Evidence map›Paper›PMID 39621192›Full record

ArticleJournal of applied genetics2025

Development of a novel gene expression panel for the characterization of MSCs for increased biological safety.

Anna M Różycka-Baczyńska, Igor M Stepaniec, Marta Warzycha, Izabela Zdolińska-Malinowska, Tomasz Oldak, Natalia Rozwadowska, Tomasz J Kolanowski

Abstract read
In one paragraph

Article in Journal of applied genetics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Review
  3. 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

7 authors.

Anna M Różycka-Baczyńska *Research and Development Department, Polski Bank Komórek Macierzystych S.A. (FamiCord Group), Warsaw, Poland.
Igor M Stepaniec *Research and Development Department, Polski Bank Komórek Macierzystych S.A. (FamiCord Group), Warsaw, Poland.
Marta WarzychaResearch and Development Department, Polski Bank Komórek Macierzystych S.A. (FamiCord Group), Warsaw, Poland.
Izabela Zdolińska-MalinowskaResearch and Development Department, Polski Bank Komórek Macierzystych S.A. (FamiCord Group), Warsaw, Poland.
Tomasz OldakResearch and Development Department, Polski Bank Komórek Macierzystych S.A. (FamiCord Group), Warsaw, Poland.
Natalia RozwadowskaInstitute of Human Genetics, Polish Academy of Sciences, Poznan, Poland. natalia.rozwadowska@igcz.poznan.pl.ORCID http://orcid.org/0000-0002-5111-0870
Tomasz J KolanowskiResearch and Development Department, Polski Bank Komórek Macierzystych S.A. (FamiCord Group), Warsaw, Poland.ORCID http://orcid.org/0000-0003-3898-8272

Funding

Ministerstwo Edukacji i Nauki DWD/6/0417/2022Narodowe Centrum Badań i Rozwoju No. POIR.01.02.00-00-00024/17-00Polski Bank Komorek Macierzystych SA (Famicord Group) internal financing
6 · The paper itself

Abstract

Mesenchymal stromal cells (MSCs) have a wide range of therapeutic applications due to their multipotency, immunomodulatory, and anti-inflammatory properties. Their ability to migrate and recolonize damaged tissues is also remarkable. However, the controversial occurrence of spontaneous tumorigenesis or malignant transformation of MSCs raises concerns about proposed cell-based therapies for patients that researchers must address. There are several in vitro and in vivo strategies for MSC safety approval, but there is still no described coherent scheme that allows the assessment of MSC oncogenic potential in a simple, robust, and reproducible manner. Here, we have developed a diagnostic panel of molecular markers that allows for the accurate verification of the quality and safety of MSCs. Moreover, presented in this article diagnostic panel that can define the origin and tumorigenicity of MSCs can be easily introduced into the routine quality control processes of MSC-based product manufacturing which will improve further clinical applications of MSCs.

Indexed as

Gene Expression ProfilingMesenchymal Stem CellsHumansCancer risk assessmentCell therapyMesenchymal stromal cellsMSCsOncogenic potential

Identifiers

PMID39621192
PMCPMC12367896

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.