Evidence map›Paper›PMID 31013696›Full record

ArticleInternational journal of molecular sciences2019

Molecular and Functional Verification of Wharton's Jelly Mesenchymal Stem Cells (WJ-MSCs) Pluripotency.

Aleksandra Musiał-Wysocka, Marta Kot, Maciej Sułkowski, Bogna Badyra, Marcin Majka

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04224207 (Management of Retinitis Pigmentosa by Wharton's Jelly Derived Mesenchymal Stem Cells), which is not on this map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
4.3field-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.

NCT04224207 phase3completednot on this map

Management of Retinitis Pigmentosa by Wharton's Jelly Derived Mesenchymal Stem Cells: Preliminary Clinical Results

TypeinterventionalSponsorAnkara Universitesi TeknokentRan2019 to 2020Enrolled32ConditionsRetinitis Pigmentosa, Inherited Retinal DystrophyArmsWharton's jelly derived mesenchymal stem cell
3 · Its place in the literature

Who cites it

38 citing papers in PubMed, 60 citations in OpenAlex.

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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

5 authors at 1 institution in 1 country.

Aleksandra Musiał-WysockaDepartment of Transplantation, Faculty of Clinical Immunology and Transplantation, Institute of Pediatrics, Collegium Medicum Jagiellonian University, Wielicka 265, 30-663 Kraków, Poland. aleksandra.musial@uj.edu.pl.ORCID 0000-0002-5366-9598
Marta KotDepartment of Transplantation, Faculty of Clinical Immunology and Transplantation, Institute of Pediatrics, Collegium Medicum Jagiellonian University, Wielicka 265, 30-663 Kraków, Poland. marta.kot@uj.edu.pl.ORCID 0000-0002-0602-0411
Maciej SułkowskiDepartment of Transplantation, Faculty of Clinical Immunology and Transplantation, Institute of Pediatrics, Collegium Medicum Jagiellonian University, Wielicka 265, 30-663 Kraków, Poland. maciek.sulkowski@uj.edu.pl.ORCID 0000-0002-7045-8258
Bogna BadyraDepartment of Transplantation, Faculty of Clinical Immunology and Transplantation, Institute of Pediatrics, Collegium Medicum Jagiellonian University, Wielicka 265, 30-663 Kraków, Poland. bogna.badyra@doctoral.uj.edu.pl.ORCID 0000-0001-9969-1144
Marcin MajkaDepartment of Transplantation, Faculty of Clinical Immunology and Transplantation, Institute of Pediatrics, Collegium Medicum Jagiellonian University, Wielicka 265, 30-663 Kraków, Poland. mmajka@cm-uj.krakow.pl.ORCID 0000-0002-0429-681X
Jagiellonian University · PL

Funding

National Center for Research and Development Strategmed2/265761/10/NCBR/2015
6 · The paper itself

Abstract

The properties of mesenchymal stem cells (MSCs), especially their self-renewal and ability to differentiate into different cell lines, are widely discussed. Considering the fact that MSCs isolated from perinatal tissues reveal higher differentiation capacity than most adult MSCs, we examined mesenchymal stem cells isolated from Wharton's jelly of umbilical cord (WJ-MSCs) in terms of pluripotency markers expression. Our studies showed that WJ-MSCs express some pluripotency markers-such as NANOG, OCT-4, and SSEA-4-but in comparison to iPS cells expression level is significantly lower. The level of expression can be raised under hypoxic conditions. Despite their high proliferation potential and ability to differentiate into different cells type, WJ-MSCs do not form tumors in vivo, the major caveat of iPS cells. Owing to their biological properties, high plasticity, proliferation capacity, and ease of isolation and culture, WJ-MSCs are turning out to be a promising tool of modern regenerative medicine.

Indexed as

Cell DifferentiationCell Self RenewalAnimalsBiomarkersCell LineCells, CulturedCell Transformation, NeoplasticFemaleGene Expression ProfilingHumansImmunophenotypingMesenchymal Stem CellsMicePluripotent Stem CellsPregnancyTranscriptomeBiomarkersiPSmesenchymal stem cellsNanogOCT-4pluripotencySSEA-4WJ-MSC

Identifiers

PMID31013696
PMCPMC6515095
OpenAlexW2936188734

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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.