Evidence map›Paper›PMID 24816239›Full record

ArticleHaematologica2014

Transcriptome analysis reveals molecular profiles associated with evolving steps of monoclonal gammopathies.

Lucía López-Corral, Luis Antonio Corchete, María Eugenia Sarasquete, María Victoria Mateos, Ramón García-Sanz, Encarna Fermiñán, Juan-José Lahuerta, Joan Bladé, Albert Oriol, Ana Isabel Teruel and 6 more

Open access · goldAbstract read
In one paragraph

Article in Haematologica, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 55 papers.

0numbers the graph read from it
0cells of the map it votes in
55citing papers in PubMed
4.5field-weighted citation impact, top 5% 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

55 citing papers in PubMed, 87 citations in OpenAlex.

  1. Trial
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  11. Genetic and Epigenetic Aberrations ofCurrent issues in molecular biology · 2025
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  20. Mouse models of human multiple myeloma subgroups.Proceedings of the National Academy of Sciences of the United States of America · 2023
    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

16 authors at 9 institutions in 1 country.

Lucía López-CorralServicio de Hematología del Hospital Universitario de Salamanca, IBSAL IBMCC (USAL-CSIC), Salamanca lucialopezcorral@usal.es.
Luis Antonio CorcheteServicio de Hematología del Hospital Universitario de Salamanca, IBSAL IBMCC (USAL-CSIC), Salamanca.
María Eugenia SarasqueteServicio de Hematología del Hospital Universitario de Salamanca, IBSAL IBMCC (USAL-CSIC), Salamanca.
María Victoria MateosServicio de Hematología del Hospital Universitario de Salamanca, IBSAL IBMCC (USAL-CSIC), Salamanca.
Ramón García-SanzServicio de Hematología del Hospital Universitario de Salamanca, IBSAL IBMCC (USAL-CSIC), Salamanca.
Encarna FermiñánCentro de Investigación del Cáncer-IBMCC (USAL-CSIC), Salamanca.
Juan-José LahuertaServicio de Hematología del Hospital 12 de Octubre, Madrid.
Joan BladéServicio de Hematología del Hospital Clinic, Barcelona.
Albert OriolServicio de Hematología del Hospital Germans Trias i Pujol, Badalona.
Ana Isabel TeruelServicio de Hematología del Hospital Universitario de Valencia.
María Luz MartinoServicio de Hematología del Hospital Virgen del Rocío, Sevilla.
José HernándezServicio de Hematología de Hospital General de Segovia.
Jesús María Hernández-RivasServicio de Hematología del Hospital Universitario de Salamanca, IBSAL IBMCC (USAL-CSIC), Salamanca.
Francisco Javier BurguilloDepartamento de Química Física, Facultad de Farmacia, Universidad de Salamanca, Spain.
Jesús F San MiguelServicio de Hematología del Hospital Universitario de Salamanca, IBSAL IBMCC (USAL-CSIC), Salamanca.
Norma C GutiérrezServicio de Hematología del Hospital Universitario de Salamanca, IBSAL IBMCC (USAL-CSIC), Salamanca.
Instituto de Investigación Biomédica de Salamanca · ESCentro de Investigación del Cáncer · ESHospital Clínic de Barcelona · ESHospital Clínico Universitario de Valencia · ESHospital General De Segovia · ESHospital Universitari Germans Trias i Pujol · ESHospital Universitario 12 De Octubre · ESHospital Universitario Virgen del Rocío · ESUniversidad de Salamanca · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A multistep model has been proposed of disease progression starting in monoclonal gammopathy of undetermined significance continuing through multiple myeloma, sometimes with an intermediate entity called smoldering myeloma, and ending in extramedullary disease. To gain further insights into the role of the transcriptome deregulation in the transition from a normal plasma cell to a clonal plasma cell, and from an indolent clonal plasma cell to a malignant plasma cell, we performed gene expression profiling in 20 patients with monoclonal gammopathy of undetermined significance, 33 with high-risk smoldering myeloma and 41 with multiple myeloma. The analysis showed that 126 genes were differentially expressed in monoclonal gammopathy of undetermined significance, smoldering myeloma and multiple myeloma as compared to normal plasma cell. Interestingly, 17 and 9 out of the 126 significant differentially expressed genes were small nucleolar RNA molecules and zinc finger proteins. Several proapoptotic genes (AKT1 and AKT2) were down-regulated and antiapoptotic genes (APAF1 and BCL2L1) were up-regulated in multiple myeloma, both symptomatic and asymptomatic, compared to monoclonal gammopathy of undetermined significance. When we looked for those genes progressively modulated through the evolving stages of monoclonal gammopathies, eight snoRNA showed a progressive increase while APAF1, VCAN and MEGF9 exhibited a progressive downregulation. In conclusion, our data show that although monoclonal gammopathy of undetermined significance, smoldering myeloma and multiple myeloma are not clearly distinguishable groups according to their gene expression profiling, several signaling pathways and genes were significantly deregulated at different steps of the transformation process.

Indexed as

AdultAgedAged, 80 and overCluster AnalysisFemaleGene Expression ProfilingHumansMaleMiddle AgedParaproteinemias

Identifiers

PMID24816239
PMCPMC4116836
OpenAlexW2131691150

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.