Evidence map›Paper›PMID 32423430›Full record

ArticleBMC cancer2020

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

Paulina Gil-Kulik, Ewa Dudzińska, Elżbieta Radzikowska-Büchner, Joanna Wawer, Mariusz Jojczuk, Adam Nogalski, Genowefa Anna Wawer, Marcin Feldo, Wojciech Kocki, Maria Cioch and 3 more

Open access · goldAbstract read
In one paragraph

Article in BMC cancer, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.3field-weighted citation impact, top 18% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

18 citing papers in PubMed, 30 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors at 3 institutions in 2 countries.

Paulina Gil-KulikDepartment of Clinical Genetics, Medical University of Lublin, 11 Radziwillowska Str, 20-080, Lublin, Poland. pgil.poczt@vp.pl.ORCID http://orcid.org/0000-0003-3119-981X
Ewa DudzińskaDepartment of Public Health, Faculty of Health Sciences, Medical University of Lublin, 1 Chodźki Str, 20-093, Lublin, Poland.
Elżbieta Radzikowska-BüchnerDepartment of Plastic Surgery, Saint Elizabeth's Hospital, 1 Goszczynskiego Str, 02-616, Warsaw, Poland.
Joanna WawerDepartment of Clinical Genetics, Medical University of Lublin, 11 Radziwillowska Str, 20-080, Lublin, Poland.
Mariusz JojczukChair and Department of Trauma Surgery and Emergency Medicine, Medical University of Lublin, 16 Staszica Str, 20-081, Lublin, Poland.
Adam NogalskiChair and Department of Trauma Surgery and Emergency Medicine, Medical University of Lublin, 16 Staszica Str, 20-081, Lublin, Poland.
Genowefa Anna WawerDepartment of Foreign Languages Medical University of Lublin, 4 Jaczewskiego Str, 20-090, Lublin, Poland.
Marcin FeldoChair and Department of Vascular Surgery and Angiology, Medical University of Lublin, 11 Staszica Str, 20-081, Lublin, Poland.
Wojciech KockiDepartment of Architecture and Urban Planning, University of Technology, 40 Nadbystrzycka Str, 20-618, Lublin, Poland.
Maria CiochChair and Department of Hematooncology and Bone Marrow Transplantation, Medical University of Lublin, 11 Staszica Str, 20-081, Lublin, Poland.
Anna Bogucka-KockaChair and Department of Biology and Genetics, Medical University of Lublin, 4a Chodźki Str, 20-093, Lublin, Poland.
Mansur RahnamaChair and Department of Dental Surgery Medical University of Lublin, 7 Karmelicka Str, 20-081, Lublin, Poland.
Janusz KockiDepartment of Clinical Genetics, Medical University of Lublin, 11 Radziwillowska Str, 20-080, Lublin, Poland.
Medical University of Lublin · PLLublin University of Technology · PLSt. Elizabeth's Hospital · PK

Funding

Narodowe Centrum Badań i Rozwoju STRATEGMED3/303570/7/NCBR/2017
6 · The paper itself

Abstract

backgroundAcute 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.

methodsThe 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.

resultsThe 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.

conclusionsOur 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.

Indexed as

Gene Expression Regulation, NeoplasticAdultAgedBiomarkers, TumorBone Marrow CellsCase-Control StudiesCell Cycle ProteinsFemaleFollow-Up StudiesHematopoietic Stem CellsHumansLeukemia, Myeloid, AcuteMaleMiddle AgedPoly (ADP-Ribose) Polymerase-1Poly(ADP-ribose) PolymerasesBiomarkers, TumorCell Cycle ProteinsPARP1 protein, humanPARP2 protein, humanPARP3 protein, humanPoly (ADP-Ribose) Polymerase-1Poly(ADP-ribose) PolymerasesTRPM2 protein, humanTRPM Cation ChannelsAMLHematopoietic stem cellsPARP1PARP2PARP3TRPM2 gene expression

Identifiers

PMID32423430
PMCPMC7236215
OpenAlexW3027289376

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.