Monosomy X as the sole cytogenetic abnormality in acute lymphoblastic leukemia: A report of two new patients

Leukemia and Lymphoma

Volumn 32, Issue 3-4, 1999, Pages 381-384

  Bueno, Jose L ^a   Watson, Ann ^b   Dainton, Melissa G ^a   Hughes, Deborah M ^c   Killick, Sally ^a   Treleaven, Jennifer G ^a   Swansbury, G John ^a  

^a INSTITUTE OF CANCER RESEARCH   (United Kingdom)

^b STOKE MANDEVILLE HOSPITAL   (United Kingdom)

^c CHURCHILL HOSPITAL   (United Kingdom)

Author keywords

Acute leukemia; AFX gene; Cytogenetics; GM CSF receptor; Monosomy X; Tumor suppressor gene

Indexed keywords

ACUTE LYMPHOBLASTIC LEUKEMIA; ADOLESCENT; ARTICLE; CASE REPORT; CLINICAL FEATURE; CYTOGENETICS; FEMALE; GENE LOCATION; HUMAN; HUMAN CELL; MONOSOMY X; MYELODYSPLASIA; PRIORITY JOURNAL; TUMOR SUPPRESSOR GENE; X CHROMOSOME;

EID: 0033022835     PISSN: 10428194     EISSN: None     Source Type: Journal    
DOI: 10.3109/10428199909167401     Document Type: Article

References (14)

1. Nowell, P.C. (1997) Genetic alterations in leukemias and lymphomas: Impressive progress and continuing complexity. Cancer Genetics and Cytogenetics, 94, 13-19.
2. Mitelman, F. (1994) Catalog of Chromosome Aberrations in Cancer. Fifth edition. pub. Wiley-Liss.
3. Riske, C.B., Morgan, R., Ondreyco, S. & Sandberg, A.A. (1994) X and Y chromosome loss as sole abnormality in acute non-lymphocytic leukemia (ANLL). Cancer Genetics and Cytogenetics, 72, 44-47.
4. Abruzzesse, E., Rao, P.N., Slatkoff, M., Cruz, J., Powell, B.L., Jackie, B & Pettenati, M.J. (1997). Monosomy X as a recurring sole cytogenetic abnormality associated with myelodysplastic disease. Cancer Genetics and Cytogenetics, 93, 140-146.
5. Heerema, N.A., Palmer, C.G. & Baehner, R.L. (1985). Karyotypic and clinical findings in a consecutive series of children with acute lymphocytic leukemia. Cancer Genetics and Cytogenetics, 17, 165-179.
6. Prigogina, E.L., Puchkova, G.P. & Mayakova, S.A. (1988). Nonrandom chromosomal abnormalities in acute lymphoblastic leukemia of childhood. Cancer Genetics and Cytogenetics, 32, 183-203.
7. Yamada, K. & Furusawa, S. (1976) Preferential Involvement of chromosomes no. 8 and no. 21 in acute leukemia and preleukemia. Blood, 47, 679-686.
8. Dewald, G.W., Brecher, M., Travis, L.B. & Stupca, P.J. (1989). Twenty-six patients with hematologic disorders and X chromosome abnormalities. Frequent idic(X)(q13) chromosomes and Xq13 anomalies associated with pathologic ringed sideroblasts. Cancer Genetics and Cytogenetics. 42, 173-185.
9. Callen, D.F., & Ford, J.H. (1983). Chromosome abnormalities in chronic lymphocytic leukemia revealed by TPA as a mitogen. Cancer Genetics and Cytogenetics, 10, 87-93
10. Bird, M.L., Ueshima, Y., Rowley, J.D., Haren, J.M., & Vardiman, J.W. (1989). Chromosome abnormalities in B cell chronic lymphocytic leukemia and their clinical correlations. Leukemia, 3, 182-191.
11. Borkhardt, A., Repp, R., Haas, O. A., Leis, T., Harbott, J., Kreuder, J., Hammermann, J, Henn, T, & Lampen, F. (1997). Cloning and characterization of AFX, the gene that fuses to MLL in acute leukemias with a t(X;11 )(q13;q23). Oncogene. 14, 195-202.
12. Mandani, A., Choukroun, V., Soulier, J., Cacheux, V., Claisse, J.F., Valensi, F., Daliphard, S., Cazin, B., Levy, V., Leblond, V., Daniel, M.T., Sigaux, F., Stem, M.H. (1996). Expression of p13MTCPI is restricted to mature T-cell proliferations with t(X;14) translocations. Blood. 87, 1923-1927.
13. Camey, L.A., Kinney, J.S., Higgins, R.R., Freeman, A.I., Hecht, B.K., Woods, G.M. (1992). X;6 translocation in a child with congenital acute lymphocytic leukemia. Cancer, 69, 799-803.
14. Gough, N.M., Gearing, N.A., Baker, E., Pritchard, M., Callen D.F., & Sutherland, G.R. (1990). Localization of the human GM-CSF gene to the X-Y pseudoautosomal region. Nature, 345, 734-6.