Evidence map›Paper›PMID 29720141›Full record

ArticleBMC complementary and alternative medicine2018

Solamargine, a bioactive steroidal alkaloid isolated from Solanum aculeastrum induces non-selective cytotoxicity and P-glycoprotein inhibition.

Trevor Burger, Tsholofelo Mokoka, Gerda Fouché, Paul Steenkamp, Vanessa Steenkamp, Werner Cordier

Open access · goldAbstract read
In one paragraph

Article in BMC complementary and alternative medicine, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed, 1 pooled it
2.5field-weighted citation impact, top 8% 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

24 citing papers in PubMed, 1 synthesis or guideline pooled it, 53 citations in OpenAlex.

  1. Pooled it
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  7. American journal of cancer research · 2024
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  14. Anticancer activity of glycoalkaloids fromFrontiers in pharmacology · 2022
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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 at 2 institutions in 1 country.

Trevor BurgerDepartment of Pharmacology, School of Medicine, Faculty of Health Sciences, University of Pretoria, P.O.Box X323, Pretoria, Arcadia, 0007, South Africa.
Tsholofelo MokokaBiosciences Division, Council of Scientific and Industrial Research, Pretoria, South Africa.
Gerda FouchéBiosciences Division, Council of Scientific and Industrial Research, Pretoria, South Africa.
Paul SteenkampBiosciences Division, Council of Scientific and Industrial Research, Pretoria, South Africa.
Vanessa SteenkampDepartment of Pharmacology, School of Medicine, Faculty of Health Sciences, University of Pretoria, P.O.Box X323, Pretoria, Arcadia, 0007, South Africa.
Werner CordierDepartment of Pharmacology, School of Medicine, Faculty of Health Sciences, University of Pretoria, P.O.Box X323, Pretoria, Arcadia, 0007, South Africa. werner.cordier@up.ac.za.ORCID http://orcid.org/0000-0002-5744-9285
Council for Scientific and Industrial Research · ZAUniversity of Pretoria · ZA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSolanum aculeastrum fruits are used by some cancer sufferers as a form of alternative treatment. Scientific literature is scarce concerning its anticancer activity, and thus the aim of the study was to assess the in vitro anticancer and P-glycoprotein inhibitory potential of extracts of S. aculeastrum fruits. Furthermore, assessment of the combinational effect with doxorubicin was also done.

methodsThe crude extract was prepared by ultrasonic maceration. Liquid-liquid extraction yielded one aqueous and two organic fractions. Bioactive constituents were isolated from the aqueous fraction by means of column chromatography, solid phase extraction and preparative thin-layer chromatography. Confirmation of bioactive constituent identity was done by nuclear magnetic resonance and ultra-performance liquid chromatography mass spectrometry. The crude extract and fractions were assessed for cytotoxicity and P-glycoprotein inhibition in both cancerous and non-cancerous cell lines using the sulforhodamine B and rhodamine-123 assays, respectively.

resultsBoth the crude extract and aqueous fraction was cytotoxic to all cell lines, with the SH-SY5Y neuroblastoma cell line being most susceptible to exposure (IC

conclusionsThe crude extract and aqueous fraction displayed potent non-selective cytotoxicity and noteworthy P-glycoprotein inhibition. These effects were attributed to solamargine. P-glycoprotein inhibitory activity was only present at concentrations higher than those inducing cytotoxicity, and thus does not appear to be the likely mechanism for the enhancement of doxorubicin's cytotoxicity. Preliminary results suggest that non-selective cytotoxicity may hinder drug development, however, further assessment of the mode of cell death is necessary to determine the route forward.

Indexed as

Antineoplastic AgentsATP Binding Cassette Transporter, Subfamily B, Member 1Cell DeathCell Line, TumorCell SurvivalDoxorubicinDrug SynergismHumansSolanaceous AlkaloidsSolanumAntineoplastic AgentsATP Binding Cassette Transporter, Subfamily B, Member 1beta-solamarineDoxorubicinSolanaceous AlkaloidsCancerP-glycoproteinSolamargineSolanum aculeastrumSolasonineSteroidal alkaloids

Identifiers

PMID29720141
PMCPMC5930800
OpenAlexW2803900295

What OpenQuestion holds

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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.