Evidence map›Paper›PMID 28584815›Full record

ArticleBioMed research international2017

From Human Mesenchymal Stem Cells to Insulin-Producing Cells: Comparison between Bone Marrow- and Adipose Tissue-Derived Cells.

Mahmoud M Gabr, Mahmoud M Zakaria, Ayman F Refaie, Engy A Abdel-Rahman, Asmaa M Reda, Sameh S Ali, Sherry M Khater, Sylvia A Ashamallah, Amani M Ismail, Hossam El-Din A Ismail and 2 more

Abstract readComparative Study
In one paragraph

Article in BioMed research international, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing 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

28 citing papers in PubMed.

  1. Article
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  7. Advanced therapy to cure diabetes: mission impossible is now possible?Frontiers in cell and developmental biology · 2024
    Review
  8. Article
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  11. Article
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  13. Article
  14. Review
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  19. Article
  20. Stem Cell Therapy for Hepatocellular Carcinoma: Future Perspectives.Advances in experimental medicine and biology · 2020
    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.

Mahmoud M GabrUrology and Nephrology Center, Mansoura, Egypt.ORCID 0000-0001-7827-8713
Mahmoud M ZakariaUrology and Nephrology Center, Mansoura, Egypt.ORCID 0000-0002-7288-8374
Ayman F RefaieUrology and Nephrology Center, Mansoura, Egypt.ORCID 0000-0002-6960-2881
Engy A Abdel-RahmanZewail City of Science and Technology, Giza, Egypt.
Asmaa M RedaZewail City of Science and Technology, Giza, Egypt.
Sameh S AliZewail City of Science and Technology, Giza, Egypt.ORCID 0000-0002-0339-6106
Sherry M KhaterUrology and Nephrology Center, Mansoura, Egypt.ORCID 0000-0001-5988-9711
Sylvia A AshamallahUrology and Nephrology Center, Mansoura, Egypt.
Amani M IsmailUrology and Nephrology Center, Mansoura, Egypt.
Hossam El-Din A IsmailDepartment of Plastic Surgery, Mansoura University, Mansoura, Egypt.
Nagwa El-BadriZewail City of Science and Technology, Giza, Egypt.
Mohamed A GhoneimUrology and Nephrology Center, Mansoura, Egypt.ORCID 0000-0003-4329-0346

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The aim of this study is to compare human bone marrow-derived mesenchymal stem cells (BM-MSCs) and adipose tissue-derived mesenchymal stem cells (AT-MSCs), for their differentiation potentials to form insulin-producing cells. BM-MSCs were obtained during elective orthotopic surgery and AT-MSCs from fatty aspirates during elective cosmetics procedures. Following their expansion, cells were characterized by phenotyping, trilineage differentiation ability, and basal gene expression of pluripotency genes and for their metabolic characteristics. Cells were differentiated according to a Trichostatin-A based protocol. The differentiated cells were evaluated by immunocytochemistry staining for insulin and c-peptide. In addition the expression of relevant pancreatic endocrine genes was determined. The release of insulin and c-peptide in response to a glucose challenge was also quantitated. There were some differences in basal gene expression and metabolic characteristics. After differentiation the proportion of the resulting insulin-producing cells (IPCs), was comparable among both cell sources. Again, there were no differences neither in the levels of gene expression nor in the amounts of insulin and c-peptide release as a function of glucose challenge. The properties, availability, and abundance of AT-MSCs render them well-suited for applications in regenerative medicine.

Indexed as

Cell DifferentiationAdipose TissueBone Marrow CellsC-PeptideHumansInsulinInsulin SecretionMesenchymal Stem CellsC-PeptideInsulin

Identifiers

PMID28584815
PMCPMC5444016

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.