Evidence map›Paper›PMID 31214616›Full record

ArticleBioMed research international2019

MiR-221 Promotes Hepatocellular Carcinoma Cells Migration via Targeting PHF2.

Yi Fu, Mingyan Liu, Fengxia Li, Li Qian, Ping Zhang, Fengwei Lv, Wenting Cheng, Ruixing Hou

Open access · hybridAbstract read
In one paragraph

Article in BioMed research international, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
2.2field-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

24 citing papers in PubMed, 40 citations in OpenAlex.

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  9. The role of AURKA/miR-199b-3p in hepatocellular carcinoma cells.Journal of clinical laboratory analysis · 2022
    Article
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  18. DNA methylation and regulation of gene expression: Guardian of our health.The Nucleus : an international journal of cytology and allied topics · 2021
    Review
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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

8 authors at 2 institutions in 1 country.

Yi FuDepartment of Human Anatomy, Histology and Embryology, School of Biology and Basic Medical Sciences, Soochow University, Suzhou 215007, China.ORCID 0000-0001-9913-5623
Mingyan LiuSchool of Medicine, Yangzhou University, Yangzhou 225001, China.
Fengxia LiSchool of Medicine, Yangzhou University, Yangzhou 225001, China.
Li QianSchool of Medicine, Yangzhou University, Yangzhou 225001, China.
Ping ZhangInstitute of Hand Surgery, Ruihua Affiliated Hospital of Soochow University, Suzhou 215007, China.
Fengwei LvSchool of Medicine, Yangzhou University, Yangzhou 225001, China.
Wenting ChengSchool of Medicine, Yangzhou University, Yangzhou 225001, China.
Ruixing HouInstitute of Hand Surgery, Ruihua Affiliated Hospital of Soochow University, Suzhou 215007, China.ORCID 0000-0002-5257-0684
Yangzhou University · CNSoochow University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

MicroRNAs (MiRNAs), which regulate the gene expression leading to translational inhibition or mRNA degradation, are involved in carcinogenesis and tumor progression. Previous studies have demonstrated that miR-221 was one of the most consistent overexpressed miRNAs in several types of cancer. However, the role of miR-221 in human liver cancer progression is not yet fully elucidated. Levels of miR-221 and plant homeodomain finger 2 (PHF2) expressions in human hepatocellular carcinoma (HCC) tissues and cell lines were detected using western blotting and quantitative real-time PCR (qRT-PCR). Cell migration was studied using the transwell assays. A dual-luciferase reporter system was used to validate the target gene of miR-221. The results indicated that miR-221 promoted HCC cell migration. By performing subsequent systematic bioinformatic analyses, we found PHF2 was the target gene of miR-221 and the direct binding relationship was further validated by dual-luciferase reporter assay. In addition, lower expression of PHF2 promoted HCC cell migration and linked to worse overall survival in HCC patients. Finally, the negative correlation between miR-221 and PHF2 expression levels in HCC specimens was further confirmed. Taken together, our findings implied that miR-221 could be a potential candidate for the therapeutics of HCC metastasis.

Indexed as

Cell MovementGene Expression Regulation, NeoplasticCarcinoma, HepatocellularFemaleHep G2 CellsHomeodomain ProteinsHumansLiver NeoplasmsMaleMicroRNAsNeoplasm MetastasisNeoplasm ProteinsRNA, NeoplasmHomeodomain ProteinsMicroRNAsMIR221, humanNeoplasm ProteinsPHF2 protein, humanRNA, Neoplasm

Identifiers

PMID31214616
PMCPMC6535842
OpenAlexW2944097021

What OpenQuestion holds

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LicenceCC BY
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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.