Evidence map›Paper›PMID 24213921›Full record

ArticleAmerican journal of physiology. Lung cellular and molecular physiology2014

Long-term effects of carbon containing engineered nanomaterials and asbestos in the lung: one year postexposure comparisons.

Anna A Shvedova, Naveena Yanamala, Elena R Kisin, Alexey V Tkach, Ashley R Murray, Ann Hubbs, Madalina M Chirila, Phouthone Keohavong, Lyudmila P Sycheva, Valerian E Kagan and 1 more

Abstract readComparative Study
In one paragraph

Article in American journal of physiology. Lung cellular and molecular physiology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
12.6field-weighted citation impact, top 1% 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

44 citing papers in PubMed, 123 citations in OpenAlex.

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  16. The asbestos-carbon nanotube analogy: An update.Toxicology and applied pharmacology · 2018
    Review
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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

11 authors at 3 institutions in 1 country.

Anna A ShvedovaNIOSH, CDC, 1095 Willowdale Rd., Morgantown, WV 26505. ats1@cdc.gov.
Naveena Yanamala
Elena R Kisin
Alexey V Tkach
Ashley R Murray
Ann Hubbs
Madalina M Chirila
Phouthone Keohavong
Lyudmila P Sycheva
Valerian E Kagan
Vincent Castranova
Centers for Disease Control and Prevention · USNational Institute for Occupational Safety and Health · USUniversity of Pittsburgh · US

Funding

Training and EducationU19AI068021 · NIAID · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI GREENBERGER, JOEL S · 2005 to 2019
$44.4M
Pulmonary Phosphatidylserine Oxidation in ApoptosisR01HL070755 · NHLBI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI KAGAN, VALERIAN E · 2002 to 2011
$3.0M
Lung Oxidative Stress/Inflammation By Carbon NanotubesR01OH008282 · OH · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI KAGAN, VALERIAN E · 2005 to 2014
$2.8M
Investigations and Mitigation of Carbon Nanomaterial ToxicityR01ES019304 · NIEHS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI STAR, ALEXANDER · 2010 to 2014
$1.9M
NHLBI NIH HHS HL-070755NIAID NIH HHS U19 AI-068021NIEHS NIH HHS R01 ES-019304NIOSH CDC HHS OH008282
6 · The paper itself

Abstract

The hallmark geometric feature of single-walled carbon nanotubes (SWCNT) and carbon nanofibers (CNF), high length to width ratio, makes them similar to a hazardous agent, asbestos. Very limited data are available concerning long-term effects of pulmonary exposure to SWCNT or CNF. Here, we compared inflammatory, fibrogenic, and genotoxic effects of CNF, SWCNT, or asbestos in mice 1 yr after pharyngeal aspiration. In addition, we compared pulmonary responses to SWCNT by bolus dosing through pharyngeal aspiration and inhalation 5 h/day for 4 days, to evaluate the effect of dose rate. The aspiration studies showed that these particles can be visualized in the lung at 1 yr postexposure, whereas some translocate to lymphatics. All these particles induced chronic bronchopneumonia and lymphadenitis, accompanied by pulmonary fibrosis. CNF and asbestos were found to promote the greatest degree of inflammation, followed by SWCNT, whereas SWCNT were the most fibrogenic of these three particles. Furthermore, SWCNT induced cytogenetic alterations seen as micronuclei formation and nuclear protrusions in vivo. Importantly, inhalation exposure to SWCNT showed significantly greater inflammatory, fibrotic, and genotoxic effects than bolus pharyngeal aspiration. Finally, SWCNT and CNF, but not asbestos exposures, increased the incidence of K-ras oncogene mutations in the lung. No increased lung tumor incidence occurred after 1 yr postexposure to SWCNT, CNF, and asbestos. Overall, our data suggest that long-term pulmonary toxicity of SWCNT, CNF, and asbestos is defined, not only by their chemical composition, but also by the specific surface area and type of exposure.

Indexed as

Administration, InhalationAnimalsAsbestosBronchoalveolar Lavage FluidBronchopneumoniaCarbonCarcinogensFemaleGenes, rasInhalation ExposureLymphadenitisMiceMice, Inbred C57BLNanotubes, CarbonPneumoniaPulmonary FibrosisAsbestosCarbonCarcinogensNanotubes, Carbonfibrosisgenotoxicityinflammationlong-term postexposurenanoparticles

Identifiers

PMID24213921
PMCPMC3920208
OpenAlexW2048456951

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.