Evidence map›Paper›PMID 40353054›Full record

ArticleAging medicine (Milton (N.S.W))2025

PseudoCell: A Multivalued Logical Regulatory Network to Investigate Premature Senescence Dynamics and Heterogeneity.

Vinícius Pierdoná, Patrícia Lavandoski, Rafael Moura Maurmann, Guilherme Antônio Borges, Jose Carlos Merino Mombach, Fátima Theresinha Costa Rodrigues Guma, Florencia María Barbé-Tuana

Abstract read
In one paragraph

Article in Aging medicine (Milton (N.S.W)), 2025. 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

7 authors.

Vinícius PierdonáPrograma de Pós-Graduação Em Ciências Biológicas: Bioquímica Do Departamento de Bioquímica Universidade Federal Do Rio Grande Do Sul Porto Alegre Rio Grande do Sul Brazil.ORCID https://orcid.org/0000-0001-5072-9789
Patrícia LavandoskiPrograma de Pós-Graduação Em Ciências Biológicas: Bioquímica Do Departamento de Bioquímica Universidade Federal Do Rio Grande Do Sul Porto Alegre Rio Grande do Sul Brazil.
Rafael Moura MaurmannPrograma de Pós-Graduação Em Biologia Celular e Molecular da Escola de Ciências da Saúde e da Vida - Pontifícia Universidade Católica Do Rio Grande Do Sul Porto Alegre Rio Grande do Sul Brazil.
Guilherme Antônio BorgesDepartamento de Engenharia Electrotécnica e de Computadores Universidade de Coimbra Coimbra Portugal.
Jose Carlos Merino MombachDepartamento de Física Universidade Federal de Santa Maria Santa Maria Rio Grande do Sul Brazil.
Fátima Theresinha Costa Rodrigues GumaPrograma de Pós-Graduação Em Ciências Biológicas: Bioquímica Do Departamento de Bioquímica Universidade Federal Do Rio Grande Do Sul Porto Alegre Rio Grande do Sul Brazil.
Florencia María Barbé-TuanaPrograma de Pós-Graduação Em Biologia Celular e Molecular da Escola de Ciências da Saúde e da Vida - Pontifícia Universidade Católica Do Rio Grande Do Sul Porto Alegre Rio Grande do Sul Brazil.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: Premature cellular senescence is a pivotal process in aging and age-related diseases, triggered by various stressors. However, this is not a homogeneous phenotype, but a heterogeneous cellular state composed of multiple senescence programs with different compositions. Therefore, understanding the complex dynamics of senescence programs requires a systemic approach. We introduce PseudoCell, a multivalued logical regulatory network designed to explore the molecular intricacies of premature senescence. Methods: PseudoCell integrates key senescence signaling pathways and molecular mechanisms, offering a versatile platform for investigating diverse premature senescence programs initiated by different stimuli. Results: Validation through simulation of classical senescence programs, including oxidative stress-induced senescence and oncogene-induced senescence, demonstrates its ability to replicate molecular signatures consistent with empirical data. Additionally, we explore the role of CCL11, a novel senescence-associated molecule, through simulations that reveal potential pathways and mechanisms underlying CCL11-mediated senescence induction. Conclusions: In conclusion, PseudoCell provides a systematic approach to dissecting premature senescence programs and uncovering novel regulatory mechanisms.

Indexed as

agingbioinformaticscellular senescencein silico modelingpremature senescence

Identifiers

PMID40353054
PMCPMC12064993

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.