Evidence map›Paper›PMID 25646699›Full record

ArticleInternational journal of oncology2015

Gallic acid exerts a protective or an anti-proliferative effect on glioma T98G cells via dose-dependent epigenetic regulation mediated by miRNAs.

Alessandro Paolini, Valeria Curti, Francesca Pasi, Giuliano Mazzini, Rosanna Nano, Enrica Capelli

Open access · hybridAbstract read
In one paragraph

Article in International journal of oncology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
4.7field-weighted citation impact, top 5% 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

27 citing papers in PubMed, 67 citations in OpenAlex.

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  8. How gallic acid regulates molecular signaling: role in cancer drug resistance.Medical oncology (Northwood, London, England) · 2023
    Review
  9. Review
  10. Review
  11. Gallic Acid: A Potential Anti-Cancer Agent.Chinese journal of integrative medicine · 2022
    Review
  12. Article
  13. Chemical and biological characteristics of propolis fromArhiv za higijenu rada i toksikologiju · 2021
    Article
  14. Article
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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 1 institution in 1 country.

Alessandro PaoliniDepartment of Biology and Biotechnology, Laboratory of Neuro Radio Experimental Biology, 'Lazzaro Spallanzani', University of Pavia, 27100 Pavia, Italy.
Valeria CurtiDepartment of Earth and Environmental Sciences, Laboratory of Immunology and Genetic Analysis, University of Pavia, 27100 Pavia, Italy.
Francesca PasiDepartment of Biology and Biotechnology, Laboratory of Neuro Radio Experimental Biology, 'Lazzaro Spallanzani', University of Pavia, 27100 Pavia, Italy.
Giuliano MazziniIGM-CNR Histochemistry and Cytometry Section, Department of Animal Biology, University of Pavia, 27100 Pavia, Italy.
Rosanna NanoDepartment of Biology and Biotechnology, Laboratory of Neuro Radio Experimental Biology, 'Lazzaro Spallanzani', University of Pavia, 27100 Pavia, Italy.
Enrica CapelliDepartment of Earth and Environmental Sciences, Laboratory of Immunology and Genetic Analysis, University of Pavia, 27100 Pavia, Italy.
University of Pavia · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Glioblastoma multiforme (GBM) is the most malignant primary brain tumor in adulthood, characterized by very high recurrence. Following the limited results for conventional therapies, novel therapeutic agents are under investigation. Among the putative new molecules, gallic acid (GA) represents a promising new anticancer drug. The anticancer effect of this drug has been based on its antioxidant effects. The aim of the present study was to investigate the toxic effects of GA on the T98G human glioblastoma cell line and its capacity to modulate the expression of microRNAs targeting the genes involved in tumor growth and invasion. Cytotoxicity, clonogenic ability and cell migration after GA treatment were tested. Moreover, the expression of miRNAs that target genes for antioxidant mitochondrial enzymes (mir-17-3p), p-21 protein (mir-21-5p) and ATM (mir-421-5p) was determined by qRT-PCR. The results confirmed in the T98G cells the anti-proliferative effect of GA reported for other glioma cell lines and showed that the miRNA expression changes depending on GA concentrations. Different GA concentrations can determine a protective or a toxic effect on tumor cells. Thus, the key for GA to induce a specific anticancer action is to use an optimal concentration that avoids these twin effects.

Indexed as

Antineoplastic AgentsBrain NeoplasmsCell Line, TumorCell MovementCell ProliferationDose-Response Relationship, DrugEpigenesis, GeneticGallic AcidGene Expression Regulation, NeoplasticGlioblastomaHumansMicroRNAsMitochondrial ProteinsAntineoplastic AgentsGallic AcidMicroRNAsMIRN17 microRNA, humanMIRN21 microRNA, humanMIRN421 microRNA, humanMitochondrial Proteins

Identifiers

PMID25646699
PMCPMC4356495
OpenAlexW2088138454

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.