Evidence map›Paper›PMID 36949664›Full record

ArticleCell proliferation2023

Progression of irradiated mesenchymal stromal cells from early to late senescence: Changes in SASP composition and anti-tumour properties.

Nicola Alessio, Mustafa Burak Acar, Tiziana Squillaro, Domenico Aprile, Şerife Ayaz-Güner, Giovanni Di Bernardo, Gianfranco Peluso, Servet Özcan, Umberto Galderisi

Open access · goldAbstract read
In one paragraph

Article in Cell proliferation, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed, 1 pooled it
4.2field-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

22 citing papers in PubMed, 1 synthesis or guideline pooled it, 24 citations in OpenAlex.

  1. Pooled it
  2. Effects of Fractionated Low Dose Ionizing Radiation on Cellular Senescence in Mouse Lung Tissue.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2026
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  11. Interrogating the regulatory epigenome of cellular senescence.Cellular and molecular life sciences : CMLS · 2025
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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

9 authors at 4 institutions in 3 countries.

Nicola AlessioDepartment of Experimental Medicine, Luigi Vanvitelli Campania University, Naples, Italy.
Mustafa Burak AcarGenome and Stem Cell Center (GENKÖK) Erciyes University, Kayseri, Turkey.
Tiziana SquillaroDepartment of Experimental Medicine, Luigi Vanvitelli Campania University, Naples, Italy.
Domenico AprileDepartment of Experimental Medicine, Luigi Vanvitelli Campania University, Naples, Italy.
Şerife Ayaz-GünerDepartment of Molecular Biology and Genetics, Faculty of Life and Natural Science, Abdullah Gül University, Kayseri, Turkey.
Giovanni Di BernardoDepartment of Experimental Medicine, Luigi Vanvitelli Campania University, Naples, Italy.
Gianfranco PelusoUniCamillus, Rome, Italy.
Servet ÖzcanGenome and Stem Cell Center (GENKÖK) Erciyes University, Kayseri, Turkey.ORCID https://orcid.org/0000-0002-9914-8843
Umberto GalderisiDepartment of Experimental Medicine, Luigi Vanvitelli Campania University, Naples, Italy.ORCID https://orcid.org/0000-0003-0909-7403
University of Campania "Luigi Vanvitelli" · ITErciyes University · TRIzmir Institute of Technology · TRSaint Camillus International University of Health and Medical Sciences · IT

Funding

Regione Campania B21C17000030007
6 · The paper itself

Abstract

Genotoxic injuries converge on senescence-executive program that promotes production of a senescence-specific secretome (SASP). The study of SASP is particularly intriguing, since through it a senescence process, triggered in a few cells, can spread to many other cells and produce either beneficial or negative consequences for health. We analysed the SASP of quiescent mesenchymal stromal cells (MSCs) following stress induced premature senescence (SIPS) by ionizing radiation exposure. We performed a proteome analysis of SASP content obtained from early and late senescent cells. The bioinformatics studies evidenced that early and late SASPs, besides some common ontologies and signalling pathways, contain specific factors. In spite of these differences, we evidenced that SASPs can block in vitro proliferation of cancer cells and promote senescence/apoptosis. It is possible to imagine that SASP always contains core components that have an anti-tumour activity, the progression from early to late senescence enriches the SASP of factors that may promote SASP tumorigenic activity only by interacting and instructing cells of the immune system. Our results on Caco-2 cancer cells incubated with late SASP in presence of peripheral white blood cells strongly support this hypothesis. We evidenced that quiescent MSCs following SIPS produced SASP that, while progressively changed its composition, preserved the capacity to block cancer growth by inducing senescence and/or apoptosis only in an autonomous manner.

Indexed as

Mesenchymal Stem CellsSecretomeCaco-2 CellsCarcinogenesisCellular SenescenceHumans

Identifiers

PMID36949664
PMCPMC10280137
OpenAlexW4360599862

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.