Study of clonality in myelodysplastic syndromes: Detection of trisomy 8 in bone marrow cell smears by fluorescence in situ hybridization

Leukemia Research

Volumn 20, Issue 7, 1996, Pages 551-557

  Abruzzese, Elisabetta ^a,b   Buss, David ^a   Rainer, Robert ^a   Rao, P Nagesh ^a   Pettenati, Mark J ^a  

^a WAKE FOREST SCHOOL OF MEDICINE   (United States)

^b Università degli Studi di Roma   (Italy)

Author keywords

Cell lineage; FISH; Myelodysplastic syndromes; Trisomy 8

Indexed keywords

ACUTE NONLYMPHOCYTIC LEUKEMIA; ADULT; AGED; APLASTIC ANEMIA; ARTICLE; BONE MARROW CELL; CELL LINEAGE; CHROMOSOME 8; CHROMOSOME ANALYSIS; CHRONIC MYELOMONOCYTIC LEUKEMIA; CLINICAL ARTICLE; CONTROLLED STUDY; DISEASE COURSE; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; HUMAN CELL; LYMPHOCYTE; MYELODYSPLASTIC SYNDROME; PLASMA CELL; PRELEUKEMIA; PRIORITY JOURNAL; TRISOMY 8;

EID: 0030199225     PISSN: 01452126     EISSN: None     Source Type: Journal    
DOI: 10.1016/0145-2126(95)00130-1     Document Type: Article

References (26)

1. 1. Bennett J. M., Catowsky D., Daniel M. T., Flandrin G., Galton D. A., Gralnick H. R. & Sultan C. (1982) Proposal for the classification of the myelodysplastic syndromes. Br. J. Haematol. 51, 189.
2. 2. Anastasi J., Feng J., Le Beau M. M., Larson R. A., Rowley J. D. & Vardiman J. W. (1993) Cytogenetic clonality in myelodysplastic syndromes studied with fluorescence in situ hybridization: lineage, response to growth factor therapy, and clone expansion. Blood 81, 1580.
3. 3. Nylund S. J., Verbeek W., Larramendy M. L., Ruutu T., Henionen K., Hallman H. & Knuutila S. (1993) 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.
4. 4. Culligan D. J., Cachia P., Whittaker J., Jacobs A. & Padua R. A. (1992) Clonal lymphocytes are detectable in only some cases of MDS. Br. J. Haematol. 81, 346.
5. 5. Gerristen W. R., Donohue J., Bauman J., Jhanwar S. C., Kernan N. A., Castro-Malaspina H., O'Reilly R. J. & 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.
6. 6. Kibbelaar R. E., Kamp H. van, Dreef E. J., Groot-Swings G. de, Kluin-Nelemans J. C., Beverstock G. C., Fibbe W. E. & Kluin P. M. (1992) Combined immunophenotyping and DNA in situ hybridization to study lineage involvement in patients with myelodysplastic syndromes. Blood 79, 1823.
7. 7. Kamp H. van, Fibbe W. E., Jansen R. P., Keur M. van der, Graaff E. de, Willemze R. & Landegent J. E. (1992) Clonal involvement of granulocytes and monocytes, but not of T and B lymphocytes and natural killer cells in patients with myelodysplasia: analysis by X-linked restriction fragment polymorphisms and polymerase chain reaction of the phosphoglycerate kinase gene. Blood 80, 1774.
8. 8. Prchal J. T., Throckmorton D. W., Carroll A. J., Fuson E. W., Gams R. A. & Prchal J. F. (1978) A common progenitor for human myeloid and lymphoid cells. Nature 274, 590.
9. 9. Fialkow P. J. (1982) Cell lineages in hematopoietic neoplasia studied with G6PD cell markers. J. Cell Physiol. 1, 37.
10. 10. Raskind W. H., Tirumali N., Jacobson R., Singer J. & Fialkow P. J. (1984) Evidence for a multistep pathogenesis of a myelodysplastic syndrome. Blood 63, 1318.
11. 11. Janssen J. W., Buschle M., Layton M., Drexler H. G., Lyons J., Berghe H. van den, Heimpel H., Kubanek B., Kleihauer E., Mufti G. J. & Bartram C. R. (1989) Clonal analysis of myelodysplastic syndromes: evidence of a multipotent stem cell origin. Blood 73, 248.
12. 12. Turhan A. G., Humphries R. K., Phillips G. L.,, Eaves A. C. & Eaves C. J. (1989) Clonal hematopoiesis demonstrated by X-linked DNA polymorphisms after allogenic bone marrow transplantation. New Engl. J. Med. 320, 1655.
13. 13. Han K., Lee W., Harris C. P., Kim W., Shim S. & Meisner L. F. (1994) Quantifying chromosome changes and lineage involvement in myelodysplastic syndrome (MDS) using fluorescent in situ hybridization (FISH). Leukemia 8, 81.
14. 14. ISCN (1985). An International System for Human Cytogenetic Nomenclature: Report of the Standing Committee on Human Cytogenetic Nomenclature (1985) (Harnden D. G. & Klinger H. P., Eds), Karger, Basel/ New York. Published in collaboration with the March of Dimes Birth Defects Foundation and Cytogenet. Cell Genet., Appendix 2.
15. 15. Koeffler H. P. (1986) Myelodysplastic syndromes (preleukemia). Semin. Hematol. 23, 284.
16. 16. Sole F., Prieto F., Badia L., Woessner S., Florensa L., Caballin M. R., Coll M. D., Besses C. & Sans-Sabrafen J. (1992) Cytogenetic studies in 112 cases of untreated myelodysplastic syndromes. Cancer Genet. Cytogenet. 64, 12.
17. 17. Lom K. van, Hagemeijer A., Smit E. M. & Lowenberg B. (1993) In situ hybridization on May-Grunwald Giemsa-stained bone marrow and blood smears of patients with hematologic disorders allow detection of cell lineage-specific cytogenetic abnormalities. Blood 82, 884.
18. 18. Kroef M. J., Fibbe W. E., Mout R., Jansen R. P., Haak H. L., Wessels J. W., Van Kamp H., Willemze R. & Landegent J. E. (1993) Myeloid but not lymphoid cells carry the 5q deletion: polymerase chain reaction analysis of loss of heterozygosity using mini repeat sequences on highly purified cell fractions. Blood 81, 1849.
19. 19. Kere J., Ruutu T. & Chapelle A de la. (1987) Monosomy 7 in granulocytes and monocytes in myelodysplastic syndrome. New Engl. J. Med. 499, 316.
20. 20. Tefferi A., Thibodeau S. N. & Solberg L. A. (1990) Clonal studies in the myelodysplastic syndrome using X-linked restriction fragment length polymorphisms. Blood 75, 1770.
21. 21. Lawrence H. J., Broudy V. C., Magenis R. E., Olson S., Tomar D., Barton S., Fitchen J. H. & Bagby G. C. (1987) Cytogenetic evidence for involvement of B lymphocytes in acquired idiopathic sideroblastic anemias. Blood 70, 1003.
22. 22. Tsukamoto N., Morita K., Maehara T., Okamoto K., Karasawa M., Omine M. & Naruse T. (1993) Clonality in myelodysplastic syndromes: demonstration of pluripotent stem cell origin using X-linked restriction fragment length polymorphisms. Br. J. Haematol. 83, 589.
23. 23. Jacobs A. (1991) Genetic lesions in preleukemia. Leukemia 5, 277.
24. 24. Nguyen L. N., Arthur D. C., Litz C. E. & Brunning R. D. (1994) Fluorescence in situ hybridization (FISH) detection of trisomy 8 in myeloid cells in chronic myeloid leukemia (CML): a study of archival blood and bone marrow smears. Leukemia 8 (10), 1654.
25. 25. United Kingdom Cancer Cytogenetic Group (1992) Primary, single, autosomal trisomies associated with hematological disorders. Leukemia Res, 16, 841.
26. 26. Garipidou V., Yamada T., Prentice H. G. & Seeker-Walker L. M. (1990) Trisomy 8 in acute lymphoblastic leukemia (ALL): a case report and update of the literature. Leukemia 4, 717.