Evidence map›Paper›PMID 29894486›Full record

ArticlePloS one2018

Mycosis fungoides progression could be regulated by microRNAs.

Rebeca Manso, Nerea Martínez-Magunacelaya, Itziar Eraña-Tomás, Verónica Monsalvez, José L Rodríguez-Peralto, Pablo-L Ortiz-Romero, Carlos Santonja, Ion Cristóbal, Miguel A Piris, Socorro M Rodríguez-Pinilla

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

13 citing papers in PubMed, 19 citations in OpenAlex.

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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

10 authors at 4 institutions in 1 country.

Rebeca MansoPathology Department, Fundación Jiménez Díaz, UAM, Madrid, CIBERONC, Madrid, Spain.ORCID 0000-0002-5450-4146
Nerea Martínez-MagunacelayaLaboratorio de Genómica del Cáncer, IDIVAL, Fundación Marques de Valdecilla, Santander, Spain.
Itziar Eraña-TomásHospital de Torrejón, Pathology Department, Madrid, Spain.
Verónica MonsalvezHospital Universitario 12 de Octubre, Dermatology Department, Madrid, Spain.
José L Rodríguez-PeraltoHospital Universitario 12 de Octubre, Pathology Department, Madrid, CIBERONC, Madrid, Spain.
Pablo-L Ortiz-RomeroHospital Universitario 12 de Octubre, Dermatology Department, Madrid, Spain.
Carlos SantonjaPathology Department, Fundación Jiménez Díaz, UAM, Madrid, CIBERONC, Madrid, Spain.ORCID 0000-0002-1335-0339
Ion CristóbalTranslational Oncology Division, Oncohealth Institute, IIS-Fundación Jiménez Díaz, UAM, Madrid, Spain.
Miguel A PirisPathology Department, Fundación Jiménez Díaz, UAM, Madrid, CIBERONC, Madrid, Spain.
Socorro M Rodríguez-PinillaPathology Department, Fundación Jiménez Díaz, UAM, Madrid, CIBERONC, Madrid, Spain.
Hospital Universitario Fundación Jiménez Díaz · ESHospital Universitario 12 De Octubre · ESFundación Marques de Valdecilla · ESHospital Universitario de Torrejón · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Differentiating early mycosis fungoides (MF) from inflammatory dermatitis is a challenge. We compare the differential expression profile of early-stage MF samples and benign inflammatory dermatoses using microRNA (miRNA) arrays. 114 miRNAs were found to be dysregulated between these entities. The seven most differentially expressed miRNAs between these two conditions were further analyzed using RT-PCR in two series comprising 38 samples of early MFs and 18 samples of inflammatory dermatitis. A series of 51 paraffin-embedded samples belonging to paired stages of 16 MF patients was also analyzed. MiRNAs 26a, 222, 181a and 146a were differentially expressed between tumoral and inflammatory conditions. Two of these miRNAs (miRNA-181a and miRNA-146a) were significantly deregulated between early and advanced MF stages. Bioinformatic analysis showed FOXP3 expression to be regulated by these miRNAs. Immunohistochemistry revealed the level of FOXP3 expression to be lower in tumoral MFs than in plaque lesions in paraffin-embedded tissue. A functional study confirmed that both miRNAs diminished FOXP3 expression when overexpressed in CTCL cells. The data presented here suggest that the analysis of a restricted number of miRNAs (26a, 222, 181a and 146a) could be sufficient to differentiate tumoral from reactive conditions. Moreover, these miRNAs seem to be involved in MF progression.

Indexed as

3' Untranslated RegionsBiomarkers, TumorCell Line, TumorDisease ProgressionFemaleForkhead Transcription FactorsGene Expression Regulation, NeoplasticHumansMaleMicroRNAsMycosis FungoidesSkin Neoplasms3' Untranslated RegionsBiomarkers, TumorForkhead Transcription FactorsFOXP3 protein, humanMicroRNAs

Identifiers

PMID29894486
PMCPMC5997347
OpenAlexW2808600002

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.