Evidence map›Paper›PMID 32033130›Full record

ArticleCells2020

A New Highlight of

Fairouz Sioud, Souheila Amor, Imène Ben Toumia, Aida Lahmar, Virginie Aires, Leila Chekir-Ghedira, Dominique Delmas

Open access · goldAbstract read
In one paragraph

Article in Cells, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
3.3field-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

17 citing papers in PubMed, 36 citations in OpenAlex.

  1. Article
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  5. Aqueous Extracts ofInternational journal of molecular sciences · 2024
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  8. The role of AlgerianSaudi journal of biological sciences · 2023
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  11. Control ofSaudi journal of biological sciences · 2022
    Article
  12. Article
  13. Article
  14. Article
  15. Essential Oils,Nutrients · 2021
    Article
  16. A Methanol Extract ofMolecules (Basel, Switzerland) · 2020
    Article
  17. 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.

Fairouz SioudResearch Unit Bioactive Natural Products and Biotechnology UR17ES49, Faculty of Dental Medicine of Monastir, University of Monastir, Avicenne street, 5000 Monastir, Tunisia.
Souheila AmorUniversité de Bourgogne Franche-Comté, F-21000 Dijon, France.
Imène Ben ToumiaResearch Unit Bioactive Natural Products and Biotechnology UR17ES49, Faculty of Dental Medicine of Monastir, University of Monastir, Avicenne street, 5000 Monastir, Tunisia.
Aida LahmarResearch Unit Bioactive Natural Products and Biotechnology UR17ES49, Faculty of Dental Medicine of Monastir, University of Monastir, Avicenne street, 5000 Monastir, Tunisia.
Virginie AiresUniversité de Bourgogne Franche-Comté, F-21000 Dijon, France.
Leila Chekir-GhediraResearch Unit Bioactive Natural Products and Biotechnology UR17ES49, Faculty of Dental Medicine of Monastir, University of Monastir, Avicenne street, 5000 Monastir, Tunisia.
Dominique DelmasUniversité de Bourgogne Franche-Comté, F-21000 Dijon, France.
Inserm · FRUniversity of Monastir · TN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Despite major advances in the last 10 years, whether in terms of prevention or treatment, the 5 year survival rate remains relatively low for a large number of cancers. These therapeutic failures can be the consequence of several factors associated with the cellular modifications or with the host by itself, especially for some anticancer drugs such as cisplatin, which induces a nephrotoxicity. In the strategy of research for active molecules capable both of exerting a protective action against the deleterious effects of cisplatin and exerting a chemosensitizing action with regard to cancer cells, we tested the potential effects of Ephedra alata Decne extract (E.A.) rich in polyphenolic compounds towards a 4T1 breast cancer model in vitro and in vivo. We showed that E.A. extract inhibited cell viability of 4T1 breast cancer cells and induced apoptosis in a caspase-dependent manner, which involved intrinsic pathways. Very interestingly, we observed a synergic antiproliferative and pro-apoptotic action with cisplatin. These events were associated with a strong decrease of breast tumor growth in mice treated with an E.A./cisplatin combination and simultaneously with a decrease of hepato- and nephrotoxicities of cisplatin.

Indexed as

Adjuvants, PharmaceuticAnimalsBreast NeoplasmsCaspasesCell DeathCell Line, TumorCell ProliferationCell SurvivalCisplatinCytochromes cDrug SynergismEnzyme ActivationEphedraFemaleInhibitory Concentration 50Mammary Neoplasms, AnimalAdjuvants, PharmaceuticCaspasesCisplatinCytochromes cPhenolsPlant ExtractsProto-Oncogene Proteins c-bcl-2breast cancerchemosensibilisationcisplatinEphedrapolyphenols

Identifiers

PMID32033130
PMCPMC7072491
OpenAlexW3004517392

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.