Evidence map›Paper›PMID 25988521›Full record

ArticleMarine drugs2015

Anti-Restenotic Roles of Dihydroaustrasulfone Alcohol Involved in Inhibiting PDGF-BB-Stimulated Proliferation and Migration of Vascular Smooth Muscle Cells.

Pei-Chuan Li, Ming-Jyh Sheu, Wei-Fen Ma, Chun-Hsu Pan, Jyh-Horng Sheu, Chieh-Hsi Wu

Abstract read
In one paragraph

Article in Marine drugs, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

11 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
  3. Cellular crosstalk in atherosclerotic plaque microenvironment.Cell communication and signaling : CCS · 2023
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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

6 authors.

Pei-Chuan LiDepartment of Pharmacology and Pharmaceutical Sciences, School of Pharmacy, University of Southern California, Los Angeles, CA 90089, USA. lipeichu@usc.edu.
Ming-Jyh SheuSchool of Pharmacy, China Medical University, Taichung 404, Taiwan. soybean13mtdtw@gmail.com.
Wei-Fen MaSchool of Nursing, China Medical University, Taichung 404, Taiwan. lhdaisy@mail.cmu.edu.tw.
Chun-Hsu PanDepartment of Pharmacy, Taipei Medical University, Taipei 110, Taiwan. panch@tmu.edu.tw.
Jyh-Horng SheuDepartment of Marine Biotechnology and Resources, National Sun Yat-sen University, Kaohsiung 804, Taiwan. sheu@mail.nsysu.edu.tw.
Chieh-Hsi WuSchool of Pharmacy, China Medical University, Taichung 404, Taiwan. chhswu@tmu.edu.tw.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Dihydroaustrasulfone alcohol (DA), an active compound firstly isolated from marine corals, has been reported to reveal anti-cancer and anti-inflammation activities. These reported activities of DA raised a possible application in anti-restenosis. Abnormal proliferation and migration of vascular smooth muscle cells (VSMCs) and the stimulation of platelet-derived growth factor (PDGF)-BB play major pathological processes involved in the development of restenosis. Experimental results showed that DA markedly reduced balloon injury-induced neointima formation in the rat carotid artery model and significantly inhibited PDGF-BB-stimulated proliferation and migration of VSMCs. Our data further demonstrated that translational and active levels of several critical signaling cascades involved in VSMC proliferation, such as extracellular signal-regulated kinase/ mitogen-activated protein kinases (ERK/MAPK), phosphatidylinositol 3-kinase (PI3K)/AKT, and signal transducer and activator of transcription (STAT), were obviously inhibited. In addition, DA also decreased the activation and expression levels of gelatinases (matrix metalloproteinase (MMP)-2 and MMP-9) involved in cell migration. In conclusion, our findings indicate that DA can reduce balloon injury-neointimal hyperplasia, the effect of which may be modulated through suppression of VSMC proliferation and migration. These results suggest that DA has potential application as an anti-restenotic agent for the prevention of restenosis.

Indexed as

AnimalsBecaplerminButanonesCell MovementCell ProliferationCoronary RestenosisExtracellular Signal-Regulated MAP KinasesMaleMAP Kinase Signaling SystemMatrix Metalloproteinase 2Matrix Metalloproteinase 9Muscle, Smooth, VascularMyocytes, Smooth MuscleNeointimaPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktBecaplerminButanonesdihydroaustrasulfone alcoholExtracellular Signal-Regulated MAP KinasesMatrix Metalloproteinase 2Matrix Metalloproteinase 9Phosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktProto-Oncogene Proteins c-sisSTAT Transcription FactorsSulfonesanti-restenosisdihydroaustrasulfone alcoholmarine originneointimal hyperplasia

Identifiers

PMID25988521
PMCPMC4446617

What Socratic 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 Socratic graph.