Evidence map›Paper›PMID 36035513›Full record

ArticleStem cells international2022

Preclinical Evaluation of the Tumorigenic and Immunomodulatory Properties of Human Bone Marrow Mesenchymal Stromal Cell Populations with Clonal Trisomy 5.

Maria Susana Joya Marodin, Juliana A Godoy, Raquel M Alves-Paiva, Kelen Alvarez, Thiago Giove Mitsugi, Ana Cristina Victorino Krepischi, Nelson Hamerschlak, Maria Augusta Tezelli Bortolini, Rodrigo Castro, Andrea T Kondo and 2 more

Abstract read
In one paragraph

Article in Stem cells international, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 1 pooled it
–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 synthesis or guideline pooled it.

  1. Pooled it
  2. Trial
  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

12 authors.

Maria Susana Joya MarodinHuman Genome and Stem Cell Research Center, Department of Genetics and Evolutionary Biology, Institute of Biosciences, University of Sao Paulo, Sao Paulo, Brazil.ORCID https://orcid.org/0000-0002-4360-8812
Juliana A GodoyDepartment of Hemotherapy and Cellular Therapy, Albert Einstein Israelite Hospital, Sao Paulo, Brazil.ORCID https://orcid.org/0000-0003-1276-4297
Raquel M Alves-PaivaDepartment of Hemotherapy and Cellular Therapy, Albert Einstein Israelite Hospital, Sao Paulo, Brazil.ORCID https://orcid.org/0000-0003-2418-4863
Kelen AlvarezDepartment of Hemotherapy and Cellular Therapy, Albert Einstein Israelite Hospital, Sao Paulo, Brazil.ORCID https://orcid.org/0000-0001-6315-6940
Thiago Giove MitsugiHuman Genome and Stem Cell Research Center, Department of Genetics and Evolutionary Biology, Institute of Biosciences, University of Sao Paulo, Sao Paulo, Brazil.ORCID https://orcid.org/0000-0001-5940-194X
Ana Cristina Victorino KrepischiHuman Genome and Stem Cell Research Center, Department of Genetics and Evolutionary Biology, Institute of Biosciences, University of Sao Paulo, Sao Paulo, Brazil.ORCID https://orcid.org/0000-0003-2931-8605
Nelson HamerschlakDepartment of Hemotherapy and Cellular Therapy, Albert Einstein Israelite Hospital, Sao Paulo, Brazil.ORCID https://orcid.org/0000-0002-5140-5310
Maria Augusta Tezelli BortoliniDepartment of Gynecology, Federal University of Sao Paulo, Sao Paulo, Brazil.ORCID https://orcid.org/0000-0002-2824-5320
Rodrigo CastroDepartment of Gynecology, Federal University of Sao Paulo, Sao Paulo, Brazil.ORCID https://orcid.org/0000-0002-0959-7363
Andrea T KondoDepartment of Hemotherapy and Cellular Therapy, Albert Einstein Israelite Hospital, Sao Paulo, Brazil.ORCID https://orcid.org/0000-0002-4228-8503
Jose Mauro KutnerDepartment of Hemotherapy and Cellular Therapy, Albert Einstein Israelite Hospital, Sao Paulo, Brazil.ORCID https://orcid.org/0000-0003-3784-6731
Oswaldo Keith OkamotoHuman Genome and Stem Cell Research Center, Department of Genetics and Evolutionary Biology, Institute of Biosciences, University of Sao Paulo, Sao Paulo, Brazil.ORCID https://orcid.org/0000-0002-8528-6225

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cytogenetic aberrations may emerge in human mesenchymal stromal cells (MSC) during ex vivo expansion for cell therapy. We have detected clonal trisomy 5 in two distinct autologous MSC products expanded from bone marrow which, based on the current quality control criteria, could not be released for clinical use. Although a safety concern, it is still unclear to what extent recurrent aneuploidies detected in MSC products may affect the threshold for neoplastic transformation or the medicinal properties of these cells. We have carried out an exploratory preclinical study to evaluate these MSC products with clonal trisomy 5, regarding their oncogenic and immunomodulatory potential. Cell population growth

Identifiers

PMID36035513
PMCPMC9417782

What OpenQuestion holds

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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.