Literature DB >> 6722761

Banded chromosome analysis in patients with treatment-associated acute nonlymphocytic leukemia.

D C Arthur, C D Bloomfield.   

Abstract

We have analyzed G-banded metaphase chromosomes from 20 patients with treatment-associated acute nonlymphocytic leukemia (t-ANLL). Nine patients were previously treated for hematologic malignancies and 11 for solid tumors. The interval from initial therapy to t-ANLL ranged from 35 to 182 mo (median 75.5 mo). Medial age at diagnosis of t-ANLL was 58.5 years. Clonal chromosome abnormalities were found in 19 patients (95%). Loss or partial deletion of the long arm of chromosomes #5 and/or #7 were most common, occurring in nine patients. These abnormalities were associated with hypodiploid complex karyotypes. Other nonrandom abnormalities recurring among karyotypes with abnormalities of chromosome #5 included loss of one #18, partial deletion of the long arm of chromosome #2, ring chromosomes, and a Philadelphia (Ph1) chromosome. We also identified a group of five patients whose only karyotypic abnormality was addition of whole chromosomes. The remaining five patients had other karyotypic abnormalities, the most common of which were structural rearrangements in a pseudodiploid clone. Combined data from our study and the three previously published large series of patients with t-ANLL studied with banding suggest a relationship between karyotype and intensity of prior therapy, with abnormalities of chromosomes #5 and #7 occurring more often in the intensively treated patients.

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Year:  1984        PMID: 6722761     DOI: 10.1016/0165-4608(84)90030-x

Source DB:  PubMed          Journal:  Cancer Genet Cytogenet        ISSN: 0165-4608


  8 in total

1.  Deletion mapping of human chromosome 5 using chromosome-specific DNA probes.

Authors:  L R Carlock; D Skarecky; S L Dana; J J Wasmuth
Journal:  Am J Hum Genet       Date:  1985-09       Impact factor: 11.025

2.  Cosegregation of hypertrophic cardiomyopathy and a fragile site on chromosome 16 in a large Italian family.

Authors:  M Ferraro; G Scarton; M Ambrosini
Journal:  J Med Genet       Date:  1990-06       Impact factor: 6.318

Review 3.  Genetic markers on chromosome 7.

Authors:  L C Tsui
Journal:  J Med Genet       Date:  1988-05       Impact factor: 6.318

4.  Chromosome breakage and recombination at fragile sites.

Authors:  T W Glover; C K Stein
Journal:  Am J Hum Genet       Date:  1988-09       Impact factor: 11.025

5.  Induction of sister chromatid exchanges at common fragile sites.

Authors:  T W Glover; C K Stein
Journal:  Am J Hum Genet       Date:  1987-11       Impact factor: 11.025

6.  Assignment of CSF-1 to 5q33.1: evidence for clustering of genes regulating hematopoiesis and for their involvement in the deletion of the long arm of chromosome 5 in myeloid disorders.

Authors:  M J Pettenati; M M Le Beau; R S Lemons; E A Shima; E S Kawasaki; R A Larson; C J Sherr; M O Diaz; J D Rowley
Journal:  Proc Natl Acad Sci U S A       Date:  1987-05       Impact factor: 11.205

7.  Loss of both CSF1R (FMS) alleles in patients with myelodysplasia and a chromosome 5 deletion.

Authors:  J Boultwood; K Rack; S Kelly; J Madden; A Y Sakaguchi; L M Wang; D G Oscier; V J Buckle; J S Wainscoat
Journal:  Proc Natl Acad Sci U S A       Date:  1991-07-15       Impact factor: 11.205

8.  Chromosomes in acute nonlymphocytic leukemia.

Authors:  E L Prigogina; E W Fleischman; G P Puchkova; S A Mayakova; M A Volkova; A K Protasova; M A Frenkel
Journal:  Hum Genet       Date:  1986-06       Impact factor: 4.132

  8 in total

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