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Different regulation of PARP1, PARP2, PARP3 and TRPM2 genes expression in acute myeloid leukemia cells

BACKGROUND: Acute myeloid leukemia (AML) is a heterogenic lethal disorder characterized by the accumulation of abnormal myeloid progenitor cells in the bone marrow which results in hematopoietic failure. Despite various efforts in detection and treatment, many patients with AML die of this cancer. T...

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Autores principales: Gil-Kulik, Paulina, Dudzińska, Ewa, Radzikowska-Büchner, Elżbieta, Wawer, Joanna, Jojczuk, Mariusz, Nogalski, Adam, Wawer, Genowefa Anna, Feldo, Marcin, Kocki, Wojciech, Cioch, Maria, Bogucka-Kocka, Anna, Rahnama, Mansur, Kocki, Janusz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7236215/
https://www.ncbi.nlm.nih.gov/pubmed/32423430
http://dx.doi.org/10.1186/s12885-020-06903-4
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author Gil-Kulik, Paulina
Dudzińska, Ewa
Radzikowska-Büchner, Elżbieta
Wawer, Joanna
Jojczuk, Mariusz
Nogalski, Adam
Wawer, Genowefa Anna
Feldo, Marcin
Kocki, Wojciech
Cioch, Maria
Bogucka-Kocka, Anna
Rahnama, Mansur
Kocki, Janusz
author_facet Gil-Kulik, Paulina
Dudzińska, Ewa
Radzikowska-Büchner, Elżbieta
Wawer, Joanna
Jojczuk, Mariusz
Nogalski, Adam
Wawer, Genowefa Anna
Feldo, Marcin
Kocki, Wojciech
Cioch, Maria
Bogucka-Kocka, Anna
Rahnama, Mansur
Kocki, Janusz
author_sort Gil-Kulik, Paulina
collection PubMed
description BACKGROUND: Acute myeloid leukemia (AML) is a heterogenic lethal disorder characterized by the accumulation of abnormal myeloid progenitor cells in the bone marrow which results in hematopoietic failure. Despite various efforts in detection and treatment, many patients with AML die of this cancer. That is why it is important to develop novel therapeutic options, employing strategic target genes involved in apoptosis and tumor progression. METHODS: The aim of the study was to evaluate PARP1, PARP2, PARP3, and TRPM2 gene expression at mRNA level using qPCR method in the cells of hematopoietic system of the bone marrow in patients with acute myeloid leukemia, bone marrow collected from healthy patients, peripheral blood of healthy individuals, and hematopoietic stem cells from the peripheral blood after mobilization. RESULTS: The results found that the bone marrow cells of the patients with acute myeloid leukemia (AML) show overexpression of PARP1 and PARP2 genes and decreased TRPM2 gene expression. In the hematopoietic stem cells derived from the normal marrow and peripheral blood after mobilization, the opposite situation was observed, i.e. TRPM2 gene showed increased expression while PARP1 and PARP2 gene expression was reduced. We observed positive correlations between PARP1, PARP2, PARP3, and TRPM2 genes expression in the group of mature mononuclear cells derived from the peripheral blood and in the group of bone marrow-derived cells. In AML cells significant correlations were not observed between the expression of the examined genes. In addition, we observed that the reduced expression of TRPM2 and overexpression of PARP1 are associated with a shorter overall survival of patients, indicating the prognostic significance of these genes expression in AML. CONCLUSIONS: Our research suggests that in physiological conditions in the cells of the hematopoietic system there is mutual positive regulation of PARP1, PARP2, PARP3, and TRPM2 genes expression. PARP1, PARP2, and TRPM2 genes at mRNA level deregulate in acute myeloid leukemia cells.
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spelling pubmed-72362152020-05-27 Different regulation of PARP1, PARP2, PARP3 and TRPM2 genes expression in acute myeloid leukemia cells Gil-Kulik, Paulina Dudzińska, Ewa Radzikowska-Büchner, Elżbieta Wawer, Joanna Jojczuk, Mariusz Nogalski, Adam Wawer, Genowefa Anna Feldo, Marcin Kocki, Wojciech Cioch, Maria Bogucka-Kocka, Anna Rahnama, Mansur Kocki, Janusz BMC Cancer Research Article BACKGROUND: Acute myeloid leukemia (AML) is a heterogenic lethal disorder characterized by the accumulation of abnormal myeloid progenitor cells in the bone marrow which results in hematopoietic failure. Despite various efforts in detection and treatment, many patients with AML die of this cancer. That is why it is important to develop novel therapeutic options, employing strategic target genes involved in apoptosis and tumor progression. METHODS: The aim of the study was to evaluate PARP1, PARP2, PARP3, and TRPM2 gene expression at mRNA level using qPCR method in the cells of hematopoietic system of the bone marrow in patients with acute myeloid leukemia, bone marrow collected from healthy patients, peripheral blood of healthy individuals, and hematopoietic stem cells from the peripheral blood after mobilization. RESULTS: The results found that the bone marrow cells of the patients with acute myeloid leukemia (AML) show overexpression of PARP1 and PARP2 genes and decreased TRPM2 gene expression. In the hematopoietic stem cells derived from the normal marrow and peripheral blood after mobilization, the opposite situation was observed, i.e. TRPM2 gene showed increased expression while PARP1 and PARP2 gene expression was reduced. We observed positive correlations between PARP1, PARP2, PARP3, and TRPM2 genes expression in the group of mature mononuclear cells derived from the peripheral blood and in the group of bone marrow-derived cells. In AML cells significant correlations were not observed between the expression of the examined genes. In addition, we observed that the reduced expression of TRPM2 and overexpression of PARP1 are associated with a shorter overall survival of patients, indicating the prognostic significance of these genes expression in AML. CONCLUSIONS: Our research suggests that in physiological conditions in the cells of the hematopoietic system there is mutual positive regulation of PARP1, PARP2, PARP3, and TRPM2 genes expression. PARP1, PARP2, and TRPM2 genes at mRNA level deregulate in acute myeloid leukemia cells. BioMed Central 2020-05-18 /pmc/articles/PMC7236215/ /pubmed/32423430 http://dx.doi.org/10.1186/s12885-020-06903-4 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. 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 in a credit line to the data.
spellingShingle Research Article
Gil-Kulik, Paulina
Dudzińska, Ewa
Radzikowska-Büchner, Elżbieta
Wawer, Joanna
Jojczuk, Mariusz
Nogalski, Adam
Wawer, Genowefa Anna
Feldo, Marcin
Kocki, Wojciech
Cioch, Maria
Bogucka-Kocka, Anna
Rahnama, Mansur
Kocki, Janusz
Different regulation of PARP1, PARP2, PARP3 and TRPM2 genes expression in acute myeloid leukemia cells
title Different regulation of PARP1, PARP2, PARP3 and TRPM2 genes expression in acute myeloid leukemia cells
title_full Different regulation of PARP1, PARP2, PARP3 and TRPM2 genes expression in acute myeloid leukemia cells
title_fullStr Different regulation of PARP1, PARP2, PARP3 and TRPM2 genes expression in acute myeloid leukemia cells
title_full_unstemmed Different regulation of PARP1, PARP2, PARP3 and TRPM2 genes expression in acute myeloid leukemia cells
title_short Different regulation of PARP1, PARP2, PARP3 and TRPM2 genes expression in acute myeloid leukemia cells
title_sort different regulation of parp1, parp2, parp3 and trpm2 genes expression in acute myeloid leukemia cells
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7236215/
https://www.ncbi.nlm.nih.gov/pubmed/32423430
http://dx.doi.org/10.1186/s12885-020-06903-4
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