Evidence map›Paper›PMID 31044566›Full record

ArticleMolecular genetics & genomic medicine2019

miR-584-5p regulates hepatocellular carcinoma cell migration and invasion through targeting KCNE2.

Huamei Wei, Jianchu Wang, Zuoming Xu, Yuan Lu, Xianjian Wu, Chenyi Zhuo, Chuan Tan, Qianli Tang, Jian Pu

Abstract read
In one paragraph

Article in Molecular genetics & genomic medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
–field-weighted citation impact
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

22 citing papers in PubMed.

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  8. Insight into the Role of the miR-584 Family in Human Cancers.International journal of molecular sciences · 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

9 authors.

Huamei WeiDepartment of Pathology, Affiliated Hospital of Youjiang Medical University for Nationalities, Baise, P. R. China.
Jianchu WangDepartment of Hepatobiliary Surgery, Affiliated Hospital of Youjiang Medical University for Nationalities, Baise, P. R. China.
Zuoming XuGraduate College of Youjiang Medical University for Nationalities, Youjiang Medical University for Nationalities, Baise, P. R. China.
Yuan LuGraduate College of Youjiang Medical University for Nationalities, Youjiang Medical University for Nationalities, Baise, P. R. China.
Xianjian WuGraduate College of Youjiang Medical University for Nationalities, Youjiang Medical University for Nationalities, Baise, P. R. China.
Chenyi ZhuoGraduate College of Youjiang Medical University for Nationalities, Youjiang Medical University for Nationalities, Baise, P. R. China.
Chuan TanGraduate College of Youjiang Medical University for Nationalities, Youjiang Medical University for Nationalities, Baise, P. R. China.
Qianli TangYoujiang Medical University for Nationalities, Baise, P. R. China.
Jian PuDepartment of Hepatobiliary Surgery, Affiliated Hospital of Youjiang Medical University for Nationalities, Baise, P. R. China.ORCID 0000-0002-9310-0195

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHepatocellular carcinoma (HCC) is one of the most commonly diagnosed cancer type. This study was aimed to investigate the role of microRNA-584-5p (miR-584-5p) in regulating HCC progression.

methodsThe expression of miR-584-5p in HCC cell lines was analyzed by quantitative real-time polymerase chain reaction. Effects of miR-584-5p depletion on HCC cell proliferation, migration, and invasion in vitro were analyzed by cell counting kit-8 assay, wound-healing assay, and transwell invasion assay. miR-584-5p targeting potassium voltage-gated channel subfamily E regulatory subunit 2 (KCNE2) was identified using bioinformatics algorithm and dual-luciferase activity reporter assay. Kaplan-Meier Plotter website was used to investigate the effect of miR-584-5p or KCNE2 expression on the overall survival of HCC patients.

resultsIn vitro functional assays showed miR-584-5p depletion decreased HCC cell proliferation, cell migration, and cell invasion. Moreover, miR-584-5p functions by directly targeting KCNE2, and it in turn, mediates the effects of miR-584-5p on HCC cell behaviors.

conclusionsThese results demonstrated that miR-584-5p functions as an oncogenic miRNA in HCC.

Indexed as

Carcinoma, HepatocellularCell LineCell Line, TumorCell MovementCell ProliferationHumansKaplan-Meier EstimateLiver NeoplasmsMicroRNAsNeoplasm InvasivenessPotassium Channels, Voltage-GatedKCNE2 protein, humanMicroRNAsMIRN584 microRNA, humanPotassium Channels, Voltage-Gatedcell behaviorshepatocellular carcinomaKCNE2miR-584-5poncogenic miRNA

Identifiers

PMID31044566
PMCPMC6565569

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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.