Evidence map›Paper›PMID 31085718›Full record

ArticleBioscience reports2019

miR-940 potentially promotes proliferation and metastasis of endometrial carcinoma through regulation of MRVI1.

Zhan Zhou, Ya-Ping Xu, Li-Juan Wang, Yan Kong

Open access · goldAbstract read
In one paragraph

Article in Bioscience reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.9field-weighted citation impact, top 15% 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

23 citing papers in PubMed, 36 citations in OpenAlex.

  1. Microrna Expression inMicroRNA (Shariqah, United Arab Emirates) · 2026
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  4. Novel Functional Features of cGMP Substrate Proteins IRAG1 and IRAG2.International journal of molecular sciences · 2023
    Review
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  6. Review
  7. Article
  8. Article
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  15. Review
  16. Non-Coding RNAs as Prognostic Markers for Endometrial Cancer.International journal of molecular sciences · 2021
    Review
  17. Review
  18. Review
  19. Article
  20. Article
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

4 authors at 1 institution in 1 country.

Zhan ZhouDepartment of Gynecology, Shandong Provincial Third Hospital, Jinan 250031, P.R. China.
Ya-Ping XuDepartment of Gynecology, Shandong Provincial Third Hospital, Jinan 250031, P.R. China.
Li-Juan WangDepartment of Gynecology, Shandong Provincial Third Hospital, Jinan 250031, P.R. China.
Yan KongDepartment of Gynecology, Shandong Provincial Third Hospital, Jinan 250031, P.R. China kyhgrm@163.com.ORCID 0000-0003-0354-8621
Shandong Provincial Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The specific functions and clinical significance of miR-940 in endometrial carcinoma (EC) have not been studied. First, we assessed the expression of miR-940 and MRVI1 in EC tissues collected from The Cancer Genome Atlas (TCGA) database and EC cell lines. miR-940 was significantly overexpressed in EC tissues and cell lines, particularly in RL95-2 cells. Correlation analysis showed that miR-940 expression level was remarkably associated with age, grade, and death. Moreover, the overall survival (OS) rate in the miR-940 low expression group was higher, compared with miR-940 high expression group. Univariate and multivariate models demonstrated that miR-940 expression, stage, and age were predictive indicators of OS. Moreover, there was no significance of the proliferation ability among the three EC cell lines (RL95-2, ISK, and KLE). To reveal the biological roles of miR-940, we respectively transfected RL95-2 cells with miR-940 mimics, miR-940 inhibitors, and control to further investigate the cell proliferation ability, and migration as well as invasion potential of RL95-2 cells. The transfection of miR-940 mimics significantly increased the proliferation and migration/invasion ability of RL95-2 cells. MRVI1 was predicted to be a potential target of miR-940 by means of

Indexed as

Cell ProliferationCell Line, TumorCell MovementEndometrial NeoplasmsFemaleHumansMembrane ProteinsMicroRNAsNeoplasm InvasivenessNeoplasm MetastasisNeoplasm ProteinsPhosphoproteinsRNA, NeoplasmIRAG1 protein, humanMembrane ProteinsMicroRNAsMIRN940 microRNA, humanNeoplasm ProteinsPhosphoproteinsRNA, Neoplasmendometrial carcinomametastasismiR-940MRVI1proliferation

Identifiers

PMID31085718
PMCPMC6559375
OpenAlexW2945283312

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.