Evidence map›Paper›PMID 36675221›Full record

ArticleInternational journal of molecular sciences2023

Prognostic Value of the miR-17~92 Cluster in Chronic Lymphocytic Leukemia.

Sylwia Chocholska, Michał Zarobkiewicz, Agata Szymańska, Natalia Lehman, Justyna Woś, Agnieszka Bojarska-Junak

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
4.9field-weighted citation impact, top 5% 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

12 citing papers in PubMed, 1 synthesis or guideline pooled it, 17 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
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  11. Article
  12. Role of microRNAs in Chronic Lymphocytic Leukemia.International journal of molecular sciences · 2023
    Review
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 1 institution in 1 country.

Sylwia ChocholskaDepartment of Haematooncology and Bone Marrow Transplantation, Medical University of Lublin, 20-080 Lublin, Poland.ORCID 0000-0002-5001-9258
Michał ZarobkiewiczDepartment of Clinical Immunology, Medical University of Lublin, 20-093 Lublin, Poland.ORCID 0000-0003-0788-6353
Agata SzymańskaDepartment of Clinical Transplantology, Medical University of Lublin, 20-093 Lublin, Poland.ORCID 0000-0002-3764-7452
Natalia LehmanDepartment of Clinical Immunology, Medical University of Lublin, 20-093 Lublin, Poland.ORCID 0000-0003-2324-5679
Justyna WośDepartment of Clinical Immunology, Medical University of Lublin, 20-093 Lublin, Poland.
Agnieszka Bojarska-JunakDepartment of Clinical Immunology, Medical University of Lublin, 20-093 Lublin, Poland.ORCID 0000-0003-2340-9442
Medical University of Lublin · PL

Funding

Medical University of Lublin DS 458
6 · The paper itself

Abstract

The aim of this study was to investigate the expression of miR-17∼92 cluster members in chronic lymphocytic leukemia (CLL) patients. Six microRNAs (miRNAs)-miR-17, miR-18a, miR-19a, miR-19b-1, miR-20a, and miR-92a-1-very poorly characterized in CLL patients, were chosen for the study to consider their possible role as cancer biomarkers. It is currently unclear to which extent miR-17~92 expression is related to other routinely measured CLL markers, and whether the findings can be of any clinical significance. To achieve this goal, we report the expression levels of these miRNAs detected by RT-qPCR in purified CD19+ B lymphocytes of 107 CLL patients and correlate them with existing clinical data. The study provides new evidence regarding the heterogeneity of miR-17~92 cluster members' expression in CLL patients. Higher miR-17-5p expression was associated with unfavorable prognostic factors (i.e., 17p and 11q deletions, CD38 and ZAP-70 expression). On the other hand, miR-19a, miR-20a, and miR-92a-1 negatively correlated with these adverse factors. The presence of del(13q) as a sole aberration was associated with a significantly lower miR-17-5p as well as higher miR-19a-3p and miR-92a-1-5p expression compared to patients carrying unfavorable genetic aberrations. Particularly, miR-20a could be considered an independent favorable prognostic factor. In a multivariate analysis, high miR-20a expression remained an independent marker predicting long TTT (time to treatment) for CLL patients.

Indexed as

Leukemia, Lymphocytic, Chronic, B-CellMicroRNAsB-LymphocytesHumansPrognosisMicroRNAsMIRN17 microRNA, humanCLLmicroRNAmiR-17∼92-clusterprognostic markers

Identifiers

PMID36675221
PMCPMC9866777
OpenAlexW4316371454

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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.