Evidence map›Paper›PMID 40731417›Full record

ArticleJournal of biological engineering2025

Capture and detection of extracellular vesicles derived from human breast cancer cells using a 3D self-assembled nanostructured SiO

Carolina Cabeza, Felipe Rojas, Lorena Lobos-González, Dominique Lemaitre, Juan Villena, María Luisa Cordero, Natalia Hassan, Rina Ortiz

Abstract read
In one paragraph

Article in Journal of biological engineering, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. Review
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

8 authors.

Carolina Cabeza *Escuela de Medicina Veterinaria, Facultad Ciencias de la Vida, Universidad Andrés Bello, Santiago, Chile.
Felipe Rojas *Instituto Universitario de Investigación y Desarrollo Tecnológico (IDT), Universidad Tecnológica Metropolitana, Santiago, Chile.
Lorena Lobos-GonzálezLaboratory of Cellular Communication, Center for studies on Exercise, Metabolism and Cancer (CEMC), Faculty of Medicine, Universidad de Chile, Santiago, Chile.
Dominique LemaitreEscuela de Medicina Veterinaria, Facultad Ciencias de la Vida, Universidad Andrés Bello, Santiago, Chile.
Juan VillenaCenter of Interdisciplinary Biomedical and Engineering Research for Health (MEDING), Escuela de Medicina, Facultad de Medicina, Universidad de Valparaíso, Angamos 655, Reñaca, Viña del Mar, 2520000, Chile.
María Luisa CorderoDepartamento de Física, FCFM, Universidad de Chile, Av. Beauchef 850, Santiago, 8370448, Chile.
Natalia HassanInstituto Universitario de Investigación y Desarrollo Tecnológico (IDT), Universidad Tecnológica Metropolitana, Santiago, Chile. nhassan@utem.cl.
Rina OrtizFacultad de Ciencias de la Vida. Carrera de Obstetricia, Universidad Viña del Mar, Viña del Mar, Chile. rina.ortiz@uvm.cl.

Funding

Fondo Nacional de Desarrollo Científico y Tecnológico 11200778Fondo Nacional de Desarrollo Científico y Tecnológico 1211223Fondo Nacional de Desarrollo Científico y Tecnológico 1230830InES Género INGE210029
6 · The paper itself

Abstract

backgroundTumor-derived extracellular vesicles offer a minimally invasive approach to evaluate tumor progression and metastasis. However, detecting biomarkers, such as extracellular vesicles in body fluids during the early stages of disease, remains a significant challenge. Conventional methods like ultracentrifugation-based isolation or Western blot protein quantification are time-consuming, require large sample volumes, and offer low yield and sensitivity. Therefore, the development of new biosensors for the specific and efficient analysis of tumor extracellular vesicles is urgently needed.

methodsMicrofluidic devices provide extraordinary benefits for bioanalysis, offering a large surface area for the contact between target molecules and the biosensor, significantly enhancing the specificity, efficiency, and speed. These devices also enable nanoscale and microscale work using reduced sample volumes. In this study, we developed a three-dimensional self-assembled SiO

resultsThe three-dimensional SiO

conclusionsThis study highlights the potential application of three-dimensional SiO

Indexed as

BiosensorsBreast cancerExtracellular vesiclesLiquid biopsyMicrofluidic chip

Identifiers

PMID40731417
PMCPMC12305923

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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 OpenQuestion graph.