Evidence map›Paper›PMID 29233192›Full record

ArticleBiological research2017

Methanolic extract of Euchelus asper exhibits in-ovo anti-angiogenic and in vitro anti-proliferative activities.

Sweta Agrawal, Sachin Chaugule, Shashank More, Gargi Rane, Madhavi Indap

Open access · goldAbstract read
In one paragraph

Article in Biological research, 2017. 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
0.4field-weighted citation impact, top 35% 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.

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  7. Endophytic Fungus Isolated FromFrontiers in oncology · 2018
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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

5 authors at 1 institution in 1 country.

Sweta AgrawalCentral Research Laboratory, D. G. Ruparel College, Senapati Bapat Marg, Mahim, Mumbai, 400 016, India.
Sachin ChauguleCentral Research Laboratory, D. G. Ruparel College, Senapati Bapat Marg, Mahim, Mumbai, 400 016, India.
Shashank MoreCentral Research Laboratory, D. G. Ruparel College, Senapati Bapat Marg, Mahim, Mumbai, 400 016, India.
Gargi RaneCentral Research Laboratory, D. G. Ruparel College, Senapati Bapat Marg, Mahim, Mumbai, 400 016, India.
Madhavi IndapCentral Research Laboratory, D. G. Ruparel College, Senapati Bapat Marg, Mahim, Mumbai, 400 016, India. madhaviindap@yahoo.com.
Central Forensic Science Laboratory · IN

Funding

University Grants Commission UGC No. F. 6-40/2011 (SA-II)
6 · The paper itself

Abstract

backgroundThe marine environment is a rich source of bioactive natural products. Many of the marine bioactive compounds have been derived successfully from molluscs. Euchelus asper is a marine mollusc which is commonly found in the intertidal rocky regions of the Mumbai coast. The present study was focused on evaluating the anti-angiogenic and anti- proliferative activities of methanolic extract of Euchelus asper (EAME).

methodsThe anti-angiogenic activity of EAME (50-800 μg/mL) was assessed by chick chorio-allantoic membrane (CAM) model wherein multiple parameters in the CAM blood vessels were analysed through morphometric and histological investigations. In vitro testing of EAME (5-20 μg/mL) included its cytotoxicity against three different cancer cell lines, its effect on cell proliferation by wound healing assay as well as their relevant molecular mechanisms. Statistical analysis was carried out by two-tailed student's t test for two unpaired groups.

resultsAnalysis of CAM revealed that the extract is effective in reducing the branching points of the 1st order blood vessels or capillaries of CAM. Histological analysis of CAM showed significant decrease in capillary plexus and compartmentalization along with increase in mesodermal blood vessels, thus establishing its anti-angiogenicity. Further, EAME exhibited moderate but significant cytotoxicity against A549 non-small cell lung carcinoma cell line. We also demonstrated that the cytotoxicity of EAME in A549 was associated with its apoptotic activity by subG1 phase arrest. Lastly, EAME significantly reduced A549 proliferation by reducing the expression of Matrix metalloproteinase-2 (MMP-2) and Matrix metalloproteinase-9 (MMP-9).

conclusionOverall, our study suggested that EAME has potential to inhibit tumour angiogenic and proliferative activity and may be a potential source for development of new anti-cancer pharmaceuticals.

Indexed as

Angiogenesis InhibitorsAnimalsBiological ProductsCell Line, TumorCell ProliferationChick EmbryoGastropodaAngiogenesis InhibitorsBiological ProductsAnti-angiogenesisAnti-cancerAnti-proliferativeCAMChorio-allantoic membraneEuchelus asperMarine bioactivesMollusc

Identifiers

PMID29233192
PMCPMC5726033
OpenAlexW2774104665

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.