Evidence map›Paper›PMID 36961799›Full record

ArticlePloS one2023

Identification of two unannotated miRNAs in classic Hodgkin lymphoma cell lines.

Adam Ustaszewski, Julia Paczkowska, Joanna Janiszewska, Stephan H Bernhart, Julia Bein, Núria Russiñol, Martin-Leo Hansmann, Vicente Chapaprieta, José I Martín-Subero, Reiner Siebert and 2 more

Open access · goldFull text read
In one paragraph

Article in PloS one, 2023. 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
0.2field-weighted citation impact, top 33% 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, 1 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

12 authors at 6 institutions in 3 countries.

Adam UstaszewskiInstitute of Human Genetics, Polish Academy of Sciences Poznan, Poznan, Poland.ORCID 0000-0002-9542-0029
Julia PaczkowskaInstitute of Human Genetics, Polish Academy of Sciences Poznan, Poznan, Poland.
Joanna JaniszewskaInstitute of Human Genetics, Polish Academy of Sciences Poznan, Poznan, Poland.
Stephan H BernhartInterdisciplinary Center for Bioinformatics, Transcriptome Bioinformatics, University of Leipzig, Leipzig, Germany.
Julia BeinDr. Senckenberg Institute of Pathology, Goethe University Frankfurt, Frankfurt am Main, Germany.
Núria RussiñolInstitut d'Investigacions Biomèdiques August Pi I Sunyer, IDIBAPS, Barcelona, Spain.
Martin-Leo HansmannFrankfurt Institute of Advanced Studies, Frankfurt am Main, Germany.
Vicente ChapaprietaInstitut d'Investigacions Biomèdiques August Pi I Sunyer, IDIBAPS, Barcelona, Spain.ORCID 0000-0002-4910-5394
José I Martín-SuberoInstitut d'Investigacions Biomèdiques August Pi I Sunyer, IDIBAPS, Barcelona, Spain.
Reiner SiebertInstitute of Human Genetics, Ulm University and Ulm University Medical Center, Ulm, Germany.
Sylvia HartmannDr. Senckenberg Institute of Pathology, Goethe University Frankfurt, Frankfurt am Main, Germany.
Maciej GiefingInstitute of Human Genetics, Polish Academy of Sciences Poznan, Poznan, Poland.ORCID 0000-0002-4760-8246
Institute of Human Genetics · PLGoethe University Frankfurt · DEConsorci Institut D'Investigacions Biomediques August Pi I Sunyer · ESInstitució Catalana de Recerca i Estudis Avançats · ESLeipzig University · DEUniversität Ulm · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

MicroRNAs (miRNAs) are small non coding RNAs responsible for posttranscriptional regulation of gene expression. Even though almost 2000 precursors have been described so far, additional miRNAs are still being discovered in normal as well as malignant cells. Alike protein coding genes, miRNAs may acquire oncogenic properties in consequence of altered expression or presence of gain or loss of function mutations. In this study we mined datasets from miRNA expression profiling (miRNA-seq) of 7 classic Hodgkin Lymphoma (cHL) cell lines, 10 non-Hodgkin lymphoma (NHL) cell lines and 56 samples of germinal center derived B-cell lymphomas. Our aim was to discover potential novel cHL oncomiRs not reported in miRBase (release 22.1) and expressed in cHL cell lines but no other B-cell lymphomas. We identified six such miRNA candidates in cHL cell lines and verified the expression of two of them encoded at chr2:212678788-212678849 and chr5:168090507-168090561 (GRCh38). Interestingly, we showed that one of the validated miRNAs (located in an intron of the TENM2 gene) is expressed together with its host gene. TENM2 is characterized by hypomethylation and open chromatin around its TSS in cHL cell lines in contrast to NHL cell lines and germinal centre B-cells respectively. It indicates an epigenetic mechanism responsible for aberrant expression of both, the TENM2 gene and the novel miRNA in cHL cell lines. Despite the GO analysis performed with the input of the in silico predicted novel miRNA target genes did not reveal ontologies typically associated with cHL pathogenesis, it pointed to several interesting candidates involved in i.e. lymphopoiesis. These include the lymphoma related BCL11A gene, the IKZF2 gene involved in lymphocyte development or the transcription initiator GTF2H1.

Indexed as

Hodgkin DiseaseLymphoma, B-CellLymphoma, Non-HodgkinMicroRNAsCell LineGene Expression Regulation, NeoplasticGerminal CenterHumansTranscription Factor TFIIHGTF2H1 protein, humanMicroRNAsTranscription Factor TFIIH

Identifiers

PMID36961799
PMCPMC10038261
OpenAlexW4324314945

What OpenQuestion holds

Textfull text, public
LicenceCC BY
reference markers read1
measurements read44
identifiers read9
Read underepoch 390

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.