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Volumn 39, Issue 3, 2015, Pages 348-354

Mutational profiling of therapy-related myelodysplastic syndromes and acute myeloid leukemia by next generation sequencing, a comparison with de novo diseases

Author keywords

AML; Karyotype; MDS; Next generation sequencing; Therapy related; TP53

Indexed keywords

APC PROTEIN; ATM PROTEIN; B RAF KINASE; CD135 ANTIGEN; CYCLIN DEPENDENT KINASE INHIBITOR 2A; DNA METHYLTRANSFERASE 3A; EPIDERMAL GROWTH FACTOR RECEPTOR; EPIDERMAL GROWTH FACTOR RECEPTOR 2; EPIDERMAL GROWTH FACTOR RECEPTOR 4; EXPORTIN 1; FIBROBLAST GROWTH FACTOR RECEPTOR 1; FIBROBLAST GROWTH FACTOR RECEPTOR 2; FIBROBLAST GROWTH FACTOR RECEPTOR 3; ISOCITRATE DEHYDROGENASE 1; ISOCITRATE DEHYDROGENASE 2; JANUS KINASE 2; JANUS KINASE 3; K RAS PROTEIN; NOTCH1 RECEPTOR; NUCLEOPHOSMIN; PLATELET DERIVED GROWTH FACTOR RECEPTOR; PROTEIN KINASE B; PROTEIN MLH1; PROTEIN TYROSINE KINASE; PROTEIN TYROSINE PHOSPHATASE SHP 2; SMAD4 PROTEIN; STEM CELL FACTOR RECEPTOR; TRANSCRIPTION FACTOR EZH2; UVOMORULIN; TUMOR PROTEIN;

EID: 84924080017     PISSN: 01452126     EISSN: 18735835     Source Type: Journal    
DOI: 10.1016/j.leukres.2014.12.006     Document Type: Article
Times cited : (108)

References (34)
  • 2
    • 77956870600 scopus 로고    scopus 로고
    • Promoter methylation of DAPK1, E-cadherin and thrombospondin-1 in de novo and therapy-related myeloid neoplasms
    • Greco M., D'Alo F., Scardocci A., Criscuolo M., Fabiani E., Guidi F., et al. Promoter methylation of DAPK1, E-cadherin and thrombospondin-1 in de novo and therapy-related myeloid neoplasms. Blood Cells, Mol, Dis 2010, 45:181-185.
    • (2010) Blood Cells, Mol, Dis , vol.45 , pp. 181-185
    • Greco, M.1    D'Alo, F.2    Scardocci, A.3    Criscuolo, M.4    Fabiani, E.5    Guidi, F.6
  • 5
    • 0038305924 scopus 로고    scopus 로고
    • Clinical-cytogenetic associations in 306 patients with therapy-related myelodysplasia and myeloid leukemia: the University of Chicago series
    • Smith S.M., Le Beau M.M., Huo D., Karrison T., Sobecks R.M., Anastasi J., et al. Clinical-cytogenetic associations in 306 patients with therapy-related myelodysplasia and myeloid leukemia: the University of Chicago series. Blood 2003, 102:43-52.
    • (2003) Blood , vol.102 , pp. 43-52
    • Smith, S.M.1    Le Beau, M.M.2    Huo, D.3    Karrison, T.4    Sobecks, R.M.5    Anastasi, J.6
  • 6
    • 84856553821 scopus 로고    scopus 로고
    • Therapy-related myeloid neoplasms following fludarabine, cyclophosphamide, and rituximab (FCR) treatment in patients with chronic lymphocytic leukemia/small lymphocytic lymphoma
    • Zhou Y., Tang G., Medeiros L.J., McDonnell T.J., Keating M.J., Wierda W.G., et al. Therapy-related myeloid neoplasms following fludarabine, cyclophosphamide, and rituximab (FCR) treatment in patients with chronic lymphocytic leukemia/small lymphocytic lymphoma. Mod Pathol 2012, 25:237-245.
    • (2012) Mod Pathol , vol.25 , pp. 237-245
    • Zhou, Y.1    Tang, G.2    Medeiros, L.J.3    McDonnell, T.J.4    Keating, M.J.5    Wierda, W.G.6
  • 7
    • 84891870816 scopus 로고    scopus 로고
    • Application of the International Prognostic Scoring System-Revised in therapy-related myelodysplastic syndromes and oligoblastic acute myeloid leukemia
    • Ok C.Y., Hasserjian R.P., Fox P.S., Stingo F., Zuo Z., Young K.H., et al. Application of the International Prognostic Scoring System-Revised in therapy-related myelodysplastic syndromes and oligoblastic acute myeloid leukemia. Leukemia 2014, 28:185-189.
    • (2014) Leukemia , vol.28 , pp. 185-189
    • Ok, C.Y.1    Hasserjian, R.P.2    Fox, P.S.3    Stingo, F.4    Zuo, Z.5    Young, K.H.6
  • 8
    • 84878900540 scopus 로고    scopus 로고
    • Clonal diversity of recurrently mutated genes in myelodysplastic syndromes
    • Walter M.J., Shen D., Shao J., Ding L., White B.S., Kandoth C., et al. Clonal diversity of recurrently mutated genes in myelodysplastic syndromes. Leukemia 2013, 27:1275-1282.
    • (2013) Leukemia , vol.27 , pp. 1275-1282
    • Walter, M.J.1    Shen, D.2    Shao, J.3    Ding, L.4    White, B.S.5    Kandoth, C.6
  • 9
    • 84878372012 scopus 로고    scopus 로고
    • Genomic and epigenomic landscapes of adult de novo acute myeloid leukemia
    • Cancer Genome Atlas Research Network Genomic and epigenomic landscapes of adult de novo acute myeloid leukemia. N Engl J Med 2013, 368:2059-2074.
    • (2013) N Engl J Med , vol.368 , pp. 2059-2074
  • 10
    • 84867806184 scopus 로고    scopus 로고
    • A novel hierarchical prognostic model of AML solely based on molecular mutations
    • Grossmann V., Schnittger S., Kohlmann A., Eder C., Roller A., Dicker F., et al. A novel hierarchical prognostic model of AML solely based on molecular mutations. Blood 2012, 120:2963-2972.
    • (2012) Blood , vol.120 , pp. 2963-2972
    • Grossmann, V.1    Schnittger, S.2    Kohlmann, A.3    Eder, C.4    Roller, A.5    Dicker, F.6
  • 11
    • 84863393263 scopus 로고    scopus 로고
    • Prognostic relevance of integrated genetic profiling in acute myeloid leukemia
    • Patel J.P., Gonen M., Figueroa M.E., Fernandez H., Sun Z., Racevskis J., et al. Prognostic relevance of integrated genetic profiling in acute myeloid leukemia. N Engl J Med 2012, 366:1079-1089.
    • (2012) N Engl J Med , vol.366 , pp. 1079-1089
    • Patel, J.P.1    Gonen, M.2    Figueroa, M.E.3    Fernandez, H.4    Sun, Z.5    Racevskis, J.6
  • 12
    • 84866749552 scopus 로고    scopus 로고
    • Validation of a prognostic model and the impact of mutations in patients with lower-risk myelodysplastic syndromes
    • Bejar R., Stevenson K.E., Caughey B.A., Abdel-Wahab O., Steensma D.P., Galili N., et al. Validation of a prognostic model and the impact of mutations in patients with lower-risk myelodysplastic syndromes. J Clin Oncol 2012, 30:3376-3382.
    • (2012) J Clin Oncol , vol.30 , pp. 3376-3382
    • Bejar, R.1    Stevenson, K.E.2    Caughey, B.A.3    Abdel-Wahab, O.4    Steensma, D.P.5    Galili, N.6
  • 13
    • 84878446656 scopus 로고    scopus 로고
    • Mutational analysis of therapy-related myelodysplastic syndromes and acute myelogenous leukemia
    • Shih A.H., Chung S.S., Dolezal E.K., Zhang S.J., Abdel-Wahab O.I., Park C.Y., et al. Mutational analysis of therapy-related myelodysplastic syndromes and acute myelogenous leukemia. Haematologica 2013, 98:908-912.
    • (2013) Haematologica , vol.98 , pp. 908-912
    • Shih, A.H.1    Chung, S.S.2    Dolezal, E.K.3    Zhang, S.J.4    Abdel-Wahab, O.I.5    Park, C.Y.6
  • 17
    • 84888069767 scopus 로고    scopus 로고
    • OncoSeek: a versatile annotation and reporting system for next generation sequencing-based clinical mutation analysis of cancer specimens. AMP 2012 Meeting Abstract
    • Abstract TT79
    • Routbort M., Handal B., Patel K.P., Singh R., Aldape K., Reddy N., et al. OncoSeek: a versatile annotation and reporting system for next generation sequencing-based clinical mutation analysis of cancer specimens. AMP 2012 Meeting Abstract. J Mol Diagn 2012, 14:637-748. Abstract TT79.
    • (2012) J Mol Diagn , vol.14 , pp. 637-748
    • Routbort, M.1    Handal, B.2    Patel, K.P.3    Singh, R.4    Aldape, K.5    Reddy, N.6
  • 18
    • 84895770396 scopus 로고    scopus 로고
    • Next-generation sequencing-based multigene mutational screening for acute myeloid leukemia using MiSeq: applicability for diagnostics and disease monitoring
    • Luthra R., Patel K.P., Reddy N.G., Haghshenas V., Routbort M.J., Harmon M.A., et al. Next-generation sequencing-based multigene mutational screening for acute myeloid leukemia using MiSeq: applicability for diagnostics and disease monitoring. Haematologica 2014, 99:465-473.
    • (2014) Haematologica , vol.99 , pp. 465-473
    • Luthra, R.1    Patel, K.P.2    Reddy, N.G.3    Haghshenas, V.4    Routbort, M.J.5    Harmon, M.A.6
  • 21
    • 0030897009 scopus 로고    scopus 로고
    • International scoring system for evaluating prognosis in myelodysplastic syndromes
    • Greenberg P., Cox C., LeBeau M.M., 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
    • 77955914238 scopus 로고    scopus 로고
    • Refinement of cytogenetic classification in acute myeloid leukemia: determination of prognostic significance of rare recurring chromosomal abnormalities among 5876 younger adult patients treated in the United Kingdom Medical Research Council trials
    • Grimwade D., Hills R.K., Moorman A.V., Walker H., Chatters S., Goldstone A.H., et al. Refinement of cytogenetic classification in acute myeloid leukemia: determination of prognostic significance of rare recurring chromosomal abnormalities among 5876 younger adult patients treated in the United Kingdom Medical Research Council trials. Blood 2010, 116:354-365.
    • (2010) Blood , vol.116 , pp. 354-365
    • Grimwade, D.1    Hills, R.K.2    Moorman, A.V.3    Walker, H.4    Chatters, S.5    Goldstone, A.H.6
  • 23
    • 84876129012 scopus 로고    scopus 로고
    • IDH1 and IDH2 mutations in therapy-related myelodysplastic syndrome and acute myeloid leukemia are associated with a normal karyotype and with der(1;7)(q10;p10)
    • Westman M.K., Pedersen-Bjergaard J., Andersen M.T., Andersen M.K. IDH1 and IDH2 mutations in therapy-related myelodysplastic syndrome and acute myeloid leukemia are associated with a normal karyotype and with der(1;7)(q10;p10). Leukemia 2013, 27:957-959.
    • (2013) Leukemia , vol.27 , pp. 957-959
    • Westman, M.K.1    Pedersen-Bjergaard, J.2    Andersen, M.T.3    Andersen, M.K.4
  • 24
    • 84893772765 scopus 로고    scopus 로고
    • Landscape of genetic lesions in 944 patients with myelodysplastic syndromes
    • Haferlach T., Nagata Y., Grossmann V., Okuno Y., Bacher U., Nagae G., et al. Landscape of genetic lesions in 944 patients with myelodysplastic syndromes. Leukemia 2014, 28:241-247.
    • (2014) Leukemia , vol.28 , pp. 241-247
    • Haferlach, T.1    Nagata, Y.2    Grossmann, V.3    Okuno, Y.4    Bacher, U.5    Nagae, G.6
  • 25
    • 84888219405 scopus 로고    scopus 로고
    • Clinical and biological implications of driver mutations in myelodysplastic syndromes
    • quiz 99
    • Papaemmanuil E., Gerstung M., Malcovati L., Tauro S., Gundem G., Van Loo P., et al. Clinical and biological implications of driver mutations in myelodysplastic syndromes. Blood 2013, 122:3616-3627. quiz 99.
    • (2013) Blood , vol.122 , pp. 3616-3627
    • Papaemmanuil, E.1    Gerstung, M.2    Malcovati, L.3    Tauro, S.4    Gundem, G.5    Van Loo, P.6
  • 26
    • 79960255863 scopus 로고    scopus 로고
    • Recurrent DNMT3A mutations in patients with myelodysplastic syndromes
    • Walter M.J., Ding L., Shen D., Shao J., Grillot M., McLellan M., et al. Recurrent DNMT3A mutations in patients with myelodysplastic syndromes. Leukemia 2011, 25:1153-1158.
    • (2011) Leukemia , vol.25 , pp. 1153-1158
    • Walter, M.J.1    Ding, L.2    Shen, D.3    Shao, J.4    Grillot, M.5    McLellan, M.6
  • 28
    • 84859856420 scopus 로고    scopus 로고
    • Frequency and prognostic impact of mutations in SRSF2, U2AF1, and ZRSR2 in patients with myelodysplastic syndromes
    • Thol F., Kade S., Schlarmann C., Loffeld P., Morgan M., Krauter J., et al. Frequency and prognostic impact of mutations in SRSF2, U2AF1, and ZRSR2 in patients with myelodysplastic syndromes. Blood 2012, 119:3578-3584.
    • (2012) Blood , vol.119 , pp. 3578-3584
    • Thol, F.1    Kade, S.2    Schlarmann, C.3    Loffeld, P.4    Morgan, M.5    Krauter, J.6
  • 29
    • 18344385476 scopus 로고    scopus 로고
    • Mutations in PTPN11, encoding the protein tyrosine phosphatase SHP-2, cause Noonan syndrome
    • Tartaglia M., Mehler E.L., Goldberg R., Zampino G., Brunner H.G., Kremer H., et al. Mutations in PTPN11, encoding the protein tyrosine phosphatase SHP-2, cause Noonan syndrome. Nat Genet 2001, 29:465-468.
    • (2001) Nat Genet , vol.29 , pp. 465-468
    • Tartaglia, M.1    Mehler, E.L.2    Goldberg, R.3    Zampino, G.4    Brunner, H.G.5    Kremer, H.6
  • 30
    • 34247518152 scopus 로고    scopus 로고
    • Mutations of the PTPN11 gene in therapy-related MDS and AML with rare balanced chromosome translocations
    • Christiansen D.H., Desta F., Andersen M.K., Pedersen-Bjergaard J. Mutations of the PTPN11 gene in therapy-related MDS and AML with rare balanced chromosome translocations. Genes, Chromosomes Cancer 2007, 46:517-521.
    • (2007) Genes, Chromosomes Cancer , vol.46 , pp. 517-521
    • Christiansen, D.H.1    Desta, F.2    Andersen, M.K.3    Pedersen-Bjergaard, J.4
  • 31
    • 79952092487 scopus 로고    scopus 로고
    • Molecular genetics of adult acute myeloid leukemia: prognostic and therapeutic implications
    • Marcucci G., Haferlach T., Dohner H. Molecular genetics of adult acute myeloid leukemia: prognostic and therapeutic implications. J Clin Oncol 2011, 29:475-486.
    • (2011) J Clin Oncol , vol.29 , pp. 475-486
    • Marcucci, G.1    Haferlach, T.2    Dohner, H.3
  • 32
    • 84872165619 scopus 로고    scopus 로고
    • Mutational landscape of AML with normal cytogenetics: biological and clinical implications
    • Martelli M.P., Sportoletti P., Tiacci E., Martelli M.F., Falini B. Mutational landscape of AML with normal cytogenetics: biological and clinical implications. Blood Rev 2013, 27:13-22.
    • (2013) Blood Rev , vol.27 , pp. 13-22
    • Martelli, M.P.1    Sportoletti, P.2    Tiacci, E.3    Martelli, M.F.4    Falini, B.5
  • 34
    • 84873381393 scopus 로고    scopus 로고
    • Patients with therapy-related myelodysplastic syndromes and acute myeloid leukemia share genetic features but can be separated by blast counts and cytogenetic risk profiles into prognostically relevant subgroups
    • Bacher U., Haferlach C., Alpermann T., Schnittger S., Kern W., Haferlach T. Patients with therapy-related myelodysplastic syndromes and acute myeloid leukemia share genetic features but can be separated by blast counts and cytogenetic risk profiles into prognostically relevant subgroups. Leuk Lymphoma 2013, 54:639-642.
    • (2013) Leuk Lymphoma , vol.54 , pp. 639-642
    • Bacher, U.1    Haferlach, C.2    Alpermann, T.3    Schnittger, S.4    Kern, W.5    Haferlach, T.6


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