Evidence map›Paper›PMID 40126346›Full record

ReviewNon-coding RNA2025

Mechanism of Action of circRNA/miRNA Network in DLBCL.

Elena Golovina, Cory Eaton, Virginia Cox, Jozef Andel, Karina Savvulidi Vargova

Abstract readReview
In one paragraph

Review in Non-coding RNA, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
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

4 citing papers in PubMed.

  1. Review
  2. METTL3-dependent mJournal of translational medicine · 2026
    Article
  3. Review
  4. Article
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

5 authors.

Elena GolovinaFirst Faculty of Medicine, Institute of Pathological Physiology, Charles University, 12108 Prague, Czech Republic.
Cory EatonFirst Faculty of Medicine, Institute of Pathological Physiology, Charles University, 12108 Prague, Czech Republic.
Virginia CoxFirst Faculty of Medicine, Institute of Pathological Physiology, Charles University, 12108 Prague, Czech Republic.
Jozef AndelFirst Faculty of Medicine, Institute of Pathological Physiology, Charles University, 12108 Prague, Czech Republic.
Karina Savvulidi VargovaFirst Faculty of Medicine, Institute of Pathological Physiology, Charles University, 12108 Prague, Czech Republic.ORCID 0000-0002-4969-4133

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Circular RNAs (circRNAs) make up approximately 10% of the human transcriptome. CircRNAs belong to the broad group of non-coding RNAs and characteristically are formed by backsplicing into a stable circular loop. Their main role is to regulate transcription through the inhibition of miRNAs' expression, termed miRNA sponging. CircRNAs promote tumorigenesis/lymphomagenesis by competitively binding to miRNAs at miRNA binding sites. In diffuse large B-cell lymphoma (DLBCL), several circRNAs have been identified and their expression is related to both progression and response to therapy. DLBCL is the most prevalent and aggressive subtype of B-cell lymphomas and accounts for about 25% to 30% of all non-Hodgkin lymphomas. DLBCL displays great heterogeneity concerning histopathology, biology, and genetics. Patients who have relapsed or have refractory disease after first-line therapy have a very poor prognosis, demonstrating an important unmet need for new treatment options. As more circRNAs are identified in the future, we will better understand their biological roles and potential use in treating cancer, including DLBCL. For example, circAmotl1 promotes nuclear translocation of

Indexed as

B-cellscircRNAgene expressionlymphomamiRNA

Identifiers

PMID40126346
PMCPMC11932212

What OpenQuestion holds

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Registered trials

None linked

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.