ArticleMethods in molecular biology (Clifton, N.J.)2025
Assessment of Angiogenic Properties of Malignant Pleural Effusion (MPE) Fluid.
Article in Methods in molecular biology (Clifton, N.J.), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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.
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.
Who cites it
1 citing paper in PubMed.
- Inhibitor of DNA binding 1 in lung cancer and the tumor microenvironment: a testable hypothesis for malignant pleural effusion formation.Frontiers in immunology · 2026Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
7 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Patients with various malignancies can develop malignant pleural effusion (MPE). MPE is the abnormal accumulation of fluid in the pleural cavity. This fluid usually contains immune cells, tumor cells, and high levels of plasma proteins. This condition is associated with impaired pleural fluid drainage and is considered an immune and angiogenic manifestation of tumors metastasized in the pleura from other thoracic and non-thoracic areas. Tumor-induced pleural vascular hyperpermeability and neoangiogenesis are crucial to pleural fluid accumulation and could be therapeutically targeted to minimize MPE development. Here, we present two methodologies required for assessing the angiogenic properties of MPE fluid-Evans' blue pulse-and-chase for evaluating increased vascular permeability and the chorioallantoic membrane (CAM) assay to assess tumor-triggered angiogenesis. We describe the steps for experimental MPE formation in mice, including MPE fluid collection, evaluation of MPE-induced vascular permeability, and assessment of MPE-induced angiogenesis.
Indexed as
Identifiers
40859084What OpenQuestion holds
Registered trials
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.