Evidence map›Paper›PMID 27809226›Full record

ArticleInternational journal of molecular sciences2016

Biophysical Properties and Motility of Human Mature Dendritic Cells Deteriorated by Vascular Endothelial Growth Factor through Cytoskeleton Remodeling.

Zu-Quan Hu, Hui Xue, Jin-Hua Long, Yun Wang, Yi Jia, Wei Qiu, Jing Zhou, Zong-Yao Wen, Wei-Juan Yao, Zhu Zeng

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.8field-weighted citation impact, top 27% 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

12 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Review
  6. Review
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. 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

10 authors at 2 institutions in 1 country.

Zu-Quan HuKey Laboratory of Biological and Medical Engineering, Guizhou Medical University, Guiyang 550025, China. huzuquan@gmc.edu.cn.
Hui XueKey Laboratory of Biological and Medical Engineering, Guizhou Medical University, Guiyang 550025, China. xuehui@bjmu.edu.cn.
Jin-Hua LongDepartment of Head and Neck, Affiliated Cancer Hospital, Guizhou Medical University, Guiyang 550025, China. longjinhua100@sina.cn.
Yun WangKey Laboratory of Biological and Medical Engineering, Guizhou Medical University, Guiyang 550025, China. wangyun@gmc.edu.cn.
Yi JiaKey Laboratory of Biological and Medical Engineering, Guizhou Medical University, Guiyang 550025, China. jiayiyouxiang@163.com.
Wei QiuKey Laboratory of Biological and Medical Engineering, Guizhou Medical University, Guiyang 550025, China. qwei407@163.com.
Jing ZhouKey Laboratory of Biological and Medical Engineering, Guizhou Medical University, Guiyang 550025, China. zhou323jing126@126.com.
Zong-Yao WenHemorheology Center, School of Basic Medical Sciences, Health Science Center of Peking University, Beijing 100191, China. rheol@bjmu.edu.cn.
Wei-Juan YaoHemorheology Center, School of Basic Medical Sciences, Health Science Center of Peking University, Beijing 100191, China. ywj01@hotmail.com.
Zhu ZengKey Laboratory of Biological and Medical Engineering, Guizhou Medical University, Guiyang 550025, China. zengzhu100@sina.com.
Guiyang Medical University · CNPeking University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Dendritic cells (DCs), the most potent antigen-presenting cells, play a central role in the initiation, regulation, and maintenance of the immune responses. Vascular endothelial growth factor (VEGF) is one of the important cytokines in the tumor microenvironment (TME) and can inhibit the differentiation and functional maturation of DCs. To elucidate the potential mechanisms of DC dysfunction induced by VEGF, the effects of VEGF on the biophysical characteristics and motility of human mature DCs (mDCs) were investigated. The results showed that VEGF had a negative influence on the biophysical properties, including electrophoretic mobility, osmotic fragility, viscoelasticity, and transmigration. Further cytoskeleton structure analysis by confocal microscope and gene expression profile analyses by gene microarray and real-time PCR indicated that the abnormal remodeling of F-actin cytoskeleton may be the main reason for the deterioration of biophysical properties, motility, and stimulatory capability of VEGF-treated mDCs. This is significant for understanding the biological behavior of DCs and the immune escape mechanism of tumors. Simultaneously, the therapeutic efficacies may be improved by blocking the signaling pathway of VEGF in an appropriate manner before the deployment of DC-based vaccinations against tumors.

Indexed as

ActinsApoptosisBiophysical PhenomenaCell DifferentiationCell MovementCytoskeletonDendritic CellsDown-RegulationElasticityElectrophoresisGene Expression ProfilingGene OntologyHumansHuman Umbilical Vein Endothelial CellsOsmotic FragilityPseudopodiaActinsRNA, MessengerVascular Endothelial Growth Factor Abiophysical characteristicsdendritic cellsimmune functionmotilityvascular endothelial growth factor

Identifiers

PMID27809226
PMCPMC5133777
OpenAlexW2543541211

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.