Evidence map›Paper›PMID 31719927›Full record

ArticleCellular and molecular bioengineering2019

Tumor Cell Mechanosensing During Incorporation into the Brain Microvascular Endothelium.

Marina A Pranda, Kelsey M Gray, Ariana Joy L DeCastro, Gregory M Dawson, Jae W Jung, Kimberly M Stroka

Open access · greenAbstract read
In one paragraph

Article in Cellular and molecular bioengineering, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.0field-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

14 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
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  6. Methods for studying mammalian aquaporin biology.Biology methods & protocols · 2023
    Review
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  14. Photodynamic Priming Modulates Endothelial Cell-Cell Junction Phenotype for Light-activated Remote Control of Drug Delivery.IEEE journal of selected topics in quantum electronics : a publication of the IEEE Lasers and Electro-optics Society
    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

6 authors at 2 institutions in 1 country.

Marina A Pranda *Fischell Department of Bioengineering, University of Maryland, College Park, College Park, MD 20742 USA.
Kelsey M Gray *Fischell Department of Bioengineering, University of Maryland, College Park, College Park, MD 20742 USA.
Ariana Joy L DeCastroFischell Department of Bioengineering, University of Maryland, College Park, College Park, MD 20742 USA.
Gregory M DawsonDepartment of Biology, University of Maryland, College Park, College Park, MD 20742 USA.
Jae W JungFischell Department of Bioengineering, University of Maryland, College Park, College Park, MD 20742 USA.
Kimberly M StrokaFischell Department of Bioengineering, University of Maryland, College Park, College Park, MD 20742 USA.ORCID 0000-0003-3314-2067
University of Maryland, College Park · USUniversity of Maryland, Baltimore · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionTumor metastasis to the brain occurs in approximately 20% of all cancer cases and often occurs due to tumor cells crossing the blood-brain barrier (BBB). The brain microenvironment is comprised of a soft hyaluronic acid (HA)-rich extracellular matrix with an elastic modulus of 0.1-1 kPa, whose crosslinking is often altered in disease states.

methodsTo explore the effects of HA crosslinking on breast tumor cell migration, we developed a biomimetic model of the human brain endothelium, consisting of brain microvascular endothelial cell (HBMEC) monolayers on HA and gelatin (HA/gelatin) films with different degrees of crosslinking, as established by varying the concentration of the crosslinker Extralink. RESULTS AND DISCUSSION: Metastatic breast tumor cell migration speed, diffusion coefficient, spreading area, and aspect ratio increased with decreasing HA crosslinking, a mechanosensing trend that correlated with tumor cell actin organization but not CD44 expression. Meanwhile, breast tumor cell incorporation into endothelial monolayers was independent of HA crosslinking density, suggesting that alterations in HA crosslinking density affect tumor cells only after they exit the vasculature. Tumor cells appeared to exploit both the paracellular and transcellular routes of trans-endothelial migration. Quantitative phenotyping of HBMEC junctions

conclusionsOverall, our quantitative results suggest that a combination of biochemical and physical factors promote tumor cell migration through the BBB.

Indexed as

Breast cancerHyaluronic acidMicrovasculatureTight junctions

Identifiers

PMID31719927
PMCPMC6816707
OpenAlexW2970203947

What OpenQuestion holds

Textmetadata
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.