Evidence map›Paper›PMID 29738532›Full record

ArticlePloS one2018

Promotion of mammalian angiogenesis by neolignans derived from soybean extracellular fluids.

Farzaneh Kordbacheh, Thomas J Carruthers, Anna Bezos, Marie Oakes, Lauren Du Fall, Charles H Hocart, Christopher R Parish, Michael A Djordjevic

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.4field-weighted citation impact, top 35% 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

2 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. 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

8 authors at 1 institution in 1 country.

Farzaneh KordbachehDepartment of Plant Sciences, Research School of Biology, Australian National University, Canberra, Australian Capital Territory, Australia.ORCID 0000-0003-2208-1414
Thomas J CarruthersResearch School of Chemistry, Australian National University, Canberra, Australian Capital Territory, Australia.
Anna BezosACRF Department of Cancer Biology and Therapeutics, The John Curtin School of Medical Research, Australian National University, Canberra, Australian Capital Territory, Australia.
Marie OakesDepartment of Plant Sciences, Research School of Biology, Australian National University, Canberra, Australian Capital Territory, Australia.
Lauren Du FallDepartment of Plant Sciences, Research School of Biology, Australian National University, Canberra, Australian Capital Territory, Australia.
Charles H HocartDepartment of Plant Sciences, Research School of Biology, Australian National University, Canberra, Australian Capital Territory, Australia.
Christopher R ParishACRF Department of Cancer Biology and Therapeutics, The John Curtin School of Medical Research, Australian National University, Canberra, Australian Capital Territory, Australia.
Michael A DjordjevicDepartment of Plant Sciences, Research School of Biology, Australian National University, Canberra, Australian Capital Territory, Australia.
Australian National University · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Excessive or insufficient angiogenesis is associated with major classes of chronic disease. Although less studied, small molecules which can promote angiogenesis are being sought as potential therapeutics for cardiovascular and peripheral arterial disease and stroke. Here we describe a bioassay-directed discovery approach utilising size exclusion and liquid chromatography to purify components of soybean xylem sap that have pro-angiogenic activity. Using high resolution accurate mass spectrometry and nuclear magnetic resonance spectroscopy, the structure of two pro-angiogenic molecules (FK1 and FK2) were identified as erythro-guaiacylglycerol-8-O-4'-(coniferyl alcohol) ether (eGGCE), and threo-guaiacylglycerol-8-O-4'-(coniferyl alcohol) ether (tGGCE). These two molecules, which are coniferyl neolignan stereoisomers, promoted in vitro angiogenesis in the μM to nM range. Independently sourced samples of eGGCE and tGGCE exhibited comparable pro-angiogenic activity to the soybean derived molecules. The cellular mode of action of these molecules was investigated by studying their effect on endothelial cell proliferation, migration, tube formation and adhesion to the extracellular matrix (ECM) components, fibronectin and vitronectin. They were found to enhance endothelial cell proliferation and endothelial cell tube formation on Matrigel, but did not affect endothelial cell migration or adhesion to fibronectin and vitronectin. Thus, this study has identified two coniferyl neolignan stereoisomers, eGGCE and tGGCE, as pro-angiogenic molecules, with eGGCE being less active than tGGCE.

Indexed as

Angiogenesis Inducing AgentsAnimalsCell AdhesionCell DivisionCell MovementCells, CulturedCollagenDrug CombinationsDrug Evaluation, PreclinicalEndothelial CellsGlycine maxHumansHuman Umbilical Vein Endothelial CellsLamininLignansMolecular StructureAngiogenesis Inducing AgentsCollagenconiferyl alcoholDrug CombinationsLamininLignansmatrigelPhenolsPlant ExtractsProteoglycans

Identifiers

PMID29738532
PMCPMC5940235
OpenAlexW2801113963

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.