메뉴 건너뛰기




Volumn 102, Issue 8, 2003, Pages 3010-3015

Formation of trisomies and their parental origin in hyperdiploid childhood acute lymphoblastic leukemia

Author keywords

[No Author keywords available]

Indexed keywords

ACUTE LYMPHOBLASTIC LEUKEMIA; ADOLESCENT; ALLELISM; ARTICLE; CELL DIVISION; CHILDHOOD LEUKEMIA; CHROMOSOME DUPLICATION; CHROMOSOME MAP; CLINICAL ARTICLE; DIPLOIDY; FEMALE; GENE DOSAGE; HUMAN; MALE; MITOSIS; PRESCHOOL CHILD; PRIORITY JOURNAL; PROGNOSIS; SCHOOL CHILD; TETRASOMY; TRISOMY; TRISOMY 8;

EID: 0141992996     PISSN: 00064971     EISSN: None     Source Type: Journal    
DOI: 10.1182/blood-2003-05-1444     Document Type: Article
Times cited : (43)

References (41)
  • 1
    • 0034518313 scopus 로고    scopus 로고
    • Acute lymphoblastic leukemia in children
    • Pui C-H. Acute lymphoblastic leukemia in children. Curr Opin Oncol. 2000;12:3-12.
    • (2000) Curr Opin Oncol , vol.12 , pp. 3-12
    • Pui, C.-H.1
  • 2
    • 0033948647 scopus 로고    scopus 로고
    • Cytogenetic and FISH studies of a single center consecutive series of 152 childhood acute lymphoblastic leukemias
    • Andreasson P, Höglund M, Békássy AN, et al. Cytogenetic and FISH studies of a single center consecutive series of 152 childhood acute lymphoblastic leukemias. Eur J Haematol. 2000;65: 40-51.
    • (2000) Eur J Haematol , vol.65 , pp. 40-51
    • Andreasson, P.1    Höglund, M.2    Békássy, A.N.3
  • 3
    • 0030294909 scopus 로고    scopus 로고
    • Dichotomy of hyperdiploid acute lymphoblastic leukemia on the basis of the distribution of gained chromosomes
    • Mertens F, Johansson B, Mitelman F. Dichotomy of hyperdiploid acute lymphoblastic leukemia on the basis of the distribution of gained chromosomes. Cancer Genet Cytogenet. 1996;92:8-10.
    • (1996) Cancer Genet Cytogenet , vol.92 , pp. 8-10
    • Mertens, F.1    Johansson, B.2    Mitelman, F.3
  • 4
    • 0033889681 scopus 로고    scopus 로고
    • Prognostic impact of karyotypic findings in childhood acute lymphoblastic leukaemia: A Nordic series comparing two treatment periods
    • Forestier E, Johansson B, Gustafsson G, et al. Prognostic impact of karyotypic findings in childhood acute lymphoblastic leukaemia: a Nordic series comparing two treatment periods. Br J Haematol. 2000;110:147-153.
    • (2000) Br J Haematol , vol.110 , pp. 147-153
    • Forestier, E.1    Johansson, B.2    Gustafsson, G.3
  • 5
    • 0004783768 scopus 로고    scopus 로고
    • Cytogenetic findings in a population-based series of 787 childhood acute lymphoblastic leukemias from the Nordic countries
    • Forestier E, Johansson B, Borgström G, Kerndrup G, Johansson J, Heim S. Cytogenetic findings in a population-based series of 787 childhood acute lymphoblastic leukemias from the Nordic countries. Eur J Haematol. 2000;64:194-200.
    • (2000) Eur J Haematol , vol.64 , pp. 194-200
    • Forestier, E.1    Johansson, B.2    Borgström, G.3    Kerndrup, G.4    Johansson, J.5    Heim, S.6
  • 7
    • 0030038426 scopus 로고    scopus 로고
    • Stroma-supported culture in childhood B-lineage acute lymphoblastic leukemia cells predicts treatment outcome
    • Kumagai M-a, Manabe A, Pui C-H, et al. Stroma-supported culture in childhood B-lineage acute lymphoblastic leukemia cells predicts treatment outcome. J Clin Invest. 1996;97:755-760.
    • (1996) J Clin Invest , vol.97 , pp. 755-760
    • Kumagai, M.-A.1    Manabe, A.2    Pui, C.-H.3
  • 8
    • 0344718439 scopus 로고    scopus 로고
    • Hyperdiploid acute lymphoblastic leukemia with 51 to 65 chromosomes: A distinct biological entity with a marked propensity to undergo apoptosis
    • Ito C, Kumagai M-a, Manabe A, et al. Hyperdiploid acute lymphoblastic leukemia with 51 to 65 chromosomes: a distinct biological entity with a marked propensity to undergo apoptosis. Blood. 1999;93:315-320.
    • (1999) Blood , vol.93 , pp. 315-320
    • Ito, C.1    Kumagai, M.-A.2    Manabe, A.3
  • 9
    • 0036221447 scopus 로고    scopus 로고
    • Increased incidence of spontaneous apoptosis in the bone marrow of hyperdiploid childhood acute lymphoblastic leukemia
    • Zhang Y, Lu J, van den Berghe J, Lee S-H. Increased incidence of spontaneous apoptosis in the bone marrow of hyperdiploid childhood acute lymphoblastic leukemia. Exp Hematol. 2002;30: 333-339.
    • (2002) Exp Hematol , vol.30 , pp. 333-339
    • Zhang, Y.1    Lu, J.2    Van den Berghe, J.3    Lee, S.-H.4
  • 10
    • 0023874363 scopus 로고
    • Correlation of karyotype and immunophenotype in childhood acute lymphoblastic leukemia
    • Pui C-H, Williams DL, Roberson PK, et al. Correlation of karyotype and immunophenotype in childhood acute lymphoblastic leukemia. J Clin Oncol. 1988;6:56-61.
    • (1988) J Clin Oncol , vol.6 , pp. 56-61
    • Pui, C.-H.1    Williams, D.L.2    Roberson, P.K.3
  • 11
    • 0035839885 scopus 로고    scopus 로고
    • Chromosomal translocation master genes, mouse models and experimental therapeutics
    • Rabbitts TH. Chromosomal translocation master genes, mouse models and experimental therapeutics. Oncogene. 2001;20:5763-5777.
    • (2001) Oncogene , vol.20 , pp. 5763-5777
    • Rabbitts, T.H.1
  • 13
    • 0026489499 scopus 로고
    • Is cancer cytogenetics reducible to the molecular genetics of cancer cells?
    • Heim S. Is cancer cytogenetics reducible to the molecular genetics of cancer cells? Genes Chromosomes Cancer. 1992;5:188-196.
    • (1992) Genes Chromosomes Cancer , vol.5 , pp. 188-196
    • Heim, S.1
  • 14
    • 0037238483 scopus 로고    scopus 로고
    • Trisomy 8 as the sole chromosomal aberration in myelocytic malignancies: A multicolor and locus-specific fluorescence in situ hybridization study
    • Paulsson K, Fioretos T, Strömbeck B, Mauritzson N, Tanke HJ, Johansson B. Trisomy 8 as the sole chromosomal aberration in myelocytic malignancies: a multicolor and locus-specific fluorescence in situ hybridization study. Cancer Genet Cytogenet. 2003;140:66-69.
    • (2003) Cancer Genet Cytogenet , vol.140 , pp. 66-69
    • Paulsson, K.1    Fioretos, T.2    Strömbeck, B.3    Mauritzson, N.4    Tanke, H.J.5    Johansson, B.6
  • 15
    • 0022632366 scopus 로고
    • Somatic shift to homozygosity for a chromosomal polymorphism in a child with acute lymphoblastic leukemia
    • Stamberg J, Shende A, Lanzkowsky P. Somatic shift to homozygosity for a chromosomal polymorphism in a child with acute lymphoblastic leukemia. Blood. 1986;67:350-353.
    • (1986) Blood , vol.67 , pp. 350-353
    • Stamberg, J.1    Shende, A.2    Lanzkowsky, P.3
  • 16
    • 0026755913 scopus 로고
    • Hyperdiploidy arising from near-haploidy in childhood acute lymphoblastic leukemia
    • Onodera N, McCabe NR, Nachman JB, et al. Hyperdiploidy arising from near-haploidy in childhood acute lymphoblastic leukemia. Genes Chromosomes Cancer. 1992;4:331-336.
    • (1992) Genes Chromosomes Cancer , vol.4 , pp. 331-336
    • Onodera, N.1    McCabe, N.R.2    Nachman, J.B.3
  • 17
    • 0026748638 scopus 로고
    • Formation of a hyperdiploid karyotype in childhood acute lymphoblastic leukemia
    • Onodera N, McCabe NR, Rubin CM. Formation of a hyperdiploid karyotype in childhood acute lymphoblastic leukemia. Blood. 1992;80:203-208.
    • (1992) Blood , vol.80 , pp. 203-208
    • Onodera, N.1    McCabe, N.R.2    Rubin, C.M.3
  • 18
    • 0036659908 scopus 로고    scopus 로고
    • Nondysjunction of chromosomes leading to hyperdiploid childhood B-cell precursor acute lymphoblastic leukemia is an early event during leukemogenesis
    • Panzer-Grümayer ER, Fasching K, Panzer S, et al. Nondysjunction of chromosomes leading to hyperdiploid childhood B-cell precursor acute lymphoblastic leukemia is an early event during leukemogenesis. Blood. 2002;100:347-349.
    • (2002) Blood , vol.100 , pp. 347-349
    • Panzer-Grümayer, E.R.1    Fasching, K.2    Panzer, S.3
  • 19
    • 0029743779 scopus 로고    scopus 로고
    • Is genomic imprinting involved in the pathogenesis of hyperdiploid and haploid acute lymphoblastic leukemia of childhood?
    • Haas OA. Is genomic imprinting involved in the pathogenesis of hyperdiploid and haploid acute lymphoblastic leukemia of childhood? Acta Genet Med Gemellol (Roma). 1996;45:239-242.
    • (1996) Acta Genet Med Gemellol (Roma) , vol.45 , pp. 239-242
    • Haas, O.A.1
  • 20
    • 0031473005 scopus 로고    scopus 로고
    • Rapid detection of aneuploidies by microsatellite and the quantitative fluorescent polymerase chain reaction
    • Adinolfi M, Pertl B, Sherlock J. Rapid detection of aneuploidies by microsatellite and the quantitative fluorescent polymerase chain reaction. Prenat Diagn. 1997;17:1299-1311.
    • (1997) Prenat Diagn , vol.17 , pp. 1299-1311
    • Adinolfi, M.1    Pertl, B.2    Sherlock, J.3
  • 21
    • 0031689134 scopus 로고    scopus 로고
    • Comparative genomic hybridization in childhood acute lymphoblastic leukemia
    • Larramendy ML, Huhta T, Vettenranta K, et al. Comparative genomic hybridization in childhood acute lymphoblastic leukemia. Leukemia. 1998; 12:1638-1644.
    • (1998) Leukemia , vol.12 , pp. 1638-1644
    • Larramendy, M.L.1    Huhta, T.2    Vettenranta, K.3
  • 22
    • 0002440928 scopus 로고
    • Molecular Cloning
    • Cold Spring Harbor, NY. Cold Spring Harbor Laboratory Press
    • Sambrook J, Fritsch EF, Maniatis T. Molecular Cloning. A Laboratory Manual. Cold Spring Harbor, NY. Cold Spring Harbor Laboratory Press; 1989.
    • (1989) A Laboratory Manual
    • Sambrook, J.1    Fritsch, E.F.2    Maniatis, T.3
  • 23
    • 0036090234 scopus 로고    scopus 로고
    • Preferential loss of maternal 9p alleles in childhood acute lymphoblastic leukemia
    • Morison IM, Ellis LM, Teague LR, Reeve AE. Preferential loss of maternal 9p alleles in childhood acute lymphoblastic leukemia. Blood. 2002; 99:375-377.
    • (2002) Blood , vol.99 , pp. 375-377
    • Morison, I.M.1    Ellis, L.M.2    Teague, L.R.3    Reeve, A.E.4
  • 24
    • 0027323518 scopus 로고
    • Deletions of the short arm of chromosome 9, including the interferon-α/-β genes, in acute lymphocytic leukemia: Studies on loss of heterozygosity, parental origin of deleted genes and prognosis
    • Heyman M, Grander D, Bröndum-Nielsen K, Liu Y, Söderhäll S, Einhorn S. Deletions of the short arm of chromosome 9, including the interferon-α/-β genes, in acute lymphocytic leukemia: studies on loss of heterozygosity, parental origin of deleted genes and prognosis. Int J Cancer. 1993; 54:748-753.
    • (1993) Int J Cancer , vol.54 , pp. 748-753
    • Heyman, M.1    Grander, D.2    Bröndum-Nielsen, K.3    Liu, Y.4    Söderhäll, S.5    Einhorn, S.6
  • 25
    • 0026678490 scopus 로고
    • Methylation of HpaII and HhaI sites near the polymorphic CAG repeat in the human androgen-receptor gene correlates with X chromosome inactivation
    • Allen RC, Zoghbi HY, Moseley AB, Rosenblatt HM, Belmont JW. Methylation of HpaII and HhaI sites near the polymorphic CAG repeat in the human androgen-receptor gene correlates with X chromosome inactivation. Am J Hum Genet. 1992;51:1229-1239.
    • (1992) Am J Hum Genet , vol.51 , pp. 1229-1239
    • Allen, R.C.1    Zoghbi, H.Y.2    Moseley, A.B.3    Rosenblatt, H.M.4    Belmont, J.W.5
  • 26
    • 0036119091 scopus 로고    scopus 로고
    • Acquired skewing of Lyonization remains stable for a prolonged period in healthy blood donors
    • van Dijk JP, Heuver L, Stevens-Linders E, et al. Acquired skewing of Lyonization remains stable for a prolonged period in healthy blood donors. Leukemia. 2002;16:362-367.
    • (2002) Leukemia , vol.16 , pp. 362-367
    • Van Dijk, J.P.1    Heuver, L.2    Stevens-Linders, E.3
  • 28
    • 0029902171 scopus 로고    scopus 로고
    • Primary vs. secondary neoplasia-associated chromosomal abnormalities-balanced rearrangements vs. genomic imbalances?
    • Johansson B, Mertens F, Mitelman F. Primary vs. secondary neoplasia-associated chromosomal abnormalities-balanced rearrangements vs. genomic imbalances? Genes Chromosomes Cancer. 1996;16:155-163.
    • (1996) Genes Chromosomes Cancer , vol.16 , pp. 155-163
    • Johansson, B.1    Mertens, F.2    Mitelman, F.3
  • 29
    • 0034101453 scopus 로고    scopus 로고
    • Trisomy 4 leading to duplication of a mutated KIT allele in acute myeloid leukemia with mast cell involvement
    • Beghini A, Ripamonti CB, Castorina P, et al. Trisomy 4 leading to duplication of a mutated KIT allele in acute myeloid leukemia with mast cell involvement. Cancer Genet Cytogenet. 2000;119: 26-31.
    • (2000) Cancer Genet Cytogenet , vol.119 , pp. 26-31
    • Beghini, A.1    Ripamonti, C.B.2    Castorina, P.3
  • 30
    • 17344373892 scopus 로고    scopus 로고
    • Trisomy 7-harbouring non-random duplication of the mutant MET allele in hereditary papillary renal carcinomas
    • Zhuang Z, Park W-S, Pack S, et al. Trisomy 7-harbouring non-random duplication of the mutant MET allele in hereditary papillary renal carcinomas. Nat Genet. 1998;20:66-69.
    • (1998) Nat Genet , vol.20 , pp. 66-69
    • Zhuang, Z.1    Park, W.-S.2    Pack, S.3
  • 31
    • 19044399684 scopus 로고    scopus 로고
    • Classification, subtype discovery, and prediction of outcome in pediatric acute lymphoblastic leukemia by gene expression profiling
    • Yeoh E-J, Ross ME, Shurtleff SA, et al. Classification, subtype discovery, and prediction of outcome in pediatric acute lymphoblastic leukemia by gene expression profiling. Cancer Cell. 2002; 1:133-143.
    • (2002) Cancer Cell , vol.1 , pp. 133-143
    • Yeoh, E.-J.1    Ross, M.E.2    Shurtleff, S.A.3
  • 32
    • 0033541448 scopus 로고    scopus 로고
    • Genomic imprinting and cancer
    • Jirtle RL. Genomic imprinting and cancer. Exp Cell Res. 1999;248:18-24.
    • (1999) Exp Cell Res , vol.248 , pp. 18-24
    • Jirtle, R.L.1
  • 33
    • 0032076307 scopus 로고    scopus 로고
    • Imprinting in Prader-Willi and Angelman syndromes
    • Nicholls RD, Saitoh S, Horsthemke B. Imprinting in Prader-Willi and Angelman syndromes. Trends Genet. 1998;14:194-200.
    • (1998) Trends Genet , vol.14 , pp. 194-200
    • Nicholls, R.D.1    Saitoh, S.2    Horsthemke, B.3
  • 34
    • 0023256838 scopus 로고
    • Nonrandom loss of maternal chromosome 11 alleles in Wilms tumors
    • Schroeder WT, Chao L-Y, Dao DD, et al. Nonrandom loss of maternal chromosome 11 alleles in Wilms tumors, Am J Hum Genet. 1987;40:413-420.
    • (1987) Am J Hum Genet , vol.40 , pp. 413-420
    • Schroeder, W.T.1    Chao, L.-Y.2    Dao, D.D.3
  • 35
    • 0036292260 scopus 로고    scopus 로고
    • Preferential loss of paternal 19q, but not 1p, alleles in oligodendrogliomas
    • Sanson M, Leuraud P, Marie Y, Delattre J-Y, Hoang-Xuan K. Preferential loss of paternal 19q, but not 1p, alleles in oligodendrogliomas. Ann Neurol. 2002;52:105-107.
    • (2002) Ann Neurol , vol.52 , pp. 105-107
    • Sanson, M.1    Leuraud, P.2    Marie, Y.3    Delattre, J.-Y.4    Hoang-Xuan, K.5
  • 36
    • 0030053298 scopus 로고    scopus 로고
    • Acquired homozygosity (isodisomy) of chromosome 3 during clonal evolution of a uveal melanoma: Association with morphologic heterogeneity
    • White VA, McNeil BK, Thiberville L, Horsman DE. Acquired homozygosity (isodisomy) of chromosome 3 during clonal evolution of a uveal melanoma: association with morphologic heterogeneity. Genes Chromosomes Cancer. 1996;15:138-143.
    • (1996) Genes Chromosomes Cancer , vol.15 , pp. 138-143
    • White, V.A.1    McNeil, B.K.2    Thiberville, L.3    Horsman, D.E.4
  • 37
    • 0031874333 scopus 로고    scopus 로고
    • High-resolution allelotype analysis of childhood B-lineage acute lymphoblastic leukemia
    • Chambon-Pautas C, Cave H, Gerard B, et al. High-resolution allelotype analysis of childhood B-lineage acute lymphoblastic leukemia. Leukemia. 1998;12:1107-1113.
    • (1998) Leukemia , vol.12 , pp. 1107-1113
    • Chambon-Pautas, C.1    Cave, H.2    Gerard, B.3
  • 38
    • 0030670674 scopus 로고    scopus 로고
    • Homozygous deletions at 9p21 in childhood acute lymphoblastic leukemia detected by microsatellite analysis
    • Takeuchi S, Koike M, Seriu T, et al. Homozygous deletions at 9p21 in childhood acute lymphoblastic leukemia detected by microsatellite analysis. Leukemia. 1997;11:1636-1640.
    • (1997) Leukemia , vol.11 , pp. 1636-1640
    • Takeuchi, S.1    Koike, M.2    Seriu, T.3
  • 39
    • 0036230566 scopus 로고    scopus 로고
    • A genome-wide screen for normally methylated human CpG islands that can identify novel imprinted genes
    • Strichman-Almashanu LZ, Lee RS, Onyango PO, et al. A genome-wide screen for normally methylated human CpG islands that can identify novel imprinted genes. Genome Res. 2002;12:543-554.
    • (2002) Genome Res , vol.12 , pp. 543-554
    • Strichman-Almashanu, L.Z.1    Lee, R.S.2    Onyango, P.O.3
  • 40
    • 0035171016 scopus 로고    scopus 로고
    • The imprinted gene and parent-of-origin effect database
    • Morison IM, Paton CJ, Cleverley SD. The imprinted gene and parent-of-origin effect database. Nucleic Acids Res. 2001;29:275-276.
    • (2001) Nucleic Acids Res , vol.29 , pp. 275-276
    • Morison, I.M.1    Paton, C.J.2    Cleverley, S.D.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.