Evidence map›Paper›PMID 31169331›Full record

ArticleCancer science2019

Vascular endothelial growth factor (VEGF) impairs the motility and immune function of human mature dendritic cells through the VEGF receptor 2-RhoA-cofilin1 pathway.

Jinhua Long, Zuquan Hu, Hui Xue, Yun Wang, Jin Chen, Fuzhou Tang, Jing Zhou, Lina Liu, Wei Qiu, Shichao Zhang and 5 more

Open access · goldAbstract read
In one paragraph

Article in Cancer science, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 51 papers.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

51 citing papers in PubMed, 66 citations in OpenAlex.

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  19. VEGF signaling: Role in angiogenesis and beyond.Biochimica et biophysica acta. Reviews on cancer · 2024
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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

15 authors at 1 institution in 1 country.

Jinhua LongDepartment of Immunology, School of Basic Medical Sciences, Guizhou Medical University, Guiyang, China.
Zuquan HuDepartment of Immunology, School of Basic Medical Sciences, Guizhou Medical University, Guiyang, China.
Hui XueImmune Cells and Antibody Engineering Research Center of Guizhou Province, Key Laboratory of Biology and Medical Engineering, School of Biology and Engineering, Guizhou Medical University, Guiyang, China.
Yun WangDepartment of Immunology, School of Basic Medical Sciences, Guizhou Medical University, Guiyang, China.
Jin ChenDepartment of Immunology, School of Basic Medical Sciences, Guizhou Medical University, Guiyang, China.
Fuzhou TangImmune Cells and Antibody Engineering Research Center of Guizhou Province, Key Laboratory of Biology and Medical Engineering, School of Biology and Engineering, Guizhou Medical University, Guiyang, China.
Jing ZhouImmune Cells and Antibody Engineering Research Center of Guizhou Province, Key Laboratory of Biology and Medical Engineering, School of Biology and Engineering, Guizhou Medical University, Guiyang, China.
Lina LiuImmune Cells and Antibody Engineering Research Center of Guizhou Province, Key Laboratory of Biology and Medical Engineering, School of Biology and Engineering, Guizhou Medical University, Guiyang, China.
Wei QiuImmune Cells and Antibody Engineering Research Center of Guizhou Province, Key Laboratory of Biology and Medical Engineering, School of Biology and Engineering, Guizhou Medical University, Guiyang, China.
Shichao ZhangImmune Cells and Antibody Engineering Research Center of Guizhou Province, Key Laboratory of Biology and Medical Engineering, School of Biology and Engineering, Guizhou Medical University, Guiyang, China.ORCID https://orcid.org/0000-0002-8760-3482
Yan OuyangImmune Cells and Antibody Engineering Research Center of Guizhou Province, Key Laboratory of Biology and Medical Engineering, School of Biology and Engineering, Guizhou Medical University, Guiyang, China.
Yuannong YeImmune Cells and Antibody Engineering Research Center of Guizhou Province, Key Laboratory of Biology and Medical Engineering, School of Biology and Engineering, Guizhou Medical University, Guiyang, China.
Guoqiang XuDepartment of Immunology, School of Basic Medical Sciences, Guizhou Medical University, Guiyang, China.
Long LiDepartment of Nephrology, The Third Affiliated Hospital of Guizhou Medical University, Duyun, China.
Zhu ZengDepartment of Immunology, School of Basic Medical Sciences, Guizhou Medical University, Guiyang, China.ORCID https://orcid.org/0000-0003-1989-5142
Guiyang Medical University · CN

Funding

2011 Collaborative Innovation Program of Guizhou Province 2015-04Cell and Gene Engineering Innovative Research Groups of Guizhou Province KY-2016-031China Postdoctoral Science Foundation 2015M582747XBKey Project of the Ministry of Education of China 210196National Natural Science Foundation of China 11762006National Natural Science Foundation of China 31660258National Natural Science Foundation of China 31771014National Natural Science Foundation of China 31860262Science and Technology Foundation of Guizhou Province 2016-5676Science and Technology Foundation of Guizhou Province 2017-5718Science and Technology Foundation of Guizhou Province 2018-1412Science and Technology Foundation of Guizhou Province 2019-1266Science and Technology Foundation of Guizhou Province 2019-2787Science and Technology Innovative Talent Team of Guizhou Province 2015-4021
6 · The paper itself

Abstract

Dendritic cells (DCs) are potent and specialized antigen presenting cells, which play a crucial role in initiating and amplifying both the innate and adaptive immune responses against cancer. Tumor cells can escape from immune attack by secreting suppressive cytokines that solely or cooperatively impair the immune function of DCs. However, the underlying mechanisms are not fully defined. Vascular endothelial growth factor (VEGF) has been identified as a major cytokine in the tumor microenvironment. To elucidate the effects of VEGF on the motility and immune function of mature DCs (mDCs), the cells were treated with 50 ng/mL VEGF and investigated by proteomics and molecular biological technologies. The results showed that VEGF can impair the migration capacity and immune function of mDCs through the RhoA-cofilin1 pathway mediated by the VEGF receptor 2, suggesting impaired motility of mDCs by VEGF is one of the aspects of immune escape mechanisms of tumors. It is clinically important to understand the biological behavior of DCs and the immune escape mechanisms of tumor as well as how to improve the efficiency of antitumor therapy based on DCs.

Indexed as

Actin Depolymerizing FactorsCell MovementCells, CulturedCytokinesDendritic CellsHumansHuman Umbilical Vein Endothelial CellsrhoA GTP-Binding ProteinSignal TransductionVascular Endothelial Growth Factor AVascular Endothelial Growth Factor Receptor-2Actin Depolymerizing FactorsCytokinesKDR protein, humanrhoA GTP-Binding ProteinRHOA protein, humanVascular Endothelial Growth Factor AVascular Endothelial Growth Factor Receptor-2VEGFA protein, humanimmune functionmature dendritic cellmotilitysignaling pathwayvascular endothelial growth factor

Identifiers

PMID31169331
PMCPMC6676124
OpenAlexW2954959338

What OpenQuestion holds

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LicenceCC BY-NC
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Registered trials

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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.