Evidence map›Paper›PMID 26580586›Full record

ArticleMolecules (Basel, Switzerland)2015

Nonprenylated Xanthones from Gentiana lutea, Frasera caroliniensis, and Centaurium erythraea as Novel Inhibitors of Vascular Smooth Muscle Cell Proliferation.

Birgit Waltenberger, Rongxia Liu, Atanas G Atanasov, Stefan Schwaiger, Elke H Heiss, Verena M Dirsch, Hermann Stuppner

Open access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2015. 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
4.1field-weighted citation impact, top 7% 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, 18 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Simultaneous Quantitative Analysis of the Major Bioactive Compounds inJournal of agricultural and food chemistry · 2022
    Article
  5. Medicinal, biological and phytochemical properties of Gentiana species.Journal of traditional and complementary medicine · 2017
    Review
  6. Article
  7. Coumarins, Xanthones and Related Compounds.Molecules (Basel, Switzerland) · 2016
    Article
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

7 authors at 2 institutions in 2 countries.

Birgit WaltenbergerInstitute of Pharmacy/Pharmacognosy, University of Innsbruck, 6020 Innsbruck, Austria. birgit.waltenberger@uibk.ac.at.
Rongxia LiuDepartment of Pharmacognosy, University of Vienna, 1090 Vienna, Austria. liurongxia107@outlook.com.
Atanas G AtanasovDepartment of Pharmacognosy, University of Vienna, 1090 Vienna, Austria. atanas.atanasov@univie.ac.at.
Stefan SchwaigerInstitute of Pharmacy/Pharmacognosy, University of Innsbruck, 6020 Innsbruck, Austria. stefan.schwaiger@uibk.ac.at.
Elke H HeissDepartment of Pharmacognosy, University of Vienna, 1090 Vienna, Austria. elke.heiss@univie.ac.at.
Verena M DirschDepartment of Pharmacognosy, University of Vienna, 1090 Vienna, Austria. verena.dirsch@univie.ac.at.
Hermann StuppnerInstitute of Pharmacy/Pharmacognosy, University of Innsbruck, 6020 Innsbruck, Austria. hermann.stuppner@uibk.ac.at.
University of Vienna · ATUniversität Innsbruck · AT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Aberrant proliferation of vascular smooth muscle cells (VSMC) plays a major role in restenosis, the pathological renarrowing of the blood vessel lumen after surgical treatment of stenosis. Since available anti-proliferative pharmaceuticals produce unfavorable side effects, there is high demand for the identification of novel VSMC proliferation inhibitors. A natural product screening approach using a resazurin conversion assay enabled the identification of gentisin (1) from Gentiana lutea as a novel inhibitor of VSMC proliferation with an IC50 value of 7.84 µM. Aiming to identify further anti-proliferative compounds, 13 additional nonprenylated xanthones, isolated from different plant species, were also tested. While some compounds showed no or moderate activity at 30 µM, 1-hydroxy-2,3,4,5-tetramethoxyxanthone (4), swerchirin (6), and methylswertianin (7) showed IC50 values between 10.2 and 12.5 µM. The anti-proliferative effect of 1, 4, 6, and 7 was confirmed by the quantification of DNA synthesis (BrdU incorporation) in VSMC. Cell death quantification (determined by LDH release in the culture medium) revealed that the compounds are not cytotoxic in the investigated concentration range. In conclusion, nonprenylated xanthones are identified as novel, non-toxic VSMC proliferation inhibitors, which might contribute to the development of new therapeutic applications to combat restenosis.

Indexed as

AnimalsCell ProliferationCells, CulturedCell SurvivalCentauriumGentianaGentianaceaeInhibitory Concentration 50Molecular StructureMuscle, Smooth, VascularMyocytes, Smooth MuscleRatsXanthonesXanthonesatherosclerosisbitter plantsCentaurium erythraeaFrasera caroliniensisGentianaceaeGentiana luteagentisinrestenosisvascular smooth muscle cell proliferationxanthones.

Identifiers

PMID26580586
PMCPMC6332299
OpenAlexW2124483254

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.