Evidence map›Paper›PMID 30518369›Full record

ArticleBMC complementary and alternative medicine2018

Anti-metastatic and anti-proliferative activity of eugenol against triple negative and HER2 positive breast cancer cells.

Mashan L Abdullah, Mohamed M Hafez, Ali Al-Hoshani, Othman Al-Shabanah

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 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
2.4field-weighted citation impact, top 10% 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

30 citing papers in PubMed, 78 citations in OpenAlex.

  1. Review
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  15. An Update on the Therapeutic Anticancer Potential ofMolecules (Basel, Switzerland) · 2023
    Review
  16. Review
  17. MAPLE Processed Nanostructures for Antimicrobial Coatings.International journal of molecular sciences · 2022
    Article
  18. Review
  19. Article
  20. Anticancer Properties of Eugenol: A Review.Molecules (Basel, Switzerland) · 2021
    Review
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

4 authors at 3 institutions in 2 countries.

Mashan L AbdullahPharmacology and toxicology department, King Saud University, Riyadh, Saudi Arabia.ORCID http://orcid.org/0000-0002-4628-1536
Mohamed M HafezCancer Biology Department,Virology and Immunology Unit, National Cancer Institute, Cairo University, Cairo, 11976, Egypt. mohhafez_2000@yahoo.com.
Ali Al-HoshaniPharmacology and toxicology department, King Saud University, Riyadh, Saudi Arabia.
Othman Al-ShabanahPharmacology and toxicology department, King Saud University, Riyadh, Saudi Arabia.
King Saud University · SACairo University · EGKing Saud bin Abdulaziz University for Health Sciences · SA

Funding

King Abdulaziz City for Science and Technology 1-17-03-001-0008
6 · The paper itself

Abstract

backgroundEugenol is a natural phenolic compound and possesses anticancer and antibacterial activities. Breast cancer is a major global health problem, and most of the chemotherapeutic agents are highly toxic with long-term side effects. Therefore, this study aimed to explore the possibility of using eugenol as an anti-metastatic and anti-proliferative agent against MDA-MB-231 and SK-BR-3 breast cancer cells.

methodsBreast cancer cell lines MDA-MB-231 and SK-BR-3 were treated with eugenol and cell proliferation was measured using a real-time cell electronic sensing system. Annexin V analysis with flow cytometry was used to detect the effect of eugenol on cell death. In MDA-MB-231 and SK-BR-3 cells, metastatic potential after eugenol treatment was examined using a wound-healing assay. Real-time PCR was used to study the effect of eugenol on the expression of anti-metastatic genes such as MMP2, MMP9, and TIMP-1, and genes involved in apoptosis including Caspase3, Caspase7, and Caspase9.

resultsTreatment with 4 μM and 8 μM eugenol for 48 h significantly inhibited cell proliferation of MDA-MB-231, with an inhibition rate of 76.4%, whereas 5 μM and 10 μM of eugenol for 48 h significantly inhibited the proliferation of SK-BR-3 cells with an inhibition rate of 68.1%. Eugenol-treated cells showed significantly decreased MMP2 and MMP9 expression and an insignificant increase in TIMP1 expression in HER2 positive and triple negative breast cancer cells. Eugenol significantly increased the proportion of MDA-MB-231 and SK-BR-3 cells in late apoptosis and increased the expression of Caspase3, Caspase7, and Caspase9.

conclusionTo the best of our knowledge, this is the first study to describe the anti-metastatic effect of eugenol against MDA-MB-231 and SK-BR-3 breast cancer cell lines.

Indexed as

Antineoplastic AgentsApoptosisBreast NeoplasmsCell Line, TumorCell ProliferationEugenolFemaleHumansTriple Negative Breast NeoplasmsAntineoplastic AgentsEugenolAnti-apoptoticAnti-proliferativeEugenolGene expressionTriple negative breast cancer

Identifiers

PMID30518369
PMCPMC6282398
OpenAlexW2902625530

What OpenQuestion holds

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LicenceCC BY
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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.