Evidence map›Paper›PMID 25598225›Full record

ArticleToxicology2015

Toxicoproteomic analysis of pulmonary carbon nanotube exposure using LC-MS/MS.

Gina M Hilton, Alexia J Taylor, Christina D McClure, Gregory N Parsons, James C Bonner, Michael S Bereman

Abstract read
In one paragraph

Article in Toxicology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.5field-weighted citation impact, top 19% 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

4 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
  2. Mechanisms of carbon nanotube-induced pulmonary fibrosis: a physicochemical characteristic perspective.Wiley interdisciplinary reviews. Nanomedicine and nanobiotechnology · 2018
    Review
  3. Systems Biology to Support Nanomaterial Grouping.Advances in experimental medicine and biology · 2017
    Review
  4. Review
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.

Gina M HiltonDepartment of Biological Sciences, Environmental and Molecular Toxicology, North Carolina State University, Raleigh, NC, United States.
Alexia J TaylorDepartment of Biological Sciences, Environmental and Molecular Toxicology, North Carolina State University, Raleigh, NC, United States.
Christina D McClureDepartment of Chemical and Biomolecular Engineering, North Carolina State University, Raleigh, NC, United States.
Gregory N ParsonsDepartment of Chemical and Biomolecular Engineering, North Carolina State University, Raleigh, NC, United States.
James C BonnerDepartment of Biological Sciences, Environmental and Molecular Toxicology, North Carolina State University, Raleigh, NC, United States.
Michael S BeremanDepartment of Biological Sciences, Environmental and Molecular Toxicology, North Carolina State University, Raleigh, NC, United States. Electronic address: michaelbereman@ncsu.edu.
North Carolina State University · US

Funding

TRAINING IN BIOCHEMICAL AND ENVIRONMENTAL TOXICOLOGYT32ES007046 · NIEHS · NORTH CAROLINA STATE UNIVERSITY RALEIGH · PI Seth William Kullman · 1985 to 2026
$5.1M
Genetic Susceptibility to Nanoparticle-Induced Respiratory DiseaseR01ES020897 · NIEHS · NORTH CAROLINA STATE UNIVERSITY RALEIGH · PI BONNER, JAMES CHRISTOPHER · 2012 to 2017
$1.7M
Lung Toxicity of Carbon Nanotubes in Models of Pre-Existing Respiratory DiseaseRC2ES018772 · NIEHS · NORTH CAROLINA STATE UNIVERSITY RALEIGH · PI BONNER, JAMES CHRISTOPHER · 2009 to 2010
$1.1M
NIEHS NIH HHS NIEHS R01ES020897NIEHS NIH HHS NIEHS RC2ES018772NIEHS NIH HHS R01 ES020897NIEHS NIH HHS RC2 ES018772NIEHS NIH HHS T32 ES007046
6 · The paper itself

Abstract

Toxicoproteomics is a developing field that utilizes global proteomic methodologies to investigate the physiological response as a result of adverse toxicant exposure. The aim of this study was to compare the protein secretion profile in lung bronchoalveolar lavage fluid (BALF) from mice exposed to non-functionalized multi-walled carbon nanotubes (U-MWCNTs) or MWCNTs functionalized by nanoscale Al2O3 coatings (A-MWCNT) formed using atomic layer deposition (ALD). Proteins were identified using liquid chromatography tandem mass spectrometry (LC-MS/MS), and quantified using a combination of two label-free proteomic methods: spectral counting and MS1 peak area analysis. On average 465 protein groups were identified per sample and proteins were first screened using spectral counting and the Fisher's exact test to determine differentially regulated species. Significant proteins by Fisher's exact test (p<0.05) were then verified by integrating the intensity under the extracted ion chromatogram from a single unique peptide for each protein across all runs. A two sample t-test based on integrated peak intensities discovered differences in 27 proteins for control versus U-MWCNT, 13 proteins for control versus A-MWCNT, and 2 proteins for U-MWCNT versus A-MWCNT. Finally, an in-vitro binding experiment was performed yielding 4 common proteins statistically different (p<0.05) for both the in-vitro and in-vivo study. Several of the proteins found to be significantly different between exposed and control groups are known to play a key role in inflammatory and immune response. A comparison between the in-vitro and in-vivo CNT exposure emphasized a true biological response to CNT exposure.

Indexed as

Acute-Phase ProteinsAnimalsBronchoalveolar Lavage FluidChromatography, LiquidComplement C3Complement C4bComplement C9HistonesLactoferrinLipocalin-2LipocalinsLungMiceMice, Inbred C57BLNanotubes, CarbonOncogene ProteinsAcute-Phase ProteinsComplement C3Complement C4bComplement C9HistonesLactoferrinLcn2 protein, mouseLipocalin-2LipocalinsNanotubes, CarbonOncogene ProteinsPeroxidaseProteomePulmonary Surfactant-Associated Protein BCarbon nanotubeLabel-free proteomicsPulmonary fibrosisToxicoproteomics

Identifiers

PMID25598225
PMCPMC4442484
OpenAlexW2017416551

What OpenQuestion holds

Textmetadata
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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.