Evidence map›Paper›PMID 28676126›Full record

Trial reportStem cell research & therapy2017

Umbilical cord-derived mesenchymal stromal cells: predictive obstetric factors for cell proliferation and chondrogenic differentiation.

Léonore Avercenc-Léger, Philippe Guerci, Jean-Marc Virion, Ghislaine Cauchois, Sébastien Hupont, Rachid Rahouadj, Jacques Magdalou, Jean-François Stoltz, Danièle Bensoussan, Céline Huselstein and 1 more

Abstract readRandomized Controlled Trial
In one paragraph

Trial report in Stem cell research & therapy, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing 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

17 citing papers in PubMed.

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  9. The in vitro treatment of mesenchymal stem cells for colorectal cancer cells.Medical oncology (Northwood, London, England) · 2023
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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

11 authors.

Léonore Avercenc-LégerUMR 7365 CNRS-Université de Lorraine, Ingénierie Moléculaire et Physiopathologie Articulaire (IMoPA), Biopôle de l'Université de Lorraine, Campus biologie-santé, Faculté de Médecine, Avenue de la Forêt de Haye, BP 184, 54500, Vandoeuvre-Les-nancy, France.
Philippe GuerciCHRU de Nancy, Maternité Régionale Universitaire, Département d'Anesthésie-Réanimation, 54000, Nancy, France.
Jean-Marc VirionCHRU de Nancy, Epidémiologie et Evaluation Cliniques, 54500, Vandœuvre-lès-Nancy, France.
Ghislaine CauchoisUMR 7365 CNRS-Université de Lorraine, Ingénierie Moléculaire et Physiopathologie Articulaire (IMoPA), Biopôle de l'Université de Lorraine, Campus biologie-santé, Faculté de Médecine, Avenue de la Forêt de Haye, BP 184, 54500, Vandoeuvre-Les-nancy, France.
Sébastien HupontFR3209 CNRS BMCT - Bio-Ingénierie Moléculaire Cellulaire et Thérapeutique, Faculté de Médecine, 54500, Vandœuvre-lès-Nancy, France.
Rachid RahouadjUniversité de Lorraine, 54000, Nancy, France.
Jacques MagdalouUMR 7365 CNRS-Université de Lorraine, Ingénierie Moléculaire et Physiopathologie Articulaire (IMoPA), Biopôle de l'Université de Lorraine, Campus biologie-santé, Faculté de Médecine, Avenue de la Forêt de Haye, BP 184, 54500, Vandoeuvre-Les-nancy, France.
Jean-François StoltzUMR 7365 CNRS-Université de Lorraine, Ingénierie Moléculaire et Physiopathologie Articulaire (IMoPA), Biopôle de l'Université de Lorraine, Campus biologie-santé, Faculté de Médecine, Avenue de la Forêt de Haye, BP 184, 54500, Vandoeuvre-Les-nancy, France.
Danièle BensoussanUMR 7365 CNRS-Université de Lorraine, Ingénierie Moléculaire et Physiopathologie Articulaire (IMoPA), Biopôle de l'Université de Lorraine, Campus biologie-santé, Faculté de Médecine, Avenue de la Forêt de Haye, BP 184, 54500, Vandoeuvre-Les-nancy, France.
Céline HuselsteinUMR 7365 CNRS-Université de Lorraine, Ingénierie Moléculaire et Physiopathologie Articulaire (IMoPA), Biopôle de l'Université de Lorraine, Campus biologie-santé, Faculté de Médecine, Avenue de la Forêt de Haye, BP 184, 54500, Vandoeuvre-Les-nancy, France.
Loïc ReppelUMR 7365 CNRS-Université de Lorraine, Ingénierie Moléculaire et Physiopathologie Articulaire (IMoPA), Biopôle de l'Université de Lorraine, Campus biologie-santé, Faculté de Médecine, Avenue de la Forêt de Haye, BP 184, 54500, Vandoeuvre-Les-nancy, France. loic.reppel@univ-lorraine.fr.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe umbilical cord is becoming a notable alternative to bone marrow (BM) as a source of mesenchymal stromal cells (MSC). Although age-dependent variations in BM-MSC are well described, less data are available for MSC isolated from Wharton's jelly (WJ-MSC). We initiated a study to identify whether obstetric factors influenced MSC properties. We aimed to evaluate the correlation between a large number of obstetric factors collected during pregnancy and until peripartum (related to the mother, the labor and delivery, and the newborn) with WJ-MSC proliferation and chondrogenic differentiation parameters.

methodsCorrelations were made between 27 obstetric factors and 8 biological indicators including doubling time at passage (P)1 and P2, the percentage of proteoglycans and collagens, and the relative transcriptional expression of Sox-9, aggrecans, and total type 2 collagen (Coll2T).

resultsAmongst the obstetric factors considered, birth weight, the number of amenorrhea weeks, placental weight, normal pregnancy, and the absence of preeclampsia were identified as relevant factors for cell expansion, using multivariate linear regression analysis. Since all the above parameters are related to term, we concluded that WJ-MSC from healthy, full-term infants exhibit greater proliferation capacity. As for chondrogenesis, we also observed that obstetric factors influencing proliferation seemed beneficial, with no negative impact on MSC differentiation.

conclusionsAwareness of obstetric factors influencing the proliferation and/or differentiation of WJ-MSC will make it possible to define criteria for collecting optimal umbilical cords with the aim of decreasing the variability of WJ-MSC batches produced for clinical use in cell and tissue engineering.

Indexed as

AmenorrheaBirth WeightCell DifferentiationCell ProliferationChondrogenesisAdultCollagen Type IIFemaleHumansMesenchymal Stem CellsPregnancyRisk FactorsSOX9 Transcription FactorUmbilical CordCollagen Type IISOX9 protein, humanSOX9 Transcription FactorChondrogenic differentiationMesenchymal stromal cellsObstetric factorsProliferationUmbilical cordWharton’s jelly

Identifiers

PMID28676126
PMCPMC5497358

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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.