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Volumn 118, Issue 11, 2012, Pages 2879-2888

Myeloid neoplasms with isolated isochromosome 17q represent a clinicopathologic entity associated with myelodysplastic/myeloproliferative features, a high risk of leukemic transformation, and wild-type TP53

Author keywords

blast transformation; isochromosome 17q; myelodysplastic; myeloid neoplasm; myeloproliferative; wild type TP53

Indexed keywords

ANTINEOPLASTIC AGENT; FLT3 LIGAND; JANUS KINASE 2; PROTEIN P53;

EID: 84861337785     PISSN: 0008543X     EISSN: 10970142     Source Type: Journal    
DOI: 10.1002/cncr.26537     Document Type: Article
Times cited : (62)

References (37)
  • 1
    • 0032870994 scopus 로고    scopus 로고
    • Isolated isochromosome 17q: A distinct type of mixed myeloproliferative disorder/myelodysplastic syndrome with an aggressive clinical course
    • McClure RF, Dewald GW, Hoyer JD, Hanson CA,. Isolated isochromosome 17q: a distinct type of mixed myeloproliferative disorder/myelodysplastic syndrome with an aggressive clinical course. Br J Haematol. 1999; 106: 445-454.
    • (1999) Br J Haematol , vol.106 , pp. 445-454
    • McClure, R.F.1    Dewald, G.W.2    Hoyer, J.D.3    Hanson, C.A.4
  • 2
    • 0018178963 scopus 로고
    • Relation among occupational exposure to potential mutagenic/carcinogenic agents, clinical findings, and bone marrow chromosomes in acute nonlymphocytic leukemia
    • Mitelman F, Brandt L, Nilsson PG,. Relation among occupational exposure to potential mutagenic/carcinogenic agents, clinical findings, and bone marrow chromosomes in acute nonlymphocytic leukemia. Blood. 1978; 52: 1229-1237.
    • (1978) Blood , vol.52 , pp. 1229-1237
    • Mitelman, F.1    Brandt, L.2    Nilsson, P.G.3
  • 3
    • 0018233126 scopus 로고
    • Chromosome studies in preleukemic states. IV. Myeloproliferative versus cytopenic disorders
    • Nowell P, Finan J,. Chromosome studies in preleukemic states. IV. Myeloproliferative versus cytopenic disorders. Cancer. 1978; 42: 2254-2261.
    • (1978) Cancer , vol.42 , pp. 2254-2261
    • Nowell, P.1    Finan, J.2
  • 4
    • 0018637403 scopus 로고
    • Isochromosome 17 in a patient with a myeloproliferative disorder terminating in eosinophilic leukemia
    • Lonnqvist B, Gahrton G, Eriksson P, Fribert K, Zech L,. Isochromosome 17 in a patient with a myeloproliferative disorder terminating in eosinophilic leukemia. Acta Med Scand. 1979; 206: 321-325.
    • (1979) Acta Med Scand , vol.206 , pp. 321-325
    • Lonnqvist, B.1    Gahrton, G.2    Eriksson, P.3    Fribert, K.4    Zech, L.5
  • 5
    • 0020407124 scopus 로고
    • Karyotype analysis in acute nonlymphocytic leukemia (ANLL): Comparison with ethnic group, age, morphology, and survival
    • Bernstein R, Pinto MR, Morcom G, et al. Karyotype analysis in acute nonlymphocytic leukemia (ANLL): comparison with ethnic group, age, morphology, and survival. Cancer Genet Cytogenet. 1982; 6: 187-199.
    • (1982) Cancer Genet Cytogenet , vol.6 , pp. 187-199
    • Bernstein, R.1    Pinto, M.R.2    Morcom, G.3
  • 6
    • 0021344857 scopus 로고
    • Chromosome patterns in 26 South African children with acute nonlymphocytic leukemia (ANLL)
    • Bernstein R, MacDougall LG, Pinto MR,. Chromosome patterns in 26 South African children with acute nonlymphocytic leukemia (ANLL). Cancer Genet Cytogenet. 1984; 11: 199-214.
    • (1984) Cancer Genet Cytogenet , vol.11 , pp. 199-214
    • Bernstein, R.1    MacDougall, L.G.2    Pinto, M.R.3
  • 7
    • 0023077363 scopus 로고
    • Isochromosome 17q in a patient with acute myeloblastic leukemia
    • Peetre C, Nilsson PG, Mitelman F,. Isochromosome 17q in a patient with acute myeloblastic leukemia. Cancer Genet Cytogenet. 1987; 24: 315-318.
    • (1987) Cancer Genet Cytogenet , vol.24 , pp. 315-318
    • Peetre, C.1    Nilsson, P.G.2    Mitelman, F.3
  • 8
    • 0023079136 scopus 로고
    • Isochromosome 17q in a case of myelofibrosis with myeloid metaplasia terminating in blastic transformation
    • Nakamura H, Sadamori N, Yamada Y, et al. Isochromosome 17q in a case of myelofibrosis with myeloid metaplasia terminating in blastic transformation. Cancer Genet Cytogenet. 1987; 24: 221-224.
    • (1987) Cancer Genet Cytogenet , vol.24 , pp. 221-224
    • Nakamura, H.1    Sadamori, N.2    Yamada, Y.3
  • 10
    • 0026096185 scopus 로고
    • P53 gene mutations in acute myeloid leukemia with 17p monosomy
    • Fenaux P, Jonveaux P, Quiquandon I, et al. p53 gene mutations in acute myeloid leukemia with 17p monosomy. Blood. 1991; 78: 1652-1657.
    • (1991) Blood , vol.78 , pp. 1652-1657
    • Fenaux, P.1    Jonveaux, P.2    Quiquandon, I.3
  • 11
    • 0027248108 scopus 로고
    • GSCF gene is expressed but not rearranged in a patient with isochromosome 17q positive acute nonlymphocytic leukemia
    • Fiedler W, Weh HJ, Hegawisch-Becker S, Hossfeld DK,. GSCF gene is expressed but not rearranged in a patient with isochromosome 17q positive acute nonlymphocytic leukemia. Cancer Genet Cytogenet. 1993; 68: 49-51.
    • (1993) Cancer Genet Cytogenet , vol.68 , pp. 49-51
    • Fiedler, W.1    Weh, H.J.2    Hegawisch-Becker, S.3    Hossfeld, D.K.4
  • 13
    • 35148884159 scopus 로고    scopus 로고
    • Exacerbation of acute leukemia bearing isolated i(17q) along with proliferation of blasts with high BMI-1 expression [in Japanese]
    • Mihara K, Kido M, Nakaju N, et al. Exacerbation of acute leukemia bearing isolated i(17q) along with proliferation of blasts with high BMI-1 expression [in Japanese]. Rinsho Ketsueki. 2007; 48: 659-663.
    • (2007) Rinsho Ketsueki , vol.48 , pp. 659-663
    • Mihara, K.1    Kido, M.2    Nakaju, N.3
  • 14
    • 42749096040 scopus 로고    scopus 로고
    • Isochromosome i(17q) as a sole cytogenetic abnormality in a case of leukemic transformation from myelodysplastic syndrome (MDS)/myeloproliferative diseases (MPD)
    • Nishida H, Ueno H, Park JW, Yano T,. Isochromosome i(17q) as a sole cytogenetic abnormality in a case of leukemic transformation from myelodysplastic syndrome (MDS)/myeloproliferative diseases (MPD). Leuk Res. 2008; 32: 1325-1327.
    • (2008) Leuk Res , vol.32 , pp. 1325-1327
    • Nishida, H.1    Ueno, H.2    Park, J.W.3    Yano, T.4
  • 15
    • 0021924742 scopus 로고
    • Isochromosome 17q in Ph-negative chronic myelocytic leukemia
    • Goh K, Rubins J,. Isochromosome 17q in Ph-negative chronic myelocytic leukemia. Cancer Genet Cytogenet. 1985; 14: 323-330.
    • (1985) Cancer Genet Cytogenet , vol.14 , pp. 323-330
    • Goh, K.1    Rubins, J.2
  • 16
    • 0027189863 scopus 로고
    • Analysis of the p53 gene in patients with isochromosome 17q and Ph-positive or -negative myeloid leukemia
    • Schutte J, Opalka B, Becher R, et al. Analysis of the p53 gene in patients with isochromosome 17q and Ph-positive or -negative myeloid leukemia. Leuk Res. 1993; 17: 533-539.
    • (1993) Leuk Res , vol.17 , pp. 533-539
    • Schutte, J.1    Opalka, B.2    Becher, R.3
  • 17
    • 57649119892 scopus 로고    scopus 로고
    • Cytogenetic abnormalities in a series of 1029 patients with primary myelodysplastic syndromes. A report from the US with a focus on some undefined single chromosomal abnormalities
    • Pozdnyakova O, Miron PM, Tang G, et al. Cytogenetic abnormalities in a series of 1029 patients with primary myelodysplastic syndromes. A report from the US with a focus on some undefined single chromosomal abnormalities. Cancer. 2008; 113: 3331-3340.
    • (2008) Cancer , vol.113 , pp. 3331-3340
    • Pozdnyakova, O.1    Miron, P.M.2    Tang, G.3
  • 18
    • 0025129559 scopus 로고
    • Acute nonlymphocytic leukemia (ANLL) with isochromosome i(17q) as the sole chromosomal anomaly: A distinct entity?
    • Weh HJ, Kuse R, Hossfeld DK,. Acute nonlymphocytic leukemia (ANLL) with isochromosome i(17q) as the sole chromosomal anomaly: a distinct entity? Eur J Haematol. 1990; 44: 312-314.
    • (1990) Eur J Haematol , vol.44 , pp. 312-314
    • Weh, H.J.1    Kuse, R.2    Hossfeld, D.K.3
  • 19
    • 0025194137 scopus 로고
    • Isochromosome 17q in Ph-negative leukemia: A clinical cytogenetic, and molecular study
    • Becher R, Carbonell F, Bartram CR,. Isochromosome 17q in Ph-negative leukemia: a clinical cytogenetic, and molecular study. Blood. 1990; 75: 1679-1683.
    • (1990) Blood , vol.75 , pp. 1679-1683
    • Becher, R.1    Carbonell, F.2    Bartram, C.R.3
  • 20
    • 0027303276 scopus 로고
    • Isochromosome 17q as a sole anomaly: A distinct myelodysplastic syndrome entity?
    • Sole F, Torrabadella M, Granada I, et al. Isochromosome 17q as a sole anomaly: a distinct myelodysplastic syndrome entity? Leuk Res. 1993; 17: 717-720.
    • (1993) Leuk Res , vol.17 , pp. 717-720
    • Sole, F.1    Torrabadella, M.2    Granada, I.3
  • 21
    • 0038125956 scopus 로고    scopus 로고
    • Isochromosome 17q in patients with myelodysplastic syndromes: 6 new cases
    • Xiao Z, Liu S, Yu M, Xu Z, Hao Y,. Isochromosome 17q in patients with myelodysplastic syndromes: 6 new cases. Haematologica. 2003; 88: 714-715.
    • (2003) Haematologica , vol.88 , pp. 714-715
    • Xiao, Z.1    Liu, S.2    Yu, M.3    Xu, Z.4    Hao, Y.5
  • 22
    • 0345299213 scopus 로고    scopus 로고
    • Isochromosome 17q in blast crisis of chronic myeloid leukemia and in other hematologic malignancies is the result of clustered breakpoints in 17p11 and is not associated with coding TP13 mutation
    • Fioretos T, Strombeck B, Sandberg T, et al. Isochromosome 17q in blast crisis of chronic myeloid leukemia and in other hematologic malignancies is the result of clustered breakpoints in 17p11 and is not associated with coding TP13 mutation. Blood. 1999; 94: 225-232.
    • (1999) Blood , vol.94 , pp. 225-232
    • Fioretos, T.1    Strombeck, B.2    Sandberg, T.3
  • 23
    • 61349104536 scopus 로고    scopus 로고
    • Introduction and overview of the classification of the myeloid neoplasms
    • Swerdlow S.H. Campo E. Harris N.L. et al, eds. Lyon, France: IARC.
    • Vardiman JW, Porwit A, Brunning RD, et al. Introduction and overview of the classification of the myeloid neoplasms. In:, Swerdlow SH, Campo E, Harris NL, et al, eds. WHO Classification of Tumours of Haematopoietic and Lymphoid Tissues. Lyon, France: IARC; 2008: 18-30.
    • (2008) WHO Classification of Tumours of Haematopoietic and Lymphoid Tissues , pp. 18-30
    • Vardiman, J.W.1    Porwit, A.2    Brunning, R.D.3
  • 25
    • 77952952862 scopus 로고    scopus 로고
    • Quantification of fibrosis and osteosclerosis in myeloproliferative neoplasms: A computer-assisted image study
    • Teman CJ, Wilson AR, Perkins SL, Hickman K, Prchal JT, Salama ME,. Quantification of fibrosis and osteosclerosis in myeloproliferative neoplasms: a computer-assisted image study. Leuk Res. 2010; 34: 871-876.
    • (2010) Leuk Res , vol.34 , pp. 871-876
    • Teman, C.J.1    Wilson, A.R.2    Perkins, S.L.3    Hickman, K.4    Prchal, J.T.5    Salama, M.E.6
  • 26
    • 15744381871 scopus 로고    scopus 로고
    • Chronic lymphocytic leukemia/small lymphocytic lymphoma associated with IgM paraprotein
    • Yin CC, Lin P, Carney DA, et al. Chronic lymphocytic leukemia/small lymphocytic lymphoma associated with IgM paraprotein. Am J Clin Pathol. 2005; 123: 594-602.
    • (2005) Am J Clin Pathol , vol.123 , pp. 594-602
    • Yin, C.C.1    Lin, P.2    Carney, D.A.3
  • 27
    • 77649274289 scopus 로고    scopus 로고
    • HDM4 is overexpressed in mantle cell lymphoma and its inhibition induces p21 expression and apoptosis
    • Liang M, Han X, Vadhan-Rai S, et al. HDM4 is overexpressed in mantle cell lymphoma and its inhibition induces p21 expression and apoptosis. Mod Pathol. 2010; 23: 381-391.
    • (2010) Mod Pathol , vol.23 , pp. 381-391
    • Liang, M.1    Han, X.2    Vadhan-Rai, S.3
  • 28
    • 0027670412 scopus 로고
    • Frequent p53 overexpression in therapy related myelodysplastic syndromes and acute myeloid leukemias: An immunohistochemical study of bone marrow biopsies
    • Orazi A, Cattoretti G, Heerema NA, Sozzi G, John K, Neiman RS,. Frequent p53 overexpression in therapy related myelodysplastic syndromes and acute myeloid leukemias: an immunohistochemical study of bone marrow biopsies. Mod Pathol. 1993; 6: 521-525.
    • (1993) Mod Pathol , vol.6 , pp. 521-525
    • Orazi, A.1    Cattoretti, G.2    Heerema, N.A.3    Sozzi, G.4    John, K.5    Neiman, R.S.6
  • 29
    • 2442702517 scopus 로고    scopus 로고
    • TaqMan RT-PCR assay coupled with capillary electrophoresis for quantification and identification of bcr-abl transcript type
    • Luthra R, Sanchez-Vega B, Medeiros LJ,. TaqMan RT-PCR assay coupled with capillary electrophoresis for quantification and identification of bcr-abl transcript type. Mod Pathol. 2004; 17: 96-103.
    • (2004) Mod Pathol , vol.17 , pp. 96-103
    • Luthra, R.1    Sanchez-Vega, B.2    Medeiros, L.J.3
  • 30
    • 74749101243 scopus 로고    scopus 로고
    • Distinct patterns of cytogenetic and clinical progression in chronic myeloproliferative neoplasms with or without JAK2 or MPL mutations
    • Millecker L, Lennon PA, Verstovsek S, et al. Distinct patterns of cytogenetic and clinical progression in chronic myeloproliferative neoplasms with or without JAK2 or MPL mutations. Cancer Genet Cytogenet. 2010; 197: 1-7.
    • (2010) Cancer Genet Cytogenet , vol.197 , pp. 1-7
    • Millecker, L.1    Lennon, P.A.2    Verstovsek, S.3
  • 31
    • 75149119465 scopus 로고    scopus 로고
    • Modeling interactions between leukemia-specific chromosomal changes, somatic mutations, and gene expression patterns during progression of core-binding factor leukemias
    • Jones D, Yao H, Ramans A, et al. Modeling interactions between leukemia-specific chromosomal changes, somatic mutations, and gene expression patterns during progression of core-binding factor leukemias. Genes Chromosomes Cancer. 2010; 49: 182-191.
    • (2010) Genes Chromosomes Cancer , vol.49 , pp. 182-191
    • Jones, D.1    Yao, H.2    Ramans, A.3
  • 32
    • 72249099452 scopus 로고    scopus 로고
    • Cuplike nuclei (prominent nuclear invaginations) in acute myeloid leukemia are highly associated with FLT3 internal tandem duplication and NPM1 mutation
    • Chen W, Konoplev S, Medeiros LJ, et al. Cuplike nuclei (prominent nuclear invaginations) in acute myeloid leukemia are highly associated with FLT3 internal tandem duplication and NPM1 mutation. Cancer. 2009; 115: 5481-5489.
    • (2009) Cancer , vol.115 , pp. 5481-5489
    • Chen, W.1    Konoplev, S.2    Medeiros, L.J.3
  • 33
    • 0035168677 scopus 로고    scopus 로고
    • Prevalence and prognostic significance of flt3 internal tandem duplication in pediatric acute myeloid leukemia
    • Meshinchi S, Woods WG, Stirewalt DL, et al. Prevalence and prognostic significance of flt3 internal tandem duplication in pediatric acute myeloid leukemia. Blood. 2001; 97: 89-94.
    • (2001) Blood , vol.97 , pp. 89-94
    • Meshinchi, S.1    Woods, W.G.2    Stirewalt, D.L.3
  • 34
    • 0035871889 scopus 로고    scopus 로고
    • Activating mutation of D835 within the activation loop of flt3 in human hematologic malignancies
    • Yamamoto Y, Kiyoi H, Nakano Y, et al. Activating mutation of D835 within the activation loop of flt3 in human hematologic malignancies. Blood. 2001; 97: 2434-2439.
    • (2001) Blood , vol.97 , pp. 2434-2439
    • Yamamoto, Y.1    Kiyoi, H.2    Nakano, Y.3
  • 35
    • 0023838764 scopus 로고
    • Localization of the human G-CSF gene to the region of a breakpoint in the translocation typical of acute promyelocytic leukemia
    • Simmers RN, Smith J, Shannon MF, et al. Localization of the human G-CSF gene to the region of a breakpoint in the translocation typical of acute promyelocytic leukemia. Hum Genet. 1988; 78: 134-136.
    • (1988) Hum Genet , vol.78 , pp. 134-136
    • Simmers, R.N.1    Smith, J.2    Shannon, M.F.3
  • 36
    • 0023640343 scopus 로고
    • The localization of the human myeloperoxydase gene is in close proximity to the translocation breakpoint in acute promyelocytic leukemia
    • Chang KS, Schroeder W, Siciliano MD, et al. The localization of the human myeloperoxydase gene is in close proximity to the translocation breakpoint in acute promyelocytic leukemia. Leukemia. 1987; 1: 458-462.
    • (1987) Leukemia , vol.1 , pp. 458-462
    • Chang, K.S.1    Schroeder, W.2    Siciliano, M.D.3


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