Evidence map›Paper›PMID 32013005›Full record

ArticleInternational journal of environmental research and public health2020

Apoptotic Effect of 1800 MHz Electromagnetic Radiation on NIH/3T3 Cells.

Dan-Yang Li, Jing-Dong Song, Zhao-Yuan Liang, Kiana Oskouei, Xiang-Qian Xiao, Wen-Zhe Hou, Jin-Tao Li, Yi-Shu Yang, Ming-Lian Wang, Manuel Murbach

Open access · goldAbstract read
In one paragraph

Article in International journal of environmental research and public health, 2020. 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
2.9field-weighted citation impact, top 9% 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, 21 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

10 authors at 3 institutions in 2 countries.

Dan-Yang LiCollege of Life Science and Bioengineering, Beijing University of Technology, Beijing 100124, China.
Jing-Dong SongState Key Laboratory of Infectious Disease Prevention and Control, National Institute for Viral Disease Control and Prevention, Chinese Center for Disease Control and Prevention, Beijing 100052, China.
Zhao-Yuan LiangCollege of Life Science and Bioengineering, Beijing University of Technology, Beijing 100124, China.
Kiana OskoueiCollege of Life Science and Bioengineering, Beijing University of Technology, Beijing 100124, China.
Xiang-Qian XiaoCollege of Life Science and Bioengineering, Beijing University of Technology, Beijing 100124, China.
Wen-Zhe HouState Key Laboratory of Infectious Disease Prevention and Control, National Institute for Viral Disease Control and Prevention, Chinese Center for Disease Control and Prevention, Beijing 100052, China.
Jin-Tao LiCollege of Life Science and Bioengineering, Beijing University of Technology, Beijing 100124, China.
Yi-Shu YangCollege of Life Science and Bioengineering, Beijing University of Technology, Beijing 100124, China.
Ming-Lian WangCollege of Life Science and Bioengineering, Beijing University of Technology, Beijing 100124, China.
Manuel MurbachIT'IS Foundation, Zeughausstrasse 43, 8004 Zurich, Switzerland.
Beijing University of Technology · CNNational Institute for Viral Disease Control and Prevention · CNFoundation for Research on Information Technologies in Society · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

To investigate the effect of 1800 MHz electromagnetic radiation (EMR) on apoptosis, we exposed NIH/3T3 cells at 1800 MHz with a specific absorption rate (SAR) of 2 W/kg intermittently for 12, 24, 36, and 48 h. After exposure, Cell Counting Kit-8 (CCK-8) and flow cytometry were used to detect cell viability and apoptosis; the expression of p53, a molecule with the key role in apoptosis, was measured by real-time qPCR, western blot, and immunofluorescence; and images of the structure of the mitochondria, directly reflecting apoptosis, were captured by electron microscopy. The results showed that the viability of cells in the 12, 36, and 48 h exposure groups significantly decreased compared with the sham groups; after 48 h of exposure, the percentage of late apoptotic cells in the exposure group was significantly higher. Real-time qPCR results showed that p53 mRNA in the 48 h exposure group was 1.4-fold of that in the sham group; significant differences of p53 protein fluorescence expression were observed between the exposure groups and the sham groups after 24 h and 48 h. The mitochondrial swelling and vesicular morphology were found in the electron microscopy images after 48 h exposure. These findings demonstrated 1800 MHz, SAR 2 W/kg EMR for 48 h may cause apoptosis in NIH/3T3 cells and that this apoptosis might be attributed to mitochondrial damage and upregulation of p53 expression.

Indexed as

ApoptosisElectromagnetic RadiationAnimalsCell SurvivalMiceMitochondriaNIH 3T3 CellsTumor Suppressor Protein p53Trp53 protein, mouseTumor Suppressor Protein p53cell apoptosiselectromagnetic radiationmitochondriap53

Identifiers

PMID32013005
PMCPMC7037840
OpenAlexW3003953110

What OpenQuestion holds

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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.