A Population-Based Single Nucleotide Polymorphism Array Analysis of Genomic Aberrations in Younger Adult Acute Lymphoblastic Leukemia Patients
(2015) In Genes, Chromosomes and Cancer 54(5). p.326-333- Abstract
- Adult acute lymphoblastic leukemia (ALL) is characterized by a high frequency of abnormal karyotypes some of which are related to outcome. Single nucleotide polymorphism (SNP) array analysis provides a highly sensitive platform to detect large and small genomic aberrations. SNP array profiling data in adult ALL are limited and further systematic studies of this patient group are needed. We performed a population-based SNP array analysis of genomic aberrations and their influence on survival in 66 Lithuanian 18-65 year old ALL patients diagnosed between 2007 and 2013. Most aberrations were detected in chromosome arm 9p, chromosome arm 6q, chromosome arm 13q, and chromosome 17. The recurrently targeted copy number abnormalities involved... (More)
- Adult acute lymphoblastic leukemia (ALL) is characterized by a high frequency of abnormal karyotypes some of which are related to outcome. Single nucleotide polymorphism (SNP) array analysis provides a highly sensitive platform to detect large and small genomic aberrations. SNP array profiling data in adult ALL are limited and further systematic studies of this patient group are needed. We performed a population-based SNP array analysis of genomic aberrations and their influence on survival in 66 Lithuanian 18-65 year old ALL patients diagnosed between 2007 and 2013. Most aberrations were detected in chromosome arm 9p, chromosome arm 6q, chromosome arm 13q, and chromosome 17. The recurrently targeted copy number abnormalities involved several leukemia-related genesCDKN2A/B, MLL, IKZF1, PAX5, RB1, TP53, and ETV6. We identified several new recurrent aberrations with possible new target genes: SMARCA4 in 19p13.2, RNASEL in 1q25.3, ARHGEF12 in 11q23.3, and LYL1 in 19p13.2. Aberrations in chromosome 13 and the RB1 gene as well as CDKN2A/B gene status were related to the outcome. (c) 2015 Wiley Periodicals, Inc. (Less)
Please use this url to cite or link to this publication:
https://lup.lub.lu.se/record/5281796
- author
- Dirse, Vaidas ; Bertasiute, Agne ; Gineikiene, Egle ; Zvirblis, Tadas ; Dambrauskiene, Ruta ; Gerbutavicius, Rolandas ; Juozaityte, Elona ; Malciute, Ligita ; Paulsson, Kajsa LU and Griskevicius, Laimonas
- organization
- publishing date
- 2015
- type
- Contribution to journal
- publication status
- published
- subject
- in
- Genes, Chromosomes and Cancer
- volume
- 54
- issue
- 5
- pages
- 326 - 333
- publisher
- John Wiley & Sons Inc.
- external identifiers
-
- wos:000351680900006
- scopus:84925371292
- ISSN
- 1045-2257
- DOI
- 10.1002/gcc.22246
- language
- English
- LU publication?
- yes
- id
- 05a221f1-6abc-4e30-9d6e-27e739f5f424 (old id 5281796)
- date added to LUP
- 2016-04-01 10:00:37
- date last changed
- 2022-04-12 01:03:52
@article{05a221f1-6abc-4e30-9d6e-27e739f5f424, abstract = {{Adult acute lymphoblastic leukemia (ALL) is characterized by a high frequency of abnormal karyotypes some of which are related to outcome. Single nucleotide polymorphism (SNP) array analysis provides a highly sensitive platform to detect large and small genomic aberrations. SNP array profiling data in adult ALL are limited and further systematic studies of this patient group are needed. We performed a population-based SNP array analysis of genomic aberrations and their influence on survival in 66 Lithuanian 18-65 year old ALL patients diagnosed between 2007 and 2013. Most aberrations were detected in chromosome arm 9p, chromosome arm 6q, chromosome arm 13q, and chromosome 17. The recurrently targeted copy number abnormalities involved several leukemia-related genesCDKN2A/B, MLL, IKZF1, PAX5, RB1, TP53, and ETV6. We identified several new recurrent aberrations with possible new target genes: SMARCA4 in 19p13.2, RNASEL in 1q25.3, ARHGEF12 in 11q23.3, and LYL1 in 19p13.2. Aberrations in chromosome 13 and the RB1 gene as well as CDKN2A/B gene status were related to the outcome. (c) 2015 Wiley Periodicals, Inc.}}, author = {{Dirse, Vaidas and Bertasiute, Agne and Gineikiene, Egle and Zvirblis, Tadas and Dambrauskiene, Ruta and Gerbutavicius, Rolandas and Juozaityte, Elona and Malciute, Ligita and Paulsson, Kajsa and Griskevicius, Laimonas}}, issn = {{1045-2257}}, language = {{eng}}, number = {{5}}, pages = {{326--333}}, publisher = {{John Wiley & Sons Inc.}}, series = {{Genes, Chromosomes and Cancer}}, title = {{A Population-Based Single Nucleotide Polymorphism Array Analysis of Genomic Aberrations in Younger Adult Acute Lymphoblastic Leukemia Patients}}, url = {{http://dx.doi.org/10.1002/gcc.22246}}, doi = {{10.1002/gcc.22246}}, volume = {{54}}, year = {{2015}}, }