Evidence map›Paper›PMID 38418133›Full record

ArticleIn vivo (Athens, Greece)

Clinical Relevance of Differential

Nikolay Kalitin, Galina Dudina, Natalia Kostritsa, Anastasiya Sivirinova, Andrey Vaiman, Aida Karamysheva

Open access · diamondAbstract read
In one paragraph

Article in In vivo (Athens, Greece). The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 98% 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

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

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

6 authors at 3 institutions in 1 country.

Nikolay KalitinLaboratory of Tumor Cell Genetics, N.N. Blokhin National Medical Research Center of Oncology, Moscow, Russian Federation; f.oskolov@mail.ru.
Galina DudinaDepartment of Oncohematology, A.S. Loginov Moscow Clinical Scientific Center, Moscow, Russian Federation.
Natalia KostritsaFaculty of Fundamental Medicine, M.V. Lomonosov Moscow State University, Moscow, Russian Federation.
Anastasiya SivirinovaFaculty of Fundamental Medicine, M.V. Lomonosov Moscow State University, Moscow, Russian Federation.
Andrey VaimanLaboratory of Tumor Cell Genetics, N.N. Blokhin National Medical Research Center of Oncology, Moscow, Russian Federation.
Aida KaramyshevaFaculty of Fundamental Medicine, M.V. Lomonosov Moscow State University, Moscow, Russian Federation.
Lomonosov Moscow State University · RURussian Cancer Research Center NN Blokhin · RUMoscow Clinical Scientific Center · RU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND/

aimMyelodysplastic syndromes (MDS) are clinically heterogeneous hematological malignancies with an increased risk of transformation to acute myeloid leukemia, emphasizing the importance of identifying new diagnostic and prognostic markers. This study sought to investigate the predictive ability of all-trans retinoic acid (ATRA)-dependent nuclear transcription factors RARα and PPARβ/δ gene expression in MDS patients. MATERIALS AND

methodsPeripheral blood specimens were collected from 49 MDS patients and 15 healthy volunteers. The specimens were further separated in Ficoll density gradient to obtain the mononuclear cells fractions. Gene expression analysis was carried out using quantitative real-time polymerase chain reaction (qRT-PCR) technique.

resultsIn the mononuclear cell fractions of MDS patients, RARα expression was increased (p<0.05) and PPARβ/δ expression was decreased (p<0.01) compared to healthy volunteers. When RARα and PPARβ/δ expression was compared in groups of MDS patients with different risks of disease progression, no statistically significant difference was found for RARα expression, while PPARβ/δ expression was significantly lower in the high-risk group of patients compared to the low-risk group (p<0.05). The expression of RARα was significantly associated with overall survival (p<0.05). ROC analysis showed that the expression of PPARβ/δ, rather than RARα expression, could have potential diagnostic value for MDS patients (AUC=0.75, p=0.003 and AUC=0.65, p=0.081, respectively).

conclusionRARα and PPARβ/δ genes are putative biomarkers that may be associated with the diagnosis and prognosis of MDS.

Indexed as

Myelodysplastic SyndromesPPAR-betaPPAR deltaClinical RelevanceHumansRetinoic Acid Receptor alphaTretinoinPPAR-betaPPAR deltaPPARD protein, humanRARA protein, humanRetinoic Acid Receptor alphaTretinoingene expressionMyelodysplastic syndromesPPARβ/δprognostic significanceRARα

Identifiers

PMID38418133
PMCPMC10905464
OpenAlexW4392250826

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.