Evidence map›Paper›PMID 32686017›Full record

ArticleMolecular biology reports2020

Anticancer and apoptotic activities of parthenolide in combination with epirubicin in mda-mb-468 breast cancer cells.

Arash Ghorbani-Abdi-Saedabad, Mohammad Yahya Hanafi-Bojd, Negin Parsamanesh, Zahra Tayarani-Najaran, Homa Mollaei, Reyhane Hoshyar

Abstract read
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In one paragraph

Article in Molecular biology reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

16 citing papers in PubMed, 29 citations in OpenAlex.

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  16. ARA-linker-TGFαL3: a novel chimera protein to target breast cancer cells.Medical oncology (Northwood, London, England) · 2021
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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 5 institutions in 2 countries.

Arash Ghorbani-Abdi-SaedabadDepartment of Biochemistry, School of Medicine, Birjand University of Medical Sciences, Birjand, Iran.
Mohammad Yahya Hanafi-BojdCellular and Molecular Research Center, Birjand University of Medical Sciences, Birjand, Iran.
Negin ParsamaneshZanjan Metabolic Diseases Research center, Zanjan University of Medical Sciences, Zanjan, Iran.
Zahra Tayarani-NajaranDepartment of Pharmacodynamics and Toxicology, School of Pharmacy, Mashhad University of Medical Sciences, Mashhad, Iran.
Homa MollaeiDepartment of Biology, Faculty of Sciences, University of Birjand, Birjand, Iran. hmollaei@birjand.ac.ir.
Reyhane HoshyarCellular and Molecular Research Center, Birjand University of Medical Sciences, Birjand, Iran. hooshyar@msu.edu.ORCID http://orcid.org/0000-0001-7713-3897
Birjand University of Medical Sciences · IRMashhad University of Medical Sciences · IRMichigan State University · USUniversity of Birjand · IRZanjan University of Medical Sciences · IR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Breast cancer is the most common malignancy in women worldwide. Unfortunately, current therapeutic methods are not completely efficient. Hence, combination therapy with medicinal plants has attracted several kinds of research. In the current study, we aimed to investigate the apoptotic and anti-cancer effect of Parthenolide in combination with Epirubicin in the MDA-MB-468 breast cancer cell line. In this study,  the anti-proliferative and pro-apoptotic effect of Parthenolide in combination with Epirubicin and without it, in the MDA-MB-468 cell line have been assessed by MTT test, Hoescht staining and flow cytometry methods. Our outcomes showed that Parthenolide treatment in the present of Epirubicin led to a decrease in the minimum toxic concentration of Parthenolide and Epirubicin in comparison with individual treatments. Then, to achieve a likely molecular mechanism of mentioned drugs Bax and Bcl2 expression level evaluated by Real-time PCR and subsequently, Western blotting has been estimated the protein level of Caspase 3. Our data indicated that the treatment of cells with Parthenolide led to up-regulation of Bax and downregulation of Bcl2 at mRNA level. Moreover, Parthenolide treatment led to the obvious alternation of Caspase3 protein level. These results indicated that Parthenolide in combination with Epirubicin have significant cytotoxicity due to targeting the main regulators of apoptosis. Hence, according to lack of cytotoxicity of Parthenolide on normal cells that lead to reduction of drug side effects, it could be suggested as an adjuvant therapy with Epirubicin after complementary research on animal model and clinical trial.

Indexed as

Anti-Inflammatory Agents, Non-SteroidalAntineoplastic Combined Chemotherapy ProtocolsApoptosisbcl-2-Associated X ProteinBreast NeoplasmsCell Line, TumorCell ProliferationCell SurvivalEpirubicinFemaleHumansProto-Oncogene Proteins c-bcl-2SesquiterpenesTopoisomerase II InhibitorsAnti-Inflammatory Agents, Non-SteroidalBAX protein, humanbcl-2-Associated X ProteinBCL2 protein, humanEpirubicinparthenolideProto-Oncogene Proteins c-bcl-2SesquiterpenesTopoisomerase II InhibitorsApoptosisBreast cancerEpirubicinParthenolide

Identifiers

PMID32686017
OpenAlexW3043569414

What OpenQuestion holds

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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.