Evidence map›Paper›PMID 30074096›Full record

ArticleJournal of materials science. Materials in medicine2018

Protection of normal cells from irradiation bystander effects by silica-flufenamic acid nanoparticles.

Giovanna Gomes Lara, Gracielle Ferreira Andrade, Marcelo Fernandes Cipreste, Wellington Marcos da Silva, Pedro Lana Gastelois, Dawidson Assis Gomes, Marcelo Coutinho de Miranda, Waldemar Augusto de Almeida Macedo, Maria Jose Neves, Edésia Martins Barros de Sousa

Abstract read
PubMed Publisher
In one paragraph

Article in Journal of materials science. Materials in medicine, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

8 citing papers in PubMed, 56 citations in OpenAlex.

  1. RHA/TiOScientific reports · 2026
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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

10 authors at 2 institutions in 1 country.

Giovanna Gomes LaraCentro de Desenvolvimento da Tecnologia Nuclear, CDTN, Belo Horizonte, 31270-901, MG, Brazil.
Gracielle Ferreira AndradeCentro de Desenvolvimento da Tecnologia Nuclear, CDTN, Belo Horizonte, 31270-901, MG, Brazil.
Marcelo Fernandes CipresteCentro de Desenvolvimento da Tecnologia Nuclear, CDTN, Belo Horizonte, 31270-901, MG, Brazil.
Wellington Marcos da SilvaCentro de Desenvolvimento da Tecnologia Nuclear, CDTN, Belo Horizonte, 31270-901, MG, Brazil.
Pedro Lana GasteloisCentro de Desenvolvimento da Tecnologia Nuclear, CDTN, Belo Horizonte, 31270-901, MG, Brazil.
Dawidson Assis GomesDepartamento de Bioquímica e Imunologia, Instituto de Ciências Biológicas, UFMG, Belo Horizonte, Brazil.
Marcelo Coutinho de MirandaDepartamento de Bioquímica e Imunologia, Instituto de Ciências Biológicas, UFMG, Belo Horizonte, Brazil.
Waldemar Augusto de Almeida MacedoCentro de Desenvolvimento da Tecnologia Nuclear, CDTN, Belo Horizonte, 31270-901, MG, Brazil.
Maria Jose NevesCentro de Desenvolvimento da Tecnologia Nuclear, CDTN, Belo Horizonte, 31270-901, MG, Brazil.
Edésia Martins Barros de SousaCentro de Desenvolvimento da Tecnologia Nuclear, CDTN, Belo Horizonte, 31270-901, MG, Brazil. sousaem@cdtn.br.
Centro de Desenvolvimento da Tecnologia Nuclear · BRUniversidade Federal de Minas Gerais · BR

Funding

FAPEMIG apq-01897-16
6 · The paper itself

Abstract

The development of a myriad of nanoparticles types has opened new possibilities for the diagnostics and treatment of many diseases, especially for cancer. However, most of the researches done so far do not focus on the protection of normal cells surrounding a tumor from irradiation bystander effects that might lead to cancer recurrence. Gap-junctions are known to be involved in this process, which leads to genomic instability of neighboring normal cells, and flufenamic acid (FFA) is included in a new group of gap-junction blockers recently discovered. The present work explores the use of mesoporous silica nanoparticles MCM-41 functionalized with 3-Aminopropyltriethoxysilane (APTES) for anchoring the flufenamic acid for its prolonged and controlled release and protection from radiation bystander effects. MCM-41 and functionalized samples were structurally and chemically characterized with multiple techniques. The biocompatibility of all samples was tested in a live/dead assay performed in cultured MRC-5 and HeLa cells. HeLa cells cultured were exposed to 50 Gy of gamma-rays and the media transferred to fibroblast cells cultured separately. Our results show that MCM-41 and functionalized samples have high biocompatibility with MCR-5 and HeLa cells, and most importantly, the FFA delivered by these NPs was able to halt apoptosis, one of main bystander effects.

Indexed as

Bystander EffectCell LineFibroblastsFlufenamic AcidGamma RaysHumansMaterials TestingMicroscopy, Electron, ScanningNanoparticlesSilicon DioxideFlufenamic AcidSilicon Dioxide

Identifiers

PMID30074096
OpenAlexW2887780628

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.