Evidence map›Paper›PMID 33506378›Full record

ArticleJournal of materials science. Materials in medicine2021

PI3K/AKT signaling drives titanium-induced angiogenic stimulus.

Bruna Rodrigues Martins, Thais Silva Pinto, Célio Junior da Costa Fernandes, Fábio Bezerra, Willian Fernando Zambuzzi

Open access · goldAbstract read
In one paragraph

Article in Journal of materials science. Materials in medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.2field-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

14 citing papers in PubMed, 32 citations in OpenAlex.

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  2. RSC advances · 2024
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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 1 institution in 1 country.

Bruna Rodrigues MartinsInstitute of Biosciences of Botucatu, Department of Chemical and Biological Sciences, UNESP - São Paulo State University, Botucatu, São Paulo, Brazil.
Thais Silva PintoInstitute of Biosciences of Botucatu, Department of Chemical and Biological Sciences, UNESP - São Paulo State University, Botucatu, São Paulo, Brazil.
Célio Junior da Costa FernandesInstitute of Biosciences of Botucatu, Department of Chemical and Biological Sciences, UNESP - São Paulo State University, Botucatu, São Paulo, Brazil.
Fábio BezerraInstitute of Biosciences of Botucatu, Department of Chemical and Biological Sciences, UNESP - São Paulo State University, Botucatu, São Paulo, Brazil.
Willian Fernando ZambuzziInstitute of Biosciences of Botucatu, Department of Chemical and Biological Sciences, UNESP - São Paulo State University, Botucatu, São Paulo, Brazil. w.zambuzzi@unesp.br.ORCID http://orcid.org/0000-0002-4149-5965
Universidade Estadual Paulista (Unesp) · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Although osseointegration and clinical success of titanium (Ti)-implanted materials depend on neovascularization in the reactional peri-implant tissue, very little has been achieved considering the Ti-molecules release on the behavior of endothelial cells. To address this issue, we challenged endothelial cells (HUVECs) with Ti-enriched medium obtained from two types of commercial titanium surfaces [presenting or not dual-acid etching (DAE)] up to 72 h to allow molecular machinery analysis. Our data show that the Ti-enriched medium provokes significant stimulus of angiogenesis-related machinery in endothelial cells by upexpressing VEGFR1, VEGFR2, VEGF, eNOS, and iNOS genes, while the PI3K/Akt signaling pathway was also significantly enhanced. As PI3K/AKT signaling was related to angiogenesis in response to vascular endothelial growth factor (VEGF), we addressed the importance of PI3K/Akt upon Ti-enriched medium responses by concomitantly treating the cells with wortmannin, a well-known PI3K inhibitor. Wortmannin suppressed the angiogenic factors, because VEGF, VEGFR1, and eNOS genes were downregulated in those cells, highlighting the importance of PI3K/AKT signaling on driving angiogenic phenotype and angiogenesis performance within the peri-implant tissue reaction. In conjunction, these data reinforce that titanium-implantable devices modify the metabolism of surrounding cells, such as endothelial cells, probably coupling osteogenesis and angiogenesis processes in peri-implant tissue and then contributing to successfully osseointegration of biomedical titanium-based devices.

Indexed as

Cell ProliferationCells, CulturedEndothelial CellsHumansHuman Umbilical Vein Endothelial CellsNeovascularization, PhysiologicPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktSignal TransductionTitaniumUp-RegulationPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktTitanium

Identifiers

PMID33506378
PMCPMC7840643
OpenAlexW3124493356

What OpenQuestion holds

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LicenceCC BY
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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.