Evidence map›Paper›PMID 32985591›Full record

ArticleScientific reports2020

Differential epigenetic regulation between the alternative promoters, PRDM1α and PRDM1β, of the tumour suppressor gene PRDM1 in human multiple myeloma cells.

Raquel Romero-García, Laura Gómez-Jaramillo, Rosa María Mateos, Gema Jiménez-Gómez, Nuria Pedreño-Horrillo, Esther Foncubierta, Juan Francisco Rodríguez-Gutiérrez, Sebastián Garzón, Francisco Mora-López, Carmen Rodríguez and 2 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2020. 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
0.3field-weighted citation impact, top 42% 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

4 citing papers in PubMed, 4 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

12 authors at 4 institutions in 1 country.

Raquel Romero-GarcíaUnidad de Investigación, Hospital Universitario Puerta del Mar, Avenida Ana de Viya 21, 11009, Cádiz, Spain.
Laura Gómez-JaramilloUnidad de Investigación, Hospital Universitario Puerta del Mar, Avenida Ana de Viya 21, 11009, Cádiz, Spain.
Rosa María MateosInstituto de Investigación e Innovación en Ciencias Biomédicas de Cádiz (INiBICA), Avenida Ana de Viya 21, 11009, Cádiz, Spain.
Gema Jiménez-GómezUnidad de Investigación, Hospital Universitario Puerta del Mar, Avenida Ana de Viya 21, 11009, Cádiz, Spain.
Nuria Pedreño-HorrilloUnidad de Investigación, Hospital Universitario Puerta del Mar, Avenida Ana de Viya 21, 11009, Cádiz, Spain.
Esther FoncubiertaUnidad de Investigación, Hospital Universitario Puerta del Mar, Avenida Ana de Viya 21, 11009, Cádiz, Spain.
Juan Francisco Rodríguez-GutiérrezInstituto de Investigación e Innovación en Ciencias Biomédicas de Cádiz (INiBICA), Avenida Ana de Viya 21, 11009, Cádiz, Spain.
Sebastián GarzónInstituto de Investigación e Innovación en Ciencias Biomédicas de Cádiz (INiBICA), Avenida Ana de Viya 21, 11009, Cádiz, Spain.
Francisco Mora-LópezInstituto de Investigación e Innovación en Ciencias Biomédicas de Cádiz (INiBICA), Avenida Ana de Viya 21, 11009, Cádiz, Spain.
Carmen RodríguezInstituto de Investigación e Innovación en Ciencias Biomédicas de Cádiz (INiBICA), Avenida Ana de Viya 21, 11009, Cádiz, Spain.
Luis M ValorUnidad de Investigación, Hospital Universitario Puerta del Mar, Avenida Ana de Viya 21, 11009, Cádiz, Spain.
Antonio Campos-CaroUnidad de Investigación, Hospital Universitario Puerta del Mar, Avenida Ana de Viya 21, 11009, Cádiz, Spain. antonio.campos@uca.es.
Hospital Universitario Puerta del Mar · ESBiomedical Research and Innovation Institute of Cadiz · ESHospital Jerez Puerta del Sur · ESUniversidad de Cádiz · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Multiple myeloma (MM) is a B-cell neoplasm that is characterized by the accumulation of malignant plasma cells in the bone marrow. The transcription factor PRDM1 is a master regulator of plasma cell development and is considered to be an oncosuppressor in several lymphoid neoplasms. The PRDM1β isoform is an alternative promoter of the PRDM1 gene that may interfere with the normal role of the PRDM1α isoform. To explain the induction of the PRDM1β isoform in MM and to offer potential therapeutic strategies to modulate its expression, we characterized the cis regulatory elements and epigenetic status of its promoter. We observed unexpected patterns of hypermethylation and hypomethylation at the PRDM1α and PRDM1β promoters, respectively, and prominent H3K4me1 and H3K9me2 enrichment at the PRDM1β promoter in non-expressing cell lines compared to PRDM1β-expressing cell lines. After treatment with drugs that inhibit DNA methylation, we were able to modify the activity of the PRDM1β promoter but not that of the PRDM1α promoter. Epigenetic drugs may offer the ability to control the expression of the PRDM1α/PRDM1β promoters as components of novel therapeutic approaches.

Indexed as

DNA MethylationPromoter Regions, GeneticApoptosisCell Line, TumorDown-RegulationEpigenesis, GeneticGene Expression Regulation, NeoplasticHumansMultiple MyelomaPositive Regulatory Domain I-Binding Factor 1Positive Regulatory Domain I-Binding Factor 1

Identifiers

PMID32985591
PMCPMC7522722
OpenAlexW3089146751

What OpenQuestion holds

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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.