Evidence map›Paper›PMID 33015045›Full record

ArticleFrontiers in cell and developmental biology2020

miR-146a-5p Plays an Oncogenic Role in NSCLC via Suppression of TRAF6.

Xiangdong Liu, Bo Liu, Ruihua Li, Fei Wang, Ning Wang, Maihe Zhang, Yang Bai, Jin Wu, Liping Liu, Dongyu Han and 11 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in cell and developmental biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
2.1field-weighted citation impact, top 12% 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

33 citing papers in PubMed, 48 citations in OpenAlex.

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  18. Involvement of FAM170B-AS1, hsa-miR-1202, and hsa-miR-146a-5p in breast cancer.Cancer biomarkers : section A of Disease markers · 2024
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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

21 authors at 6 institutions in 2 countries.

Xiangdong LiuInstitute for Genome Engineered Animal Models of Human Diseases, Dalian Medical University, Dalian, China.
Bo LiuInstitute for Genome Engineered Animal Models of Human Diseases, Dalian Medical University, Dalian, China.
Ruihua LiDepartment of Clinical Laboratory, Second Affiliated Hospital of Dalian Medical University, Liaoning, China.
Fei WangInstitute for Genome Engineered Animal Models of Human Diseases, Dalian Medical University, Dalian, China.
Ning WangInstitute for Genome Engineered Animal Models of Human Diseases, Dalian Medical University, Dalian, China.
Maihe ZhangInstitute for Genome Engineered Animal Models of Human Diseases, Dalian Medical University, Dalian, China.
Yang BaiInstitute for Genome Engineered Animal Models of Human Diseases, Dalian Medical University, Dalian, China.
Jin WuInstitute for Genome Engineered Animal Models of Human Diseases, Dalian Medical University, Dalian, China.
Liping LiuInstitute for Genome Engineered Animal Models of Human Diseases, Dalian Medical University, Dalian, China.
Dongyu HanInstitute for Genome Engineered Animal Models of Human Diseases, Dalian Medical University, Dalian, China.
Zhiguang LiCenter of Genome and Personalized Medicine, Institute of Cancer Stem Cell, Cancer Center, Dalian Medical University, Dalian, China.
Bin FengDepartment of Biotechnology, Dalian Medical University, Dalian, China.
Guangbiao ZhouInstitute of Zoology, Chinese Academy of Sciences, Beijing, China.
Shujing WangLiaoning Provence Key Lab of Genome Engineered Animal Models, Dalian Medical University, Dalian, China.
Li ZengInstitute for Genome Engineered Animal Models of Human Diseases, Dalian Medical University, Dalian, China.
Jian MiaoDivision of Hepatobiliary and Pancreatic Surgery, Department of General Surgery, Second Affiliated Hospital of Dalian Medical University, Liaoning, China.
Yiqun YaoDepartment of Thyroid and Breast Surgery, Affiliated Zhongshan Hospital of Dalian University, Dalian, China.
Bin LiangSchool of Life Sciences, Yunnan University, Kunming, China.
Lin HuangLiaoning Provence Key Lab of Genome Engineered Animal Models, Dalian Medical University, Dalian, China.
Qi WangDepartment of Respiratory Medicine, Second Affiliated Hospital of Dalian Medical University, Liaoning, China.
Yingjie WuInstitute for Genome Engineered Animal Models of Human Diseases, Dalian Medical University, Dalian, China.
Dalian Medical University · CNAffiliated Zhongshan Hospital of Dalian University · CNIcahn School of Medicine at Mount Sinai · USInstitute of Zoology · CNSecond Affiliated Hospital of Dalian Medical University · CNYunnan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Non-small cell lung cancer (NSCLC) is the most deadly cancer in the world due to its often delayed diagnosis. Identification of biomarkers with high sensitivity, specificity, and accessibility for early detection, such as circulating microRNAs, is therefore of utmost importance. In the present study, we identified a significantly higher expression of miR-146a-5p in the serum and tissue samples of NSCLC patients than that of the healthy controls. In parallel, miR-146a-5p was also highly expressed in three human NSCLC adenocarcinoma-cell lines (A549, H1299, and H1975) compared to the human bronchial epithelium cell line (HBE). By dual-luciferase reporter assay and manipulation of the expressions of miR-146a-5p and its target gene, tumor necrosis factor receptor-associated factor 6 (TRAF6), we showed that the functional effects of miR-146a-5p on NSCLC cell survival and migration were mediated by direct binding to and suppression of TRAF6. Overexpression of TRAF6 sufficiently reversed miR-146a-5p-induced cancer cell proliferation, migration, and apoptosis resistance. Our data implied that miR-146a-5p/TRAF6/NF-κB-p65 axis could be a promising diagnostic marker and a therapeutic target for NSCLC.

Indexed as

apoptosismigrationmiR-146a-5pnon-small cell lung cancerTRAF6

Identifiers

PMID33015045
PMCPMC7493784
OpenAlexW3082982041

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.