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RECQ helicases are deregulated in hematological malignancies in association with a prognostic value
BACKGROUND: RECQ helicase family members act as guardians of the genome to assure proper DNA metabolism in response to genotoxic stress. Hematological malignancies are characterized by genomic instability that is possibly related to underlying defects in DNA repair of genomic stability maintenance....
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4752763/ https://www.ncbi.nlm.nih.gov/pubmed/26877874 http://dx.doi.org/10.1186/s40364-016-0057-4 |
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author | Viziteu, Elena Kassambara, Alboukadel Pasero, Philippe Klein, Bernard Moreaux, Jerome |
author_facet | Viziteu, Elena Kassambara, Alboukadel Pasero, Philippe Klein, Bernard Moreaux, Jerome |
author_sort | Viziteu, Elena |
collection | PubMed |
description | BACKGROUND: RECQ helicase family members act as guardians of the genome to assure proper DNA metabolism in response to genotoxic stress. Hematological malignancies are characterized by genomic instability that is possibly related to underlying defects in DNA repair of genomic stability maintenance. METHODS: We have investigated the expression of RECQ helicases in different hematological malignancies and in their normal counterparts using publicly available gene expression data. Furthermore, we explored whether RECQ helicases expression could be associated with tumor progression and prognosis. RESULTS: Expression of at least one RECQ helicase family member was found significantly deregulated in all hematological malignancies investigated when compared to their normal counterparts. In addition, RECQ helicase expression was associated with a prognostic value in acute myeloid leukemia, chronic lymphocytic leukemia, lymphoma and multiple myeloma. CONCLUSION: RECQ helicase expression is deregulated in hematological malignancies compared to their normal counterparts in association with a prognostic value. Deregulation of RECQ helicases appears to play a role in tumorigenesis and represent potent therapeutic targets for synthetic lethal approaches in hematological malignancies. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s40364-016-0057-4) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4752763 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-47527632016-02-14 RECQ helicases are deregulated in hematological malignancies in association with a prognostic value Viziteu, Elena Kassambara, Alboukadel Pasero, Philippe Klein, Bernard Moreaux, Jerome Biomark Res Research BACKGROUND: RECQ helicase family members act as guardians of the genome to assure proper DNA metabolism in response to genotoxic stress. Hematological malignancies are characterized by genomic instability that is possibly related to underlying defects in DNA repair of genomic stability maintenance. METHODS: We have investigated the expression of RECQ helicases in different hematological malignancies and in their normal counterparts using publicly available gene expression data. Furthermore, we explored whether RECQ helicases expression could be associated with tumor progression and prognosis. RESULTS: Expression of at least one RECQ helicase family member was found significantly deregulated in all hematological malignancies investigated when compared to their normal counterparts. In addition, RECQ helicase expression was associated with a prognostic value in acute myeloid leukemia, chronic lymphocytic leukemia, lymphoma and multiple myeloma. CONCLUSION: RECQ helicase expression is deregulated in hematological malignancies compared to their normal counterparts in association with a prognostic value. Deregulation of RECQ helicases appears to play a role in tumorigenesis and represent potent therapeutic targets for synthetic lethal approaches in hematological malignancies. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s40364-016-0057-4) contains supplementary material, which is available to authorized users. BioMed Central 2016-02-13 /pmc/articles/PMC4752763/ /pubmed/26877874 http://dx.doi.org/10.1186/s40364-016-0057-4 Text en © Viziteu et al. 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Viziteu, Elena Kassambara, Alboukadel Pasero, Philippe Klein, Bernard Moreaux, Jerome RECQ helicases are deregulated in hematological malignancies in association with a prognostic value |
title | RECQ helicases are deregulated in hematological malignancies in association with a prognostic value |
title_full | RECQ helicases are deregulated in hematological malignancies in association with a prognostic value |
title_fullStr | RECQ helicases are deregulated in hematological malignancies in association with a prognostic value |
title_full_unstemmed | RECQ helicases are deregulated in hematological malignancies in association with a prognostic value |
title_short | RECQ helicases are deregulated in hematological malignancies in association with a prognostic value |
title_sort | recq helicases are deregulated in hematological malignancies in association with a prognostic value |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4752763/ https://www.ncbi.nlm.nih.gov/pubmed/26877874 http://dx.doi.org/10.1186/s40364-016-0057-4 |
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