Evidence map›Paper›PMID 30819137›Full record

ArticleBMC cancer2019

VEGFR2 promotes tumorigenesis and metastasis in a pro-angiogenic-independent way in gastric cancer.

Lian Lian, Xiang-Li Li, Meng-Dan Xu, Xian-Min Li, Meng-Yao Wu, Yan Zhang, Min Tao, Wei Li, Xiao-Ming Shen, Chong Zhou and 1 more

Open access · goldAbstract read
In one paragraph

Article in BMC cancer, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 75 papers.

0numbers the graph read from it
0cells of the map it votes in
75citing papers in PubMed
5.7field-weighted citation impact, top 3% of its field
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

75 citing papers in PubMed, 139 citations in OpenAlex.

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  15. Antiangiogenic potential ofOpen medicine (Warsaw, Poland) · 2025
    Article
  16. Advanced biomedical research · 2025
    Review
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15 more citing papers are in PubMed but not listed here.

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

11 authors at 3 institutions in 1 country.

Lian LianDepartment of Oncology, Suzhou Xiangcheng People's Hospital, Suzhou, 215131, China.
Xiang-Li LiDepartment of General Surgery, Suzhou Xiangcheng People's Hospital, Suzhou, 215131, China.
Meng-Dan XuDepartment of Oncology, the First Affiliated Hospital of Soochow University, Suzhou, 215006, China.
Xian-Min LiDepartment of Oncology, Suzhou Xiangcheng People's Hospital, Suzhou, 215131, China.
Meng-Yao WuDepartment of Oncology, the First Affiliated Hospital of Soochow University, Suzhou, 215006, China.
Yan ZhangDepartment of Oncology, the First Affiliated Hospital of Soochow University, Suzhou, 215006, China.
Min TaoDepartment of Oncology, the First Affiliated Hospital of Soochow University, Suzhou, 215006, China.
Wei LiDepartment of Oncology, the First Affiliated Hospital of Soochow University, Suzhou, 215006, China.
Xiao-Ming ShenDepartment of Oncology, Suzhou Xiangcheng People's Hospital, Suzhou, 215131, China. shenxiaoming909@sohu.com.
Chong ZhouDepartment of Radiation Oncology, Xuzhou Central Hospital, Xuzhou, 221009, China. zhouchongsuda@163.com.
Min JiangDepartment of Oncology, the First Affiliated Hospital of Soochow University, Suzhou, 215006, China. jiangmin1023@suda.edu.cn.
Soochow University · CNFirst Affiliated Hospital of Soochow University · CNXuzhou Central Hospital · CN

Funding

National Natural Science Foundation of China 81200369National Natural Science Foundation of China 81402093National Natural Science Foundation of China 81402176National Natural Science Foundation of China 81472296National Natural Science Foundation of China 81501970National Natural Science Foundation of China 81602091
6 · The paper itself

Abstract

backgroundVEGF/VEGFR2 pathway is the central therapeutic target in anti-angiogenic treatment in multiple cancers. However, little work has been carried out concerning the pro-malignancy functions of VEGFR2 that are independent of its pro-angiogenesis effects in gastric cancer. Here, we demonstrated that VEGFR2 up-regulation in gastric cancer tissues was a prognostic marker for poor disease-free survival and overall survival of gastric cancer patients.

methodsImmunohistochemistry was used to detect VEGFR2 and VTN expressions in specimens. Kaplan-Meier curves were constructed for survival analysis. Stably knockdown cell lines and overexpression cell lines were constructed by small interfering RNA and plasmids transfection. Real-time PCR and Western blot were used to confirm the expressions of target genes at both RNA and protein levels. Cell proliferation was measured by using Cell Counting Kit-8 and xenograft models. Microarray and bioinformatic analysis were also performed to identify the relationship between Vitronectin (VTN) and VEGFR2.

resultsWhen overexpressed in gastric cancer cells, VEGFR2 increased cellular proliferation and invasion in vitro and tumor formation in xenograft models. By using integrating microarray and bioinformatic analysis, we identifiedVTN as a downstream of VEGFR2 pathway. In gain- and loss-of function analysis in gastric cancer cells, VTN was further verified in consistent with VEGFR2 in expression levels and in regulating cell growth and motility in vitro and in vivo. Moreover, in gastric cancer samples, VTN was as also revealed as a poor prognostic factor.

conclusionsOur present findings defined a novel activity for VEGFR2 in promoting tumorogenicity, motility and indicating a poor survival in gastric cancer beyond its known pro-angiogenic effects. IMPLICATIONS: Our present findings defined a novel activity for VEGFR2 in promoting tumorogenicity, motility and indicating a poor survival in gastric cancer beyond its known pro-angiogenic effects, which may provide a new and valuable target for design of therapies for intervention and a new cognitive perspective for the anti-angiogenesis therapies.

Indexed as

Signal TransductionAgedAged, 80 and overAnimalsBiomarkers, TumorCell Line, TumorCell MovementCell ProliferationCell Transformation, NeoplasticComputational BiologyFemaleGene ExpressionGene Expression Regulation, NeoplasticGene Regulatory NetworksHumansImmunohistochemistryBiomarkers, TumorVascular Endothelial Growth Factor Receptor-2Gastric cancerVEGFR2VTN

Identifiers

PMID30819137
PMCPMC6393973
OpenAlexW2920683253

What OpenQuestion holds

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LicenceCC BY
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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.