Evidence map›Paper›PMID 42344694›Full record

ArticleFrontiers in oncology2026

Chronic military stress and glandular epithelial tumor biology: an integrative neuroendocrine-inflammatory framework with insights from microgravity gene discovery.

David Laván, Natalia Argüelles, Rosa Rea, José Morales, Sofia Montes, Daniel Huaman, Alexis Lluncor, Juan Moyano, Milton Peña, Vilma Herencia-Reyes and 4 more

Abstract read
In one paragraph

Article in Frontiers in oncology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

14 authors.

David LavánInstituto de Investigaciones en Ciencias Biomédicas, Facultad de Medicina Humana, Universidad Ricardo Palma, Lima, Peru.
Natalia ArgüellesDepartment of Research, Development and Innovation, BioTechCell Sociedad Anónima Cerrada (SAC), Lima, Peru.
Rosa ReaDepartment of Research, Development and Innovation, BioTechCell Sociedad Anónima Cerrada (SAC), Lima, Peru.
José MoralesDepartment of Research, Development and Innovation, BioTechCell Sociedad Anónima Cerrada (SAC), Lima, Peru.
Sofia MontesEscuela de Biología, Facultad de Ciencias Biológicas, Universidad Ricardo Palma, Lima, Peru.
Daniel HuamanDepartment of Research, Development and Innovation, BioTechCell Sociedad Anónima Cerrada (SAC), Lima, Peru.
Alexis LluncorFaculty of Natural and Mathematical Sciences, National University Federico Villareal, Lima, Peru.
Juan MoyanoEscuela de Medicina Humana, Universidad Señor de Sipán, Chiclayo, Peru.
Milton PeñaEscuela de Ingeniería Electrónica, Facultad de Ingeniería, Universidad Ricardo Palma, Lima, Peru.
Vilma Herencia-ReyesEscuela de Medicina Humana, Facultad de Medicina Humana, Universidad Ricardo Palma, Lima, Peru.
Alcides GuerraEscuela de Biología, Facultad de Ciencias Biológicas, Universidad Ricardo Palma, Lima, Peru.
Gabriela CalderónDepartment of International Clinical Oncology, Clínica Internacional, Lima, Peru.
José M Vela-RuizInstituto de Investigaciones en Ciencias Biomédicas, Facultad de Medicina Humana, Universidad Ricardo Palma, Lima, Peru.
Aly GalloCenter for Research in Precision Medicine, Genomics, and Human Performance, Lima, Peru.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Exposure to extreme stress within military contexts such as combat, captivity, survival training, or blast exposure triggers complex neurobiological responses that, in susceptible individuals, culminate in conditions such as Post-Traumatic Stress Disorder (PTSD). This inter-individual variability is rooted in profound genetic and epigenetic foundations. This manuscript reviews the critical relationship between chronic military stress and five key molecules: the glucocorticoid receptor (NR3C1), the FK506-binding protein 5 (FKBP5), brain-derived neurotrophic factor (BDNF), neuropeptide Y (NPY), and interleukin-6 (IL6). We examine how the dysregulation of this allostatic network predisposes individuals to PTSD and generates an altered systemic inflammatory and neuroendocrine microenvironment. Seeking an integrative biological perspective, this pathogenic model is linked to discoveries derived from extreme physical environments. Previous investigations by our group involving

Indexed as

BDNFchronic stressepithelial-mesenchymal transitionFKBP5glandular epithelial neoplasmshypothalamic-pituitary-adrenal axisIL-6military personnel

Identifiers

PMID42344694
PMCPMC13288269

What Socratic 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 Socratic graph.