Fluorescence in situ hybridization to assess aneuploidy for chromosomes 7 and 8 in hematologic disorders

Cancer Genetics and Cytogenetics

Volumn 102, Issue 2, 1998, Pages 114-124

  Wyandt, Herman E ^a   Chinnappan, Dharmaraj ^a   Ioannidou, Sophia ^a   Salama, Magdy ^a   O'Hara, Carl ^a  

^a BOSTON UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ANEUPLOIDY; ARTICLE; CHROMOSOME 7; CHROMOSOME 8; CYTOGENETICS; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; HUMAN CELL; MONOSOMY; MYELODYSPLASTIC SYNDROME; PRIORITY JOURNAL; TRISOMY;

ANEUPLOIDY; CHROMOSOME ABERRATIONS; CHROMOSOMES, HUMAN, PAIR 7; CHROMOSOMES, HUMAN, PAIR 8; CYTOGENETICS; DNA PROBES; FEMALE; HEMATOLOGIC DISEASES; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INTERPHASE; MALE; METAPHASE; MYELODYSPLASTIC SYNDROMES;

CUCURBITA;

EID: 0032055599     PISSN: 01654608     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0165-4608(97)00355-5     Document Type: Article

References (23)

1. Cremer T, Lichter P, Borden J, Ward DC, Manuelidis L (1988): Detection of chromosome aberrations in metaphase and interphase tumor cells by in situ hybridization using chromosome-specific library probes. Hum Genet 80:235-246.
2. Poddighe PJ, Moesker O, Smeets D, Awwad BH, Ramaekers CS, Hopman AHN (1991): Interphase cytogenetics of hematological cancer: comparison of classical karyotyping and in situ hybridization using a panel of eleven chromosome-specific DNA probes. Cancer Res 51:1959-1967.
3. Arnoldus EP, Noordermeer IA, Peters ACB, Voormolen JHC, Bots GTAM, Raap AK, van der Ploeg M (1991): Interphase cytogenetics of brain tumors. Genes Chromosom Cancer 3:101-107.
4. Anastasi J (1991): Interphase cytogenetic analysis in the diagnosis and study of neoplastic disorders. Am J Clin Pathol 95 (suppl 1):S22-S28.
5. Meloni AM, Peier AM, Haddad FS, Powell IJ, Block AMW, Huben RP, Todd I, Potter W, Sandberg AA (1993): A new approach in the diagnosis and follow-up of bladder cancer. FISH analysis of urine, bladder washings and tumors. Cancer Genet Cytogenet 71:105-118.
6. Willemze R, Fibbe WE, Falkenburg JHF, Kluin-Nelemans JC, Kluin PM, Landegant JE (1993): Biology and treatment of myelodysplastic syndromes - developments in the past decade. Ann Hemat 66:107-115.
7. Clare N, Hansen K (1994): Cytogenetics in the diagnosis of hematological malignancies. Diag Hemat 8:785-807.
8. Kibbelaar RE, van Kamp H, Dreef EJ, de Groot-Swings G, Kluin-Nelemans JC, Beverstock GC, Fibbe WE, Kuin PM (1992): Combined immunophenotyping and DNA in situ hybridization to study lineage involvement in patients with myelodysplastic syndromes. Blood 79:1823-1828.
9. Zhao L, van Oort J, Cork A, Liang JC (1993): Comparison between interphase and metaphase cytogenetics in detecting chromosome 7 defects in hematological neoplasias. Am J Hemat 43:205-211.
10. Kadam P, Masterson M, Soukup S, Moore C, Raza A, Lampkin B (1994): Detection of unexpected clones of monosomy 7 in childhood acute lymphoblastic leukemia using fluorescence in situ hybridization. Anticancer Res 14:545-548.
11. Han K, Lee W, Harris CP, Kim W, Shim S, Meisner L (1994): Quantifying chromosome changes and lineage involvement in myelodysplastic syndrome (MDS) using fluorescent in situ hybridization (FISH). Leukemia 8:81-86.
12. Flactif M, Lai JL, Preudhomme C, Feneaux P (1994): Fluorescence in situ hybridization improves the detection of monosomy 7 in myelodysplastic syndromes. Leukemia 8:1012-1018.
13. Brizard F, Brizard A, Guilhot F, Tanzer J, Berger R (1994): Detection of monosomy 7 and trisomies 8 and 11 in myelo-dysplastic disorders by interphase fluorescent in situ hybridization. Comparison with acute non-lymphocytic leukemias. Leukemia 8:1005-1011.
14. Kibbelaar RE, Mulder JWR, Dreef EJ, van Kamp H, Fibbe WE, Wessels JW, Beverstock GC, Haak HL, Kluin PM (1993): Detection of monosomy 7 and trisomy 8 in myeloid neoplasia: a comparison of banding and fluorescence in situ hybridization. Blood 82:904-913.
15. Jenkins RB, LeBeau MM, Kraker WJ, Borell TJ, Stalboerger PG, Davis EM, Penland L, Fernald A, Espinosa R, Schaid DJ, Noel P, Dewald G (1992): Fluorescence in situ hybridization: a sensitive method for trisomy 8 detection in bone marrow specimens. Blood 79:3307-3315.
16. ISCN (1995): An International System for Human Cytogenetic Nomenclature. F Mitelman, ed. S. Karger, Basel.
17. Chinnappan D, Wyandt HE, Rastogi A, Blanchard R, Milunsky A (1995): Discrepant cytogenetic and FISH results in a 26-year-old male with early T-cell ALL. Am J Hum Genet 57:A62.
18. Jacobs RH, Cornbleet MA, Vardiman JW, Larson RA, LeBeau MM, Rowley JD (1986): Prognostic implications of morphology and karyotyping in primary myelo-displastic syndromes. Blood 67:1765-1772.
19. Arranz E, Renedo M, Ramos C, Martinez B, Prieto E, Benitez J (1994): Aplicación de la hybridación in situ fluorescente (FISH) interfásica en 4 casos de neoplasias mieloides con alteraciones del cromosoma 7. Sangre 34:457-460.
20. Gerritsen WR, Donohue J, Bauman J, Jhanwar SC, Kernan NA, Castro-Malaspina H, O'Reilly RJ, Bourhis J-H (1992): Clonal analysis of myelodysplastic syndrome: monosomy 7 is expressed in the myeloid lineage, but not in the lymphoid lineage as detected by fluorescent in situ hybridization. Blood 80:217-224.
21. Stanley WS, Devine GC, Murphy BA, Seibel N, Dinnforf P (1992): Longitudinal cytogenetic study of metaphase and interphase cells in childhood monosomy 7 syndrome. Cancer Genet Cytogenet 62:160-165.
22. Harrison KJ, Massing B, McKenna C, Kalousek DK (1995): Molecular cytogenetic analysis of monosomy 7 in pediatric patients with myelodysplastic syndrome. Am J Hemat 48:88-91.
23. Fugazza G, Bruzzone R, Dejana AM, Gobbi M, Ghio R, Patrone F, Rattenni S, Sessarego M (1995): Cytogenetic clonality in chronic myelomonocytic leukemia studied with fluorescence in situ hybridization. Leukemia 9:109-114.