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Allelic Imbalances in Radiation—Associated Acute Myeloid Leukemia

Acute myeloid leukemia (AML) can develop as a secondary malignancy following radiotherapy, but also following low-dose environmental or occupational radiation exposure. Therapy-related AML frequently carries deletions of chromosome 5q and/or 7, but for low-dose exposure associated AML this has not b...

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Autores principales: Klymenko, Sergiy V., Smida, Jan, Atkinson, Michael J., Bebeshko, Volodymir G., Nathrath, Michaela, Rosemann, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3424488/
https://www.ncbi.nlm.nih.gov/pubmed/22924110
http://dx.doi.org/10.3390/genes2020384
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author Klymenko, Sergiy V.
Smida, Jan
Atkinson, Michael J.
Bebeshko, Volodymir G.
Nathrath, Michaela
Rosemann, Michael
author_facet Klymenko, Sergiy V.
Smida, Jan
Atkinson, Michael J.
Bebeshko, Volodymir G.
Nathrath, Michaela
Rosemann, Michael
author_sort Klymenko, Sergiy V.
collection PubMed
description Acute myeloid leukemia (AML) can develop as a secondary malignancy following radiotherapy, but also following low-dose environmental or occupational radiation exposure. Therapy-related AML frequently carries deletions of chromosome 5q and/or 7, but for low-dose exposure associated AML this has not been described. For the present study we performed genome-wide screens for loss-of-heterozygosity (LOH) in a set of 19 AML cases that developed after radiation-exposure following the Chernobyl accident. Using Affymetrix SNP arrays we found large regions of LOH in 16 of the cases. Eight cases (42%) demonstrated LOH at 5q and/or 7, which is a known marker of complex karyotypic changes and poor prognosis. We could show here for the first time that exposure to low-dose ionizing radiation induces AML with molecular alterations similar to those seen in therapy-related cases.
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spelling pubmed-34244882012-08-22 Allelic Imbalances in Radiation—Associated Acute Myeloid Leukemia Klymenko, Sergiy V. Smida, Jan Atkinson, Michael J. Bebeshko, Volodymir G. Nathrath, Michaela Rosemann, Michael Genes (Basel) Article Acute myeloid leukemia (AML) can develop as a secondary malignancy following radiotherapy, but also following low-dose environmental or occupational radiation exposure. Therapy-related AML frequently carries deletions of chromosome 5q and/or 7, but for low-dose exposure associated AML this has not been described. For the present study we performed genome-wide screens for loss-of-heterozygosity (LOH) in a set of 19 AML cases that developed after radiation-exposure following the Chernobyl accident. Using Affymetrix SNP arrays we found large regions of LOH in 16 of the cases. Eight cases (42%) demonstrated LOH at 5q and/or 7, which is a known marker of complex karyotypic changes and poor prognosis. We could show here for the first time that exposure to low-dose ionizing radiation induces AML with molecular alterations similar to those seen in therapy-related cases. MDPI 2011-05-31 /pmc/articles/PMC3424488/ /pubmed/22924110 http://dx.doi.org/10.3390/genes2020384 Text en © 2011 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Article
Klymenko, Sergiy V.
Smida, Jan
Atkinson, Michael J.
Bebeshko, Volodymir G.
Nathrath, Michaela
Rosemann, Michael
Allelic Imbalances in Radiation—Associated Acute Myeloid Leukemia
title Allelic Imbalances in Radiation—Associated Acute Myeloid Leukemia
title_full Allelic Imbalances in Radiation—Associated Acute Myeloid Leukemia
title_fullStr Allelic Imbalances in Radiation—Associated Acute Myeloid Leukemia
title_full_unstemmed Allelic Imbalances in Radiation—Associated Acute Myeloid Leukemia
title_short Allelic Imbalances in Radiation—Associated Acute Myeloid Leukemia
title_sort allelic imbalances in radiation—associated acute myeloid leukemia
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3424488/
https://www.ncbi.nlm.nih.gov/pubmed/22924110
http://dx.doi.org/10.3390/genes2020384
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