Evidence map›Paper›PMID 29228869›Full record

ArticleCell cycle (Georgetown, Tex.)2018

Tumour-suppressive microRNA-424-5p directly targets CCNE1 as potential prognostic markers in epithelial ovarian cancer.

Jingjing Liu, Zhenpeng Gu, Yujie Tang, Junmei Hao, Cuiping Zhang, Xingsheng Yang

Open access · bronzeAbstract read
In one paragraph

Article in Cell cycle (Georgetown, Tex.), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
3.4field-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

36 citing papers in PubMed, 64 citations in OpenAlex.

  1. Review
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  4. Role of miR-424 in the carcinogenesis.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2024
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  9. Sequence Requirements for miR-424-5p Regulating and Function in Cancers.International journal of molecular sciences · 2022
    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

6 authors at 4 institutions in 1 country.

Jingjing Liua Department of Obstetrics and Gynecology , Qilu Hospital of Shandong University , Jinan , China.ORCID 0000-0002-3828-1608
Zhenpeng Guc Department of Obstetrics and Gynecology , Binzhou Medical University Hospital , Binzhou , China.
Yujie Tanga Department of Obstetrics and Gynecology , Qilu Hospital of Shandong University , Jinan , China.
Junmei Haoe Department of Pathology , Yantai Affiliated Hospital of Bin Zhou Medical University , Yantai , China.ORCID 0000-0002-9600-8554
Cuiping Zhange Department of Pathology , Yantai Affiliated Hospital of Bin Zhou Medical University , Yantai , China.
Xingsheng Yanga Department of Obstetrics and Gynecology , Qilu Hospital of Shandong University , Jinan , China.ORCID 0000-0002-4946-2033
Binzhou University · CNBinzhou Medical University · CNCentral Hospital of Zibo · CNQilu Hospital of Shandong University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

An accumulated evidence supports that MicroRNAs (miRNAs) have shown a prominent role in pathological processes and different tumor onset. However, to date, the potential functional roles and molecular mechanisms by how microRNA-424-5p(miR-424-5p) affects cancer cell proliferation are greatly unclear, especially in epithelial ovarian cancer(EOC).In this study, we demonstrated that miR-424-5p was significantly down-regulated in EOC tissues and cell lines. The level of miR-424-5p was negatively correlated with tumor size, TNM stage, pathological grade, lymphatic metastasis of EOC. Restoring miR-424-5p expression in EOC cells dramatically suppressed cell proliferation and caused an accumulation of cells in G1 phase, and thus contributed to better prognosis of EOC patients. Mechanistically, miR-424-5p inhibits CCNE1 expression through targeting CCNE1 3'UTR, and subsequent arrest cell cycle in G1/G0 phase by inhibiting E2F1-pRb pathway. This study revealed functional and mechanistic links between miR-424-5p and CCNE1 in the progression of EOC and provide an important insight into that miR-424-5p may serve as a therapeutic target in EOC.

Indexed as

3' Untranslated RegionsBase SequenceBiomarkers, TumorCarcinoma, Ovarian EpithelialCell CycleCell Line, TumorCell ProliferationCell SurvivalCyclin EFemaleGene Expression Regulation, NeoplasticHumansMicroRNAsMiddle AgedModels, BiologicalOncogene Proteins3' Untranslated RegionsBiomarkers, TumorCCNE1 protein, humanCyclin EMicroRNAsMIRN424 microrna, humanOncogene ProteinsCCNE1cell proliferationepithelial ovarian cancermiR-424-5pprognosis

Identifiers

PMID29228869
PMCPMC5914728
OpenAlexW2774079887

What OpenQuestion holds

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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.