Evidence map›Paper›PMID 25244013›Full record

ArticleInternational journal of molecular sciences2014

A novel poly-naphthol compound ST104P suppresses angiogenesis by attenuating matrix metalloproteinase-2 expression in endothelial cells.

Yi-Ling Ma, Shih-Wei Lin, Hua-Chang Fang, Kang-Ju Chou, Youn-Shen Bee, Tian-Huei Chu, Ming-Chi Chang, Wen-Tsan Weng, Chang-Yi Wu, Chung-Lung Cho and 1 more

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.3field-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

10 citing papers in PubMed, 12 citations in OpenAlex.

  1. Nitrobenzoate-Derived Compound X8 Impairs Vascular Development in Zebrafish.International journal of molecular sciences · 2022
    Article
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  5. Ftr82 Is Critical for Vascular Patterning during Zebrafish Development.International journal of molecular sciences · 2017
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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

11 authors at 4 institutions in 1 country.

Yi-Ling MaDepartment of Biological Sciences, National Sun Yat-Sen University, Kaohsiung 804, Taiwan. ylma@vghks.gov.tw.
Shih-Wei LinNational Sun Yat-sen University and Academia Sinica Doctoral Degree Program in Marine Biotechnology, National Sun Yat-Sen University, Kaohsiung 804, Taiwan. shiwey0214@gmail.com.
Hua-Chang FangDivision of Nephrology, Kaohsiung Veterans General Hospital, Kaohsiung 813, Taiwan. hcfang@vghks.gov.tw.
Kang-Ju ChouDivision of Nephrology, Kaohsiung Veterans General Hospital, Kaohsiung 813, Taiwan. kjchou@vghks.gov.tw.
Youn-Shen BeeDepartment of Ophthalmology, Kaohsiung Veterans General Hospital, Kaohsiung 804, Taiwan. ysbee@vghks.gov.tw.
Tian-Huei ChuInstitute of Biomedical Sciences, National Sun Yat-Sen University, Kaohsiung 804, Taiwan. skbboyz0817@gmail.com.
Ming-Chi ChangDivision of Colorectal Surgery, Kaohsiung Veterans General Hospital, Kaohsiung 813, Taiwan. mcchang@vghks.gov.tw.
Wen-Tsan WengInstitute of Basic Medical Sciences, National Cheng Kung University, Tainan 701, Taiwan. bpvincent@gmail.com.
Chang-Yi WuDepartment of Biological Sciences, National Sun Yat-Sen University, Kaohsiung 804, Taiwan. cywu@mail.nsysu.edu.tw.
Chung-Lung ChoDepartment of Biological Sciences, National Sun Yat-Sen University, Kaohsiung 804, Taiwan. clcho@mail.nsysu.edu.tw.
Ming-Hong TaiDepartment of Biological Sciences, National Sun Yat-Sen University, Kaohsiung 804, Taiwan. minghongtai@gmail.com.
National Sun Yat-sen University · TWKaohsiung Veterans General Hospital · TWAcademia Sinica · TWNational Cheng Kung University · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Angiogenesis, the process of neovascularization, plays an important role in physiological and pathological conditions. ST104P is a soluble polysulfated-cyclo-tetrachromotropylene compound with anti-viral and anti-thrombotic activities. However, the functions of ST104P in angiogenesis have never been explored. In this study, we investigated the effects of ST104P in angiogenesis in vitro and in vivo. Application of ST104P potently suppressed the microvessels sprouting in aortic rings ex vivo. Furthermore, ST104P treatment significantly disrupted the vessels' development in transgenic zebrafish in vivo. Above all, repeated administration of ST104P resulted in delayed tumor growth and prolonged the life span of mice bearing Lewis lung carcinoma. Mechanistic studies revealed that ST104P potently inhibited the migration, tube formation and wound closure of human umbilical endothelial cells (HUVECs). Moreover, ST104P treatment inhibited the secretion and expression of matrix metalloproteinase-2 (MMP-2) in a dose-dependent manner. Together, these results suggest that ST104P is a potent angiogenesis inhibitor and may hold potential for treatment of diseases due to excessive angiogenesis including cancer.

Indexed as

Angiogenesis InhibitorsAnimalsAnimals, Genetically ModifiedAortaCarcinoma, Lewis LungCell MovementDown-RegulationDrug Evaluation, PreclinicalEmbryo, NonmammalianEndothelium, VascularEnzyme InductionHumansHuman Umbilical Vein Endothelial CellsMacrocyclic CompoundsMatrix Metalloproteinase 2MiceAngiogenesis InhibitorsMacrocyclic CompoundsMatrix Metalloproteinase 2NaphthalenesulfonatesST104P compound

Identifiers

PMID25244013
PMCPMC4200753
OpenAlexW2062192077

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.