Evidence map›Paper›PMID 39625294›Full record

ArticleBiology open2024

Effect of cigarette smoke on the proliferation, viability, gene expression, and cellular functions of adipose-derived mesenchymal stem cells from smoking and non-smoking donors.

Bareqa Salah, Diana Shahin, Momen Sarhan, Joud Al-Karmi, Ban Al-Kurdi, Renata Al-Atoom, Mohammad A Ismail, Nouran Hammad, Hanan Jafar, Abdalla Awidi and 1 more

Abstract read
In one paragraph

Article in Biology open, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Trial
  2. Review
  3. Article
  4. Article
  5. 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

11 authors.

Bareqa SalahGeneral Surgery Department/Plastic & Reconstructive, Jordan University Hospital, the University of Jordan, 11942.
Diana ShahinCell Therapy Center, the University of Jordan, Amman, Jordan, 11942.
Momen SarhanCell Therapy Center, the University of Jordan, Amman, Jordan, 11942.
Joud Al-KarmiSchool of Medicine, the University of Jordan, Amman, Jordan, 11942.
Ban Al-KurdiCell Therapy Center, the University of Jordan, Amman, Jordan, 11942.
Renata Al-AtoomCell Therapy Center, the University of Jordan, Amman, Jordan, 11942.
Mohammad A IsmailCell Therapy Center, the University of Jordan, Amman, Jordan, 11942.
Nouran HammadSchool of Medicine , Jordan University of Science and Technology, Al-Ramtha, Jordan, 22110.
Hanan JafarCell Therapy Center, the University of Jordan, Amman, Jordan, 11942.
Abdalla AwidiCell Therapy Center, the University of Jordan, Amman, Jordan, 11942.
Nidaa A AbabnehCell Therapy Center, the University of Jordan, Amman, Jordan, 11942.ORCID 0000-0002-2155-3013

Funding

Deanship of Scientific research/University of Jordan
6 · The paper itself

Abstract

Cigarette smoking negatively impacts mesenchymal stem cell functionality, including proliferation, viability, and differentiation potential. Adipose-derived mesenchymal stem cells (ADMSCs) are increasingly used for therapeutic purposes, but the specific effects of smoking in vivo on these cells are poorly understood. This study investigates the effects of cigarette smoke on the proliferation, viability, gene expression, and cellular functions of ADMSCs from smoking and non-smoking donors. In this study, ADMSCs were isolated from healthy smokers and non-smokers, and cell proliferation was assessed using the MTT assay, viability with apoptosis assays, mitochondrial membrane potential (MMP), and gene expression related to oxidative stress and cellular functions. Cell cycle analysis was also conducted. Our findings reveal a significant decrease in the proliferation of ADMSCs from smokers. Apoptosis assays showed reduced viable cells in smokers without a significant change in MMP, suggesting alternative pathways contributing to decreased viability. Gene expression analysis indicated the upregulation of genes associated with oxidative stress response and cellular defense mechanisms and the downregulation of genes related to inflammatory signaling, detoxification, and cellular metabolism. Cell cycle analysis indicates cycle arrest or delay in smokers, possibly due to stress and potential DNA damage. Smoking negatively affects ADMSCs' proliferation, viability, and function through oxidative stress and gene expression alterations. These findings highlight the importance of considering smoking status in ADMSC therapies and the need for further research to mitigate the effect of smoking on stem cells.

Indexed as

Adipose TissueCell ProliferationCell SurvivalGene Expression RegulationMesenchymal Stem CellsAdultApoptosisBiomarkersCell DifferentiationCells, CulturedCigarette SmokingFemaleGene Expression ProfilingHumansMembrane Potential, MitochondrialOxidative StressBiomarkersSmokeAdipose-derived MSCs (ADMSCs)Cigarette smokingOxidative stressStem cells

Identifiers

PMID39625294
PMCPMC11646114

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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.