Evidence map›Paper›PMID 30648805›Full record

ArticleJournal of cellular and molecular medicine2019

Fucoxanthin inhibits tumour-related lymphangiogenesis and growth of breast cancer.

Jia Wang, Yanhong Ma, Jingshi Yang, Lu Jin, Zixiang Gao, Lingyun Xue, Lin Hou, Linlin Sui, Jing Liu, Xiangyang Zou

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 44 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed, 2 pooled it
4.3field-weighted citation impact, top 5% 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

44 citing papers in PubMed, 2 syntheses or guidelines pooled it, 89 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 2 institutions in 1 country.

Jia WangRegenerative Medicine Center, The First Affiliated Hospital of Dalian Medical University, Dalian, China.ORCID 0000-0003-1603-7361
Yanhong MaDepartment of Biotechnology, Dalian Medical University, Dalian, China.
Jingshi YangDepartment of Biotechnology, Dalian Medical University, Dalian, China.
Lu JinDepartment of Biotechnology, Dalian Medical University, Dalian, China.
Zixiang GaoDepartment of Biotechnology, Dalian Medical University, Dalian, China.
Lingyun XueINNOBIO Corporation Limited, Dalian, China.
Lin HouCollege of Life Sciences, Liaoning Normal University, Dalian, China.
Linlin SuiDepartment of Biotechnology, Dalian Medical University, Dalian, China.
Jing LiuRegenerative Medicine Center, The First Affiliated Hospital of Dalian Medical University, Dalian, China.
Xiangyang ZouDepartment of Biotechnology, Dalian Medical University, Dalian, China.
Dalian Medical University · CNLiaoning Normal University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tumour lymphangiogenesis plays an important role in promoting the growth and lymphatic metastasis of tumours. The process is associated with cell proliferation, migration and tube-like structure formation in lymphatic endothelial cells (LEC), but no antilymphangiogenic agent is currently used in clinical practice. Fucoxanthin is a material found in brown algae that holds promise in the context of drug development. Fucoxanthin is a carotenoid with variety of pharmacological functions, including antitumour and anti-inflammatory effects. The ability of fucoxanthin to inhibit lymphangiogenesis remains unclear. The results of experiments performed as part of this study show that fucoxanthin, extracted from Undaria pinnatifida (Wakame), inhibits proliferation, migration and formation of tube-like structures in human LEC (HLEC). In this study, fucoxanthin also suppressed the malignant phenotype in human breast cancer MDA-MB-231 cells and decreased tumour-induced lymphangiogenesis when used in combination with a conditional medium culture system. Fucoxanthin significantly decreased levels of vascular endothelial growth factor (VEGF)-C, VEGF receptor-3, nuclear factor kappa B, phospho-Akt and phospho-PI3K in HLEC. Fucoxanthin also decreased micro-lymphatic vascular density (micro-LVD) in a MDA-MB-231 nude mouse model of breast cancer. These findings suggest that fucoxanthin inhibits tumour-induced lymphangiogenesis in vitro and in vivo, highlighting its potential use as an antilymphangiogenic agent for antitumour metastatic comprehensive therapy in patients with breast cancer.

Indexed as

Xenograft Model Antitumor AssaysAnimalsBreast NeoplasmsCell Line, TumorCell MovementCell ProliferationEndothelial CellsFemaleHumansLymphangiogenesisLymphatic VesselsMice, Inbred BALB CMice, NudePhaeophyceaeVascular Endothelial Growth Factor CVascular Endothelial Growth Factor Receptor-3fucoxanthinVascular Endothelial Growth Factor CVascular Endothelial Growth Factor Receptor-3Xanthophyllsfucoxanthinlymphatic metastasisMDA-MB-231 cellstumour-induced lymphangiogenesis

Identifiers

PMID30648805
PMCPMC6378177
OpenAlexW2910271798

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.