Evidence map›Paper›PMID 39180066›Full record

ArticleCancer cell international2024

Extracellular vesicle-bound VEGF in oral squamous cell carcinoma and its role in resistance to Bevacizumab Therapy.

Jiasheng Zhou, Xue Liu, Qi Dong, Jiao Li, Weidong Niu, Tingjiao Liu

Abstract read
In one paragraph

Article in Cancer cell international, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Extracellular vesicles as modulators of cancer metabolism and microenvironment.Extracellular vesicles and circulating nucleic acids · 2026
    Review
  5. Article
  6. Review
  7. Review
  8. Review
  9. Article
  10. 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

6 authors.

Jiasheng ZhouSchool of Stomatology, Dalian Medical University, West Section No.9, South Road of Lvshun, Dalian, 116044, China.
Xue LiuDepartment of Oral Pathology, School of Stomatology, Shanghai Stomatological Hospital, Fudan University, Tianjin Road No.2, Huangpu District, Shanghai, 200001, China.
Qi DongSchool of Stomatology, Dalian Medical University, West Section No.9, South Road of Lvshun, Dalian, 116044, China.
Jiao LiDepartment of Oral Pathology, School of Stomatology, Shanghai Stomatological Hospital, Fudan University, Tianjin Road No.2, Huangpu District, Shanghai, 200001, China.
Weidong NiuSchool of Stomatology, Dalian Medical University, West Section No.9, South Road of Lvshun, Dalian, 116044, China. niu.wd.endo@dmu.edu.cn.
Tingjiao LiuDepartment of Oral Pathology, School of Stomatology, Shanghai Stomatological Hospital, Fudan University, Tianjin Road No.2, Huangpu District, Shanghai, 200001, China. tingjiao_liu@fudan.edu.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundVascular endothelial growth factor (VEGF) is an important proangiogenic factor and has been considered as a key target of antiangiogenetic therapy in oral squamous cell carcinoma (OSCC). However, clinical application of bevacizumab, a specific VEGF antibody, didn't improve the survival rate of OSCC patients. One possible explanation is that VEGF gene expresses diverse isoforms, which associate with extracellular vesicles (EVs), and EVs potentially contribute to VEGF resistance to bevacizumab. However, clear solution is lacking in addressing this issue.

methodsExpression of VEGF isoforms in OSCC cells was confirmed by reverse transcription and polymerase chain reaction (RT-PCR) and western blot. EVs isolated from OSCC cell's conditioned medium (CM) were characterized by western blot, transmission electron microscopy (TEM) and nanoparticle tracking analysis (NTA). Flow cytometry, immunogold labeling and western blot were applied to study the VEGF on EVs. Tube formation assay and Matrigel plug angiogenesis assay were used for analyzing the angiogenesis capacity of EV-VEGF.

resultsThe most popular isoforms expressed by VEGF gene are VEGF

conclusionAntagonists targeting HSPG might potentially overcome the resistance of EV-VEGF to bevacizumab and serve as an alternative for anti-VEGF therapy in OSCC.

Indexed as

BevacizumabExtracellular vesiclesHeparan sulfate proteoglycansOral squamous cell carcinomaVascular endothelial growth factor

Identifiers

PMID39180066
PMCPMC11344308

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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.