Molecular characterization of the 7q deletion in myeloid disorders

British Journal of Haematology

Volumn 93, Issue 1, 1996, Pages 75-80

  Lewis, Sian ^a   Abrahamson, Gail ^a   Boultwood, Jacqueline ^a   Fidler, Carrie ^a   Potter, Alison ^a   Wainscoat, James S ^a  

^a JOHN RADCLIFFE HOSPITAL   (United Kingdom)

Author keywords

chromosome 7; chromosome deletion; myelodysplasia; secondary leukaemia

Indexed keywords

ANTINEOPLASTIC AGENT; CYCLOPHOSPHAMIDE; DOXORUBICIN; VINCRISTINE;

ADULT; AGED; ARTICLE; CHROMOSOME 7Q; CHROMOSOME DELETION; CLINICAL ARTICLE; FEMALE; HUMAN; HUMAN CELL; LEUKEMIA; MALE; MYELODYSPLASIA; MYELOID LEUKEMIA; PRIORITY JOURNAL; SECOND CANCER;

ADULT; AGED; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 7; ELECTROPHORESIS, GEL, PULSED-FIELD; FEMALE; GENE DOSAGE; HUMANS; MALE; MIDDLE AGED; MYELODYSPLASTIC SYNDROMES; POLYMORPHISM, RESTRICTION FRAGMENT LENGTH;

EID: 0029987983     PISSN: 00071048     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1365-2141.1996.4841025.x     Document Type: Article

References (34)

1. Barker, D., Green, P., Knowlton, R., Schumm, J., Lander, E.,. Oliphant, A., Willard, H., Akots, G., Brown, V., Gravius, T., Helms, C., Nelson, C., Parker, C., Rediker, K., Rising, M., Watt, M., Weiffenbach, B. & Donis-Keller, H. (1987) Genetic linkage map of human chromosome 7 with 63 DNA markers. Proceedings of the National Academy of Sciences of the United States of America, 84, 8006-8010.
2. Bennett, J.M., Catovsky, D., Daniel, M.T., Flandrin, G., Galton, D.A.G., Gralnick, H.R. & Sultan, C. (1976) Proposals for the classification of acute leukaemias. British Journal of Haematotogy, 33, 451-458.
3. Bennett, J.M., Catovsky, D., Daniel, M.T., Flandrin, G., Galton, D.A.G., Gralnick, H.R. & Sultan, C. (1982) Proposals for the classification of the myelodysplastic syndromes. British Journal of Haematology, 51, 189-199.
4. Borgstrom, G.H., Teerenhovi, L., Vuopio, P., de la Chapelle, A., Van den Berghe, H., Brandt, L., Golomb, H.M., Louwagie, A., Mitelman, F., Rowley, J.D. & Sandberg, A.A. (1980) Clinical implications of monosomy 7 in acute nonlymphocytic leukaemia. Cancer Genetics and Cytogenetics, 2, 115-126.
5. Borrensen, A.L., Moller, P. & Berg, K. (1988) Linkage disequlibrium analyses and restriction mapping of four RFLPs at the pro alpha 2 collagen locus: lack of correlation between linkage disequilibrium and physical distance. Human Genetics, 78, 216-221.
6. Boultwood, J., Rack, K., Kelly, S., Madden, J., Sakaguchi, A.Y., Wang, L.-M., Oscier, D.G., Buckle, V.J. & Wainscoat, J.S. (1991) Loss of both CSF1R (FMS) alleles in patients with myelodysplasia and a chromosome 5 deletion. Proceedings of the National Academy of Sciences of the United States of America, 88, 6167-6180.
7. Boyum, A. (1986) Isolation of mononuclear cells and granulocytes from human blood: isolation of mononuclear cells by one centrifugation and of granulocytes by combining centrifugation and sedimentation at 1 g. Scandinavian Journal of Clinical and Laboratory Investigation, 97, (Suppl.), 77-89.
8. Cohen-Haguenauer, O., Soubrier, F., Van Cong, N., Gross, M.S., Jegou, C., Corval, P. & Frezal, J. (1987) Confirmation of the chromosomal assignment of the renin gene to human chomosome 1 and regional assignment using in situ hybridization. Cytogenetics and Cell Genetics, 46, 597-599.
9. Dean, M., Park, M., Le Beau, M.M., Robins, T.S., Diaz, M.O., Rowley, J.D., Blair, D.G. & Van de Woude, G.F. (1985) The human met oncogene is related to the tyrosine kinase oncogenes. Nature, 318, 318-322.
10. Ehrlich, G., Viegas-Pequignot, E., Ginzberg, D., Sindel, L., Soreq, H. & Zakut, H. (1992) Mapping the acetylcholinesterase gene to chromosome 7q22 by fluorescent in situ hybridization coupled with selective PCR amplification from a somatic hybrid cell panel and chromosome-sorted libraries. Genomics, 13, 1192-1197.
11. Fazio, M.J., Mattet, M-G., Passage, E., Chu, M-L., Black, D., Solomon, E., Davidson, J.M. & Uitto, J. (1991) Human elastin gene: new evidence for localisation to the long arm of chromosome 7. American Journal of Human Genetics, 48, 696-703.
12. Fourth International Workshop on Chromosomes in Leukemia 1982 (1984) Abnormalities of chromosome 7 resulting in monosomy 7 or in deletion of the long arm (7q-): review of translocations, breakpoints and associated abnormalities. Cancer Genetics and Cytogenetics, 11, 251-360.
13. Harrison, C.J., Rooney, D.E. & Czepulkowski, B. (eds) (1986) Human Genetics, pp. 135-161. IRL Press, Oxford.
14. Horiike, S., Taniwaki, M., Misawa, S. & Abe, T. (1988) Chromosome abnormalities and karyotypic evolution in 83 patients with myelodysplastic syndrome and predictive value for prognosis. Cancer, 62, 1129-1138.
15. Johansson, B., Mertens, F., Heim, S., Kristoffersson, K. & Mitelman, F. (1991) Cytogenetics of secondary myelodysplasia (sMDS) and acute non-lymphocytic leukaemia (sANLL). European Journal of Haematology, 47, 17-27.
16. Johansson, B., Mertens, F. & Mitelman, F. (1993) Cytogenetic deletion maps of hematologic neoplasms: circumstantial evidence for tumor suppressor loci. Genes, Chromosomes and Cancer, 8, 205-218.
17. Kaplan, M.E. & Clark, C.J. (1974) An improved rosseting assay for detection of human T-lymphocytes. Journal of Immunological Methods, 5, 131-134.
18. Kere, J. (1989) Chromosome 7 long arm deletion breakpoints in preleukemia: mapping by pulsed field gel electrophoresis. Nucleic Acids Research, 17, 1511-1520.
19. Kere, J., Donis-Keller, H., Ruutu, T. & de la Chapelle, A. (1989b) Chromosome 7 long arm deletions in myeloid disorders: terminal DNA sequences are commonly conserved and breakpoints vary, Cytogenetics and Cell Genetics, 50, 226-229.
20. Kere, J., Ruutu, T., Davies, K.A., Roninson, I.B., Walkins, P.C. Winqvist, R. & de lu Chapelle, A. (1989b) Chromosome 7 long arm deletion in myeloid disrorders: a narrow breakpoint region in 7q22 defined by molecular mapping. Blood, 73, 230-234.
21. Klinger, K.W., Winqvist, R., Riccio, A., Andreasen, A., Satorio, R., Nielsen, L.S., Stuart, N., Stanislovitis, P., Watkins, P., Douglas, R., Grzeschik, K.H., & Alitalo, K. (1987) Plasminogen activator inhibitor type 1 gene is located at region q21.3-q22 of chromosome 7 and genetically linked with cystic fibrosis. Proceedings of the National Academy of Sciences of the United States of America, 84, 8548-8552.
22. Lapidot-Lifson, Y., Prody, C.A., Ginzberg, D., Meytes, D., Zukut, H. & Soreq, H. (1989) Co-amplitication of human acetylcholinesterase genes in blood cells: correlation with various leukemias and abnormal megakaryopoiesis. Proceedings of the Journal Academy of Sciences of the United Stales of America, 86, 4715-4719.
23. Le Beau, M.M., Diaz, M.O., Rowley, J.D. & Mak, T.W. (1985) Chromosomal localisation of the human T cell receptor beta-chain gene. Cell, 41, 335.
24. Nakai, H., Inoue, S., Miyazaki, H., Murakami, K. & Tada, K. (1988) Human renin gene assigned to chromosome band 1q42 by in situ hybridisation. Cytogenetics and Cell Genetics, 47, 90-91.
25. Pederson-Bjergaard, J., Preben, P., Larsen, O., Jensen, G. & Byrsting, K. (1990) Chromosome aberrations and prognostic factors in therapy-related myelodysplasia and acute nonlymphocytic leukemia. Blood, 76, 1083-1091.
26. Sambrook, J., Fritsch, E.F. & Maniatis, T. (1989) Molecular Cloning: a laboratory Manual. Cold Spring Harbor Laboratory Press, Cold Spring Harbor, New York.
27. Scherer, S.W., Neufeld, E.J., Lievens, P.M.J., Orkin, S.H. & Tsui, L.C. (1993) Regional localization of the CCAAT displacement protein gene (CUTL1) to 7q22 by analysis of somatic cell hybrids. Genomics, 15, 695-696.
28. Schiffer, C.A., Lee, E.J., Tomiyasu, T., Wiernick, P.H. & Testa, J.R. (1989) Prognostic impact of cytogenic abnormalities in patients with de novo acute non-lymphocytic leukemia. Blood, 73, 263-270.
29. Shannon, K.M., Turhan, G.M., Rogers, P.C.J. & Kan, Y.W. (1992) Evidence implicating heterogenous deletion of chromosome 7 in the pathogenesis of familial leukemia associated with monosomy 7. Genomics, 51, 170-177.
30. Skalnik, D.G., Strauss, E.C. & Orkin, S.H. (1991) CCAAT displacement protein as a repressor of the myelomonocytic-specific gp91-phox gene promoter. Journal of Biological Chemistry, 266, 16736-16744.
31. Testa, J.R., Kanofsky, J.R., Rowley, J.D., Baron, J.M. & Vardimann, J.W. (1981) Karyotype patterns and their clinical significance in polycythemia vera. American Journal of Hematology, 11, 29-45.
32. Watkins, P.C., Hoffman, N., Stanislovitis, P., Beck, A.K., Galli, J., Vellucci, V., Gusella, J.F. & Shows, T.B. (1986) Regional assignment of the erythropoietin gene to human chromosome region 7pter-q11. Cytogenetics and Cell Genetics, 42, 214-218.
33. Whang-Peng, J., Lee, E.C., Longo, D.L., Schechter, G.P. & Devita, V.T. (1988) Cytogenetic studies in patients with secondary leukemia/dysmyelopoietic syndrome after different treatment modalities. Blood, 71, 403-414.
34. Yunis, J.J., Rydell, R.E., Oken, M.M., Arnesen, M.A., Mayer, M.G. & Lobell, M. (1986) Refined chromosome analysis as an independent prognostic indicator in de novo myelodysplastic syndromes. Blood, 67, 1721-1730.