Abstract |
The C-band heterochromatin polymorphism of chromosomes 1, 9, and 16 was studied in lymphocytes from 53 patients with Ph1-positive chronic myeloid leukemia (CML) and 183 control persons. The patients had significantly larger heterochromatic blocks on chromosome 16 (p less than 0.01) and fewer partial inversions of chromosome 9 (p less than 0.05) than the control persons, whereas no differences were found for the symmetry/asymmetry pattern. We suggest that the increased constitutive heterochromatin regions may, via sister chromosome exchange, facilitate homo- or hemizygotization of genes which favor neoplasia development and/or progression.
|
Authors | U Kristoffersson, A Bernheim, R Berger, B Nilsson, S Heim, N Mandahl, F Mitelman |
Journal | Hereditas
(Hereditas)
Vol. 110
Issue 2
Pg. 145-8
( 1989)
ISSN: 0018-0661 [Print] England |
PMID | 2745151
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
|
Chemical References |
|
Topics |
- Chromosome Aberrations
- Chromosome Banding
- Chromosome Inversion
- Chromosomes, Human, Pair 1
(ultrastructure)
- Chromosomes, Human, Pair 16
(ultrastructure)
- Chromosomes, Human, Pair 9
(ultrastructure)
- Heterochromatin
(ultrastructure)
- Humans
- Leukemia, Myelogenous, Chronic, BCR-ABL Positive
(genetics)
- Polymorphism, Genetic
- Sister Chromatid Exchange
|