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Volumn 54, Issue 4, 2013, Pages 867-870

Quantitative detection of IDH2 mutation for minimal residual disease monitoring in patients with acute myeloid leukemia and its comparison with mutations in NPM1 gene

Author keywords

[No Author keywords available]

Indexed keywords

CYTARABINE; DAUNORUBICIN; ISOCITRATE DEHYDROGENASE 2; MITOXANTRONE; NUCLEOPHOSMIN;

EID: 84879544462     PISSN: 10428194     EISSN: 10292403     Source Type: Journal    
DOI: 10.3109/10428194.2012.727414     Document Type: Letter
Times cited : (12)

References (15)
  • 1
    • 77954658823 scopus 로고    scopus 로고
    • IDH1 and IDH2 mutation studies in 1473 patients with chronic-, fi brotic-or blast-phase essential trombocythemia, polycythemia vera or myelofi brosis
    • Teff eri A, Lasho T L, Abdel-Wahab O, et al. IDH1 and IDH2 mutation studies in 1473 patients with chronic-, fi brotic-or blast-phase essential trombocythemia, polycythemia vera or myelofi brosis. Leukemia 2010; 24: 1302-1309.
    • (2010) Leukemia , vol.24 , pp. 1302-1309
    • Tefferi, A.1    Lasho, T.L.2    Abdel-Wahab, O.3
  • 2
    • 77957806536 scopus 로고    scopus 로고
    • IDH1 mutations in patients with myelodysplastic syndromes are associated with an unfavorable prognosis
    • Th ol F, Weissinger EM, Krauter J, et al. IDH1 mutations in patients with myelodysplastic syndromes are associated with an unfavorable prognosis. Haematologica 2010; 95: 1668-1674.
    • (2010) Haematologica , vol.95 , pp. 1668-1674
    • Thol, F.1    Weissinger, E.M.2    Krauter, J.3
  • 3
    • 70149093912 scopus 로고    scopus 로고
    • Recurring mutations found by sequencing an acute myeloid leukemia genome
    • Mardis D, Ding L, Dooling DJ, et al. Recurring mutations found by sequencing an acute myeloid leukemia genome. N Engl J Med 2009; 361: 1058-1066.
    • (2009) N Engl J Med , vol.361 , pp. 1058-1066
    • Mardis, D.1    Ding, L.2    Dooling, D.J.3
  • 4
    • 77955907891 scopus 로고    scopus 로고
    • IDH1 and IDH2 mutations are frequent genetic alterations in acute myeloid leukemia and confer adverse prognosis in cytogenetically normal acute myeloid leukemia with NPM1 mutation without FLT3 internal tandem duplication
    • Paschka P, Schlenk RF, Gaidzik VI, et al. IDH1 and IDH2 mutations are frequent genetic alterations in acute myeloid leukemia and confer adverse prognosis in cytogenetically normal acute myeloid leukemia with NPM1 mutation without FLT3 internal tandem duplication. J Clin Oncol 2010; 28: 3636-3643.
    • (2010) J Clin Oncol , vol.28 , pp. 3636-3643
    • Paschka, P.1    Schlenk, R.F.2    Gaidzik, V.I.3
  • 5
    • 77149134353 scopus 로고    scopus 로고
    • Cancer-associated metabolite 2-hydroxyglutarate accumulates in acute myelogenous leukemia with isocitrate dehydrogenase 1 and 2 mutations
    • Gross S, Cairns RA, Minden MR, et al. Cancer-associated metabolite 2-hydroxyglutarate accumulates in acute myelogenous leukemia with isocitrate dehydrogenase 1 and 2 mutations. J Exp Med 2010; 207: 339-344.
    • (2010) J Exp Med , vol.207 , pp. 339-344
    • Gross, S.1    Cairns, R.A.2    Minden, M.R.3
  • 6
    • 77649305610 scopus 로고    scopus 로고
    • The common feature of leukemiaassociated IDH1 and IDH2 mutations is a neomorphic enzyme activity converting 〈 ketoglutarate to 2-hydroxyglutarate
    • Ward PS, Patel J, Wise DR, et al. The common feature of leukemiaassociated IDH1 and IDH2 mutations is a neomorphic enzyme activity converting 〈 -ketoglutarate to 2-hydroxyglutarate. Cancer Cell 2010; 17: 225-234.
    • (2010) Cancer Cell , vol.17 , pp. 225-234
    • Ward, P.S.1    Patel, J.2    Wise, D.R.3
  • 7
    • 84857997263 scopus 로고    scopus 로고
    • IDH mutations in primary myelofi brosis predict leukemic transformation and shortened survival: Clinical evidence for leukemogenic collaboration with JAK2V617F
    • Teff eri A, Jimma T, Sulai N H, et al. IDH mutations in primary myelofi brosis predict leukemic transformation and shortened survival: Clinical evidence for leukemogenic collaboration with JAK2V617F. Leukemia 2012; 26: 475-480.
    • (2012) Leukemia , vol.26 , pp. 475-480
    • Tefferi, A.1    Jimma, T.2    Sulai, N.H.3
  • 8
    • 77956050251 scopus 로고    scopus 로고
    • Prognostic impact of IDH2 mutations in cytogenetically normal acute myeloid leukemia
    • Th ol F, Damm F, Wagner K, et al. Prognostic impact of IDH2 mutations in cytogenetically normal acute myeloid leukemia. Blood 2010; 116: 614-616.
    • (2010) Blood , vol.116 , pp. 614-616
    • Thol, F.1    Damm, F.2    Wagner, K.3
  • 9
    • 79960534917 scopus 로고    scopus 로고
    • The prognostic signifi cance of IDH2 mutations in AML depends on the location of the mutation
    • Green CL, Evans CM, Zhao L, et al. The prognostic signifi cance of IDH2 mutations in AML depends on the location of the mutation. Blood 2011; 118: 409-412.
    • (2011) Blood , vol.118 , pp. 409-412
    • Green, C.L.1    Evans, C.M.2    Zhao, L.3
  • 10
    • 84857995946 scopus 로고    scopus 로고
    • Persistence of mutant isocitrate dehydrogenase in patients with acute myeloid leukemia in remission
    • Chou WC, Peng KY, Lei WC, et al. Persistence of mutant isocitrate dehydrogenase in patients with acute myeloid leukemia in remission. Leukemia 2011; 26: 527-529.
    • (2011) Leukemia , vol.26 , pp. 527-529
    • Chou, W.C.1    Peng, K.Y.2    Lei, W.C.3
  • 11
    • 78650036450 scopus 로고    scopus 로고
    • IDH2 mutations in patients with acute myeloid leukemia: Missense p.R140 mutations are linked to disease status
    • Jeziskova I, Razga F, Bajerova M, et al. IDH2 mutations in patients with acute myeloid leukemia: Missense p.R140 mutations are linked to disease status. Leuk Lymphoma 2010; 51: 2285-2287.
    • (2010) Leuk Lymphoma , vol.51 , pp. 2285-2287
    • Jeziskova, I.1    Razga, F.2    Bajerova, M.3
  • 12
    • 78649502291 scopus 로고    scopus 로고
    • Monitoring of minimal residual disease in acute myeloid leukemia with frequent and rare patient-specific NPM1 mutations
    • Dvorakova D, Racil Z, Jeziskova I, et al. Monitoring of minimal residual disease in acute myeloid leukemia with frequent and rare patient-specific NPM1 mutations. Am J Hematol 2010; 85: 926-929.
    • (2010) Am J Hematol , vol.85 , pp. 926-929
    • Dvorakova, D.1    Racil, Z.2    Jeziskova, I.3
  • 13
    • 0035057567 scopus 로고    scopus 로고
    • Determination of RhD zygosity: Comparison of a double amplifi cation refractory mutation system approach and a multiplex real-time quantitative PCR approach
    • Chiu RWK, Murphy MF, Fidler C, et al. Determination of RhD zygosity: Comparison of a double amplifi cation refractory mutation system approach and a multiplex real-time quantitative PCR approach. Clin Chem 2001; 47: 667-672.
    • (2001) Clin Chem , vol.47 , pp. 667-672
    • Chiu, R.W.K.1    Murphy, M.F.2    Fidler, C.3
  • 14
    • 77449159028 scopus 로고    scopus 로고
    • Diagnosis and management of acute myeloid leukemia in adults: Recommendations from an international expert panel, on behalf of the European LeukemiaNet
    • Dohner H, Estey EH, Amadori S, et al. Diagnosis and management of acute myeloid leukemia in adults: Recommendations from an international expert panel, on behalf of the European LeukemiaNet. Blood 2010; 115: 453-474.
    • (2010) Blood , vol.115 , pp. 453-474
    • Dohner, H.1    Estey, E.H.2    Amadori, S.3
  • 15
    • 78649990315 scopus 로고    scopus 로고
    • Cancer-associated IDH mutations: Biomarker and therapeutic opportunities
    • Yen K E, Bittinger M A, S u S M, et al. Cancer-associated IDH mutations: Biomarker and therapeutic opportunities. Oncogene 2010; 29: 6409-6417.
    • (2010) Oncogene , vol.29 , pp. 6409-6417
    • Yen, K.E.1    Bittinger, M.A.2    Su, S.M.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.