Evidence map›Paper›PMID 34340715›Full record

ArticleGenes and environment : the official journal of the Japanese Environmental Mutagen Society2021

miR221 regulates cell migration by targeting annexin a1 expression in human mesothelial MeT-5A cells neoplastic-like transformed by multi-walled carbon nanotube.

Li Ju, Lijin Zhu, Hao Wu, Min Yu, Xianhong Yin, Zhenyu Jia, Lingfang Feng, Shibo Ying, Hailing Xia, Shuzhi Zhang and 2 more

Open access · goldAbstract read
In one paragraph

Article in Genes and environment : the official journal of the Japanese Environmental Mutagen Society, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.2field-weighted citation impact, top 51% 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

2 citing papers in PubMed, 2 citations in OpenAlex.

  1. Article
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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 2 institutions in 1 country.

Li JuHangzhou Medical College, Hangzhou, 310013, China.
Lijin ZhuHangzhou Medical College, Hangzhou, 310013, China.
Hao WuHangzhou Medical College, Hangzhou, 310013, China.
Min YuHangzhou Medical College, Hangzhou, 310013, China.
Xianhong YinJiading District Center for Disease Control and Prevention, Shanghai, 201800, China.
Zhenyu JiaHangzhou Medical College, Hangzhou, 310013, China.
Lingfang FengHangzhou Medical College, Hangzhou, 310013, China.
Shibo YingHangzhou Medical College, Hangzhou, 310013, China.
Hailing XiaHangzhou Medical College, Hangzhou, 310013, China.
Shuzhi ZhangHangzhou Medical College, Hangzhou, 310013, China.
Jianlin LouHangzhou Medical College, Hangzhou, 310013, China. jianlinlou@163.com.
Jun YangHangzhou Normal University, School of Public Health, Hangzhou, 310036, China. junyanghzzju@163.com.
Hangzhou Medical College · CNHangzhou Normal University · CN

Funding

Natural Science Foundation of Zhejiang Province (CN) LQY18H260001 and LZ19H260001the Health and Family Planning Commission of Zhejiang Province 2019ZD026the Health and Family Planning Commission of Zhejiang Province (CN) 2018KY343 and 2017ZD014Young Scientists Fund 31971138 and 81973011Young Scientists Fund 81402718Young Scientists Fund 81502794
6 · The paper itself

Abstract

backgroundMulti-walled carbon nanotube (MWCNT) is one of the most widely used manufactured nanomaterials, however, its potential harmful effect on human health is of great concern. Previously we have shown the acute and chronic exposure to MWCNT induced different responses in human mesothelial MeT-5A cells. In the current study, MeT-5A cells were continuously subjected to MWCNT exposure at 10 μg/cm

resultsAfter one-year MWCNT treatment, MeT-5A cells exhibited neoplastic-like properties, including morphological changes, anchorage-independent growth, increased cell proliferation and cell migration. Further examination revealed the expression of microRNA 221 (miR221) was gradually decreased, while the annexin a1 expression was increased at both the mRNA and protein level during the exposure. Bioinformatic analysis indicated that annexin a1 is a target for miR221 regulation, and it was confirmed by transfecting cells with miR221 mimics, which resulted in the downregulation of annexin a1. Detailed analyses demonstrated miR221 was involved in the regulation of cell migration, e.g., downregulation of miR221 or overexpression of ANNEXIN A1, contributed to the increased cell migration. In contrast, overexpression of miR221 or downregulation of ANNEXIN A1 slowed cell migration.

conclusionsTaken together, these results point to a neoplastic-transforming property of MWCNT, and the miR221-annexin a1 axis is involved in the regulation of cell migration in the transformed cells.

Indexed as

Annexin a1Long-term exposureMulti-walled carbon nanotubes (MWCNT)Neoplastic-like transformation

Identifiers

PMID34340715
PMCPMC8327461
OpenAlexW3187954694

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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.