Tetrasomy 8 is associated with a major cellular proliferative advantage and a poor prognosistwo cases of myeloid hematologic disorders and review of the literature

Cancer Genetics and Cytogenetics

Volumn 125, Issue 1, 2001, Pages 14-20

  Yan, Ju ^a   Marceau, Danièle ^b   Drouin, Régen ^a  

^a Dept of Med Biol   (Canada)

^b LAVAL UNIVERSITY   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

ACUTE GRANULOCYTIC LEUKEMIA; ADULT; AGED; ARTICLE; CASE REPORT; CHROMOSOME 8; CHROMOSOME ABERRATION; DISOMY; FISH; HUMAN; INTERPHASE; MALE; METAPHASE; PRIMED IN SITU LABELING; PRIORITY JOURNAL; PROGNOSIS; TETRASOMY; TRISOMY 18; TRISOMY 8; Y CHROMOSOME;

AGED; BASE SEQUENCE; CHROMOSOME ABERRATIONS; CHROMOSOME DISORDERS; CHROMOSOMES, HUMAN, PAIR 8; DNA PRIMERS; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; KARYOTYPING; LEUKEMIA, NONLYMPHOCYTIC, ACUTE; MALE; MIDDLE AGED;

EID: 0035067405     PISSN: 01654608     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0165-4608(00)00352-6     Document Type: Article

References (29)

1. Somatic shift to homozygosity for a chromosomal polymorphism in a child with acute lymphoblastic leukemia
2. Tetrasomy of chromosome 8; an interesting and rare cytogenetic phenomenon in acute nonlymphocytic leukemia
3. Tetrasomy 8 in acute myelomonocytic leukemia developing after a gastric cancer operation
4. A new case of isolated tetrasomy of chromosome 8 in a patient with therapy-related myelodysplastic syndrome; confirmation by chromosome painting in metaphase and interphase nuclei
5. A further case of acute nonlymphocytic leukemia with tetrasomy 8
6. Tetrasomy 8 in acute monoblastic leukemia (AML-M5a) with myelosarcomatosis of the skin
7. Tetrasomy 8 as a clonal anomaly in myeloid neoplasias
8. Cytogenetic and FISH investigations on tetrasomy 8 in ANLL
9. Tetrasomy of chromosome 8 in a patient with acute myeloid leukemia
10. Tetrasomy 8 and t(1;11)(p32;q24) in acute myelo-monocytic leukemia with extensive leukemic cutaneous involvement
11. Tetrasomy 8 in a patient with acute nonlymphocytic leukemia; a metaphase and interphase study with fluorescence in situ hybridization
12. Tetrasomy 8 detected by interphase cytogenetics in a child with acute lymphocytic leukemia
13. Coexistence of tetrasomy 8 and trisomy 8 in a case with myeloid metaplasia with myelofibrosis
14. Chromosome 8 tetrasomies and pentasomies-a clonal abnormality closely associated with acute monocytic leukaemia
15. Isolated tetrasomy 8 in minimally differentiated acute myeloid leukemia (AML-M0)
16. Translocation (15;17)(q22;q21) as a secondary chromosomal abnormality in a case of acute monoblastic leukemia with tetrasomy 8
17. A rapid banding technique for human chromosomes
18. Construction of a panel of chromosome-specific oligonucleotide probes (PRINS-primers) useful for the identification of individual human chromosomes in situ
19. Assessment of aneuploidy for chromosomes 8, 9, 13, 16, and 21 in human sperm by using primed in situ labeling technique
20. Selection of chromosome-specific primers and their use in simple and double PRINS techniques for rapid in situ identification of human chromosomes
21. Trisomy 8 and monosomy 7 detected in bone marrow using primed in situ labeling (PRINS), fluorescence in situ hybridization (FISH) and conventional cytogenetic analyses; a study of 54 cases of hematological disorders
22. In vitro proliferative advantage of bone marrow cells with tetrasomy 8 in Ewing sarcoma
23. Fluorescence in situ hybridization of progenitor cells obtained by fluorescence-activated cell sorting for the detection of cells affected by chromosome abnormality trisomy 8 in patients with myelodysplastic syndromes
24. Cell lineage specific involvement in acute promyelocytic leukaemia (APL) using a combination of May-Grunwald-Giemsa staining and fluorescence in situ hybridization techniques for the detection of the translocation t(15;17)(q22;q12)
25. Refined chromosome study helps define prognostic subgroups in most patients with primary myelodysplastic syndrome and acute myelogenous leukaemia