Evidence map›Paper›PMID 28229277›Full record

ArticleEuropean journal of nutrition2018

Ginger extract adjuvant to doxorubicin in mammary carcinoma: study of some molecular mechanisms.

Nahla E El-Ashmawy, Naglaa F Khedr, Hoda A El-Bahrawy, Hend E Abo Mansour

Abstract readComparative Study
PubMed Publisher
In one paragraph

Article in European journal of nutrition, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 1 pooled it
3.3field-weighted citation impact, top 9% 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, 1 synthesis or guideline pooled it, 47 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Article
  5. Anticancer Effect ofMolecules (Basel, Switzerland) · 2024
    Article
  6. Review
  7. Article
  8. Review
  9. Article
  10. Review
  11. Review
  12. Article
  13. Article
  14. Bioactive Compounds and Bioactivities of Ginger (Foods (Basel, Switzerland) · 2019
    Review
  15. Article
  16. Article
  17. Anticancer activity of salicin and fenofibrate.Naunyn-Schmiedeberg's archives of pharmacology · 2017
    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

4 authors at 1 institution in 1 country.

Nahla E El-AshmawyDepartment of Biochemistry, Faculty of Pharmacy, Tanta University, 31527, Tanta, Egypt.
Naglaa F KhedrDepartment of Biochemistry, Faculty of Pharmacy, Tanta University, 31527, Tanta, Egypt.
Hoda A El-BahrawyDepartment of Biochemistry, Faculty of Pharmacy, Tanta University, 31527, Tanta, Egypt.
Hend E Abo MansourDepartment of Biochemistry, Faculty of Pharmacy, Tanta University, 31527, Tanta, Egypt. hend_elsayed_2010@yahoo.com.
Tanta University · EG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeThe present study aimed to investigate the molecular mechanisms underlying the anticancer properties of ginger extract (GE) in mice bearing solid Ehrlich carcinoma (SEC) and to evaluate the use of GE in combination with doxorubicin (DOX) as a complementary therapy against SEC.

methodsSEC was induced in 60 female mice. Mice were divided into four equal groups: SEC, GE, DOX and GE + DOX. GE (100 mg/kg orally day after day) and DOX (4 mg/kg i.p. for 4 cycles every 5 days) were given to mice starting on day 12 of inoculation. On the 28th day, blood samples were collected, mice were scarified, tumor volume was measured, and tumor tissues were excised.

resultsThe anti-cancer effect of GE was mediated by activation of adenosine monophosphate protein kinase (AMPK) and down-regulation of cyclin D1 gene expression. GE also showed pro-apoptotic properties as evidenced by elevation of the P53 and suppression of nuclear factor-kappa B (NF-κB) content in tumor tissue. Co-administration of GE alongside DOX markedly increased survival rate, decreased tumor volume, and increased the level of phosphorylated AMPK (PAMPK) and improved related pathways compared to DOX group. In addition, the histopathological results demonstrated enhanced apoptosis and absence of multinucleated cells in tumor tissue of GE + DOX group.

conclusionAMPK pathway and cyclin D1 gene expression could be a molecular therapeutic target for the anticancer effect of GE in mice bearing SEC. Combining GE and DOX revealed a greater efficacy as anticancer therapeutic regimen.

Indexed as

AMP-Activated Protein KinasesAnimalsAntibiotics, AntineoplasticAntineoplastic Agents, PhytogenicApoptosisBiomarkers, TumorCarcinoma, Ehrlich TumorCombined Modality TherapyCyclin D1Dietary SupplementsDoxorubicinEnzyme ActivationFemaleGene Expression Regulation, NeoplasticMammary Glands, AnimalMammary Neoplasms, ExperimentalAMP-Activated Protein KinasesAntibiotics, AntineoplasticAntineoplastic Agents, PhytogenicBiomarkers, TumorCcnd1 protein, ratCyclin D1DoxorubicinNeoplasm ProteinsPlant ExtractsAMPKCyclin D1DoxorubicinGingerMammary carcinomaSolid Ehrlich carcinoma

Identifiers

PMID28229277
OpenAlexW2589786476

What OpenQuestion holds

Textmetadata
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.