Evidence map›Paper›PMID 34206901›Full record

ArticlePharmaceuticals (Basel, Switzerland)2021

3,4-Difluorobenzocurcumin Inhibits Vegfc-Vegfr3-Erk Signalling to Block Developmental Lymphangiogenesis in Zebrafish.

Kazuhide S Okuda, Mei Fong Ng, Nur Faizah Ruslan, Neil I Bower, Dedrick Soon Seng Song, Huijun Chen, Sungmin Baek, Philip S Crosier, Katarzyna Koltowska, Jonathan W Astin and 3 more

Open access · goldAbstract read
In one paragraph

Article in Pharmaceuticals (Basel, Switzerland), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed, 8 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

13 authors at 5 institutions in 5 countries.

Kazuhide S OkudaOrganogenesis and Cancer Program, Peter MacCallum Cancer Centre, Melbourne, VIC 3000, Australia.ORCID 0000-0002-8060-0377
Mei Fong NgCancer Research Malaysia, Subang Jaya 47500, Selangor, Malaysia.
Nur Faizah RuslanCancer Research Malaysia, Subang Jaya 47500, Selangor, Malaysia.
Neil I BowerDivision of Genomics of Development and Disease, Institute for Molecular Bioscience, The University of Queensland, St Lucia, QLD 4072, Australia.
Dedrick Soon Seng SongCancer Research Malaysia, Subang Jaya 47500, Selangor, Malaysia.
Huijun ChenDivision of Genomics of Development and Disease, Institute for Molecular Bioscience, The University of Queensland, St Lucia, QLD 4072, Australia.
Sungmin BaekDivision of Genomics of Development and Disease, Institute for Molecular Bioscience, The University of Queensland, St Lucia, QLD 4072, Australia.
Philip S CrosierDepartment of Molecular Medicine & Pathology, School of Medical Sciences, The University of Auckland, Auckland 1010, New Zealand.
Katarzyna KoltowskaDivision of Genomics of Development and Disease, Institute for Molecular Bioscience, The University of Queensland, St Lucia, QLD 4072, Australia.
Jonathan W AstinDepartment of Molecular Medicine & Pathology, School of Medical Sciences, The University of Auckland, Auckland 1010, New Zealand.ORCID 0000-0002-3554-0133
Pei Jean TanCancer Research Malaysia, Subang Jaya 47500, Selangor, Malaysia.ORCID 0000-0002-7953-0965
Benjamin M HoganOrganogenesis and Cancer Program, Peter MacCallum Cancer Centre, Melbourne, VIC 3000, Australia.
Vyomesh PatelCancer Research Malaysia, Subang Jaya 47500, Selangor, Malaysia.
Cancer Research Malaysia · MYThe University of Queensland · AUUniversity of Auckland · NZStowers Institute for Medical Research · USUppsala University · SE

Funding

Internal grant by the Cancer Research Malaysia Not providedNational Heart Foundation/NHMRC Career Development Fellowship BH, 1083811Terry Fox Run Kuala Lumpur grant not provided
6 · The paper itself

Abstract

Lymphangiogenesis, the formation of new lymphatic vessels from pre-existing vasculature, plays critical roles in disease, including in cancer metastasis and chronic inflammation. Preclinical and recent clinical studies have now demonstrated therapeutic utility for several anti-lymphangiogenic agents, but optimal agents and efficacy in different settings remain to be determined. We tested the anti-lymphangiogenic property of 3,4-Difluorobenzocurcumin (CDF), which has previously been implicated as an anti-cancer agent, using zebrafish embryos and cultured vascular endothelial cells. We used transgenic zebrafish labelling the lymphatic system and found that CDF potently inhibits lymphangiogenesis during embryonic development. We also found that the parent compound, Curcumin, does not inhibit lymphangiogenesis. CDF blocked lymphatic and venous sprouting, and lymphatic migration in the head and trunk of the embryo. Mechanistically, CDF impaired VEGFC-VEGFR3-ERK signalling in vitro and in vivo. In an in vivo pathological model of Vegfc-overexpression

Indexed as

3,4-DifluorobenzocurcuminErklymphaticVegfcVegfr3zebrafish

Identifiers

PMID34206901
PMCPMC8308560
OpenAlexW3177453169

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.