A pooled analysis of karyotypic patterns, breakpoints and imbalances in 783 cytogenetically abnormal multiple myelomas reveals frequently involved chromosome segments as well as significant age- and sex-related differences.
Nilsson, Therese LU ; Höglund, Mattias LU ; Lenhoff, Stig ; Rylander, Lars LU
; Turesson, Ingemar
LU
; Westin, Jan
LU
; Mitelman, Felix
LU
and Johansson, Bertil
LU
(2003)
In British Journal of Haematology
120(6).
p.960-969
- Abstract
- The cytogenetic features (ploidy, complexity, breakpoints, imbalances) were ascertained in 783 abnormal multiple myeloma (MM) cases to identify frequently involved chromosomal regions as well as a possible impact of age/sex. The series included MM patients from the Mitelman Database of Chromosome Aberrations in Cancer and from our own laboratory. Hyperdiploidy was most common, followed by hypodiploidy, pseudodiploidy and tri-/tetraploidy. Most cases were complex, with a median of eight changes per patient. The distribution of modal numbers differed between younger and older patients, but was not related to sex. No sex- or age-related differences regarding the number of anomalies were found. The most frequent genomic breakpoints were 14q32,... (More)
- The cytogenetic features (ploidy, complexity, breakpoints, imbalances) were ascertained in 783 abnormal multiple myeloma (MM) cases to identify frequently involved chromosomal regions as well as a possible impact of age/sex. The series included MM patients from the Mitelman Database of Chromosome Aberrations in Cancer and from our own laboratory. Hyperdiploidy was most common, followed by hypodiploidy, pseudodiploidy and tri-/tetraploidy. Most cases were complex, with a median of eight changes per patient. The distribution of modal numbers differed between younger and older patients, but was not related to sex. No sex- or age-related differences regarding the number of anomalies were found. The most frequent genomic breakpoints were 14q32, 11q13, 1q10, 8q24, 1p11, 1q21, 22q11, 1p13, 1q11, 19q13, 1p22, 6q21 and 17p11. Breaks in 1p13, 6q21 and 11q13 were more common in the younger age group. The most frequent imbalances were + 9, - 13, + 15, + 19, + 11 and - Y. Trisomy 11 and monosomy 16 were more common among men, while -X was more frequent among women. Loss of Y as the sole change and + 5 were more common in elderly patients, and - 14 was more frequent in the younger age group. The present findings strongly suggest that some karyotypic features of MM are influenced by endogenous and/or exogenous factors. (Less)
Please use this url to cite or link to this publication:
https://lup.lub.lu.se/record/112686
- author
- Nilsson, Therese
LU
; Höglund, Mattias
LU
; Lenhoff, Stig
; Rylander, Lars
LU
; Turesson, Ingemar
LU
; Westin, Jan
LU
; Mitelman, Felix
LU
and Johansson, Bertil
LU
- organization
- publishing date
- 2003
- type
- Contribution to journal
- publication status
- published
- subject
- in
- British Journal of Haematology
- volume
- 120
- issue
- 6
- pages
- 960 - 969
- publisher
- Wiley-Blackwell
- external identifiers
-
- pmid:12648065
- wos:000181633900006
- scopus:0037353820
- ISSN
- 0007-1048
- DOI
- 10.1046/j.1365-2141.2003.04221.x
- language
- English
- LU publication?
- yes
- id
- ffe9e1ae-909d-427e-8e29-66e3cbc0e09f (old id 112686)
- date added to LUP
- 2016-04-01 12:05:12
- date last changed
- 2022-08-28 08:05:32
@article{ffe9e1ae-909d-427e-8e29-66e3cbc0e09f,
abstract = {{The cytogenetic features (ploidy, complexity, breakpoints, imbalances) were ascertained in 783 abnormal multiple myeloma (MM) cases to identify frequently involved chromosomal regions as well as a possible impact of age/sex. The series included MM patients from the Mitelman Database of Chromosome Aberrations in Cancer and from our own laboratory. Hyperdiploidy was most common, followed by hypodiploidy, pseudodiploidy and tri-/tetraploidy. Most cases were complex, with a median of eight changes per patient. The distribution of modal numbers differed between younger and older patients, but was not related to sex. No sex- or age-related differences regarding the number of anomalies were found. The most frequent genomic breakpoints were 14q32, 11q13, 1q10, 8q24, 1p11, 1q21, 22q11, 1p13, 1q11, 19q13, 1p22, 6q21 and 17p11. Breaks in 1p13, 6q21 and 11q13 were more common in the younger age group. The most frequent imbalances were + 9, - 13, + 15, + 19, + 11 and - Y. Trisomy 11 and monosomy 16 were more common among men, while -X was more frequent among women. Loss of Y as the sole change and + 5 were more common in elderly patients, and - 14 was more frequent in the younger age group. The present findings strongly suggest that some karyotypic features of MM are influenced by endogenous and/or exogenous factors.}},
author = {{Nilsson, Therese and Höglund, Mattias and Lenhoff, Stig and Rylander, Lars and Turesson, Ingemar and Westin, Jan and Mitelman, Felix and Johansson, Bertil}},
issn = {{0007-1048}},
language = {{eng}},
number = {{6}},
pages = {{960--969}},
publisher = {{Wiley-Blackwell}},
series = {{British Journal of Haematology}},
title = {{A pooled analysis of karyotypic patterns, breakpoints and imbalances in 783 cytogenetically abnormal multiple myelomas reveals frequently involved chromosome segments as well as significant age- and sex-related differences.}},
url = {{https://lup.lub.lu.se/search/files/2775195/623713.pdf}},
doi = {{10.1046/j.1365-2141.2003.04221.x}},
volume = {{120}},
year = {{2003}},
}