Evidence map›Paper›PMID 28044136›Full record

ArticleBioMed research international2016

Cytotoxicity of Titanate-Calcium Complexes to MC3T3 Osteoblast-Like Cells.

Yen-Wei Chen, Jeanie L Drury, Joelle Moussi, Kathryn M L Taylor-Pashow, David T Hobbs, John C Wataha

Abstract read
In one paragraph

Article in BioMed research international, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Yen-Wei ChenDepartment of Restorative Dentistry, University of Washington School of Dentistry, Seattle, WA 98195-7456, USA.ORCID 0000-0003-1209-1168
Jeanie L DruryDepartment of Restorative Dentistry, University of Washington School of Dentistry, Seattle, WA 98195-7456, USA.
Joelle MoussiDepartment of Restorative Dentistry, University of Washington School of Dentistry, Seattle, WA 98195-7456, USA.
Kathryn M L Taylor-PashowSavannah River National Laboratory, Aiken, SC 29808, USA.
David T HobbsSavannah River National Laboratory, Aiken, SC 29808, USA.ORCID 0000-0003-1287-0233
John C WatahaDepartment of Restorative Dentistry, University of Washington School of Dentistry, Seattle, WA 98195-7456, USA.ORCID 0000-0003-3195-2197

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Monosodium titanates (MST) are a relatively novel form of particulate titanium dioxide that have been proposed for biological use as metal sorbents or delivery agents, most recently calcium (II). In these roles, the toxicity of the titanate or its metal complex is crucial to its biological utility. The aim of this study was to determine the cytotoxicity of MST and MST-calcium complexes with MC3T3 osteoblast-like cells; MST-Ca(II) complexes could be useful to promote bone formation in various hard tissue applications. MC3T3 cells were exposed to native MST or MST-Ca(II) complexes for 24-72 h. A CellTiter-Blue® assay was employed to assess the metabolic activity of the cells. The results showed that MST and MST-Ca(II) suppressed MC3T3 metabolic activity significantly in a dose-, time-, and cell-density-dependent fashion. MST-Ca(II) suppressed MC3T3 metabolism in a statistically identical manner as native MST at all concentrations. We concluded that MST and MST-Ca(II) are significantly cytotoxic to MC3T3 cells through a mechanism yet unknown; this is a potential problem to the biological utility of these complexes.

Indexed as

AnimalsCalciumCell DifferentiationCell LineMiceOsteoblastsOsteogenesisTitaniumCalciumTitaniumtitanium dioxide

Identifiers

PMID28044136
PMCPMC5156824

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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.