 scopus 로고    scopus 로고
    • Refractory anemia with ringed sideroblasts associated with marked thrombocytosis (RARS-T), another myeloproliferative condition characterized by JAK2 V617F mutation
    • Szpurka, H., Tiu, R., Murugesan, G., Aboudola, S., Hsi, E.D., Theil, K.S., Sekeres, M.A. & Maciejewski, J.P. (2006) Refractory anemia with ringed sideroblasts associated with marked thrombocytosis (RARS-T), another myeloproliferative condition characterized by JAK2 V617F mutation. Blood, 108, 2173-2181.
    • (2006) Blood , vol.108 , pp. 2173-2181
    • Szpurka, H.1    Tiu, R.2    Murugesan, G.3    Aboudola, S.4    Hsi, E.D.5    Theil, K.S.6    Sekeres, M.A.7    Maciejewski, J.P.8
  • 45
    • 77954581139 scopus 로고    scopus 로고
    • Novel mutations and their functional and clinical relevance in myeloproliferative neoplasms: JAK2, MPL, TET2, ASXL1, CBL, IDH and IKZF1
    • Tefferi, A. (2010) Novel mutations and their functional and clinical relevance in myeloproliferative neoplasms: JAK2, MPL, TET2, ASXL1, CBL, IDH and IKZF1. Leukemia, 24, 1128-1138.
    • (2010) Leukemia , vol.24 , pp. 1128-1138
    • Tefferi, A.1
  • 46
    • 70149103800 scopus 로고    scopus 로고
    • Mutation in TET2 in myeloid cancers
    • author reply 1117-1118.
    • Tefferi, A., Lim, K.H. & Levine, R. (2009) Mutation in TET2 in myeloid cancers. New England Journal of Medicine, 361, 1117; author reply 1117-1118.
    • (2009) New England Journal of Medicine , vol.361 , pp. 1117
    • Tefferi, A.1    Lim, K.H.2    Levine, R.3
  • 47
    • 27144432878 scopus 로고    scopus 로고
    • JAK2 Val617Phe activating tyrosine kinase mutation in juvenile myelomonocytic leukemia
    • Tono, C., Xu, G., Toki, T., Takahashi, Y., Sasaki, S., Terui, K. & Ito, E. (2005) JAK2 Val617Phe activating tyrosine kinase mutation in juvenile myelomonocytic leukemia. Leukemia, 19, 1843-1844.
    • (2005) Leukemia , vol.19 , pp. 1843-1844
    • Tono, C.1    Xu, G.2    Toki, T.3    Takahashi, Y.4    Sasaki, S.5    Terui, K.6    Ito, E.7


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.