Evidence map›Paper›PMID 42304274›Full record

ArticleBMC cancer2026

Ultrasonographic characterization of malignant pleural effusion in a murine experimental model.

Amanda Jardim Mello, Enrico Fortunato, Karina Rocha Pereira, Carlos Sérgio Rocha Silva, Roberta Karla Barbosa Sales, Suelen Cristina Russafa Nascimento, Lisete Ribeiro Teixeira, Milena Marques Pagliarelli Acencio

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Article in BMC cancer, 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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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.

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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

8 authors.

Amanda Jardim MelloUnidade de Doencas Pleurais, Divisao de Pneumologia, Instituto do Coracao (InCor), Hospital das Clinicas HCFMUSP, Faculdade de Medicina, Universidade de Sao Paulo, Sao Paulo, SP, Brazil. mello_amanda@usp.br.
Enrico FortunatoUnidade de Doencas Pleurais, Divisao de Pneumologia, Instituto do Coracao (InCor), Hospital das Clinicas HCFMUSP, Faculdade de Medicina, Universidade de Sao Paulo, Sao Paulo, SP, Brazil.
Karina Rocha PereiraUnidade de Doencas Pleurais, Divisao de Pneumologia, Instituto do Coracao (InCor), Hospital das Clinicas HCFMUSP, Faculdade de Medicina, Universidade de Sao Paulo, Sao Paulo, SP, Brazil.
Carlos Sérgio Rocha SilvaUnidade de Doencas Pleurais, Divisao de Pneumologia, Instituto do Coracao (InCor), Hospital das Clinicas HCFMUSP, Faculdade de Medicina, Universidade de Sao Paulo, Sao Paulo, SP, Brazil.
Roberta Karla Barbosa SalesUnidade de Doencas Pleurais, Divisao de Pneumologia, Instituto do Coracao (InCor), Hospital das Clinicas HCFMUSP, Faculdade de Medicina, Universidade de Sao Paulo, Sao Paulo, SP, Brazil.
Suelen Cristina Russafa NascimentoDivisao de Cardiologia, Instituto do Coracao (InCor), Hospital das Clinicas HCFMUSP, Faculdade de Medicina, Universidade de Sao Paulo, Sao Paulo, SP, Brazil.
Lisete Ribeiro TeixeiraUnidade de Doencas Pleurais, Divisao de Pneumologia, Instituto do Coracao (InCor), Hospital das Clinicas HCFMUSP, Faculdade de Medicina, Universidade de Sao Paulo, Sao Paulo, SP, Brazil.
Milena Marques Pagliarelli AcencioUnidade de Doencas Pleurais, Divisao de Pneumologia, Instituto do Coracao (InCor), Hospital das Clinicas HCFMUSP, Faculdade de Medicina, Universidade de Sao Paulo, Sao Paulo, SP, Brazil.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMalignant pleural effusion (MPE) is a common manifestation of advanced malignancies and is associated with high morbidity and poor prognosis. Thoracic ultrasound (TUS) has emerged as a sensitive, non-invasive imaging modality for pleural evaluation; however, standardized ultrasonographic criteria for MPE in murine experimental model remains limited. The aim of this study was to describe and characterize the TUS findings of MPE in an experimental murine model.

methodsMPE was induced in C57Bl/6 mice by intrapleural injection of Lewis lung carcinoma (LLC) cells. TUS examinations were performed longitudinally at predefined time points to assess pleural fluid depth, pleural line characteristics, pleural thickening, nodules, subpleural consolidations, lung parenchymal alterations, and ultrasound artifacts. Pleural fluid volume, cytology, and histological analyses were obtained after euthanasia and correlated with ultrasonographic findings.

resultsTUS detected early pleural changes as early as day 7, preceding large-volume effusion. Pleural fluid depth measured by TUS showed a strong correlation with pleural fluid volume obtained by direct puncture (R = 0.927, p < 0.001). Progressive pleural thickening and nodularity (R = 0.704 e p = 0.002) correlated with histopathological tumor involvement.

conclusionTUS reliably characterizes and quantifies MPE progression in a murine model, closely reproducing human disease patterns. This experimental model supports translational research by enabling longitudinal and non-invasive assessment of biological and pathological processes over time, thereby allowing repeated evaluations within the same subject and significantly reducing the need for animal euthanasia at multiple experimental endpoints, while also providing a robust framework that may corroborate and facilitate future studies in related research fields.

Indexed as

Carcinoma, Lewis LungPleural Effusion, MalignantAnimalsDisease Models, AnimalMaleMiceMice, Inbred C57BLUltrasonographyExperimental modelMalignant pleural effusionThoracic ultrasoundTranslational research

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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.