Evidence map›Paper›PMID 40045008›Full record

ArticleEuropean radiology experimental2025

Microvascular heterogeneity exploration in core and invasive zones of orthotopic rat glioblastoma via ultrasound localization microscopy.

Xing Hu, Gaobo Zhang, Yong Wang, Xiandi Zhang, Rong Xie, Xin Liu, Hong Ding

Abstract read
In one paragraph

Article in European radiology experimental, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. 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

7 authors.

Xing Hu *Department of Ultrasound, Huashan Hospital, Fudan Univertity, Shanghai, China.
Gaobo Zhang *Department of Biomedical Engineering, School of Information Science and Technology, Fudan University, Shanghai, China.
Yong WangDepartment of Ultrasound, Huashan Hospital, Fudan Univertity, Shanghai, China.
Xiandi ZhangDepartment of Ultrasound, Huashan Hospital, Fudan Univertity, Shanghai, China.
Rong XieDepartment of Neurosurgery, Huashan Hospital, E Fudan Univertity, Shanghai, China.
Xin LiuAcademy for Engineering and Technology, Fudan University, Shanghai, China. xin_liu@fudan.edu.cn.
Hong DingDepartment of Ultrasound, Huashan Hospital, Fudan Univertity, Shanghai, China. ding_hong@fudan.edu.cn.ORCID http://orcid.org/0000-0002-9998-0904

Funding

National Natural Science Foundation of China 82272017
6 · The paper itself

Abstract

backgroundWe studied the microvascular structure and function of in situ glioblastoma using ultrasound localization microscopy (ULM).

methodsThe in vivo study was conducted via craniotomy in six Sprague-Dawley rats. Capillary pattern, capillary hemodynamics, and functional quantitative parameters were compared among tumor core, invasive zone, and normal brain tissue with ex vivo micro-computed tomography (micro-CT) and scanning electron microscopy. Correlations between quantitative parameters and histopathological vascular density (VD-H), proliferation index, and histopathological vascular maturity index (VMI-H) were evaluated. Kruskal-Wallis H, ANOVA, Mann-Whitney U, Pearson, and Spearman correlation statistics were used.

resultsCompared to the tumor core, the invasive zone exhibited higher microvascularity structural disorder and complexity, increased hemodynamic heterogeneity, higher local blood flow perfusion (p ≤ 0.033), and slightly lower average flow velocity (p = 0.873). Significant differences were observed between the invasive zone and normal brain tissue across all parameters (p ≤ 0.001). ULM demonstrated higher microstructural resolution compared to micro-CT and a nonsignificant difference compared to scanning electron microscopy. The invasive zone vascular density correlated with VD-H (r = 0.781, p < 0.001). Vessel diameter (r = 0.960, p < 0.001), curvature (r = 0.438, p = 0.047), blood flow velocity (r = 0.487, p = 0.025), and blood flow volume (r = 0.858, p < 0.001) correlated with proliferation index. Vascular density (r = -0.444, p = 0.044) and fractal dimension (r = -0.933, p < 0.001) correlated with VMI-H.

conclusionULM provided high-resolution, noninvasive imaging of glioblastoma microvascularity, offering insights into structural/functional abnormalities. RELEVANCE STATEMENT: ULM technology based on ultrafast ultrasound can accurately quantify the microvessels of glioblastoma, providing a new method for evaluating the effectiveness of antiangiogenic therapy and visualizing disease progression. This method may facilitate early therapeutic assessment. KEY POINTS: ULM reliably captures the vascular structures and hemodynamic features of glioblastoma in rats. Micro-CT and scanning electron microscopy validated its effectiveness in microvascular non-invasion characterization. ULM is expected to effectively evaluate glioblastoma anti-vascular therapy response.

Indexed as

Brain NeoplasmsGlioblastomaMicroscopy, AcousticMicrovesselsAnimalsMaleMicroscopy, Electron, ScanningNeoplasm InvasivenessRatsRats, Sprague-DawleyX-Ray MicrotomographyGlioblastomaHeterogeneityInvasiveMicrovascularUltrasound localization microscopy

Identifiers

PMID40045008
PMCPMC11882483

What OpenQuestion 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 OpenQuestion graph.