Evidence map›Paper›PMID 28762752›Full record

ReviewAntioxidants & redox signaling2018

Oxidative Stress in Mesenchymal Stem Cell Senescence: Regulation by Coding and Noncoding RNAs.

Rosa Vono, Eva Jover Garcia, Gaia Spinetti, Paolo Madeddu

Open access · bronzeAbstract readReview
In one paragraph

Review in Antioxidants & redox signaling, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 62 papers.

0numbers the graph read from it
0cells of the map it votes in
62citing papers in PubMed
4.5field-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.

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

62 citing papers in PubMed, 108 citations in OpenAlex.

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  16. International journal of molecular sciences · 2024
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2 more citing papers are in PubMed but not listed here.

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

4 authors at 3 institutions in 2 countries.

Rosa Vono1 Laboratory of Cardiovascular Research , IRCCS MultiMedica, Milan, Italy .
Eva Jover Garcia2 School of Clinical Sciences, Bristol Heart Institute, University of Bristol , United Kingdom .
Gaia Spinetti1 Laboratory of Cardiovascular Research , IRCCS MultiMedica, Milan, Italy .
Paolo Madeddu2 School of Clinical Sciences, Bristol Heart Institute, University of Bristol , United Kingdom .
University of Bristol · GBIstituti di Ricovero e Cura a Carattere Scientifico · ITMultiMedica · IT

Funding

HISTAMINE MODULATION T-CELL IMMOBILIZATION IN THE LUNGK08HL001317 · NHLBI · BOSTON UNIVERSITY MEDICAL CAMPUS · PI BERMAN, JEFFREY S · 1985 to 1988
–
British Heart Foundation RG/13/17/30545
6 · The paper itself

Abstract

significanceMesenchymal stem cells (MSCs), adult stem cells with the potential of differentiation into mesodermal lineages, play an important role in tissue homeostasis and regeneration. In different organs, a subpopulation of MSCs is located near the vasculature and possibly represents the original source of lineage-committed mesenchymal progenitors. Recent Advances: The plasticity and immune characteristics of MSCs render them a preferential tool for regenerative cell therapy. CRITICAL ISSUES: The culture expansion needed before MSC transplantation is associated with cellular senescence. Moreover, accelerated senescence of the total and perivascular MSC pool has been observed in humans and mouse models of premature aging disorders. MSC dysfunction is acknowledged as a culprit for the aging-associated degeneration of mesodermal tissues, but the underlying epigenetic pathways remain elusive. This article reviews current understanding of mechanisms impinging on MSC health, including oxidative stress, Nrf2-antioxidant responsive element activity, sirtuins, noncoding RNAs, and PKCs. FUTURE DIRECTIONS: We provide evidence that epigenetic profiling of MSCs is utilitarian to the prediction of therapeutic outcomes. In addition, strategies that target oxidative stress-associated mechanisms represent promising approaches to counteract the detrimental effect of age and senescence in MSCs.-Antioxid. Redox Signal. 29, 864-879.

Indexed as

AnimalsCellular SenescenceHumansMesenchymal Stem CellsOxidative StressRNA, UntranslatedRNA, Untranslatedcell therapymesenchymal stem cellspericytesreactive oxygen speciessenescence

Identifiers

PMID28762752
PMCPMC6080119
OpenAlexW2740168400

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.