Evidence map›Paper›PMID 35458590›Full record

ArticleMolecules (Basel, Switzerland)2022

Evening Primrose Oil Enhances Tamoxifen's Anticancer Activity against Breast Cancer Cells by Inducing Apoptosis, Inhibiting Angiogenesis, and Arresting the Cell Cycle.

Mohammad M Abd-Alhaseeb, Sarah M Massoud, Fatma Elsayed, Gamal A Omran, Ahmad Salahuddin

Open access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
2.4field-weighted citation impact, top 12% 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

9 citing papers in PubMed, 15 citations in OpenAlex.

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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 2 institutions in 1 country.

Mohammad M Abd-AlhaseebDepartment of Pharmacology & Toxicology, Faculty of Pharmacy, Damanhour University, Damanhour 22511, Egypt.ORCID 0000-0001-5388-5250
Sarah M MassoudDepartment of Biochemistry, Faculty of Pharmacy, Damanhour University, Damanhour 22511, Egypt.
Fatma ElsayedCell Culture Unit, Medical Research Institute, Alexandria University, Alexandria 21648, Egypt.
Gamal A OmranDepartment of Biochemistry, Faculty of Pharmacy, Damanhour University, Damanhour 22511, Egypt.ORCID 0000-0002-1609-8802
Ahmad SalahuddinDepartment of Biochemistry, Faculty of Pharmacy, Damanhour University, Damanhour 22511, Egypt.ORCID 0000-0002-7382-4284
Damanhour University · EGAlexandria University · EG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDespite advancements in cancer treatment, breast cancer (BC) is still one of the leading causes of death among women. The majority of anti-breast-cancer medications induce serious side effects and multidrug resistance. Although several natural compounds, such as evening primrose oil (EPO), have been shown to have anticancer properties when used alone, their combination with the anticancer medicine tamoxifen (TAM) has yet to be investigated. The present study aimed to investigate the anticancer efficacy of EPO, alone or in combination with TAM, in the BC cell lines MCF-7 and MDA-MB-231, as well as to elucidate the mechanism of action.

methodsThe MTT assay was used to investigate the cytotoxic effect of EPO on the two cell lines, and we discovered an acceptable IC

resultsThe combination of EPO and TAM suppressed the VEGF level, VEGF gene expression and Cyclin D1 signaling pathways, arrested the cell cycle, and induced the apoptotic signaling pathways by increasing the Bax/Bcl-2 ratio and caspase 3 activity; this revealed significant anti-tumor activity.

conclusionsThe most significant finding of this study was the confirmation of the anticancer activity of the natural product EPO, which potentiated the activity of the anticancer drug TAM against MCF-7 and MDA-MB-231 BC cell lines through the induction of apoptosis, inhibiting angiogenesis and halting cell proliferation.

Indexed as

Antineoplastic AgentsBreast Neoplasmsgamma-Linolenic AcidOenothera biennisPlant OilsTamoxifenAngiogenesis InhibitorsApoptosisCell CycleCell Line, TumorCell ProliferationFemaleHumansLinoleic AcidsMCF-7 CellsVascular Endothelial Growth Factor AAngiogenesis InhibitorsAntineoplastic Agentsevening primrose oilgamma-Linolenic AcidLinoleic AcidsPlant OilsTamoxifenVascular Endothelial Growth Factor Abreast cancerevening primrose oilMCF-7MDA-MB-231tamoxifen

Identifiers

PMID35458590
PMCPMC9031472
OpenAlexW4224238638

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Registered trials

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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.