Evidence map›Paper›PMID 42812937›Full record

ArticleFrontiers in pharmacology2026

Exploratory proteomic characterization of

José Luis Marcos, Ricardo Campos-Soto, Rina Ortiz, Yerko Olivares, Joan Villena, Mario Párraga, Ramón Sotomayor-Zárate, Luis Constandil, Heine Müller

Abstract read
In one paragraph

Article in Frontiers in pharmacology, 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

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

9 authors.

José Luis Marcos *Departamento de Ciencias Veterinarias, Facultad de Ciencias de la Vida, Universidad Viña del Mar, Viña del Mar, Chile.
Ricardo Campos-SotoDepartamento de Ciencias Veterinarias, Facultad de Ciencias de la Vida, Universidad Viña del Mar, Viña del Mar, Chile.
Rina Ortiz *Escuela de Medicina Veterinaria, Facultad Ciencias de La Vida, Universidad Andres Bello, Viña del Mar, Chile.
Yerko OlivaresDepartamento de Ciencias Veterinarias, Facultad de Ciencias de la Vida, Universidad Viña del Mar, Viña del Mar, Chile.
Joan VillenaMagíster en Ciencias Médicas mención Biología Celular y Molecular, Escuela de Medicina, Facultad de Medicina, Universidad de Valparaíso, Valparaíso, Chile.
Mario PárragaMagíster en Ciencias Médicas mención Biología Celular y Molecular, Escuela de Medicina, Facultad de Medicina, Universidad de Valparaíso, Valparaíso, Chile.
Ramón Sotomayor-ZárateCentro de Neurobiología y Fisiopatología Integrativa (CENFI), Instituto de Fisiología, Facultad de Ciencias, Universidad de Valparaíso, Valparaíso, Chile.
Luis ConstandilLaboratory of Neurobiology, Department of Biology, Faculty of Chemistry and Biology, University of Santiago de Chile, Santiago, Chile.
Heine MüllerAnaesthesiology and Intensive-Care, Clinical Centre for Small Animal Health and Research, Clinical Department for Small Animals and Horses, University of Veterinary Medicine Vienna, Vienna, Austria.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Bee venom ( Methods: Venom from multiple Results: Overall, 679 proteins were identified. Principal component analysis and hierarchical clustering showed reproducible grouping of analytical duplicates by geographic origin, indicating distinct proteomic profiles among zones. Differential abundance analysis identified proteins with significant abundance changes between regions, particularly between Sea Level and Inland Valley. Classical venom components, including melittin and phospholipase A2, predominated across samples, whereas proteins associated with stress response, redox regulation, metabolism, and secretion showed geographic variation. Conclusion: Bee venom from geographically distinct areas of central Chile exhibited exploratory proteomic differences, primarily in protein abundance patterns. Although the absence of independent biological replicates limits population-level inference, these patterns suggest environmentally associated proteomic plasticity potentially relevant to biological activity and pharmacological standardization. Further studies incorporating biological replication, targeted validation, and functional assays are required to confirm these findings.

Indexed as

Apis melliferabee venom proteomicsbioactive peptideschemical ecologydrug discovery potentialecological venom variationLC–MS/MS proteomicsvenom pharmacology

Identifiers

PMID42812937
PMCPMC13621212

What OpenQuestion holds

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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.