Chromosomal changes detected by flourescence in situ hybridization in patients with acute lymphoblastic leukemia

Chinese Medical Journal

Volumn 116, Issue 9, 2003, Pages 1298-1303

  Zhang, Lijun ^a,b   Parkhurst, J B ^a   Kern, W F ^a   Scott, K V ^a   Niccum, D ^a   Mulvihill, J J ^a   Li, Shibo ^a  

^a UNIVERSITY OF OKLAHOMA   (United States)

^b CHINA MEDICAL UNIVERSITY   (China)

Author keywords

Acute lymphoblastic leukemia; Chromosome rearrangements; Fluorescence in situ hybridization

Indexed keywords

BCR ABL PROTEIN;

ACUTE LYMPHOBLASTIC LEUKEMIA; ADOLESCENT; ADULT; AGED; ARTICLE; B CELL LEUKEMIA; CANCER CELL CULTURE; CELL LINEAGE; CENTROMERE; CHILD; CHROMOSOME 10; CHROMOSOME 12P; CHROMOSOME 17; CHROMOSOME 21; CHROMOSOME 4; CHROMOSOME ABERRATION; CHROMOSOME DELETION; CHROMOSOME DUPLICATION; CHROMOSOME MOSAICISM; CHROMOSOME PAINTING; CHROMOSOME REARRANGEMENT; CHROMOSOME TRANSLOCATION 12; CHROMOSOME TRANSLOCATION 21; COMPUTER PROGRAM; CONTROLLED STUDY; CYTOGENETICS; DNA PROBE; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE FUSION; GENE LOCUS; HUMAN; IMAGE ANALYSIS; INFANT; MAJOR CLINICAL STUDY; MALE; METAPHASE; MONOSOMY; PHILADELPHIA 1 CHROMOSOME; RING CHROMOSOME; T CELL LEUKEMIA;

ADOLESCENT; ADULT; AGED; ARTIFICIAL GENE FUSION; CHILD; CHILD, PRESCHOOL; CHROMOSOME ABERRATIONS; CHROMOSOMES, HUMAN, PAIR 10; CHROMOSOMES, HUMAN, PAIR 17; CHROMOSOMES, HUMAN, PAIR 21; CHROMOSOMES, HUMAN, PAIR 4; FEMALE; GENE REARRANGEMENT; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INFANT; LEUKEMIA, LYMPHOCYTIC, ACUTE; MALE; MIDDLE AGED;

EID: 0141838030     PISSN: 03666999     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (18)

1. Adolfo A, Ferrando A, Thomas L, et al. Clinical implications of recurring chromosomal and associated molecular abnormalities in acute lymphoblastic leukemia. Semin Hematol 2000;37:381-395.
2. Amare P, Gladstone B, Varghese C, et al. Clinical significance of cytogenetic findings at diagnosis and in remission in childhood and adult acute lymphoblastic leukemia: Experience from India. Cancer Genet Cytogenet 1999;110:44-46.
3. Amland B, Glassman MD. Chromosomal abnormalities in acute leukemia. Clin Lab Med 2000;20:39-48.
4. Luke S, Shepelsky M. FISH: Recent Advances and Diagnostic Aspects. Cell Vision 1998;5:49-53.
5. Minenori EI, Mariko E, Eiichi I, et al. Breakage and fusion of the TEL (ETV6) gene in immature B lymphocytes induced by apoptogenic signals. Blood 2001;97:737-743.
6. Mignon LL, Lewis B, Silverman ML, et al. Incidence of TEL/AML1 fusion in children with relapsed acute lymphoblastic leukemia. Blood 1998;92:4792-4797.
7. Harrison CJ. The genetics of childhood acute lymphoblastic practleukaemia. Best Pract Clin Haematol 2000;427-439.
8. Srinivals T, Peter D, Aplan D, et al. Molecular biology of acute lymphocytic leukemia. Semin Oncol 1997;24:45-56.
9. McLean TW, Ringold S, Neuberg D, et al. TEL/AML-1 dimerizes and is associated with a favorable outcome in childhood acute lymphoblastic leukemia. Blood 1996; 88: 4252-4258.
10. Harris MB, Shuster JJ, Carroll A, et al. Trisomy of leukemic cell chromosomes 4 and 10 identifies children with B-progenitor cell acute lymphoblastic leukemia with a very low risk of treatment failure: a pediatric oncology group study. Blood 1992;79:3316-3324.
11. Heerema NA, Sather HN, Sensel MG, et al. Prognostic impact of trisomies of chromosomes 10, 17, and 5 among children with acute lymphoblastic leukemia and Highhyperdiploidy (>50 chromosomes). J Clin Oncol 2000; 18:1876-1887.
12. Look AT, Roberson PK, Williams DL, et al. Prognositic importance of blast cell DNA content in childhood acute lymphoblastic leukemia. Blood 1985;65:1079-1086.
13. Trueworthy R, Shuster J, Look T, et al. Ploidy of lymphoblasts is the strongest predictor of treatment outcome in B-progenitor cell acute lymphoblastic leukemia of childhood: A Pediatric Onceology Group study. J Clin Oncol 1992;10: 606-613.
14. Bloomfield CD, Secker-Walker LM, Goldman SI, et al. Six-year follow-up the clinical significance of karyotype in acute lymphoblastic leukemia. Cancer Genet Cytogenet 1989;40: 171-185.
15. Raimondi SC, Roberson PK, Pui, et al. Hyperdiploid (47-50) acute lymphobla stic leukemia in children. Blood 1995; 79:3245-3252.
16. Raimondi SC, Pui CH, Hancock ML, et al. Heterogeneity of hyperdiploid (51-67) childhood acute lymphoblastic leukemia. Leukemia 1996;10:213-224.
17. Fletcher JA, Lynch EA, Kimball VM, et al. Translocation (9; 22) is associated with extremely poor prognosis in intensively treated children with acute lymphoblastic leukemia. Blood 1991;77:435-439.
18. Heerema NA, Arthur DC, Sather H, et al. Cytogenetic features of infants less than 12 months of age at diagnosis of acute lymphoblastic leukemia: impact of the 11 q23 breakpoint on outcome: a report of the Childrens Cancer Group. Blood 1994;83:2274-2284.