Evidence map›Paper›PMID 42448671›Full record

ArticleCell death discovery2026

Piceatannol as a safe senotherapeutic: ameliorating senescence-associated markers in a radiation-induced murine model.

Alessia Ambrosino, Claudia Moriello, Nicola Alessio, Domenico Aprile, Salvatore Cappabianca, Nicolamaria Tarantino, Gianfranco Peluso, Giovanni Di Bernardo, Umberto Galderisi

Abstract read
In one paragraph

Article in Cell death discovery, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

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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

0 citing papers in PubMed.

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4 · The record

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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.

Alessia AmbrosinoDepartment of Experimental Medicine, University of Campania "Luigi Vanvitelli", Naples, Italy.
Claudia MorielloDepartment of Experimental Medicine, University of Campania "Luigi Vanvitelli", Naples, Italy.
Nicola AlessioDepartment of Experimental Medicine, University of Campania "Luigi Vanvitelli", Naples, Italy.
Domenico AprileDepartment of Experimental Medicine, University of Campania "Luigi Vanvitelli", Naples, Italy.
Salvatore CappabiancaDepartment of Precision Medicine, University of Campania "Luigi Vanvitelli", Naples, Italy.
Nicolamaria TarantinoDepartment of Precision Medicine, University of Campania "Luigi Vanvitelli", Naples, Italy.
Gianfranco PelusoSaint Camillus International University of Health and Medical Sciences, Rome, Italy.
Giovanni Di BernardoDepartment of Experimental Medicine, University of Campania "Luigi Vanvitelli", Naples, Italy. gianni.dibernardo@unicampania.it.ORCID http://orcid.org/0000-0002-4985-4029
Umberto GalderisiDepartment of Experimental Medicine, University of Campania "Luigi Vanvitelli", Naples, Italy. umberto.galderisi@unicampania.it.ORCID http://orcid.org/0000-0003-0909-7403

Funding

Ministero dell'Istruzione, dell'Università e della Ricerca (Ministry of Education, University and Research) PRIN2022
6 · The paper itself

Abstract

Cellular senescence is a key driver of age-associated tissue dysfunction through the secretion of pro-inflammatory and pro-senescent factors (SASP). Among these, insulin-like growth factor binding proteins (IGFBPs) have emerged as causal mediators of senescence propagation. Piceatannol (PCT), a naturally occurring stilbene and resveratrol metabolite with superior pharmacokinetic properties, exhibits senomorphic activity in vitro, but its in vivo senotherapeutic potential remains poorly defined. We established a murine model of mild aging using sublethal X-ray irradiation, in which organ function remains largely preserved but molecular and cellular hallmarks of aging, such as senescent cell accumulation, SASP factor elevation, tissue remodeling, and low-grade inflammation, are detectable. This controlled model mimics the early stage of aging seen in many healthy middle-aged individuals, particularly prevalent in Western societies, and provides a relevant platform for testing preventive senotherapeutics. Mice were treated with oral PCT at a human-translatable dose and evaluated for behavioral performance, circulating SASP factors, tissue senescence, inflammation and fibrosis. PCT significantly improved motor coordination and spatial memory while reducing systemic inflammation and circulating SASP factors, including the senescence-propagating IGFBPs IGFBP4, IGFBP5, and IGFBP7. In kidney and heart, the organs most affected by radiation-induced aging, PCT reduced senescent cell burden, CD68⁺ inflammatory foci, fibrotic remodeling, and the senescence markers P53 and P21. PCT also preserved mesenchymal stromal cell clonogenic capacity. These multi-organ benefits were achieved without detectable toxicity in healthy animals. Our findings position PCT as a promising, safe, nutritionally derived senotherapeutic candidate for delaying aging-associated deterioration. This mild aging model, capturing preclinical senescence without overt organ failure, may accelerate the development of interventions aimed at preserving health span in middle-aged populations.

Identifiers

PMID42448671
PMCPMC13646293

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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.