Evidence map›Paper›PMID 31146342›Full record

ArticleInternational journal of molecular sciences2019

Multi-Walled Carbon Nanotube-Induced Gene Expression Biomarkers for Medical and Occupational Surveillance.

Brandi N Snyder-Talkington, Chunlin Dong, Salvi Singh, Rebecca Raese, Yong Qian, Dale W Porter, Michael G Wolfarth, Nancy L Guo

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.8field-weighted citation impact, top 29% 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

9 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
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  8. Review
  9. Progress in Research on the Role of Flavonoids in Lung Cancer.International journal of molecular sciences · 2019
    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

8 authors at 2 institutions in 1 country.

Brandi N Snyder-TalkingtonWest Virginia University Cancer Institute, West Virginia University, Morgantown, WV 26506, USA. brandi@branditalkington.com.
Chunlin DongWest Virginia University Cancer Institute, West Virginia University, Morgantown, WV 26506, USA. lindadong2004@yahoo.com.
Salvi SinghWest Virginia University Cancer Institute, West Virginia University, Morgantown, WV 26506, USA. ss0083@mix.wvu.edu.
Rebecca RaeseWest Virginia University Cancer Institute, West Virginia University, Morgantown, WV 26506, USA. rebecca.raese@gmail.com.
Yong QianNational Institute for Occupational and Environmental Safety and Health, 1095 Willowdale Rd., Morgantown, WV 26505, USA. yaq2@cdc.gov.
Dale W PorterNational Institute for Occupational and Environmental Safety and Health, 1095 Willowdale Rd., Morgantown, WV 26505, USA. dhp7@cdc.gov.
Michael G WolfarthNational Institute for Occupational and Environmental Safety and Health, 1095 Willowdale Rd., Morgantown, WV 26505, USA. mgz1@cdc.gov.
Nancy L GuoWest Virginia University Cancer Institute, West Virginia University, Morgantown, WV 26506, USA. lguo@hsc.wvu.edu.
West Virginia University · USNational Institute for Occupational Safety and Health · US

Funding

Systematic assessment of multi-walled carbon nanotubes in pulmonary diseaseR01ES021764 · NIEHS · WEST VIRGINIA UNIVERSITY · PI GUO, NANCY LAN · 2012 to 2016
$1.7M
National Institutes of Health R01ES021764NIEHS NIH HHS R01 ES021764
6 · The paper itself

Abstract

As the demand for multi-walled carbon nanotube (MWCNT) incorporation into industrial and biomedical applications increases, so does the potential for unintentional pulmonary MWCNT exposure, particularly among workers during manufacturing. Pulmonary exposure to MWCNTs raises the potential for development of lung inflammation, fibrosis, and cancer among those exposed; however, there are currently no effective biomarkers for detecting lung fibrosis or predicting the risk of lung cancer resulting from MWCNT exposure. To uncover potential mRNAs and miRNAs that could be used as markers of exposure, this study compared in vivo mRNA and miRNA expression in lung tissue and blood of mice exposed to MWCNTs with in vitro mRNA and miRNA expression from a co-culture model of human lung epithelial and microvascular cells, a system previously shown to have a higher overall genome-scale correlation with mRNA expression in mouse lungs than either cell type grown separately. Concordant mRNAs and miRNAs identified by this study could be used to drive future studies confirming human biomarkers of MWCNT exposure. These potential biomarkers could be used to assess overall worker health and predict the occurrence of MWCNT-induced diseases.

Indexed as

AnimalsBiomarkersCell LineCells, CulturedHumansLungLung DiseasesMaleMiceMice, Inbred C57BLMicroRNAsNanotubes, CarbonOccupational ExposureRNA, MessengerBiomarkersMicroRNAsNanotubes, CarbonRNA, Messengerbiomarkerslung fibrosismulti-walled carbon nanotubesMWCNT

Identifiers

PMID31146342
PMCPMC6600433
OpenAlexW2947084579

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.