Evidence map›Paper›PMID 31035725›Full record

ArticleMarine drugs2019

The Inhibitory Effect of Propylene Glycol Alginate Sodium Sulfate on Fibroblast Growth Factor 2-Mediated Angiogenesis and Invasion in Murine Melanoma B16-F10 Cells In Vitro.

He Ma, Peiju Qiu, Huixin Xu, Ximing Xu, Meng Xin, Yanyan Chu, Huashi Guan, Chunxia Li, Jinbo Yang

Open access · goldAbstract read
In one paragraph

Article in Marine drugs, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 2 pooled it
0.5field-weighted citation impact, top 36% 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

6 citing papers in PubMed, 2 syntheses or guidelines pooled it, 11 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Article
  4. Article
  5. Baicalein restrains proliferation, migration, and invasion of human malignant melanoma cells by down-regulating colon cancer associated transcript-1.Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologica · 2019
    Article
  6. Mechanisms of resistance to anti-angiogenic treatments.Cancer drug resistance (Alhambra, Calif.) · 2019
    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

9 authors at 2 institutions in 1 country.

He MaKey Laboratory of Marine Drugs of Ministry of Education, Shandong Provincial, Key Laboratory of Glycoscience and Glycotechnology, School of Medicine and Pharmacy, Ocean University of China, Qingdao 266003, China. mahe1992mahe@163.com.
Peiju QiuKey Laboratory of Marine Drugs of Ministry of Education, Shandong Provincial, Key Laboratory of Glycoscience and Glycotechnology, School of Medicine and Pharmacy, Ocean University of China, Qingdao 266003, China. peijuqiu@ouc.edu.cn.
Huixin XuKey Laboratory of Marine Drugs of Ministry of Education, Shandong Provincial, Key Laboratory of Glycoscience and Glycotechnology, School of Medicine and Pharmacy, Ocean University of China, Qingdao 266003, China. xvhuixin@hotmail.com.
Ximing XuKey Laboratory of Marine Drugs of Ministry of Education, Shandong Provincial, Key Laboratory of Glycoscience and Glycotechnology, School of Medicine and Pharmacy, Ocean University of China, Qingdao 266003, China. xuximing@ouc.edu.cn.
Meng XinKey Laboratory of Marine Drugs of Ministry of Education, Shandong Provincial, Key Laboratory of Glycoscience and Glycotechnology, School of Medicine and Pharmacy, Ocean University of China, Qingdao 266003, China. xinmeng512@126.com.
Yanyan ChuKey Laboratory of Marine Drugs of Ministry of Education, Shandong Provincial, Key Laboratory of Glycoscience and Glycotechnology, School of Medicine and Pharmacy, Ocean University of China, Qingdao 266003, China. mary0312332@126.com.
Huashi GuanKey Laboratory of Marine Drugs of Ministry of Education, Shandong Provincial, Key Laboratory of Glycoscience and Glycotechnology, School of Medicine and Pharmacy, Ocean University of China, Qingdao 266003, China. hsguan@ouc.edu.cn.
Chunxia LiKey Laboratory of Marine Drugs of Ministry of Education, Shandong Provincial, Key Laboratory of Glycoscience and Glycotechnology, School of Medicine and Pharmacy, Ocean University of China, Qingdao 266003, China. lchunxia@ouc.edu.cn.ORCID 0000-0001-8102-137X
Jinbo YangKey Laboratory of Marine Drugs of Ministry of Education, Shandong Provincial, Key Laboratory of Glycoscience and Glycotechnology, School of Medicine and Pharmacy, Ocean University of China, Qingdao 266003, China. yangjb@ouc.edu.cn.
Qingdao National Laboratory for Marine Science and Technology · CNOcean University of China · CN

Funding

"Ao Shan Talents" Program Supported by Qingdao National Laboratory for Marine Science and Technology 2017ASTCP-OS11Qingdao Leading Talents Program 16-8-3-11-zhcShandong Science and Technology Project 2014GGH215001The Marine S&T Fund of Shandong Province for Pilot National Laboratory for Marine Science and Technology (Qingdao) 2018SDKJ0404-4The National Natural Science Fund 31701221
6 · The paper itself

Abstract

Melanoma is one of the most malignant and aggressive types of cancer worldwide. Fibroblast growth factor 2 (FGF2) is one of the critical regulators of melanoma angiogenesis and metastasis; thus, it might be an effective anti-cancer strategy to explore FGF2-targeting drug candidates from existing drugs. In this study, we evaluate the effect of the marine drug propylene glycol alginate sodium sulfate (PSS) on FGF2-mediated angiogenesis and invasion. The data shows that FGF2 selectively bound to PSS with high affinity. PSS inhibited FGF2-mediated angiogenesis in a rat aortic ring model and suppressed FGF2-mediated invasion, but not the migration of murine melanoma B16-F10 cells. The further mechanism study indicates that PSS decreased the expression of activated matrix metalloproteinase 2 (MMP-2) and matrix metalloproteinase 9 (MMP-9), and also suppressed their activity. In addition, PSS was found to decrease the level of Vimentin in B16-F10 cells, which is known to participate in the epithelial-mesenchymal transition. Notably, PSS did not elicit any changes in cancer cell viability. Based on the results above, we conclude that PSS might be a potential drug to regulate the tumor microenvironment in order to facilitate the recovery of melanoma patients.

Indexed as

AlginatesAnimalsAortaAquatic OrganismsCell Line, TumorCell MovementCell SurvivalChick EmbryoChorioallantoic MembraneDrug Evaluation, PreclinicalEpithelial-Mesenchymal TransitionFibroblast Growth Factor 2HumansLaminariaMelanoma, ExperimentalMiceAlginatesFibroblast Growth Factor 2propylene glycol alginate sodium sulfateangiogenesisFGF2invasionMMP-2MMP-9propylene glycol alginate sodium sulfate

Identifiers

PMID31035725
PMCPMC6562581
OpenAlexW2941324368

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.