Evidence map›Paper›PMID 31748515›Full record

ArticleBlood cancer journal2019

Transcriptome analysis reveals significant differences between primary plasma cell leukemia and multiple myeloma even when sharing a similar genetic background.

Elizabeta A Rojas, Luis A Corchete, María Victoria Mateos, Ramón García-Sanz, Irena Misiewicz-Krzeminska, Norma C Gutiérrez

Open access · goldAbstract read
In one paragraph

Article in Blood cancer journal, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 1 pooled it
2.5field-weighted citation impact, top 10% 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

18 citing papers in PubMed, 1 synthesis or guideline pooled it, 22 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Identification of High-Risk Multiple Myeloma With a Plasma Cell Leukemia-Like Transcriptomic Profile.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2022
    Article
  11. [Update on biology of primary plasma cell leukemia].Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi · 2022
    Article
  12. Review
  13. Review
  14. Review
  15. Article
  16. Review
  17. The Role ofCancers · 2020
    Review
  18. 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

6 authors at 2 institutions in 2 countries.

Elizabeta A RojasCancer Research Center-IBMCC (USAL-CSIC), Salamanca, Spain.
Luis A CorcheteCancer Research Center-IBMCC (USAL-CSIC), Salamanca, Spain.ORCID http://orcid.org/0000-0003-4577-8599
María Victoria MateosCancer Research Center-IBMCC (USAL-CSIC), Salamanca, Spain.
Ramón García-SanzCancer Research Center-IBMCC (USAL-CSIC), Salamanca, Spain.ORCID http://orcid.org/0000-0003-4120-2787
Irena Misiewicz-KrzeminskaCancer Research Center-IBMCC (USAL-CSIC), Salamanca, Spain.
Norma C GutiérrezCancer Research Center-IBMCC (USAL-CSIC), Salamanca, Spain. normagu@usal.es.
Instituto de Investigación Biomédica de Salamanca · ESUniversidad de Salamanca · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Primary plasma cell leukemia (pPCL) is a highly aggressive plasma cell dyscrasia characterised by short remissions and very poor survival. Although the 17p deletion is associated with poor outcome and extramedullary disease in MM, its presence does not confer the degree of aggressiveness observed in pPCL. The comprehensive exploration of isoform expression and RNA splicing events may provide novel information about biological differences between the two diseases. Transcriptomic studies were carried out in nine newly diagnosed pPCL and ten MM samples, all of which harbored the 17p deletion. Unsupervised cluster analysis clearly distinguished pPCL from MM samples. In total 3584 genes and 20033 isoforms were found to be deregulated between pPCL and MM. There were 2727 significantly deregulated isoforms of non-differentially expressed genes. Strangely enough, significant differences were observed in the expression of spliceosomal machinery components between pPCL and MM, in respect of the gene, isoform and the alternative splicing events expression. In summary, transcriptome analysis revealed significant differences in the relative abundance of isoforms between pPCL and MM, even when they both had the 17p deletion. The mRNA processing pathway including RNA splicing machinery emerged as one of the most remarkable mechanisms underlying the biological differences between the two entities.

Indexed as

Genetic BackgroundGenetic Predisposition to DiseaseTranscriptomeAgedAged, 80 and overAlternative SplicingBiomarkers, TumorChromosome AberrationsFemaleGene Expression ProfilingGene Expression Regulation, NeoplasticGenetic Association StudiesHumansLeukemia, Plasma CellMaleMiddle AgedBiomarkers, Tumor

Identifiers

PMID31748515
PMCPMC6868169
OpenAlexW2990797792

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.