Evidence map›Paper›PMID 25634356›Full record

ArticleThe Journal of investigative dermatology2015

The High Expression of the microRNA 17-92 Cluster and its Paralogs, and the Downregulation of the Target Gene PTEN, Is Associated with Primary Cutaneous B-Cell Lymphoma Progression.

Maxime Battistella, Martha Romero, Luis-Jaime Castro-Vega, Guillaume Gapihan, Fatiha Bouhidel, Martine Bagot, Jean-Paul Feugeas, Anne Janin

Abstract read
PubMed Publisher
In one paragraph

Article in The Journal of investigative dermatology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed, 1 pooled it
6.0field-weighted citation impact, top 3% 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

23 citing papers in PubMed, 1 synthesis or guideline pooled it, 42 citations in OpenAlex.

  1. Pooled it
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  8. Alkylating anticancer agents and their relations to microRNAs.Cancer drug resistance (Alhambra, Calif.) · 2019
    Review
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  19. The roles of microRNAs in Wilms' tumors.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2016
    Review
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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

8 authors at 7 institutions in 2 countries.

Maxime BattistellaInserm U1165, Institut Universitaire d'Hématologie, Hôpital Saint Louis, Paris, France; Université Paris Diderot, Sorbonne Paris Cité, Laboratoire de Pathologie, UMR-S 1165, Paris, France; AP-HP, Hôpital Saint-Louis, Department of Pathology, Paris, France. Electronic address: maxime.battistella@sls.aphp.fr.
Martha RomeroInserm U1165, Institut Universitaire d'Hématologie, Hôpital Saint Louis, Paris, France; Department of Pathology, Hospital Universitario Fundacion Santa Fe de Bogota, Bogota, Colombia.
Luis-Jaime Castro-VegaINSERM, UMR970, Paris-Cardiovascular Research Center, Paris, France; Université Paris Descartes, Sorbonne Paris Cité, Faculté de Médecine, Paris, France.
Guillaume GapihanInserm U1165, Institut Universitaire d'Hématologie, Hôpital Saint Louis, Paris, France; Université Paris Diderot, Sorbonne Paris Cité, Laboratoire de Pathologie, UMR-S 1165, Paris, France.
Fatiha BouhidelInserm U1165, Institut Universitaire d'Hématologie, Hôpital Saint Louis, Paris, France; Université Paris Diderot, Sorbonne Paris Cité, Laboratoire de Pathologie, UMR-S 1165, Paris, France; AP-HP, Hôpital Saint-Louis, Department of Pathology, Paris, France.
Martine BagotAP-HP, Hôpital Saint-Louis, Department of Dermatology, Paris, France; Inserm, U 976, Paris, France; Université Paris Diderot, Sorbonne Paris Cité, Faculté de Médecine, Paris, France.
Jean-Paul FeugeasINSERM, IAME, UMR 1137, Université Paris Diderot, Paris, France.
Anne JaninInserm U1165, Institut Universitaire d'Hématologie, Hôpital Saint Louis, Paris, France; Université Paris Diderot, Sorbonne Paris Cité, Laboratoire de Pathologie, UMR-S 1165, Paris, France; AP-HP, Hôpital Saint-Louis, Department of Pathology, Paris, France.
Assistance Publique – Hôpitaux de Paris · FRDélégation Paris 7 · FRFundación Santa Fe de Bogotá · COHôpital Saint-Louis · FRInserm · FRSorbonne Paris Cité · FRUniversité Paris Cité · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The oncogenic microRNA (miR) 17-92 cluster has a causative role in the lymphomagenesis of nodal B-cell lymphomas, by activating proliferation and inhibiting apoptosis. Here we analyzed primary cutaneous B-cell lymphomas for the miR-17-92 cluster and its paralogs miR-106a-363 and miR-106b-25. In 22 primary cutaneous diffuse large B-cell lymphomas, leg type (PCLBCL-LT) compared with 22 primary cutaneous follicle center lymphomas (PCFCLs), we found that miR-20a and miR-106a were overexpressed. Multivariate Cox analysis showed that higher miR-20a and miR-20b expression levels were associated with shorter disease-free and overall survival, independently from histological type. Gene expression profiling also showed a downregulation of 8 candidate target genes of miR-20a, miR-20b, and miR-106a in PCLBCL-LT compared with PCFCL. Among the candidate target genes, PTEN, NCOA3, and CAPRIN2 were confirmed to be underexpressed in PCLBCL-LT using quantitative reverse transcriptase-PCR on CD20-positive laser-microdissected tumor cells. In multivariate Cox analysis, lower PTEN mRNA expression level was associated with shorter disease-free survival (DFS), independently from the histological type. Altogether, this molecular and bioinformatic study of 44 patient skin biopsy samples showed that the oncogenic miR-17-92 cluster and its paralogs were involved in cutaneous B-cell lymphoma progression, and that the downregulation of the target gene PTEN was associated with shorter DFS.

Indexed as

Multigene FamilyAdultAgedAged, 80 and overAntigens, CD20ApoptosisBiopsyComputational BiologyDisease-Free SurvivalDisease ProgressionFemaleGene Expression ProfilingGene Expression Regulation, NeoplasticHumansLymphoma, Large B-Cell, DiffuseMaleAntigens, CD20MicroRNAsMIR17HG, humanPTEN PhosphohydrolasePTEN protein, humanRNA, Long NoncodingRNA, Messenger

Identifiers

PMID25634356
OpenAlexW2065022923

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.