Evidence map›Paper›PMID 29890947›Full record

ArticleBMC cancer2018

Dynamic Hyaluronan drives liver endothelial cells towards angiogenesis.

Sampa Ghose, Subhrajit Biswas, Kasturi Datta, Rakesh K Tyagi

Open access · goldAbstract read
In one paragraph

Article in BMC cancer, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.4field-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

9 citing papers in PubMed, 26 citations in OpenAlex.

  1. Review
  2. Article
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  5. Article
  6. hapln1aNature communications · 2023
    Article
  7. Article
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  9. Review
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

4 authors at 2 institutions in 2 countries.

Sampa GhoseDepartment of Medical Oncology, All India Institute of Medical Sciences, Ansari Nagar, New Delhi, 110029, India. sampaghose@gmail.com.ORCID http://orcid.org/0000-0001-8262-4949
Subhrajit BiswasAmity Institute of Molecular Medicine and Stem Cell Research, Amity University Uttar Pradesh (AUUP), Sector 125, NOIDA, Uttar Pradesh, 201313, India. sbiswas2@amity.edu.
Kasturi DattaSchool of Environmental Sciences, Jawaharlal Nehru University, New Delhi, India.
Rakesh K TyagiSpecial Centre for Molecular Medicine, Jawaharlal Nehru University, New Delhi, India.
Jawaharlal Nehru University · INAmity University · AE

Funding

Council of Scientific and Industrial Research 13(8600-A)/2012-PoolDepartment of Biotechnology , Ministry of Science and Technology BT/PR15011/MED/30/1578/2015Science and Engineering Research Board YSS/2015/000092
6 · The paper itself

Abstract

backgroundAngiogenesis, the formation of new blood vessels from pre-existing vasculature is essential in a number of physiological processes such as embryonic development, wound healing as well as pathological conditions like, tumor growth and metastasis. Hyaluronic acid (HA), a high molecular weight polysaccharide, major component of extracellular matrix is known to associate with malignant phenotypes in melanomas and various other carcinomas. Hyaluronic acid binding protein 1 (HABP1) has been previously reported to trigger enhanced cellular proliferation in human liver cancer cells upon its over-expression. In the present study, we have identified the HA mediated cellular behaviour of liver endothelial cells during angiogenesis.

methodsEndothelial cells have been isolated from perfused liver of mice. Cell proliferation was studied using microwell plates with tetrazole dye. Cell migration was evaluated by measuring endothelial monolayer wound repair as well as through transwell migration assay. Alterations in proteins and mRNA expression were estimated by immunobloting and quantitative real time PCR using Applied Biosystems. The paraformaldehyde fixed endothelial cells were used for immuno- florescence staining and F-actin detection with conjugated antibodies. The images were captured by using Olympus florescence microscope (IX71).

resultsWe observed that administration of HA enhanced cell proliferation, adhesion, tubular sprout formation as well as migration of liver endothelial cells (ECs). The effect of HA in the rearrangement of the actins confirmed HA -mediated cytoskeleton re-organization and cell migration. Further, we confirmed enhanced expression of angiogenic factors like VEGF-A and VEGFR1 in endothelial cells upon HA treatment. HA supplementation led to elevated expression of HABP1 in murine endothelial cells. It was interesting to note that, although protein levels of β- catenin remained unaltered, but translocation of this protein from membrane to nucleus was observed upon HA treatment, suggesting its role not only in vessel formation but also its involvement in angiogenesis signalling.

conclusionsThe elucidation of molecular mechanism (s) responsible for HA mediated regulation of endothelial cells and angiogenesis contributes not only to our understanding the mechanism of disease progression but also offer new avenues for therapeutic intervention.

Indexed as

AnimalsCells, CulturedEndothelial CellsHyaluronic AcidLiverMiceMitochondrial ProteinsNeovascularization, PathologicNeovascularization, PhysiologicVascular Endothelial Growth Factor AVascular Endothelial Growth Factor Receptor-1C1qbp protein, mouseHyaluronic AcidMitochondrial ProteinsVascular Endothelial Growth Factor AVascular Endothelial Growth Factor Receptor-1AngiogenesisHyaluronic acid or HyaluronanLiver endothelial cells

Identifiers

PMID29890947
PMCPMC5996548
OpenAlexW2807896387

What OpenQuestion holds

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LicenceCC BY
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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.