Evidence map›Paper›PMID 33173348›Full record

ArticleCancer management and research2020

The Long Noncoding RNA Linc01833 Enhances Lung Adenocarcinoma Progression via MiR-519e-3p/S100A4 Axis.

Yuan Zhang, Wenhua Li, Zongxiang Lin, Jingfeng Hu, Jingpu Wang, Yukai Ren, BoChong Wei, Yuxia Fan, Yang Yang

Open access · goldAbstract read
In one paragraph

Article in Cancer management and research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
3.0field-weighted citation impact, top 7% 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

15 citing papers in PubMed, 38 citations in OpenAlex.

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  10. Construction and analysis of the ceRNA networkAnnals of translational medicine · 2021
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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

9 authors at 1 institution in 1 country.

Yuan Zhang *Department of Thoracic Surgery, The First Affiliated Hospital, Zhengzhou University, Zhengzhou 450052, People's Republic of China.ORCID 0000-0002-1550-8769
Wenhua Li *Department of Thoracic Surgery, The First Affiliated Hospital, Zhengzhou University, Zhengzhou 450052, People's Republic of China.
Zongxiang LinDepartment of Thoracic Surgery, The First Affiliated Hospital, Zhengzhou University, Zhengzhou 450052, People's Republic of China.
Jingfeng HuDepartment of Thoracic Surgery, The First Affiliated Hospital, Zhengzhou University, Zhengzhou 450052, People's Republic of China.
Jingpu WangDepartment of Thoracic Surgery, The First Affiliated Hospital, Zhengzhou University, Zhengzhou 450052, People's Republic of China.
Yukai RenDepartment of Thoracic Surgery, The First Affiliated Hospital, Zhengzhou University, Zhengzhou 450052, People's Republic of China.
BoChong WeiDepartment of Thoracic Surgery, The First Affiliated Hospital, Zhengzhou University, Zhengzhou 450052, People's Republic of China.
Yuxia FanDepartment of Thyroid Surgery, The First Affiliated Hospital of Zhengzhou University, Zhengzhou 450052, People's Republic of China.
Yang YangDepartment of Thoracic Surgery, The First Affiliated Hospital, Zhengzhou University, Zhengzhou 450052, People's Republic of China.
First Affiliated Hospital of Zhengzhou University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionLung cancer (LC) is among the most prevalent malignancies worldwide, with extremely high morbidity and mortality rates. Mounting evidence has suggested that the abnormally expressed long noncoding RNA (lncRNA) in lung cancer tissues may play vital roles in tumor progression. In the present research, we aimed to examine the functions and underlying mechanism of linc01833 in lung adenocarcinoma (LUAD).

methodsqRT-PCR was employed to determine transfection efficiency. CCK-8, transwell invasion assay, Western blotting analysis and qRT-PCR were used to detect proliferation as well as migration of different LUAD cell lines, and were also applied to determine the changes during epithelial-mesenchymal transformation (EMT). Afterwards, bioinformatics and dual-luciferase reporter assay were utilized to explore and to identify the potential corresponding targets of linc01833 and miR-519e-3p.

resultsLinc01833 OE can significantly improve proliferation as well as invasion ability of LC cells and promote the EMT process. Dual-luciferase reporter assay demonstrated that linc01833 could directly bind to miR-519e-3p, thereby inhibiting its expression. Further experiments showed that S100A4 was a direct target of miR-519e-3p. Rescue assay demonstrated that linc01833 acted on the miR-519e-3p/S100A4 axis.

conclusionWe verified the mechanism of linc01833 in promoting infiltration and metastasis in LUAD. To be specific, linc01833 can function as a competitive endogenous RNA (ceRNA) to adsorb miR-519e-3p through a sponge and regulate S100A4 in lung cancer, thereby being involved in LUAD progression. Collectively, our research provides new insights towards the in-depth understanding of LC progression mechanisms.

Indexed as

EMTlinc01833lung cancermiR-519e-3pS100A4

Identifiers

PMID33173348
PMCPMC7648568
OpenAlexW3095750695

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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.