Evidence map›Paper›PMID 26484208›Full record

ArticleGenomics data2015

Transcriptome analysis of bone marrow mesenchymal stromal cells from patients with primary myelofibrosis.

Christophe Martinaud, Christophe Desterke, Johanna Konopacki, Alessandro M Vannucchi, Lisa Pieri, Paola Guglielmelli, Brigitte Dupriez, Jean-Christophe Ianotto, Laetitia Boutin, Jean-Jacques Lataillade and 1 more

Open access · goldAbstract read
In one paragraph

Article in Genomics data, 2015. 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
0.7field-weighted citation impact, top 28% 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, 5 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Review
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

11 authors at 4 institutions in 2 countries.

Christophe MartinaudINSERM Unit 1197 and UMS33, Paul Brousse Hospital, Andre Lwoff Institute, France.
Christophe DesterkeINSERM Unit 1197 and UMS33, Paul Brousse Hospital, Andre Lwoff Institute, France.
Johanna KonopackiINSERM Unit 1197 and UMS33, Paul Brousse Hospital, Andre Lwoff Institute, France.
Alessandro M VannucchiINSERM Unit 1197 and UMS33, Paul Brousse Hospital, Andre Lwoff Institute, France.
Lisa PieriINSERM Unit 1197 and UMS33, Paul Brousse Hospital, Andre Lwoff Institute, France.
Paola GuglielmelliINSERM Unit 1197 and UMS33, Paul Brousse Hospital, Andre Lwoff Institute, France.
Brigitte DupriezINSERM Unit 1197 and UMS33, Paul Brousse Hospital, Andre Lwoff Institute, France.
Jean-Christophe IanottoINSERM Unit 1197 and UMS33, Paul Brousse Hospital, Andre Lwoff Institute, France.
Laetitia BoutinINSERM Unit 1197 and UMS33, Paul Brousse Hospital, Andre Lwoff Institute, France.
Jean-Jacques LatailladeINSERM Unit 1197 and UMS33, Paul Brousse Hospital, Andre Lwoff Institute, France.
Marie-Caroline Le Bousse-KerdilèsINSERM Unit 1197 and UMS33, Paul Brousse Hospital, Andre Lwoff Institute, France.
Centre Hospitalier Régional Universitaire de Brest · FRCentre Hospitalier de Lens · FRUniversity of Florence · ITInserm · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Primary myelofibrosis (PMF) is a clonal myeloproliferative neoplasm whose severity and treatment complexity are attributed to the presence of bone marrow (BM) fibrosis and alterations of stroma impairing the production of normal blood cells. Despite the recently discovered mutations including the JAK2V617F mutation in about half of patients, the primitive event responsible for the clonal proliferation is still unknown. In the highly inflammatory context of PMF, the presence of fibrosis associated with a neoangiogenesis and an osteosclerosis concomitant to the myeloproliferation and to the increase number of circulating hematopoietic progenitors suggests that the crosstalk between hematopoietic and stromal cells is deregulated in the PMF BM microenvironmental niches. Within these niches, mesenchymal stromal cells (BM-MSC) play a hematopoietic supportive role in the production of growth factors and extracellular matrix which regulate the proliferation, differentiation, adhesion and migration of hematopoietic stem/progenitor cells. A transcriptome analysis of BM-MSC in PMF patients will help to characterize their molecular alterations and to understand their involvement in the hematopoietic stem/progenitor cell deregulation that features PMF.

Indexed as

Bone marrowMesenchymal stroma cellsMyeloproliferative disordersPrimary myelofibrosis

Identifiers

PMID26484208
PMCPMC4583614
OpenAlexW2153979886

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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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.