Evidence map›Paper›PMID 34088266›Full record

ArticleBMC genomics2021

Long non-coding RNA exploration for mesenchymal stem cell characterisation.

Sébastien Riquier, Marc Mathieu, Chloé Bessiere, Anthony Boureux, Florence Ruffle, Jean-Marc Lemaitre, Farida Djouad, Nicolas Gilbert, Thérèse Commes

Abstract read
In one paragraph

Article in BMC genomics, 2021. 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
–field-weighted citation impact
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.

  1. Article
  2. Article
  3. Article
  4. Kmerator Suite: design of specificNAR genomics and bioinformatics · 2021
    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

9 authors.

Sébastien RiquierIRMB, University of Montpellier, INSERM, 80 rue Augustin Fliche, Montpellier, France.
Marc MathieuIRMB, University of Montpellier, INSERM, 80 rue Augustin Fliche, Montpellier, France.
Chloé BessiereIRMB, University of Montpellier, INSERM, 80 rue Augustin Fliche, Montpellier, France.
Anthony BoureuxIRMB, University of Montpellier, INSERM, 80 rue Augustin Fliche, Montpellier, France.
Florence RuffleIRMB, University of Montpellier, INSERM, 80 rue Augustin Fliche, Montpellier, France.
Jean-Marc LemaitreIRMB, University of Montpellier, INSERM, 80 rue Augustin Fliche, Montpellier, France.
Farida DjouadIRMB, University of Montpellier, INSERM, 80 rue Augustin Fliche, Montpellier, France.
Nicolas GilbertIRMB, University of Montpellier, INSERM, 80 rue Augustin Fliche, Montpellier, France.
Thérèse CommesIRMB, University of Montpellier, INSERM, 80 rue Augustin Fliche, Montpellier, France. therese.commes@inserm.fr.

Funding

Agence Nationale de la Recherche 18-CE45-0020-02Agence Nationale de la Recherche ANR-10-INBS-09Canceropole Grand-Sud-Ouest 2017-EM24
6 · The paper itself

Abstract

backgroundThe development of RNA sequencing (RNAseq) and the corresponding emergence of public datasets have created new avenues of transcriptional marker search. The long non-coding RNAs (lncRNAs) constitute an emerging class of transcripts with a potential for high tissue specificity and function. Therefore, we tested the biomarker potential of lncRNAs on Mesenchymal Stem Cells (MSCs), a complex type of adult multipotent stem cells of diverse tissue origins, that is frequently used in clinics but which is lacking extensive characterization.

resultsWe developed a dedicated bioinformatics pipeline for the purpose of building a cell-specific catalogue of unannotated lncRNAs. The pipeline performs ab initio transcript identification, pseudoalignment and uses new methodologies such as a specific k-mer approach for naive quantification of expression in numerous RNAseq data. We next applied it on MSCs, and our pipeline was able to highlight novel lncRNAs with high cell specificity. Furthermore, with original and efficient approaches for functional prediction, we demonstrated that each candidate represents one specific state of MSCs biology.

conclusionsWe showed that our approach can be employed to harness lncRNAs as cell markers. More specifically, our results suggest different candidates as potential actors in MSCs biology and propose promising directions for future experimental investigations.

Indexed as

Mesenchymal Stem CellsRNA, Long NoncodingBase SequenceComputational BiologySequence Analysis, RNARNA, Long NoncodingBioinformaticsLong non-coding RNAMesenchymal stem cellNGS analysisRNAseqTranscriptomics

Identifiers

PMID34088266
PMCPMC8178833

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.