Evidence map›Paper›PMID 29216917›Full record

ArticleLipids in health and disease2017

Unexpected profile of sphingolipid contents in blood and bone marrow plasma collected from patients diagnosed with acute myeloid leukemia.

Marzena Wątek, Bonita Durnaś, Tomasz Wollny, Marcin Pasiarski, Stanisław Góźdź, Michał Marzec, Anna Chabowska, Przemysław Wolak, Małgorzata Żendzian-Piotrowska, Robert Bucki

Open access · goldAbstract read
In one paragraph

Article in Lipids in health and disease, 2017. 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 19% 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, 27 citations in OpenAlex.

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  15. Hypogelsolinemia in Patients Diagnosed with Acute Myeloid Leukemia at Initial Stage of Sepsis.Medical science monitor : international medical journal of experimental and clinical research · 2019
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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

10 authors at 4 institutions in 2 countries.

Marzena WątekDepartment of Hematology, Holy Cross Oncology Center of Kielce, Artwińskiego 3, 25-734, Kielce, Poland.
Bonita DurnaśFaculty of Medicine and Health Sciences of the Jan Kochanowski University in Kielce, Kielce, Poland.
Tomasz WollnyDepartment of Hematology, Holy Cross Oncology Center of Kielce, Artwińskiego 3, 25-734, Kielce, Poland.
Marcin PasiarskiDepartment of Hematology, Holy Cross Oncology Center of Kielce, Artwińskiego 3, 25-734, Kielce, Poland.
Stanisław GóźdźDepartment of Hematology, Holy Cross Oncology Center of Kielce, Artwińskiego 3, 25-734, Kielce, Poland.
Michał MarzecDepartment of Pathology and Laboratory Medicine, University of Pennsylvania, Philadelphia, PA, USA.
Anna ChabowskaRegional Blood Transfusion Center in Bialystok, 15-950, Bialystok, Poland.
Przemysław WolakFaculty of Medicine and Health Sciences of the Jan Kochanowski University in Kielce, Kielce, Poland.
Małgorzata Żendzian-PiotrowskaDepartment of Hygiene, Epidemiology and Ergonomics Department Medical University of Bialystok, 15-222, Bialystok, Poland.
Robert BuckiFaculty of Medicine and Health Sciences of the Jan Kochanowski University in Kielce, Kielce, Poland. buckirobert@gmail.com.ORCID http://orcid.org/0000-0001-7664-9226
Jan Kochanowski University · PLHoly Cross University · PLMedical University of Białystok · PLUniversity of Pennsylvania · US

Funding

NCN Poland UMO-2015/17/B/NZ6/03473Uniwersytet Medyczny w Bialymstoku N/ST/ZB/16/003/1118
6 · The paper itself

Abstract

backgroundImpaired apoptotic pathways in leukemic cells enable them to grow in an uncontrolled way. Moreover, aberrations in the apoptotic pathways are the main factor of leukemic cells drug resistance.

methodsTo assess the presence of potential abnormalities that might promote dysfunction of leukemic cells growth, HPLC system was used to determine sphingosine (SFO), sphinganine (SFA), sphingosine-1-phosphate (S1P) and ceramide (CER) concentration in the blood collected from patients diagnose with acute myeloblastic leukemia (AML; n = 49) and compare to values of control (healthily) group (n = 51). Additionally, in AML group concentration of SFO, SFA, S1P and CER was determined in bone marrow plasma and compared to respective values in blood plasma. The concentration of S1P and CER binding protein - plasma gelsolin (GSN) was also assessed in collected samples using immunoblotting assay.

resultsWe observed that in AML patients the average SFO, SFA and CER concentration in blood plasma was significantly higher (p < 0.001) compare to control group, when blood plasma S1P concentration was significantly lower (p < 0.001). At the same time the CER/S1P ratio in AML patient (44.5 ± 19.4) was about 54% higher compare to control group (20.9 ± 13.1). Interestingly the average concentration of S1P in blood plasma (196 ± 13 pmol/ml) was higher compare to its concentration in plasma collected from bone marrow (154 ± 21 pmol/ml).

conclusionsWe hypothesize that changes in profile of sphingolipids concentration and some of their binding protein partners such as GSN in extracellular environment of blood and bone marrow cells in leukemic patients can be targeted to develop new AML treatment method(s).

Indexed as

AdultAgedAged, 80 and overBone MarrowCase-Control StudiesCeramidesFemaleGelsolinHumansLeukemia, Myeloid, AcuteLysophospholipidsMaleMiddle AgedSphingosineCeramidesGelsolinLysophospholipidssafingolSphingosinesphingosine 1-phosphateAcute myeloid leukemiaCeramideHematological malignanciesPlasma gelsolinS1PSphingolipids

Identifiers

PMID29216917
PMCPMC5721620
OpenAlexW2772394332

What OpenQuestion holds

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LicenceCC BY
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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.