Evidence map›Paper›PMID 19880535›Full record

ArticleExperimental physiology2010

Vascular endothelial growth factor enhances cancer cell adhesion to microvascular endothelium in vivo.

Shang Shen, Jie Fan, Bin Cai, Yonggang Lv, Min Zeng, Yanyan Hao, Filippo G Giancotti, Bingmei M Fu

Open access · bronzeAbstract read
In one paragraph

Article in Experimental physiology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.3field-weighted citation impact, top 21% 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

23 citing papers in PubMed, 35 citations in OpenAlex.

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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

8 authors at 4 institutions in 1 country.

Shang ShenDepartment of Mechanical Engineering, University of Nevada, Las Vegas, 4505 Maryland Parkway, Box 454027, Las Vegas, NV 89154, USA.
Jie Fan
Bin Cai
Yonggang Lv
Min Zeng
Yanyan Hao
Filippo G Giancotti
Bingmei M Fu
City College · USMemorial Sloan Kettering Cancer Center · USUniversity of Nevada, Las Vegas · USCity College of New York · US

Funding

Training and Career Development and Education CoreU54CA137788 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI Daniel Alan Heller · 2008 to 2026
$28.1M
CCNY/MSKCC Biomedical Engineering PartnershipP20CA118861 · NCI · CITY COLLEGE OF NEW YORK · PI TARBELL, JOHN M · 2005 to 2007
$731k
MICROVESSEL PERMEABILITY AND TUMOR METASTASISR15CA086847 · NCI · UNIVERSITY OF NEVADA LAS VEGAS · PI FU, BINGMEI M. · 2000 to 2000
$150k
NCI NIH HHS 011U54CA137788-01NCI NIH HHS P20 CA118861NCI NIH HHS P20CA118861-0NCI NIH HHS R15 CA086847NCI NIH HHS R15CA86847NCI NIH HHS R37CA58597NCI NIH HHS U54 CA137788PHS HHS R01129023
6 · The paper itself

Abstract

To investigate whether vascular endothelial growth factor (VEGF) enhances cancer cell adhesion to normal microvessels, we used in vivo video microscopy to measure adhesion rates of MDA-MB-435s human breast cancer cells and ErbB2-transformed mouse mammary carcinomas in the postcapillary venules of rat mesentery. An individual postcapillary venule in the mesentery was injected via a glass micropipette with cancer cells either in a perfusate of mammalian Ringer solution containing 1% bovine serum albumin as a control, or with the addition of 1 nm VEGF for test measurements. Cell adhesion was measured as either the number of adherent cells or the fluorescence intensity of adherent cells in a vessel segment for 60 min. Our results showed that during both control and VEGF treatments, the number of adherent cells increased almost linearly with time over 60 min. The VEGF treatment increased the adhesion rates of human tumour cells and mouse carcinomas 1.9-fold and 1.8-fold, respectively, over those in control conditions. We also measured cancer cell adhesion after pretreatment of cells with an antibody blocking VEGF or an antibody blocking alpha 6 integrin, and pretreatment of the microvessel with VEGF receptor (KDR/Flk-1) inhibitor, SU1498, or anti-integrin extracellular matrix ligand antibody, anti-laminin-5. All antibodies and inhibitor significantly reduced adhesion, with anti-VEGF and SU1498 reducing it the most. Our results indicate that VEGF enhances cancer cell adhesion to the normal microvessel wall, and further suggest that VEGF and its receptor, KDR/Flk-1, as well as integrins of tumour cells and their ligands at the endothelium, contribute to mammary cancer cell adhesion to vascular endothelium in vivo.

Indexed as

AnimalsBreast NeoplasmsCell AdhesionCell Line, TumorDose-Response Relationship, DrugEndothelium, VascularFemaleHumansMiceRatsVascular Endothelial Growth Factor AVascular Endothelial Growth Factor AVEGFA protein, human

Identifiers

PMID19880535
PMCPMC2859456
OpenAlexW1495435581

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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.