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Volumn 25, Issue 4, 2005, Pages 2979-2984

Impact of cytogenetic and molecular cytogenetic studies on hematologic malignancies

Author keywords

Chromosome abnormalities; Hematologic malignancies; Karyotype; Molecular cytogenetics; Review

Indexed keywords

MEMBRANE ANTIGEN;

EID: 22944458534     PISSN: 02507005     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Review
Times cited : (17)

References (56)
  • 1
    • 0033068058 scopus 로고    scopus 로고
    • The impact of the new fish technologies on the cytogenetics of haematological malignancies
    • Kearney L: The impact of the new fish technologies on the cytogenetics of haematological malignancies. Br J Haematol 4: 648-658, 1999.
    • (1999) Br J Haematol , vol.4 , pp. 648-658
    • Kearney, L.1
  • 2
    • 0037202151 scopus 로고    scopus 로고
    • Molecular cytogenetic aspects of hematologic malignancies: Clinical implications
    • Chen Z and Sanderbrg AA: Molecular cytogenetic aspects of hematologic malignancies: clinical implications. Am J Med Genet 115: 130-141, 2002.
    • (2002) Am J Med Genet , vol.115 , pp. 130-141
    • Chen, Z.1    Sanderbrg, A.A.2
  • 3
    • 0032784783 scopus 로고    scopus 로고
    • World Health Organization classification of neoplastic diseases of the hematopoietic and lymphoid tissues: Report of the Clinical Advisory Committee meeting-Airlie House, Virginia
    • Harris NL, Jaffe ES, Diebold J, Frandrin G, Muller-Hermelink HK, Vardiman J, Lister TA and Bloomfield CD: World Health Organization classification of neoplastic diseases of the hematopoietic and lymphoid tissues: report of the Clinical Advisory Committee meeting-Airlie House, Virginia. Clin Oncol 17: 3835-3849, 1997.
    • (1997) Clin Oncol , vol.17 , pp. 3835-3849
    • Harris, N.L.1    Jaffe, E.S.2    Diebold, J.3    Frandrin, G.4    Muller-Hermelink, H.K.5    Vardiman, J.6    Lister, T.A.7    Bloomfield, C.D.8
  • 5
    • 0036786901 scopus 로고    scopus 로고
    • The World Health Organization (WHO) classification of the myeloid neoplasms
    • Vardiman JW, Harris NL and Brunning RD: The World Health Organization (WHO) classification of the myeloid neoplasms. Blood 100: 2292-2302, 2002.
    • (2002) Blood , vol.100 , pp. 2292-2302
    • Vardiman, J.W.1    Harris, N.L.2    Brunning, R.D.3
  • 6
    • 0021264226 scopus 로고
    • Fourth International Workshop on Chromosomes in Leukemia: Clinical significance of chromosomal abnormalities in acute non lymphoblastic leukemia
    • Bloomfield CD, Goldman A, Hossfeld D and de la Chapelle A: Fourth International Workshop on Chromosomes in Leukemia: clinical significance of chromosomal abnormalities in acute non lymphoblastic leukemia. Cancer Genet Cytogenet 11: 332-350, 1984.
    • (1984) Cancer Genet Cytogenet , vol.11 , pp. 332-350
    • Bloomfield, C.D.1    Goldman, A.2    Hossfeld, D.3    De La Chapelle, A.4
  • 7
    • 0034758836 scopus 로고    scopus 로고
    • The clinical significance of cytogenetic abnormalities in acute myeloid leukemia
    • Grimwade D: The clinical significance of cytogenetic abnormalities in acute myeloid leukemia. Best Pract Res Clin Haematol 14: 497-529, 2001.
    • (2001) Best Pract Res Clin Haematol , vol.14 , pp. 497-529
    • Grimwade, D.1
  • 8
    • 0035339877 scopus 로고    scopus 로고
    • Comparison of cytogenetic and molecular genetic detection of t (8;21) and inv (16) in a prospective series of adults with de novo acute myeloid leukemia: A Cancer and Leukemia Group B study
    • Mrozek K, Prior TW, Edwards C et al: Comparison of cytogenetic and molecular genetic detection of t (8;21) and inv (16) in a prospective series of adults with de novo acute myeloid leukemia: a Cancer and Leukemia Group B study. J Clin Oncol 19: 2482-2492, 2001.
    • (2001) J Clin Oncol , vol.19 , pp. 2482-2492
    • Mrozek, K.1    Prior, T.W.2    Edwards, C.3
  • 9
    • 0037269184 scopus 로고    scopus 로고
    • Acute myeloid leukemia with MLL rearrangements: Clinicobiological features, prognostic impact and value of flowcytometry in the detection of residual leukemic cells
    • Minoz L, Nomded JF, Villamor N et al: Acute myeloid leukemia with MLL rearrangements: clinicobiological features, prognostic impact and value of flowcytometry in the detection of residual leukemic cells. Leukemia 17: 76-82, 2003.
    • (2003) Leukemia , vol.17 , pp. 76-82
    • Minoz, L.1    Nomded, J.F.2    Villamor, N.3
  • 10
    • 0015246254 scopus 로고
    • A rapid banding technique for human chromosomes
    • Seabright M: A rapid banding technique for human chromosomes. Lancet 30: 971-972, 1971
    • (1971) Lancet , vol.30 , pp. 971-972
    • Seabright, M.1
  • 11
    • 0017258328 scopus 로고
    • High resolution of human chromosomes
    • Yunis JG: High resolution of human chromosomes. Science 26: 1268-1270, 1976.
    • (1976) Science , vol.26 , pp. 1268-1270
    • Yunis, J.G.1
  • 12
    • 0001745242 scopus 로고    scopus 로고
    • Molecular cytogenetics of contiguous gene syndromes: Mechanisms and consequences of gene dosage imbalance
    • Scriver CR, Beaudet AL, Sly WS, Valle D, Childs B, Kinzler KW, Vogelstein B (eds.) MacGraw Hill, New York, NY, Chap. 65
    • Shaffer LG, Ledbetter DH and Lupski JR: Molecular cytogenetics of contiguous gene syndromes: mechanisms and consequences of gene dosage imbalance. In: Scriver CR, Beaudet AL, Sly WS, Valle D, Childs B, Kinzler KW, Vogelstein B (eds.) Metabolic and Molecular Basis of Inherited Disease, 8th edition, MacGraw Hill, New York, NY, Chap. 65, 1999.
    • (1999) Metabolic and Molecular Basis of Inherited Disease, 8th Edition
    • Shaffer, L.G.1    Ledbetter, D.H.2    Lupski, J.R.3
  • 14
    • 0022916663 scopus 로고
    • Detection of chromosome aberrations in the human interphase nucleus by visualization of specific target DNAs with radioactive and non-radioactive in situ hybridization techniques: Detection of trisomy 18 with probe L1. 84
    • Cremer T, Landegent J and Bruckner A: Detection of chromosome aberrations in the human interphase nucleus by visualization of specific target DNAs with radioactive and non-radioactive in situ hybridization techniques: detection of trisomy 18 with probe L1. 84. Human Genetics 74: 346-352, 1986.
    • (1986) Human Genetics , vol.74 , pp. 346-352
    • Cremer, T.1    Landegent, J.2    Bruckner, A.3
  • 15
    • 0029843439 scopus 로고    scopus 로고
    • Deciding and validation of DNA probe sets for a comprehensive interphase cytogenetic analysis of acute myeloid leukemia
    • Fischer K, Scholl C, Salat J, Frohling S, Schénk K, Bentz M, Stilgenbauer S, Lichter P and Dohner H: Deciding and validation of DNA probe sets for a comprehensive interphase cytogenetic analysis of acute myeloid leukemia. Blood 88: 3962-3971, 1996.
    • (1996) Blood , vol.88 , pp. 3962-3971
    • Fischer, K.1    Scholl, C.2    Salat, J.3    Frohling, S.4    Schénk, K.5    Bentz, M.6    Stilgenbauer, S.7    Lichter, P.8    Dohner, H.9
  • 16
    • 0026533307 scopus 로고
    • Detection of trisomy 12 in chronic lymphocytic leukemia by fluorescence in situ hybridization to interphase cells: A simple and sensitive method
    • Anastasi J, Le Beau MM, Vardiman JW, Fernald AA, Larson RA and Rowley JD: Detection of trisomy 12 in chronic lymphocytic leukemia by fluorescence in situ hybridization to interphase cells: a simple and sensitive method. Blood 79: 1796-1801, 1992.
    • (1992) Blood , vol.79 , pp. 1796-1801
    • Anastasi, J.1    Le Beau, M.M.2    Vardiman, J.W.3    Fernald, A.A.4    Larson, R.A.5    Rowley, J.D.6
  • 18
    • 0029099360 scopus 로고
    • Heterogeneity of deletions involving RB-1 and the D13S25 locus in B-cell chronic lymphocytic leukemia revealed by fluorescence in situ hybridization
    • Stilgenbauer S, Leupolt E, Ohl S, Weiss G, Schröder M, Fischer K, Bentz M, Lichter P and Döhner H: Heterogeneity of deletions involving RB-1 and the D13S25 locus in B-cell chronic lymphocytic leukemia revealed by fluorescence in situ hybridization. Cancer Res 55: 3475-3477, 1995.
    • (1995) Cancer Res , vol.55 , pp. 3475-3477
    • Stilgenbauer, S.1    Leupolt, E.2    Ohl, S.3    Weiss, G.4    Schröder, M.5    Fischer, K.6    Bentz, M.7    Lichter, P.8    Döhner, H.9
  • 19
    • 0027457275 scopus 로고
    • High frequency of monoallelic retinoblastoma gene deletion in B-cell chronic lymphoid leukemia shown by interphase cytogenetics
    • Stilgenbauer S, Dohner H, Bulgay-Morschel M, Weitz S, Bentz M and Lichter P: High frequency of monoallelic retinoblastoma gene deletion in B-cell chronic lymphoid leukemia shown by interphase cytogenetics. Blood 81: 2118-2124, 1993.
    • (1993) Blood , vol.81 , pp. 2118-2124
    • Stilgenbauer, S.1    Dohner, H.2    Bulgay-Morschel, M.3    Weitz, S.4    Bentz, M.5    Lichter, P.6
  • 23
    • 0026023565 scopus 로고
    • Interphase cytogenetic analysis detects minimal residual disease in a case of acute lymphoblastic leukemia and resolves the question of relapse after allogeneic bone marrow transplantation
    • Anastasi J, Thangavely M, Vardiman JW, Hooberman AL, Bian ML, Larson RA and Le Beau MM: Interphase cytogenetic analysis detects minimal residual disease in a case of acute lymphoblastic leukemia and resolves the question of relapse after allogeneic bone marrow transplantation. Blood 77: 1087-1091, 1991.
    • (1991) Blood , vol.77 , pp. 1087-1091
    • Anastasi, J.1    Thangavely, M.2    Vardiman, J.W.3    Hooberman, A.L.4    Bian, M.L.5    Larson, R.A.6    Le Beau, M.M.7
  • 24
    • 0027401551 scopus 로고
    • Detection of residual host cells after bone marrow transplantation using non-isotopic in situ hybridisation and karyotype analysis
    • Wessman M, Popp S, Ruutu T, Volin L, Cremer T and Knuutila S: Detection of residual host cells after bone marrow transplantation using non-isotopic in situ hybridisation and karyotype analysis. Bone Marrow Transplant 11: 279-284, 1993.
    • (1993) Bone Marrow Transplant , vol.11 , pp. 279-284
    • Wessman, M.1    Popp, S.2    Ruutu, T.3    Volin, L.4    Cremer, T.5    Knuutila, S.6
  • 25
    • 0030974970 scopus 로고    scopus 로고
    • Increased sensitivity of minimal residual disease detection by interphase FISH in acute lymphoblastic leukemia with hyperdiploidy
    • Kasprzyk A and Seeker-Walker LM: Increased sensitivity of minimal residual disease detection by interphase FISH in acute lymphoblastic leukemia with hyperdiploidy. Leukemia 11: 429-135, 1997.
    • (1997) Leukemia , vol.11 , pp. 429-1135
    • Kasprzyk, A.1    Seeker-Walker, L.M.2
  • 26
    • 0026736660 scopus 로고
    • Simultaneous genotypic and immunophenotypic analysis of interphase cells using dual-colour fluorescence: A demonstration of lineage involvement in polycythemia vera
    • Price CM, Kanfer EJ, Colman SM, Westwood N, Barret AJ and Greaves MF: Simultaneous genotypic and immunophenotypic analysis of interphase cells using dual-colour fluorescence: a demonstration of lineage involvement in polycythemia vera. Blood 80: 1033-1038, 1992.
    • (1992) Blood , vol.80 , pp. 1033-1038
    • Price, C.M.1    Kanfer, E.J.2    Colman, S.M.3    Westwood, N.4    Barret, A.J.5    Greaves, M.F.6
  • 27
    • 0027524856 scopus 로고
    • Cell lineage involvement in four patients with myelodysplastic syndrome and t (1;7) or trisomy 8 studied by simultaneous immunophenotyping and fluorescence in situ hybridization
    • Nylund SJ, Verbeek W, Larramendy ML, Ruutu T, Heinonen K, Hallman H and Knuutila S: Cell lineage involvement in four patients with myelodysplastic syndrome and t (1;7) or trisomy 8 studied by simultaneous immunophenotyping and fluorescence in situ hybridization. Cancer Genet Cytogenet 70: 120-124, 1993.
    • (1993) Cancer Genet Cytogenet , vol.70 , pp. 120-124
    • Nylund, S.J.1    Verbeek, W.2    Larramendy, M.L.3    Ruutu, T.4    Heinonen, K.5    Hallman, H.6    Knuutila, S.7
  • 28
    • 0027984279 scopus 로고
    • Direct detection of the Philadelphia chromosome in CD20-positive lymphocytes in chronic myeloid leukemia by tri-color immunophenotyping/FISH
    • Torlakovic E, Litz CE, McClure JS and Brunning RD: Direct detection of the Philadelphia chromosome in CD20-positive lymphocytes in chronic myeloid leukemia by tri-color immunophenotyping/FISH. Leukemia 8: 1940-1943, 1994.
    • (1994) Leukemia , vol.8 , pp. 1940-1943
    • Torlakovic, E.1    Litz, C.E.2    McClure, J.S.3    Brunning, R.D.4
  • 29
    • 0029032664 scopus 로고
    • Combined immunophenotying and in situ hybridization (FICTION): A rapid method to study cell lineage involvment in myelodysplastic syndromes
    • Soenen V, Fenaux P, Flactif M, Lepelley P, Lai JL, Cosson A and Preudhomme C: Combined immunophenotying and in situ hybridization (FICTION): a rapid method to study cell lineage involvment in myelodysplastic syndromes. Br J Haematol 90: 701-706, 1995.
    • (1995) Br J Haematol , vol.90 , pp. 701-706
    • Soenen, V.1    Fenaux, P.2    Flactif, M.3    Lepelley, P.4    Lai, J.L.5    Cosson, A.6    Preudhomme, C.7
  • 31
    • 0027494194 scopus 로고
    • Leukaemia arising in donor cells following allegeneic bone marrow transplantation for thalassaemia demonstrated by immunological, DNA and cytogenetic analysis
    • Katz F, Reeves BR, Alexander S, Kearney L and Chessells J: Leukaemia arising in donor cells following allegeneic bone marrow transplantation for thalassaemia demonstrated by immunological, DNA and cytogenetic analysis. Br J Haematol 85: 326-331, 1993.
    • (1993) Br J Haematol , vol.85 , pp. 326-331
    • Katz, F.1    Reeves, B.R.2    Alexander, S.3    Kearney, L.4    Chessells, J.5
  • 33
    • 0026345679 scopus 로고
    • Construction and characterization of plasmid libraries enriched in sequences from single human chromosomes
    • Collins C, Kuo WL, Segraves R, Fuscoe J, Pinkel D and Gray JW: Construction and characterization of plasmid libraries enriched in sequences from single human chromosomes. Genomics 11: 997-1006, 1991.
    • (1991) Genomics , vol.11 , pp. 997-1006
    • Collins, C.1    Kuo, W.L.2    Segraves, R.3    Fuscoe, J.4    Pinkel, D.5    Gray, J.W.6
  • 35
    • 0027365062 scopus 로고
    • Libraries for each human chromosome, constructed from sorter-enriched chromosomes by using linker-adaptor PCR
    • Vooijs M, Yu LC, Tkachuk D, Pinkel D, Johnson D and Gray JW: Libraries for each human chromosome, constructed from sorter-enriched chromosomes by using linker-adaptor PCR. Am J Hum Genet 52: 586-597, 1993.
    • (1993) Am J Hum Genet , vol.52 , pp. 586-597
    • Vooijs, M.1    Yu, L.C.2    Tkachuk, D.3    Pinkel, D.4    Johnson, D.5    Gray, J.W.6
  • 37
    • 0026948875 scopus 로고
    • Multiple colors by fluorescence in situ hybridization using radiolabelled DNA probes create a molecular karyotype
    • Dauwerse JG, Wiegant J, Raap AK, Breuning MH and van Ommen GJB: Multiple colors by fluorescence in situ hybridization using radiolabelled DNA probes create a molecular karyotype. Hum Mol Genet 1: 593-598, 1992.
    • (1992) Hum Mol Genet , vol.1 , pp. 593-598
    • Dauwerse, J.G.1    Wiegant, J.2    Raap, A.K.3    Breuning, M.H.4    Van Ommen, G.J.B.5
  • 38
    • 0026454451 scopus 로고
    • Involvement of a homolog of Drosophila trithorax by 11q23 chromosomal translocations in acute leukemias
    • Tkachuk DC, Kohler S and Cleary ML: Involvement of a homolog of Drosophila trithorax by 11q23 chromosomal translocations in acute leukemias. Cell 71: 691-700, 1992.
    • (1992) Cell , vol.71 , pp. 691-700
    • Tkachuk, D.C.1    Kohler, S.2    Cleary, M.L.3
  • 39
    • 0028908542 scopus 로고
    • Interphase cytogenetics of the t 8;21 (q22;q22) associated with acute mylogenous leukemia by two-color fluorescence in situ hybridisation
    • Sacchi N, Magnani I, Kearney L, Wijsman J, Hagemeijer A and Darfler M: Interphase cytogenetics of the t 8;21) (q22;q22) associated with acute mylogenous leukemia by two-color fluorescence in situ hybridisation. Cancer Genet Cytogenet 79: 97-103, 1995.
    • (1995) Cancer Genet Cytogenet , vol.79 , pp. 97-103
    • Sacchi, N.1    Magnani, I.2    Kearney, L.3    Wijsman, J.4    Hagemeijer, A.5    Darfler, M.6
  • 41
    • 0030960829 scopus 로고    scopus 로고
    • Development and clinical application of an innovative fluorescence in situ hybridization technique which detects submicroscopic rearrangements involving telomeres
    • Knight SJL, Horsley SW, Regan R, Lawrie M, Maher EJ, Cardy DLN, Flint J and Kearney L: Development and clinical application of an innovative fluorescence in situ hybridization technique which detects submicroscopic rearrangements involving telomeres. Eur J Hum Genet 5: 1-8, 1997.
    • (1997) Eur J Hum Genet , vol.5 , pp. 1-8
    • Knight, S.J.L.1    Horsley, S.W.2    Regan, R.3    Lawrie, M.4    Maher, E.J.5    Cardy, D.L.N.6    Flint, J.7    Kearney, L.8
  • 42
    • 0029912473 scopus 로고    scopus 로고
    • Karyotyping human chromosomes by combinatorial multi-fluor FISH
    • Speicher MR, Ballard SG and Ward DC: Karyotyping human chromosomes by combinatorial multi-fluor FISH. Nat Genet 12: 368-375, 1996.
    • (1996) Nat Genet , vol.12 , pp. 368-375
    • Speicher, M.R.1    Ballard, S.G.2    Ward, D.C.3
  • 48
    • 0029079152 scopus 로고
    • Comparative genomic hybridization in chronic B-cell leukemias shows a high incidence of chromosomal gains and losses
    • Bentz M, Huck K, du Manoir S, Joos S, Werner CA, Fischer K, Döhner H and Lichter P: Comparative genomic hybridization in chronic B-cell leukemias shows a high incidence of chromosomal gains and losses. Blood 85: 3610-3618, 1995b.
    • (1995) Blood , vol.85 , pp. 3610-3618
    • Bentz, M.1    Huck, K.2    Du Manoir, S.3    Joos, S.4    Werner, C.A.5    Fischer, K.6    Döhner, H.7    Lichter, P.8
  • 49
    • 0030041048 scopus 로고    scopus 로고
    • Primary mediastinal (thymic) B-cell lymphoma is characterized by gains of chromosomal material including 9p and amplification of the REL gene
    • Joos S, Otãno-Joos MI, Ziegler S, Brüderlein S, du Manior S, Bentz M, Möller P and Lichter P: Primary mediastinal (thymic) B-cell lymphoma is characterized by gains of chromosomal material including 9p and amplification of the REL gene. Blood 87: 1571-1578, 1996.
    • (1996) Blood , vol.87 , pp. 1571-1578
    • Joos, S.1    Otãno-Joos, M.I.2    Ziegler, S.3    Brüderlein, S.4    Du Manior, S.5    Bentz, M.6    Möller, P.7    Lichter, P.8
  • 50
    • 0029904295 scopus 로고    scopus 로고
    • DNA copy number changes in diffuse large B-cell lymphoma: Comparative genomic hybridization study
    • Monni O, Joensuu H, Franssila K and Knuutila S: DNA copy number changes in diffuse large B-cell lymphoma: comparative genomic hybridization study. Blood 87: 5269-5278, 1996.
    • (1996) Blood , vol.87 , pp. 5269-5278
    • Monni, O.1    Joensuu, H.2    Franssila, K.3    Knuutila, S.4
  • 51
    • 0030795838 scopus 로고    scopus 로고
    • Chromosomal breakpoints and changes in DNA copy number in refractory acute myeloid leukemia
    • El-Rifai W, Elonen E, Larramendy M, Ruutu T and Knuutila S: Chromosomal breakpoints and changes in DNA copy number in refractory acute myeloid leukemia. Leukemia 11: 958-963, 1997.
    • (1997) Leukemia , vol.11 , pp. 958-963
    • El-Rifai, W.1    Elonen, E.2    Larramendy, M.3    Ruutu, T.4    Knuutila, S.5
  • 55
    • 2942575149 scopus 로고    scopus 로고
    • A cytogeneticist's perspective on genomic microarrays
    • Shaffer LG and Bejjani BA: A cytogeneticist's perspective on genomic microarrays. Hum Reprod Update 10(3): 221-226, 2004.
    • (2004) Hum Reprod Update , vol.10 , Issue.3 , pp. 221-226
    • Shaffer, L.G.1    Bejjani, B.A.2


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