Evidence map›Paper›PMID 24454774›Full record

ArticlePloS one2014

Proteomic analysis of cellular response induced by multi-walled carbon nanotubes exposure in A549 cells.

Li Ju, Guanglin Zhang, Xing Zhang, Zhenyu Jia, Xiangjing Gao, Ying Jiang, Chunlan Yan, Penelope J Duerksen-Hughes, Fanqing Frank Chen, Hongjuan Li and 2 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. 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
3.6field-weighted citation impact, top 6% 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, 41 citations in OpenAlex.

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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

12 authors at 7 institutions in 2 countries.

Li JuCollaborative Innovation Center for Diagnosis and Treatment of Infectious Diseases, State Key Laboratory for Infectious Diseases Diagnosis and Therapy, The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China ; Department of Toxicology, Zhejiang University School of Public Health, Hangzhou, China ; Zhejiang Academy of Medical Sciences, Hangzhou, China.
Guanglin ZhangCollaborative Innovation Center for Diagnosis and Treatment of Infectious Diseases, State Key Laboratory for Infectious Diseases Diagnosis and Therapy, The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China ; Department of Toxicology, Zhejiang University School of Public Health, Hangzhou, China.
Xing ZhangZhejiang Academy of Medical Sciences, Hangzhou, China.
Zhenyu JiaZhejiang Academy of Medical Sciences, Hangzhou, China.
Xiangjing GaoCollaborative Innovation Center for Diagnosis and Treatment of Infectious Diseases, State Key Laboratory for Infectious Diseases Diagnosis and Therapy, The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China ; Department of Toxicology, Zhejiang University School of Public Health, Hangzhou, China.
Ying JiangCollaborative Innovation Center for Diagnosis and Treatment of Infectious Diseases, State Key Laboratory for Infectious Diseases Diagnosis and Therapy, The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China ; Department of Toxicology, Zhejiang University School of Public Health, Hangzhou, China.
Chunlan YanCollaborative Innovation Center for Diagnosis and Treatment of Infectious Diseases, State Key Laboratory for Infectious Diseases Diagnosis and Therapy, The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China ; Department of Toxicology, Zhejiang University School of Public Health, Hangzhou, China.
Penelope J Duerksen-HughesDepartment of Basic Science, Division of Biochemistry, Loma Linda University School of Medicine, Loma Linda, California, United States of America.
Fanqing Frank ChenLife Science Division, Lawrence Berkeley National Laboratory, Berkeley, California, United States of America.
Hongjuan LiHangzhou Normal University School of Public Health, Hangzhou, China.
Xinqiang ZhuDepartment of Toxicology, Zhejiang University School of Public Health, Hangzhou, China.
Jun YangCollaborative Innovation Center for Diagnosis and Treatment of Infectious Diseases, State Key Laboratory for Infectious Diseases Diagnosis and Therapy, The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China ; College of Biotechnology, Zhejiang Agriculture and Forestry University, Hangzhou, China.
First Affiliated Hospital Zhejiang University · CNZhejiang University · CNZhejiang Academy of Medical Sciences · CNHangzhou Normal University · CNLawrence Berkeley National Laboratory · USLoma Linda University · USZhejiang A & F University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The wide application of multi-walled carbon nanotubes (MWCNT) has raised serious concerns about their safety on human health and the environment. However, the potential harmful effects of MWCNT remain unclear and contradictory. To clarify the potentially toxic effects of MWCNT and to elucidate the associated underlying mechanisms, the effects of MWCNT on human lung adenocarcinoma A549 cells were examined at both the cellular and the protein level. Cytotoxicity and genotoxicity were examined, followed by a proteomic analysis (2-DE coupled with LC-MS/MS) of the cellular response to MWCNT. Our results demonstrate that MWCNT induces cytotoxicity in A549 cells only at relatively high concentrations and longer exposure time. Within a relatively low dosage range (30 µg/ml) and short time period (24 h), MWCNT treatment does not induce significant cytotoxicity, cell cycle changes, apoptosis, or DNA damage. However, at these low doses and times, MWCNT treatment causes significant changes in protein expression. A total of 106 proteins show altered expression at various time points and dosages, and of these, 52 proteins were further identified by MS. Identified proteins are involved in several cellular processes including proliferation, stress, and cellular skeleton organization. In particular, MWCNT treatment causes increases in actin expression. This increase has the potential to contribute to increased migration capacity and may be mediated by reactive oxygen species (ROS).

Indexed as

ProteomicsApoptosisCell CycleCell Line, TumorCell MovementCell ProliferationCytokinesDose-Response Relationship, DrugHumansNanotubes, CarbonReactive Oxygen SpeciesTh1 CellsTh2 CellsTime FactorsCytokinesNanotubes, CarbonReactive Oxygen Species

Identifiers

PMID24454774
PMCPMC3891800
OpenAlexW2028472766

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.