Evidence map›Paper›PMID 42801224›Full record

ReviewInternational journal of nanomedicine2026

Nanoparticle-Based Tools to Study Hallmarks of Aging at the Molecular Level.

Shuai Yao, Guangxun Shen, Jingmin Zhao

Abstract readReview
In one paragraph

Review in International journal of nanomedicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

3 authors.

Shuai YaoDepartment of Neurology, China-Japan Union Hospital of Jilin University, Changchun, People's Republic of China.
Guangxun ShenDepartment of Neurology, China-Japan Union Hospital of Jilin University, Changchun, People's Republic of China.
Jingmin ZhaoDepartment of Neurology, China-Japan Union Hospital of Jilin University, Changchun, People's Republic of China.ORCID 0000-0003-2660-1122

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Aging is characterized by the cumulative damage to the genome, proteome, epigenome, and organelles, which ultimately leads to telomere attrition, loss of proteostasis, genomic instability, mitochondrial dysfunction, cellular senescence, altered intracellular communication, chronic inflammation, and dysregulated nutrient sensing. Nanoparticle-based technologies are revolutionizing the ability to study the hallmark of aging at the molecular level. Due to the key limitation of conventional genomic, epigenomic, transcriptomic, proteomic, and metabolomic tools, nanoparticles play a vital role in the diagnosis and treatment of hallmarks of aging. This review aims to provide a comprehensive overview of recent progress on the role of nanoparticles and their applications in the diagnosis and treatment of aging and age-associated disease (AAD). In the first part of this review, we summarized aging and its hallmarks. Then, we described different types of molecular tools used in the diagnosis of aging and age-associated Diseases as well as their limitation. Finally, we reviewed the applications of each kind of nanoparticle with respect to the hallmarks. Collectively, this review provides the importance of nanoparticle platforms as a versatile toolbox to detect, visualize, and fine-tune aging hallmarks, connecting mechanistic studies with translational anti-aging interventions.

Indexed as

AgingNanoparticlesAnimalsCellular SenescenceHumansNanotechnologyage-associated diseaseaginghallmarks of agingmolecular pathwaysnanomaterialnanoparticlesnanotechnology

Identifiers

PMID42801224
PMCPMC13615805

What OpenQuestion holds

Textmetadata
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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.